Abstract
Background
Many cancer patients suffer from cancer-related fatigue (CRF) both during and after their treatment. CRF can arise at any point in the course of the disease and can be either self-limited or persistent, sometimes for years. It gives rise to a vicious circle of impaired physical performance, avoidance of exertion, inactivity, inadequate physical recovery, helplessness, and depressed mood. Its hallmarks are tiredness, exhaustion, and lack of energy; it can impair performance so severely that the patient is unable to work. It is associated with increased mortality. Cancer patients are hardly ever systematically asked about the symptoms and signs of CRF. The stress and impairments that it produces are often inadequately appreciated, and the opportunities for treatment often neglected.
Method
Selective review of the pertinent literature, including published guidelines from Germany and abroad.
Results
The pathogenesis of CRF is complex, involving an interaction of somatic, emotional, cognitive, and psychosocial factors, with a highly variable pattern of clinical expression. Clinical history-taking plays a key role in diagnostic assessment. Depressive disorders must be considered in the differential diagnosis. Many randomized trials and meta-analyses have documented the efficacy of pharmacological and non-pharmacological treatments for CRF.
Conclusion
Cancer-related fatigue is a serious problem that impairs patients physically, mentally, and socially. Physicians need to know how to recognize and treat it.
Awide variety of complex diagnostic and therapeutic techniques that have arisen through advances in modern oncology now enable more frequent cures, or at least longer survival and a better quality of life, for patients with cancer. Unfortunately, however, for many patients this also means that they will have to endure arduous treatment regimens, and in addition may suffer long term sequelae subsequent to their illness and its treatment.
Fatigue, lack of energy, exhaustion, and impaired physical performance are among the most common symptoms in cancer patients and can have severe physical, emotional, and social effects. The syndrome of fatigue and exhaustion in cancer patients is commonly described as “cancer-related fatigue” (CRF) by oncologists around the world (1).
Learning objectives
In this article, we discuss the following aspects of CRF:
clinical features,
epidemiology,
etiology and pathogenesis,
diagnostic evaluation and differential diagnosis, and
pharmacological and non-pharmacological treatments of CRF.
Main features of cancer-related fatigue.
The most common symptoms are fatigue, lack of energy, exhaustion, and impaired physical performance.
Methods
This article is based on a selective review of the pertinent literature (retrieved by searches in the Cochrane Library, Embase, and Medline), also taking account of the guidelines of the National Comprehensive Cancer Network (NCCN, [2]) and the German College of General Practitioners and Family Physicians (Deutsche Gesellschaft für Allgemeinmedizin und Familienmedizin [DEGAM], [3]), as well as a consensus statement of the European Association for Palliative Care (EAPC, [4]).
Clinical features
The multifarious manifestations of CRF include feelings of exhaustion and lack of energy, loss of drive and personal interests, and impaired memory and concentration. The affected patients vary widely in their manner of expressing and describing the problems that they experience. Qualitative studies have shown that the clinical features are highly individual, and hardly any two patients are alike (5, e1). Typically, no clear relation exists between the symptoms and whatever activities immediately precede them; moreover, unlike normal fatigue and exhaustion, CRF often fails to improve, or does so only slightly, after rest or sleep (6). Many patients also suffer from pain, sleep disturbances, and emotional distress, including anxiety and depression (7– 9) (Box 1).
Box 1. Clinical features of cancer-related fatigue.
CRF involves a vicious circle of diminished physical performance, inactivity, avoidance of effort, absence of regeneration, helplessness, and depressed mood.
The more severe the symptoms of CRF are during cancer treatment, the more likely they are to persist or recur afterward.
-
The following are risk factors for CRF:
pain
nausea
pre-existing depressive disorders
other emotional disturbances and stressors
Among all symptoms that tend to affect cancer patients in particular—e.g., pain, sleep disturbances, lack of appetite, or nausea—those of CRF are perceived as most distressing (e2, e3). CRF markedly impairs the quality of life and the physical performance ability of many of the affected patients (10, e3, e4).
Risk factors for cancer-related fatigue.
Pain
Nausea
Pre-existing depressive disorder
Other emotional disturbances and stressors
Multiple prospective studies have shown an association of the manifestations of CRF with shorter survival and increased mortality (e5, e6). CRF can arise at any point in the course of the disease: It may be an early symptom even before the cancer is diagnosed, or it may arise during the treatment, long after the treatment is over, or when the disease recurs or progresses. Its symptoms may be temporary, but they may also persist, remaining present in some cases for years after the end of treatment (e7). The worse the symptoms of CRF are during the treatment phase (chemotherapy and/or radiotherapy), the more likely they are to persist or recur once the treatment is over (e8).
Effects
Depending on the course and severity of the underlying disease, the effects of CRF can range from temporary indisposition to inadequate coping with everyday life and social withdrawal (e9) all the way to the inability to perform one’s job and earn a living, leading to economic hardship for the patient and an additional economic burden for society at large (e10, e11). Thus, CRF clearly poses a problem not only for the patients themselves, but also for the persons around them (e12).
Many studies have shown that physicians generally fail to ask cancer patients systematically about the symptoms and signs of CRF. Therefore, the treating teams often do not realize the extent of stress and impairment caused by CRF and consequently underestimate the need for treatment (11, 12). There are reasons for inadequate communication about CRF on both sides of the physician–patient relationship. Patients may not volunteer information about the symptoms of CRF for fear of seeming to complain too much, or they may think these are “normal” side effects of their disease and its treatment. They may also fear that such symptoms herald a recurrence of cancer, or that mentioning them could delay treatment (e13, e14). On the other hand, treating teams may miss the opportunity to communicate appropriately about CRF because of time pressure or because of inadequate acquaintance with the diagnosis and treatment of CRF (11). Not least, both the treating physician(s) and the patient’s family and friends may wrongly compare the patient’s symptoms with their own everyday fatigue and fail to take the manifestations of CRF seriously (e15, e16).
A vicious circle.
The worse the symptoms of CRF are during the treatment phase (chemotherapy and/or radiotherapy), the more likely they are to persist or recur once the treatment is over.
Prevalence
When interpreting epidemiological figures about cancer-related fatigue (CRF), one must bear in mind that CRF is not a single nosological entity, even though it is characterized by a typical constellation of symptoms and signs. In epidemiological studies, the frequency of CRF is often gauged with the aid of self-assessment questionnaires. Those that include items about the various dimensions of CRF (somatic, affective, and cognitive), such as the Multidimensional Fatigue Inventory (MFI), are considered the “gold standard” (e17). In reality, however, many different types of questionnaires are used, and the thresholds for the assignment of a diagnosis of CRF vary widely as well, with the result that the reported prevalence figures are distributed over a wide range. In a recent longitudinal study of CRF in a representative sample of cancer patients in Germany, symptoms of fatigue and exhaustion that were markedly worse than those of a control group of healthy individuals (as measured on the “general fatigue” subscale of the MFI) were found in 32% of patients on their admission to the hospital, 40% on discharge, and 36% six months later (13). In a further study by Kuhnt et al., 48% of patients still had symptoms and signs of CRF—and 12% had very severe signs and symptoms of CRF—two years after completing their initial treatment (e18). Studies in other countries have yielded comparable findings (e19– e21).
Etiology and pathogenesis
Possible pathophysiological factors.
Dysregulation of inflammatory cytokines
Disturbance of hypothalamic regulatory circuits • Changes in the CNS serotoninergic system
A disturbance of circadian melatonin secretion
Gene polymorphisms for regulatory proteins
All explanatory models of the causes and mechanisms of fatigue and exhaustion proceed from the assumption of a complex, multifactorial process. The causes and mechanisms of CRF may be associated with the tumor itself or with its treatment, or indeed with a potential genetic predisposition, an accompanying physical or mental illness, or behavioral and environmental factors (14, 15). Thus, a wide range of possible causes and influences—somatic, affective, cognitive, and psychosocial—that often cannot easily be separated from one another share cancer-related fatigue as a final common pathway. The following underlying pathophysiological factors are discussed in the literature:
a disturbance of hypothalamic regulatory circuits (e26– e28),
a disturbance of circadian melatonin secretion and the sleep-wake rhythm (e31– e33), and
gene polymorphisms for regulatory proteins of oxidative phosphorylation, signal transduction in B cells, the expression of pro-inflammatory cytokines, and catecholamine metabolism (e34– e37).
The causes of reduced physical performance ability, which is a common problem, are thought to lie in changes in the cortical and spinal sensorimotor centers (e38), in energy metabolism, and in the process of muscular activation (e39).
Diagnostic evaluation.
According to the National Comprehensive Cancer Network (NCCN) guideline, all cancer patients should be directly asked about symptoms of fatigue and exhaustion at regular intervals during their treatment and their further follow-up.
Diagnostic evaluation
According to the NCCN guideline, all cancer patients should be directly asked about symptoms of fatigue and exhaustion at regular intervals during their treatment and their further follow-up (2). The use of a visual analogue scale is recommended for recording the intensity of symptoms in the week leading up to the moment of inquiry (0 = no fatigue; 10 = worst fatigue you can imagine). A reported intensity of 4 or above is taken as the threshold value for further diagnostic assessment. The use of visual analogue scales is also recommended for assessing the degree to which CRF impairs the patient in various areas of everyday life; values of 5 and above are taken to imply a severe limitation of the patient’s social functioning that must be taken seriously (e40). If symptoms and signs suggesting CRF are, in fact, present, the further diagnostic assessment can be complicated by the following difficulties:
The symptoms and signs of CRF are not specific, as they may also be due to other diseases or functional impairments.
The clinical picture of CRF is defined solely by the affected patient’s subjective assessment of his or her symptoms and impairments.
Persons with CRF often do not seem to be ill, even if CRF has severe effects on them.
The type and extent of symptoms varies markedly from one patient to another and can change over time as well.
There is no reliable laboratory test or functional study for CRF.
The two-question test for depressive disorders.
The two-question test should be adminstered as part of the diagnostic assessment, as CRF may be an expression of pre-existing depression.
The complexity of this situation necessitates a deliberate and practically conceived approach whose main goal is to identify treatable causes and contributing factors (Figure 1).
Figure 1.
Cancer-related fatigue: treatable causes and contributing factors (after Ref. [e81]). (From: Mortimer JE, et al.: Studying cancer-related fatigue: Report of the NCCN Scientific Research Committee. J Natl Compr Canc Netw 2010; 8: 1331–9; Reprinted with permission from JNCCN—Journal of the National Comprehensive Cancer Network)
History-taking plays a central role in the diagnostic process. The physician should ask specifically about the type, severity, and temporal course of the patient’s symptoms, paying attention to their possible relationship to vegetative functions (e.g. sleep pattern) and other factors such as the following:
social and environmental factors
medications (including self-administered ones)
alcohol, tobacco, recreational drugs
past medical history
physical exercise.
The physician should also ask whether the symptoms are felt to be new or unusual. The history, in combination with the physical examination, can provide clues to possible causes or contributing factors (3) (Figure 2). If the history, physical examination, and basic laboratory tests yield no evidence of any underlying functional disturbance, further laboratory testing and ancillary studies are generally of little use. Therefore, according to the DEGAM guidelines, these should only be performed if the basic diagnostic assessment yields unequivocally abnormal findings (3).
Figure 2.
Basic and detailed diagnostic assessment
History-taking.
When taking the history, the physician should inquire about the nature, severity, and temporal course of symptoms and their possible relationship to vegetative functions.
With regard to the differential diagnosis of CRF, physicians are often faced with the important task of determining its possible relationship to a depressive disorder. The symptoms of fatigue and exhaustion have been found to be correlated with those of depressivity in nearly all studies that have addressed the question (8); this is hardly surprising, as easy fatigability and a lack of drive are considered to be among the main symptoms of depressive disorders. Nonetheless, according to the findings of two studies, only about one-third of persons suffering from severe CRF also have major depression, as defined by the DSM-IV (e41, e42). In clinical practice, a depressive disorder that may underlie CRF can be detected rapidly and sensitively with two questions (e43): If the patient answers both questions affirmatively, a depressive disorder is very likely to be present and therefore merits further, specialized diagnostic evaluation (Box 2). \
Box 2. The two-question test for depressive disorders, to be administered during history-taking.
Cancer-related fatigue can be an expression of (pre-existing) depression and can also be a cause of depression.
The two-question test consists of the following questions:
“In the last month, have you often felt dejected, sad, depressed, or hopeless?”
“In the last month, have you gotten much less pleasure than usual out of the things that you normally like to do?”
Differential diagnosis.
The possible presence of a depressive disorder must be investigated.
Treatment.
The causes of the patient’s symptoms can be treated both pharmacologically and non-pharmacologically.
Clinical experience with CRF patients indicates that many of them have no identifiable somatic or psychosocial cause for their symptoms. Physicians must beware of writing off the symptoms of CRF as “illegitimate” solely because of this. Rather, it is precisely this fact that makes it all the more important for the physician to take the patient’s symptoms and stresses seriously, and to show a readiness to talk about them and treat them. Repeated follow-up—even weeks or months after initial evaluation—often reveals additional information that may help establish or confirm a diagnosis (3).
Initiation of Treatment.
Treatment should be initiated early to prevent chronification.
Treatment
In most cases, CRF must be treated in the absence of a clearly diagnosed cause, but with the knowledge of a number of potential contributing factors (Figure 3). The treatment should be initiated early, to prevent CRF from turning into a chronic problem (e8). Multiple treatment approaches should be jointly applied, with an orientation toward the individual pattern of physical, mental, and cognitive symptoms, the extent of functional impairment, and the patient’s own conceptualization of the problem. The important persons in the patient’s life should also be included in treatment planning (e44).
Figure 3.
Treatment algorithm (modified from Radbruch et al [4]); TRH, thyrotropin-releasing hormone; ESA, erythropoiesis-stimulating agent. (From: Radbruch L, et al.: Fatigue in palliative care patients—an EAPC approach. Palliat Med 2008; 22: 13–32; with the kind permission of SAGE Publications)
The central goals of treatment are:
alleviating any factors that may be worsening the patient’s CRF,
offering individualized help so that the patient can cope with the symptoms and stresses of CRF,
activating the patient’s strengths and resources,
and working toward a shared biopsychosocial conception of the situation that takes its many different aspects into account.
The central goals of treatment.
Alleviate factors that worsen CRF
Help the patient cope with symptoms & stresses
Activate the patient’s strengths and resources
Maintain a biopsychosocial view
As as first step, the patient should be comprehensively informed about CRF and given appropriate counseling. Many patients are unaware that there is such a thing as CRF and cannot understand why they are so exhausted—especially if they seem to have achieved cure. Many patients find that the people around them cannot understand the problem either. Just knowing that their symptoms have a name and can be treated can give patients a large measure of emotional relief (e45). It is also important to tell patients that CRF need not have a bad outcome (e46). The physician can alleviate or prevent fears of prolonged and intractable fatigue by discussing CRF prophylactically before the treatment of the tumor is begun (e8).
All of the suggestions below for treating CRF with medications, or with non-pharmacological measures, are derived from randomized controlled trials and/or summaries of such trials in review articles and meta-analyses. They thus correspond to evidence levels 1 and 2 of the Oxford Centre for Evidence-Based Medicine.
Non-pharmacological treatments
There are many ways to alleviate the symptoms and stresses of CRF without recourse to medications.
The findings of two recent meta-analyses and numerous randomized controlled trials enable us to recommend certain specific psychosocial interventions and special types of physical exercise (16, 17).
Psychosocial interventions—The main interventions of this type that can alleviate CRF include cognitive behavioral therapeutic approaches (16, 17, e47); psychoeducation and directed, topical counseling (16, 17); energy conservation and activity management; and methods for the promotion and reinforcement of regeneration (17, e48, e49) (Table 1).
Non-pharmacological treatments of CRF supported by evidence from systematic reviews (SR), meta-analyses (MA), and randomized controlled clinical trials (RCT).
| Type of intervention | Description | Sources of evidence |
| Exercise | Endurance and strength training at moderate intensity several times a week for 30 to 45 minutes, gradually increasing intensity, individualized exercises, supervision by physician or physical therapist desirable (necessary for strength training) | SR/MA: (e70– e72) |
| RCT: (e73, e74) | ||
| Psychoeducation, cognitive behavioral therapy | Targeted information and counseling about CRF, stress reduction, identification of adaptive and maladaptive attitudes, relief of anxiety, assistance in coping with stress, promotion of active problem-centered coping strategies, learning of control techniques | SR/MA: (e71, e75, e76) |
| RCT: (e47, e77) | ||
| Activity and energy management | Rational apportionment of physical effort, task planning, taking of breaks and rest periods, health-promoting measures | SR/MA: (e76) |
| RCT: (e48, e49) | ||
| Relaxation techniques, mindfulness | Progressive muscle relaxation, mindfulness-based stress reduction (MBSR) | RCT: (e78, e79) |
While behavioral therapy (including cognitive behavioral therapy) and so-called mindfulness-based stress reduction (MBSR) are specialized techniques that must be carried out by trained experts, the remaining interventions can be incorporated into routine general medical practice, as long as the necessary infrastructure is available.
The physician–patient relationship.
Psychoeducational interventions and topic-centered counseling are important elements of a supportive treatment plan.
Energy conservation and activity management are intended to help patients economize with their physical resources, e.g., by doing only the most important tasks themselves, resting at appropriate intervals, and planning time for pleasant diversions (e.g., going to the movies, meeting friends, or listening to music).
Physical exercise.
Strength and endurance training helps the patient escape from the vicious circle of physical inactivity, deconditioning, and rapid exhaustion; it can be recommended to all patients with CRF, as long as no contraindications are present.
Psychoeducation and topical counseling are important elements of a supportive treatment plan. Directed cognitive behavioral therapeutic approaches have proven particularly useful (17, e47); the aim of such approaches is to illuminate the relationship of the physical symptoms with the way they are subjectively assessed (e.g., as “unpleasant” versus “catastrophic”), the resulting emotional states (e.g., worry versus despair), and patterns of behavior. Patients should be helped to understand that an appropriate assessment of the situation can improve their quality of life. Cognitive behavioral therapy and MBSR can also alleviate the hypersomnia and insomnia that often accompany CRF (2). In addition, they can equip the patient with ways to cope with the illness and the consequences of its treatment and limit emotional distress in the form of fears, mood shifts, and so forth.
Physical exercise—Strength and endurance training programs help the patient escape from the vicious circle of physical inactivity, deconditioning, and rapid exhaustion; they can be recommended to all patients with CRF (18, e50), as long as no contraindications are present (Box 3). The German Society for Sports Medicine and Prevention (Deutsche Gesellschaft für Sportmedizin und Prävention) and the German Cancer Society (Deutsche Krebsgesellschaft) have issued guidelines for training and exercise prorgrams for cancer patients (19).
Box 3. Calculation of the maximal heart rate, according to Lagerstrøm (Ref. [15]).
In the acute-care hospital: 180 minus age in years
In the rehabilitation phase, for endurance sports such as cycling and rowing: 220 minus age
In the rehabilitation phase, for non-strength-oriented sports such as swimming and jogging: 220 minus 2/3 of age
These are only rules of thumb; beware of demanding excessive effort from patients!
Pharmacotherapy.
Medications with various mechanisms of action are used to treat CRF, including psychostimulants, phytotherapeutic agents, growth factors, and corticosteroids.
Ideally, medically prescribed physical exercise sessions should take place several times per week, with daily endurance exercises and twice-weekly exercises to improve strength. Each training session should last 30 to 45 minutes (20) (Box 4). From the patient’s point of view, there are often multiple hindrances to the implementation of an ideal exercise program of this type, which should, in the best case, be continued for life: These include physical limitations, lack of interest, and purported lack of opportunity (e51). The physician should detect any such hindrances by directed history-taking and endeavor to overcome them with appropriate counseling or behavioral therapeutic approaches, so that physical exercise becomes a regular part of the patient’s daily routine. It is useful to encourage patients to do their own favorite types of physical exercise and to adapt the intensity and duration of each training session to their current capabilities and illness situation, with a gradual increase over four to six weeks (21). At the end of this period, the degree of physical exertion during exercise should not exceed 70% to 80% of the patient’s maximal capacity (maximal heart rate or maximal force). Strength training should generally take place in a facility where it can be overseen by a physical therapist or physician, while moderate endurance training can be introduced as part of routine clinical practice. Effective training involves elevating the heart rate to 70% to 80% of maximum. As a rule, exercise should not be so vigorous as to make the patient short of breath (22).
Box 4. Contraindications to exercise in patients with cancer*1.
-
Absolute contraindications
acute illnesses
acute worsening or decompensation of chronic illness
fever above 38°C
pain
inadequately controlled arterial hypertension
-
Relative contraindications
anemia (hemoglobin below 8 g/dL)
thrombocytopenia, coagulopathy
bone metastases
accompanying illnesses such as coronary heart disease, occlusive peripheral arterial disease, arterial hypertension, diabetes mellitus, arthrosis
administration of cytostatic agents on the same day
mediastinal/cardiac radiation therapy
flu-like symptoms under immunotherapy
epilepsy
Pharmacotherapy
Medications with various mechanisms of action are used to treat CRF, including psychostimulants, phytotherapeutic agents, growth factors, corticosteroids, and antidepressants. Trials of antidepressants to date have not yielded any improvement in CRF (e52). It follows that these should be used only if there is clear evidence for, or a definitive diagnosis of, a depressive disorder.
In the following sections, we will discuss only those forms of treatment whose safety and efficacy have been studied in randomized controlled trials, corresponding to evidence levels 1 and 2 in the scheme of the Oxford Centre for Evidence-Based Medicine (Table 2).
Table 2. Randomized controlled double-blind drug intervention trials showing efficacy against CRF as the primary endpoint.
| Trial | Design | Patients (number and type) | Intervention | Effect on CRF (primary outcome measure) |
| Roth 2010 (e58) | Two-armed, parallel, placebo-controlled | 68Advanced prostate cancer | Methylphenidate, initially 5 mg po qd, increase by 5 mg/day every 2–3 days possible, maximum dose 15 mg po bid | Improvement after 6 weeks of treatment(BFI) |
| Lower 2009 (e59) | Two-armed, parallel, placebo-controlled | 152Mainly breast and ovarian cancer, all stages | D-MP, initially 5 mg po bid, weekly dose increases possible up to a maximum of 50 mg/day | Improvement after 8 weeks of treatment (FACIT-F) |
| Jean-Pierre 2010 (e61) | Two-armed, parallel, placebo-controlled | 867Various types of cancer, all stages, during chemotherapy | Modafinil, 100 mg po qd, increase to 200 mg/day after 3 days of treatment, maximum dose 400 mg/day | Improvement after 8–12 weeks of treatment among patients with severe CRF (BFI) |
| Younus 2003 (e66) | Two-armed, parallel, placebo-controlled | 20Various types of cancer, various stages, during chemotherapy | Panax ginseng po, dose not indicated, taken daily | Improvement after 9–12 weeks of treatment (BFI) |
| Barton 2010 (e65) | Four-armed, parallel, placebo-controlled | 290 Various types of cancer, all stages, during chemotherapy | Panax quinquefolius, 750–2000 mg/day po | Improvement after 4, resp. 8 weeks in the groups taking 1000 und 2000 mg/day (BFI) |
| Campos 2011 (e68) | Two-armed, parallel, placebo-controlled | 75Breast cancer, all stages, during chemotherapy | Guarana 50 mg po bid | Improvement after 3 and 7 weeks of treatment (FACIT-F) |
| Kamath 2011 (e63) | Two-armed, crossover, placebo-controlled | 9Various types of cancer, various stages | TRH 0.5 mg IV 1x/week,then 1.5 mg IV 1x/week | Improvement 3, 7, & 24 hr after TRH administration, lasting up to 1 week (VAS) |
D-MP, dextromethylphenidate; BFI, Brief Fatigue Inventory; FACIT-F, Functional Assessment of Chronic Illness Therapy—Fatigue; VAS, Visual Analogue Scale; TRH, thyrotropin-releasing hormone
Hematopoietic growth factors—The administration of erythropoiesis-stimulating agents (ESA) can relieve CRF in anemic patients undergoing chemotherapy (e53). The expected treatment effect is seen in only a minority of patients, as most patients with CRF are not anemic (e52, e54, e55). A meta-analysis of individual patient data indicated that the administration of ESA during chemotherapy is associated with higher mortality, and that ESA elevate the frequency of thrombotic and thromboembolic events (e56); thus, the benefits and risks of treating CRF with ESA must be critically weighed in every case (e57).
Psychostimulants.
The psychostimulants methylphenidate and modafinil are potentially useful especially for patients with severe CRF that has not responded satisfactorily to other forms of treatment.
Psychostimulants—The psychostimulants methylphenidate (MP) and modafinil (MF) can relieve CRF (23– 25). In Germany, these medications may only be given off-label, or in the setting of a clinical trial, to treat CRF. They are potentially useful especially for patients with severe CRF that has not responded satisfactorily to other forms of treatment. They can only be given in the absence of contraindications such as poorly controlled arterial hypertension, symptomatic coronary heart disease, arrhythmia, or epilepsy (for methylphenidate), or psychosis and severe affective disorders (for modafinil).
Thyreoliberin.
The findings of an initial randomized trial suggest that intravenously administered thyreoliberin (thyrotropin-releasing hormone [TRH]) may be a safe and effective way to treat CRF.
Methylphenidate has been found to relieve moderate-to-severe CRF significantly better than placebo in patients with advanced prostate cancer (e58) and gynecological tumors (e59) (Table 2). A retrospective analysis of trial data suggests that methylphenidate is most effective for patients with severe CRF; that the D-(+) form of methylphenidate is more effective than other forms; and that patients who already benefit from the drug in the first few days of treatment will benefit more from it overall (e60).
Ginseng.
The results of scientific studies permit the tentative conclusion that both Panax quinquefolius and Panax ginseng may effectively alleviate CRF.
The findings of a recent study imply that modafinil is only effective against severe CRF (e61) (Table 2). In any case, in the past year, the European Medicines Agency (EMA) has restricted its use to the treatment of adults with excessive sleepiness, because of the occurrence of psychiatric manifestations and cutaneous reactions (erythema multiforme, Stevens-Johnson syndrome).
Corticosteroids—In palliative situations, corticosteroids can temporarily improve CRF and increase patients’ physical activity (e62). Therefore, the National Comprehensive Cancer Network (NCCN) and the European Association for Palliative Care (EAPC) recommend considering corticosteroids for use in such situations, but for a limited time only, in view of the risk that steroid-induced myopathy might worsen CRF with prolonged use (2, 4).
Thyreoliberin—The findings of an initial randomized trial suggest that intravenously administered thyreoliberin (thyrotropin-releasing hormone [TRH]) may be a safe and effective way to treat CRF (e63). In this trial, the patients’ manifestations of exhaustion improved within a few hours of treatment, and the improvement was sustained for several days (Table 2). In Germany, however, TRH preparations are approved only for diagnostic purposes, not for treatment.
Phytotherapeutic agents—Ginseng is traditionally given to treat states of exhaustion of all kinds (e64). American ginseng (Panax quinquefolius) (e65) and Asian ginseng (Panax ginseng C.A. Meyer) (e66) have both been studied scientifically; the results permit the tentative conclusion that both may be effective against CRF (Table 2). In Germany, Panax ginseng preparations are approved for the treatment of states of exhaustion (e67).
Regarding the putative efficacy of guarana (Paullinia cupana), there is initial positive evidence from a randomized trial, in which guarana improved CRF in women undergoing chemotherapy for breast cancer (e68) (Table 2). The main active ingredient of guarana is caffeine; in the trial just cited, the dose of guarana that was given contained about the same amount of caffeine as two cups of strong coffee, but caffeine is said to be released more slowly from guarana than from coffee (e69).
Guarana.
Regarding the putative efficacy of guarana (Paullinia cupana), there is initial positive evidence from a randomized trial, in which guarana improved CRF in women undergoing chemotherapy for breast cancer.
Further information on CME.
This article has been certified by the North Rhine Academy for Postgraduate and Continuing Medical Education. Deutsches Ärzteblatt provides certified continuing medical education (CME) in accordance with the requirements of the Medical Associations of the German federal states (Länder). CME points of the Medical Associations can be acquired only through the Internet, not by mail or fax, by the use of the German version of the CME questionnaire within 6 weeks of publication of the article. See the following website: cme.aerzteblatt.de
Participants in the CME program can manage their CME points with their 15-digit “uniform CME number” (einheitliche Fortbildungsnummer, EFN). The EFN must be entered in the appropriate field in the cme.aerzteblatt.de website under “meine Daten” (“my data”), or upon registration. The EFN appears on each participant’s CME certificate. The solutions to the following questions will be published in issue 17/2012.
The CME unit “Functional Bowel Disorders in Adults” (issue 5/2012) can be accessed until 16 March 2012.
For issue 13/2012, we plan to offer the topic “Insect Stings: Clinical Features and Management.”
Solutions to the CME questionnaire in issue 1–2/2012:
Kiefer M, Unterberg A: The Differential Diagnosis and Treatment of Normal-Pressure Hydrocephalus.
Solutions: 1c, 2a, 3e, 4d, 5e, 6b, 7a, 8a, 9e, 10b
Please answer the following questions to participate in our certified Continuing Medical Education program. Only one answer is possible per question. Please select the answer that is most appropriate.
Question 1
Which of the following may be a manifestation of cancer-related fatigue?
Impaired memory and concentration
Recurrent tension headache
Tremor and altered gait
Lymphadenopathy and skin irritation
Ptosis and diplopia
Question 2
What initial laboratory tests are useful for differential diagnosis in patients who first present with symptoms of cancer-related fatigue?
EBV, borrelia, hepatitis viruses, M. tuberculosis, herpes viruses
Complete blood count, adrenocortical hormones, tumor markers
Vitamins, selenium, vitamin D, magnesium, manganese, heavy metals
Blood count, electrolytes, glucose, transaminases, ?-GT, CRP, TSH
Serotonin, cortisol, melatonin, cytokines, catecholamines
Question 3
Roughly what percentage of patients with severe CRF meet the DSM-IV criteria for major depression?
Less than 5%
˜ 10%
˜ 30%
˜ 50–80%
More than 80%
Question 4
What temporal relation does CRF have to cancer?
CRF usually arises before cancer is diagnosed.
CRF usually arises after diagnosis and before the initiation of treatment.
CRF usually arises immediately after the end of chemotherapy.
CRF usually arises after the completion of radiotherapy.
CRF can arise at any point in the course of cancer and its treatment.
Question 5
Which of the following is a known risk factor for CRF?
Emotional stress
Irritable bowel syndrome
Fibromyalgia
Migraine
Disturbances of impulse control
Question 6
Which of the following statements from the patient points to CRF as the leading element of the differential diagnosis?
“All my muscles hurt all the time. I have continuous cramping pain.”
“When I come home from shopping, I am so tired that I have to lie down.”
“I can hardly fall asleep any more, because so many things are going through my head.”
“I have no appetite any more; then again, I can hardly keep any food down, either.”
“Every little thing makes me upset now. I feel totally stressed out.”
Question 7
Which of the following absolutely contraindicates physical exercise in a patient with CRF?
Anemia with a hemoglobin concentration below 8 g/dL
Bone metastases
Accompanying illnesses such as coronary heart disease, diabetes mellitus, and arthritis
Fever above 38°C
Flu-like symptoms under immunotherapy
Question 8
What percentage of maximum capacity (i.e., maximum heart rate or maximum force) is the recommended upper limit of exertion for CRF patients doing physical exercise?
50%
60%
70%
80%
90%
Question 9
What non-pharmacological intervention is suitable for the treatment of patients with CRF?
Qigong
Cognitive behavioral therapy
Whole foods diet
Relex zone massage
Kinesiology
Question 10
Which of the following preparations is approved in Germany for the treatment of states of exhaustion?
Mistletoe
Paroxetine
Panax ginseng
St. John’s wort oil
Methylphenidate
Acknowledgments
Translated from the original German by Ethan Taub, M.D.
Footnotes
Conflict of interest statement
Prof. Weis has received honoraria for lectures at symposia sponsored by the following pharmaceutical companies: Novartis, Roche, Astra Zeneca, and Ipsen.
PD Dr. Rüffer owns stock in Sanofi Aventis and serves as an advisor for Hexal.
PD Dr. Dimeo has received reimbursement of travel and accommodation expenses from Chugai and Amgen and lecture honoraria from Pfizer, Amgen, and Chugai. He has received money from Pfizer for a research project that he initiated.
Dr. Horneber has received lecture honoraria from Novartis.
Dr. Fischer states that she has no conflict of interest.
References
- 1.Weis J. Cancer-related fatigue: prevalence, assessment and treatment strategies. Expert Rev Pharmacoecon Outcomes Res. 2011;11:441–446. doi: 10.1586/erp.11.44. [DOI] [PubMed] [Google Scholar]
- 2.Berger AM, Abernethy AP, Atkinson A, et al. Cancer-related fatigue. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines TM) Version 1. 2011 [Google Scholar]
- 3.Donner-Banzhoff N, Maisel P, Dörr C, Baum E. Deutsche Gesellschaft für Allgemeinmedizin und Familienmedizin (DEGAM) Göttingen: Stand 2006; Müdigkeit - DEGAM Leitlinie Nr 2. AWMF Register Nr.053/002. [Google Scholar]
- 4.Radbruch L, Strasser F, Elsner F, et al. Fatigue in palliative care patients - an EAPC approach. Palliat Med. 2008;22:13–32. doi: 10.1177/0269216307085183. [DOI] [PubMed] [Google Scholar]
- 5.Scott JA, Lasch KE, Barsevick AM, Piault-Louis E. Patients’ experiences with cancer-related fatigue: a review and synthesis of qualitative research. Oncol Nurs Forum. 2011;38:191–203. doi: 10.1188/11.ONF.E191-E203. [DOI] [PubMed] [Google Scholar]
- 6.Piper BF, Cella D. Cancer-related fatigue: definitions and clinical subtypes. J Natl Compr Canc Netw. 2010;8:958–966. doi: 10.6004/jnccn.2010.0070. [DOI] [PubMed] [Google Scholar]
- 7.Ancoli-Israel S, Moore PJ, Jones V. The relationship between fatigue and sleep in cancer patients: a review. Eur J Cancer Care. 2001;10:245–255. doi: 10.1046/j.1365-2354.2001.00263.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Brown LF, Kroenke K. Cancer-related fatigue and its associations with depression and anxiety: a systematic review. Psychosomatics. 2009;50:440–447. doi: 10.1176/appi.psy.50.5.440. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Rüffer JU, Flechtner H, Tralls P, Josting A, Sieber M, Lathan B, et al. Fatigue in long-term survivors of Hodgkin’s lymphoma; a report from the German Hodgkin Lymphoma Study Group (GHSG) Eur J Cancer. 2003;39:2179–2186. doi: 10.1016/s0959-8049(03)00545-8. [DOI] [PubMed] [Google Scholar]
- 10.Cheng KK, Lee DT. Effects of pain, fatigue, insomnia, and mood disturbance on functional status and quality of life of elderly patients with cancer. Crit Rev Oncol Hematol. 2011;78:127–137. doi: 10.1016/j.critrevonc.2010.03.002. [DOI] [PubMed] [Google Scholar]
- 11.Vogelzang NJ, Breitbart W, Cella D, et al. Patient, caregiver, and oncologist perceptions of cancer-related fatigue. Results of a tripart assessment survey. Semin Hematol. 1997;34:4–12. [PubMed] [Google Scholar]
- 12.Newell S, Sanson-Fisher RW, Girgis A, Bonaventura A. How well do medical oncologists’ perceptions reflect their patients’ reported physical and psychosocial problems? Data from a survey of five oncologists. Cancer. 1998;83:1640–1651. [PubMed] [Google Scholar]
- 13.Singer S, Kuhnt S, Zwerenz R, et al. Age- and sex-standardised prevalence rates of fatigue in a large hospital-based sample of cancer patients. Br J Cancer. 2011;105:445–451. doi: 10.1038/bjc.2011.251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Bruera E. Cancer-related fatigue: a multidimensional syndrome. J Support Oncol. 2010;8:175–176. [PubMed] [Google Scholar]
- 15.Barsevick A, Frost M, Zwinderman A, Hall P, Halyard M. I’m so tired: biological and genetic mechanisms of cancer-related fatigue. Qual Life Res. 2010;19:1419–1427. doi: 10.1007/s11136-010-9757-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Kangas M, Bovbjerg DH, Montgomery GH. Cancer-related fatigue: a systematic and meta-analytic review of non-pharmacological therapies for cancer patients. Psychol Bull. 2008;134:700–741. doi: 10.1037/a0012825. [DOI] [PubMed] [Google Scholar]
- 17.Goedendorp MM, Gielissen MF, Verhagen CA, Bleijenberg G. Psychosocial interventions for reducing fatigue during cancer treatment in adults. Cochrane Database Syst Rev. 2009 doi: 10.1002/14651858.CD006953.pub2. CD006953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Dimeo FC. Effects of exercise on cancer-related fatigue. Cancer. 2001;92:1689–1693. doi: 10.1002/1097-0142(20010915)92:6+<1689::aid-cncr1498>3.0.co;2-h. [DOI] [PubMed] [Google Scholar]
- 19.Deutsche Krebsgesellschaft. Richtlinien für die Anwendung von Sport und körperlicher Aktivität in der Prävention, supportiver Therapie und Rehabilitation neoplastischer Erkrankungen Teil II. FORUM. 2011;5:9–12. [Google Scholar]
- 20.Dimeo F. Standards in der Sportmedizin: Körperliche Aktivität und Krebs. Zeitschrift für Sportmedizin. 2004;4:106–107. [Google Scholar]
- 21.McNeely ML, Courneya KS. Exercise programs for cancer-related fatigue: evidence and clinical guidelines. J Natl Compr Canc Netw. 2010;8:945–953. doi: 10.6004/jnccn.2010.0069. [DOI] [PubMed] [Google Scholar]
- 22.Baumann FT. Ausdauertraining mit Krebspatienten: Bewegungstherapie und Sport bei Krebs. In: Baumann FT, Schüle K, editors. Leitfaden für die Praxis. Köln: Deutscher Ärzte-Verlag GmbH; 2008. pp. 33–55. [Google Scholar]
- 23.Breitbart W, Alici Y. Psychostimulants for cancer-related fatigue. J Natl Compr Canc Netw. 2010;8:933–942. doi: 10.6004/jnccn.2010.0068. [DOI] [PubMed] [Google Scholar]
- 24.Minton O, Richardson A, Sharpe M, Hotopf M, Stone PC. Psychostimulants for the management of cancer-related fatigue: A systematic review and meta-analysis. J Pain Symptom Manage. 2011;41:761–767. doi: 10.1016/j.jpainsymman.2010.06.020. [DOI] [PubMed] [Google Scholar]
- 25.Cooper MR, Bird HM, Steinberg M. Efficacy and safety of modafinil in the treatment of cancer-related fatigue. Ann Pharmacother. 2009;43:721–725. doi: 10.1345/aph.1L532. [DOI] [PubMed] [Google Scholar]
- e1.Holley S. Cancer-related fatigue. Suffering a different fatigue. Cancer Pract. 2000;8:87–95. doi: 10.1046/j.1523-5394.2000.82007.x. [DOI] [PubMed] [Google Scholar]
- e2.Tishelman C, Degner LF, Rudman A, et al. Symptoms in patients with lung carcinoma: distinguishing distress from intensity. Cancer. 2005;104:2013–2021. doi: 10.1002/cncr.21398. [DOI] [PubMed] [Google Scholar]
- e3.Shi Q, Smith TG, Michonski JD, Stein KD, Kaw C, Cleeland CS. Symptom burden in cancer survivors 1 year after diagnosis: A Report from the american cancer society’s studies of cancer survivors. Cancer. 2011;117:2779–2790. doi: 10.1002/cncr.26146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e4.Scott JA, Lasch KE, Barsevick AM, Piault-Louis E. Patients’ experiences with cancer-related fatigue: a review and synthesis of qualitative research. Oncol Nurs Forum. 2011;38:E191–E203. doi: 10.1188/11.ONF.E191-E203. [DOI] [PubMed] [Google Scholar]
- e5.Gotay CC, Kawamoto CT, Bottomley A, Efficace F. The prognostic significance of patient-reported outcomes in cancer clinical trials. J Clin Oncol. 2008;26:1355–1363. doi: 10.1200/JCO.2007.13.3439. [DOI] [PubMed] [Google Scholar]
- e6.Montazeri A. Quality of life data as prognostic indicators of survival in cancer patients: an overview of the literature from 1982 to 2008. Health Qual Life Outcomes. 2009;7 doi: 10.1186/1477-7525-7-102. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e7.Servaes P, Gielissen MF, Verhagen S, Bleijenberg G. The course of severe fatigue in disease-free breast cancer patients: a longitudinal study. Psychooncology. 2007;16:787–795. doi: 10.1002/pon.1120. [DOI] [PubMed] [Google Scholar]
- e8.Kuhnt S, Ehrensperger C, Singer S, et al. Prädiktoren tumorassoziierter Fatigue. Psychotherapeut. 2011;56:216–223. [Google Scholar]
- e9.Smith SK, Herndon JE, Lyerly HK, et al. Correlates of quality of life-related outcomes in breast cancer patients participating in the Pathfinders pilot study. Psychooncology. 2011;20:559–564. doi: 10.1002/pon.1770. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e10.Spelten ER, Sprangers MA, Verbeek JH. Factors reported to influence the return to work of cancer survivors: a literature review. Psychooncology. 2002;11:124–131. doi: 10.1002/pon.585. [DOI] [PubMed] [Google Scholar]
- e11.Tiedtke C, de Rijk A, Dierckx de Casterlé B, Christiaens MR, Donceel P. Experiences and concerns about ’returning to work’ for women breast cancer survivors: a literature review. Psychooncology. 2010;19:677–683. doi: 10.1002/pon.1633. [DOI] [PubMed] [Google Scholar]
- e12.Oktay JS, Bellin MH, Scarvalone S, Appling S, Helzlsouer KJ. Managing the impact of posttreatment fatigue on the family: Breast cancer survivors share their experiences. Fam Syst Health. 2011;29:127–137. doi: 10.1037/a0023947. [DOI] [PubMed] [Google Scholar]
- e13.Shun SC, Lai YH, Hsiao FH. Patient-related barriers to fatigue communication in cancer patients receiving active treatment. Oncologist. 2009;14:936–943. doi: 10.1634/theoncologist.2009-0048. [DOI] [PubMed] [Google Scholar]
- e14.Westerman MJ, The AM, Sprangers MA, Groen HJ, van der Wal G, Hak T. Small-cell lung cancer patients are just ’a little bit’ tired: response shift and self-presentation in the measurement of fatigue. Qual Life Res. 2007;16:853–861. doi: 10.1007/s11136-007-9178-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e15.Pearce S, Richardson A. Fatigue in cancer: a phenomenological perspective. Eur J Cancer Care. 1996;5:111–115. doi: 10.1111/j.1365-2354.1996.tb00217.x. [DOI] [PubMed] [Google Scholar]
- e16.Passik SD, Kirsh KL, Donaghy K, et al. Patient-related barriers to fatigue communication: initial validation of the fatigue management barriers questionnaire. J Pain Symptom Manage. 2002;24:481–493. doi: 10.1016/s0885-3924(02)00518-3. [DOI] [PubMed] [Google Scholar]
- e17.Smets EM, Garssen B, Bonke B, de Haes JC. The Multidimensional Fatigue Inventory (MFI) psychometric qualities of an instrument to assess fatigue. J Psychosom Res. 1995;39:315–325. doi: 10.1016/0022-3999(94)00125-o. [DOI] [PubMed] [Google Scholar]
- e18.Kuhnt S, Ernst J, Singer S, et al. Fatigue in cancer survivors—prevalence and correlates. Onkologie. 2009;32:312–317. doi: 10.1159/000215943. [DOI] [PubMed] [Google Scholar]
- e19.Schultz SL, Dalton SO, Christensen J, Carlsen K, Ross L, Johansen C. Factors correlated with fatigue in breast cancer survivors undergoing a rehabilitation course, Denmark, 2002-2005. Psychooncology. 2010;20:352–360. doi: 10.1002/pon.1739. [DOI] [PubMed] [Google Scholar]
- e20.Cella D, Davis K, Breitbart W, Curt G. Cancer-related fatigue: prevalence of proposed diagnostic criteria in a United States sample of cancer survivors. J Clin Oncol. 2001;19:3385–3391. doi: 10.1200/JCO.2001.19.14.3385. [DOI] [PubMed] [Google Scholar]
- e21.Knobel H, Havard LJ, Brit LM, Forfang K, Nome O, Kaasa S. Late medical complications and fatigue in Hodgkin’s disease survivors. J Clin Oncol. 2001;19:3226–3233. doi: 10.1200/JCO.2001.19.13.3226. [DOI] [PubMed] [Google Scholar]
- e22.Bower JE, Ganz PA, Irwin MR, Kwan L, Breen EC, Cole SW. Inflammation and behavioral symptoms after breast cancer treatment: do fatigue, depression, and sleep disturbance share a common underlying mechanism? J Clin Oncol. 2011;29:3517–3522. doi: 10.1200/JCO.2011.36.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e23.Bower JE, Ganz PA, Aziz N, Olmstead R, Irwin MR, Cole SW. Inflammatory responses to psychological stress in fatigued breast cancer survivors: relationship to glucocorticoids. Brain Behav Immun. 2007;21:251–258. doi: 10.1016/j.bbi.2006.08.001. [DOI] [PubMed] [Google Scholar]
- e24.Schubert C, Hong S, Natarajan L, Mills PJ, Dimsdale JE. The association between fatigue and inflammatory marker levels in cancer patients: a quantitative review. Brain Behav Immun. 2007;21:413–427. doi: 10.1016/j.bbi.2006.11.004. [DOI] [PubMed] [Google Scholar]
- e25.Jager A, Sleijfer S, van der Rijt CC. The pathogenesis of cancer related fatigue: could increased activity of pro-inflammatory cytokines be the common denominator? Eur J Cancer. 2008;44:175–181. doi: 10.1016/j.ejca.2007.11.023. [DOI] [PubMed] [Google Scholar]
- e26.Kamath J, Yarbrough GG, Prange AJ, Jr, Winokur A. The thyrotropin-releasing hormone (TRH)-immune system homeostatic hypothesis. Pharmacol Ther. 2009;121:20–28. doi: 10.1016/j.pharmthera.2008.09.004. [DOI] [PubMed] [Google Scholar]
- e27.Kamath J, Yarbrough GG, Prange AJ, Jr, Winokur A. Thyrotropin-releasing hormone can relieve cancer-related fatigue: hypothesis and preliminary observations. J Int Med Res. 2009;37:1152–1157. doi: 10.1177/147323000903700420. [DOI] [PubMed] [Google Scholar]
- e28.Strasser F, Palmer JL, Schover LR, et al. The impact of hypogonadism and autonomic dysfunction on fatigue, emotional function, and sexual desire in male patients with advanced cancer: a pilot study. Cancer. 2006;107:2949–2957. doi: 10.1002/cncr.22339. [DOI] [PubMed] [Google Scholar]
- e29.Bower JE. Cancer-related fatigue: links with inflammation in cancer patients and survivors. Brain Behav Immun. 2007;21:863–871. doi: 10.1016/j.bbi.2007.03.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e30.Alexander S, Stone P, White S, Andrews P, Nussey S, Bano G. Evaluation of central serotonin sensitivity in breast cancer survivors with cancer-related fatigue syndrome. J Pain Symptom Manage. 2010;40:892–898. doi: 10.1016/j.jpainsymman.2010.03.023. [DOI] [PubMed] [Google Scholar]
- e31.Payne JK. Altered Circadian Rhythms and Cancer-Related Fatigue Outcomes. Integr Cancer Ther. 2011;10:32–21. doi: 10.1177/1534735410392581. 233 doi: 10.1177/1534735410392581. Epub 2011 Mar 7. [DOI] [PubMed] [Google Scholar]
- e32.Berger AM, Wielgus K, Hertzog M, Fischer P, Farr L. Patterns of circadian activity rhythms and their relationships with fatigue and anxiety/depression in women treated with breast cancer adjuvant chemotherapy. Support Care Cancer. 2009;18 doi: 10.1007/s00520-009-0636-0. [DOI] [PubMed] [Google Scholar]
- e33.Rich TA. Symptom clusters in cancer patients and their relation to EGFR ligand modulation of the circadian axis. J Support Oncol. 2007;5:167–174. [PubMed] [Google Scholar]
- e34.Sprangers MA, Bartels M, Veenhoven R, et al. Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states. Qual Life Res. 2010;19:1429–1437. doi: 10.1007/s11136-010-9652-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e35.Whistler T, Taylor R, Craddock RC, Broderick G, Klimas N, Unger ER. Gene expression correlates of unexplained fatigue. Pharmacogenomics. 2006;7:395–405. doi: 10.2217/14622416.7.3.395. [DOI] [PubMed] [Google Scholar]
- e36.Reinertsen KV, Grenaker Alnaes GI, Landmark-Hoyvik H, et al. Fatigued breast cancer survivors and gene polymorphisms in the inflammatory pathway. Brain Behav Immun. 2011;25:1376–1383. doi: 10.1016/j.bbi.2011.04.001. [DOI] [PubMed] [Google Scholar]
- e37.Bower JE, Ganz PA, Irwin MR, Arevalo JM, Cole SW. Fatigue and gene expression in human leukocytes: increased NF-kappaB and decreased glucocorticoid signaling in breast cancer survivors with persistent fatigue. Brain Behav Immun. 2011;25:147–150. doi: 10.1016/j.bbi.2010.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e38.Yavuzsen T, Davis MP, Ranganathan VK, et al. Cancer-related fatigue: central or peripheral? J Pain Symptom Manage. 2009;38:587–596. doi: 10.1016/j.jpainsymman.2008.12.003. [DOI] [PubMed] [Google Scholar]
- e39.Ng AV. The underrecognized role of impaired muscle function in cancer-related fatigue. J Support Oncol. 2010;8:177–178. [PubMed] [Google Scholar]
- e40.Given B, Given CW, Sikorskii A, et al. Establishing mild, moderate, and severe scores for cancer-related symptoms: how consistent and clinically meaningful are interference-based severity cut-points? J Pain Symptom Manage. 2008;35:126–135. doi: 10.1016/j.jpainsymman.2007.03.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e41.Andrykowski MA, Donovan KA, Laronga C, Jacobsen PB. Prevalence, predictors, and characteristics of off-treatment fatigue in breast cancer survivors. Cancer. 2010;116:5740–5748. doi: 10.1002/cncr.25294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e42.Murphy H, Alexander S, Stone P. Investigation of diagnostic criteria for cancer-related fatigue syndrome in patients with advanced cancer: a feasibility study. Palliat Med. 2006;20:413–418. doi: 10.1191/0269216306pm1145oa. [DOI] [PubMed] [Google Scholar]
- e43.Rudolf S, Bermejo I, Schweiger U, Hohagen F, Härter M. Diagnostik depressiver Störungen. Dtsch Arztebl. 2006;103:A1754–A1762. [Google Scholar]
- e44.Escalante CP, Kallen MA, Valdres RU, Morrow PK, Manzullo EF. Outcomes of a cancer-related fatigue clinic in a comprehensive cancer center. J Pain Symptom Manage. 2010;39:691–701. doi: 10.1016/j.jpainsymman.2009.09.010. [DOI] [PubMed] [Google Scholar]
- e45.Kuhnt S, Brähler E. Tumorassoziierte Fatigue. Psychother Psychosom Med Psychol. 2010;60:402–408. doi: 10.1055/s-0030-1248590. [DOI] [PubMed] [Google Scholar]
- e46.Glaus A, Frei IA, Knipping C, Ream E, Browne N. Attitude of cancer patients to fatigue: patient attitude in Switzerland and England. Pflege. 2002;15:187–194. doi: 10.1024/1012-5302.15.5.187. [DOI] [PubMed] [Google Scholar]
- e47.Gielissen MF, Verhagen S, Witjes F, Bleijenberg G. Effects of cognitive behavior therapy in severely fatigued disease-free cancer patients compared with patients waiting for cognitive behavior therapy: a randomized controlled trial. J Clin Oncol. 2006;24:4882–4887. doi: 10.1200/JCO.2006.06.8270. [DOI] [PubMed] [Google Scholar]
- e48.Barsevick AM, Dudley W, Beck S, Sweeney C, Whitmer K, Nail L. A randomized clinical trial of energy conservation for patients with cancer-related fatigue. Cancer. 2004;100:1302–1310. doi: 10.1002/cncr.20111. [DOI] [PubMed] [Google Scholar]
- e49.Yuen HK, Mitcham M, Morgan L. Managing post-therapy fatigue for cancer survivors using energy conservation training. J Allied Health. 2006;35:121E–139E. [PubMed] [Google Scholar]
- e50.Schmitz KH, Courneya KS, Matthews C, et al. American college of sports medicine roundtable on exercise guidelines for cancer survivors. Med Sci Sports Exerc. 2010;42:1409–1426. doi: 10.1249/MSS.0b013e3181e0c112. [DOI] [PubMed] [Google Scholar]
- e51.Blaney J, Lowe-Strong A, Rankin J, Campbell A, Allen J, Gracey J. The cancer rehabilitation Journey: Barriers to and facilitators of exercise among patients with cancer-related fatigue. Phys Ther. 2010;90:1135–1147. doi: 10.2522/ptj.20090278. [DOI] [PubMed] [Google Scholar]
- e52.Minton O, Stone P, Richardson A, Sharpe M, Hotopf M. Drug therapy for the management of cancer related fatigue. Cochrane Database Syst Rev. 2010;7 doi: 10.1002/14651858.CD006704.pub3. CD006704. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e53.Eton DT, Cella D. Do erythropoietic-stimulating agents relieve fatigue? A review of reviews. Cancer Treat Res. 2011;157:181–194. doi: 10.1007/978-1-4419-7073-2_11. [DOI] [PubMed] [Google Scholar]
- e54.Dimeo F, Schmittel A, Fietz T, et al. Physical performance, depression, immune status and fatigue in patients with hematological malignancies after treatment. Ann Oncol. 2004;15:1237–1242. doi: 10.1093/annonc/mdh314. [DOI] [PubMed] [Google Scholar]
- e55.Geinitz H, Zimmermann FB, Stoll P, et al. Fatigue, serum cytokine levels, and blood cell counts during radiotherapy of patients with breast cancer. Int J Radiat Oncol Biol Phys. 2001;51:691–698. doi: 10.1016/s0360-3016(01)01657-1. [DOI] [PubMed] [Google Scholar]
- e56.Bohlius J, Schmidlin K, Brillant C, et al. Recombinant human erythropoiesis-stimulating agents and mortality in patients with cancer: a meta-analysis of randomised trials. Lancet. 2009;373:1532–1542. doi: 10.1016/S0140-6736(09)60502-X. [DOI] [PubMed] [Google Scholar]
- e57.Rizzo JD, Brouwers M, Hurley P, et al. American Society of Clinical Oncology/American Society of Hematology clinical practice guideline update on the use of epoetin and darbepoetin in adult patients with cancer. J Clin Oncol. 2010;28(33):4996–5010. doi: 10.1200/JCO.2010.29.2201. [DOI] [PubMed] [Google Scholar]
- e58.Roth AJ, Nelson C, Rosenfeld B, et al. Methylphenidate for fatigue in ambulatory men with prostate cancer. Cancer. 2010;116:5102–5110. doi: 10.1002/cncr.25424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e59.Lower EE, Fleishman S, Cooper A, et al. Efficacy of dexmethyl-phenidate for the treatment of fatigue after cancer chemotherapy: a randomized clinical trial. J Pain Symptom Manage. 2009;38:650–662. doi: 10.1016/j.jpainsymman.2009.03.011. [DOI] [PubMed] [Google Scholar]
- e60.Yennurajalingam S, Palmer JL, Chacko R, Bruera E. Factors associated with response to methylphenidate in advanced cancer patients. Oncologist. 2011;16:246–253. doi: 10.1634/theoncologist.2010-0214. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e61.Jean-Pierre P, Morrow GR, Roscoe JA, et al. A Phase 3 randomized, placebo-controlled, double-blind, clinical trial of the effect of Modafinil on cancer-related fatigue among 631 patients receiving chemotherapy. Cancer. 2010;15:3513–3520. doi: 10.1002/cncr.25083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e62.Lundholm K, Gelin J, Hyltander A, et al. Anti-inflammatory treatment may prolong survival in undernourished patients with metastatic solid tumors. Cancer Res. 1994;54:5602–5606. [PubMed] [Google Scholar]
- e63.Kamath J, Feinn R, Winokur A. Thyrotropin-releasing hormone as a treatment for cancer-related fatigue: a randomized controlled study. Support Care Cancer. 2011 doi: 10.1007/s00520-011-1268-8. [DOI] [PubMed] [Google Scholar]
- e64.Jia L, Zhao Y. Current evaluation of the millennium phytomedicine—ginseng (I): etymology, pharmacognosy, phytochemistry, market and regulations. Curr Med Chem. 2009;16:2475–2484. doi: 10.2174/092986709788682146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e65.Barton DL, Soori GS, Bauer BA, et al. Pilot study of Panax quinquefolius (American ginseng) to improve cancer-related fatigue: a randomized, double-blind, dose-finding evaluation: NCCTG trial N03CA. Support Care Cancer. 2010;18:179–187. doi: 10.1007/s00520-009-0642-2. (Epub 2009 May 6) [DOI] [PMC free article] [PubMed] [Google Scholar]
- e66.Younus J, Collins A, Wang X, et al. A double blind placebo controlled pilot study to evaluate the effect of ginseng on fatigue and quality of life in adult chemo-naïve cancer patients. Proc Am Soc Clin Oncol. 2003;22 [abstr 2947] [Google Scholar]
- e67.Fischer I, Boehm K, Horneber M CAM-Cancer Consortium. Ginseng [online document] www.cam-cancer.org/CAM-Summaries/Biologically-Based-Practices/Ginseng. Last accessed on 12 July 2010. [Google Scholar]
- e68.de Oliveira Campos MP, Riechelmann R, Martins LC, Hassan BJ, Casa FB, Giglio AD. Guarana (Paullinia cupana) Improves Fatigue in Breast Cancer Patients Undergoing Systemic Chemotherapy. J Altern Complement Med. 2011;17:505–512. doi: 10.1089/acm.2010.0571. [DOI] [PubMed] [Google Scholar]
- e69.Hänsel R, Sticher O. 8th edition. Heidelberg: Springer Medizin Verlag; 2007. Pharmakognosie Phytopharmazie. [Google Scholar]
- e70.Brown JC, Huedo-Medina TB, Pescatello LS, Pescatello SM, Ferrer RA, Johnson BT. Efficacy of Exercise interventions in modulating cancer-related fatigue among adult cancer survivors: A meta-analysis. Cancer Epidemiol Biomarkers Prev. 2011;20:123–133. doi: 10.1158/1055-9965.EPI-10-0988. Epub 2010 Nov 4. [DOI] [PubMed] [Google Scholar]
- e71.Duijts SF, Faber MM, Oldenburg HS, van Beurden M, Aaronson NK. Effectiveness of behavioral techniques and physical exercise on psychosocial functioning and health-related quality of life in breast cancer patients and survivors—a meta-analysis. Psychooncology. 2011;20:115–126. doi: 10.1002/pon.1728. [DOI] [PubMed] [Google Scholar]
- e72.Velthuis MJ, Agasi-Idenburg SC, Aufdemkampe G, Wittink HM. The effect of physical exercise on cancer-related fatigue during cancer treatment: a meta-analysis of randomised controlled trials. Clin Oncol (R Coll Radiol) 2010;22:208–221. doi: 10.1016/j.clon.2009.12.005. [DOI] [PubMed] [Google Scholar]
- e73.Dimeo F, Schwartz S, Wesel N, Voigt A, Thiel E. Effects of an endurance and resistance exercise program on persistent cancer-related fatigue after treatment. Ann Oncol. 2008;19:1495–1499. doi: 10.1093/annonc/mdn068. [DOI] [PubMed] [Google Scholar]
- e74.Dimeo FC, Stieglitz RD, Novelli-Fischer U, Fetscher S, Keul J. Effects of physical activity on the fatigue and psychologic status of cancer patients during chemotherapy. Cancer. 1999;85:2273–2277. [PubMed] [Google Scholar]
- e75.Goedendorp MM, Gielissen MF, Verhagen CA, Bleijenberg G. Psychosocial interventions for reducing fatigue during cancer treatment in adults. Cochrane Database Syst Rev. 2009 doi: 10.1002/14651858.CD006953.pub2. CD006953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- e76.Kangas M, Bovbjerg DH, Montgomery GH. Cancer-related fatigue: a systematic and meta-analytic review of non-pharmacological therapies for cancer patients. Psychol Bull. 2008;134:700–741. doi: 10.1037/a0012825. [DOI] [PubMed] [Google Scholar]
- e77.van der Lee ML, Garssen B. Mindfulness-based cognitive therapy reduces chronic cancer-related fatigue: a treatment study. Psycho-oncology. 2010 Dec 19; doi: 10.1002/pon.1890. [Epub ahead of print] [DOI] [PubMed] [Google Scholar]
- e78.Dimeo FC, Thomas F, Raabe-Menssen C, Propper F, Mathias M. Effect of aerobic exercise and relaxation training on fatigue and physical performance of cancer patients after surgery. A randomised controlled trial. Support Care Cancer. 2004;12:774–779. doi: 10.1007/s00520-004-0676-4. [DOI] [PubMed] [Google Scholar]
- e79.Carlson LE, Garland SN. Impact of mindfulness-based stress reduction (MBSR) on sleep, mood, stress and fatigue symptoms in cancer outpatients. Int J Behav Med. 2005;12:278–285. doi: 10.1207/s15327558ijbm1204_9. [DOI] [PubMed] [Google Scholar]
- e80.Dimeo FC. Bewegung im eigenen Takt - Körperliche Aktivität und Sport bei Tumorerkrankungen. Im Focus Onkologie. 2010;5:60–66. [Google Scholar]
- e81.Mortimer JE, Barsevick AM, Bennett CL, et al. Studying cancer-related fatigue: Report of the NCCN Scientific Research Committee. J Natl Compr Canc Netw. 2010;8:1331–1339. doi: 10.6004/jnccn.2010.0101. [DOI] [PubMed] [Google Scholar]



