Skip to main content
Springer logoLink to Springer
. 2021 Feb 4;38(2):20. doi: 10.1007/s12032-021-01460-7

Quality of life, symptoms and dietary habits in oncology outpatients with malnutrition: A cross-sectional study

Mira Sonneborn-Papakostopoulos 1, Clara Dubois 1, Viktoria Mathies 3,, Mara Heß 1, Nicole Erickson 2, Thomas Ernst 1, Jutta Huebner 1
PMCID: PMC7862192  PMID: 33543336

Abstract

Cancer-related malnutrition has a high prevalence, reduces survival and increases side effects. The aim of this study was to assess oncology outpatients and risk of malnutrition. Reported symptoms and quality of life (QoL) in patients found to be at risk of malnutrition or malnourished were compared to patients without malnutrition. Using a standardized questionnaire, the European Organization for Research and Treatment of Cancer Questionnaire for Quality of Life and the Mini Nutritional Assessment (MNA), patients in an outpatient cancer clinic undergoing chemotherapy treatment at a German University Hospital were assessed for nutrition, risk of malnutrition and quality of life. Based on the MNA, 39 (45.9%) patients were categorized as malnourished or at risk for malnutrition. Loss of appetite (n = 37.6%, p < 0.001) and altered taste sensation (n = 30,3%, p < 0.001) were the symptoms most frequently associated with reduced food intake. Patients with risk of malnutrition scored lower on the global health status (n = 48.15%, p = 0.001). Side effects of cancer treatments lead to a higher risk of malnutrition and as a consequence lower QoL. These side effects should be addressed more efficiently in cancer care.

Keywords: Malnutrition, Cancer, Dietary habits, Screening, Side effects of cancer treatments

Introduction

Many cancer patients suffer from malnutrition: a lack of adequate calories, protein, or other nutrients needed for tissue maintenance and repair [1]. This condition is defined by The European Society of Clinical Nutrition and Metabolism (ESPEN) by two options. Body mass index (BMI, kg/m2) <18.5 or the combination of unintentional weight loss (either >10% of habitual weight indefinite of time, or > 5% over 3 months) combined with either a reduced age specific BMI or a low fat free mass index using sex specific cut-offs [2]. For cancer patients, malnutrition is considered to be an important prognostic factor. Affected patients suffer from a negative clinical outcome up to premature death [39]. About 20–30% of patients with malignancies die due to tumor-related malnutrition [10]. Reduced quality of life is another important aspect associated to a poor nutritional status [1113]. Therefore, malnutrition is highly relevant for everyday clinical practice in oncology and effective assessment, prevention, intervention and reevaluation are of major importance.

Despite the awareness that nutrition-related sides effects contribute largely to a reduced energy intake during cancer therapies, physicians often oversee nutritional issues, have limited knowledge how to calculate nutrition needs and do not routinely refer patients to a dietitian [1418]. A variety of validated tools are a reliable method to detect the risk of malnutrition in cancer patients [1921]. These include the Patient Generated-Subjective Global Assessment (PG-SGA), the Malnutrition Universal Screening Tool (MUST), the Nutritional Risk Screening (NRS-2002) and the Mini Nutritional Assessment (MNA). All these tools rely on measurable items like weight loss over defined time periods and assess the presence of symptoms associated with the disease [21, 22]. All of these tools are non-invasive, quick to apply, low in cost, easily feasible, and can be performed by any health professional. The PG-SGA short form is the only one which is completed by the patient, thus appropriate in settings where health professional’s time is limited. Du et al. compared screening tools and proposed that not only a comprehensive nutritional assessment tool should be recommended to all cancer patients but also that none of them should be implemented without follow-up care [23].

In a cross-sectional investigation, we aimed to compare differences in patient-reported symptoms regarding nutritional issues in patients with cancer undergoing chemotherapy who were well nourished compared to the patients identified at-risk of malnutrition or malnourished according to the MNA criteria [5, 24]. We also explored quality of life for both groups in order to evaluate the association of malnutrition and wellbeing. The results should help increase oncologists’ awareness to the importance of systematic screening for malnutrition, repeated re-evaluation during treatment, and to symptoms associated with malnutrition. Furthermore, the data may provide insights which strategies should be prioritized in the prevention of malnutrition through early interventions.

Patients and methods

Patients

During a two-week period in February 2018, 110 patients with any cancer undergoing chemotherapy treatment were asked to complete the questionnaires during their visit to the outpatient clinic of oncology at the University Hospital in Jena.

All patients attending chemotherapy during these days were asked to participate. Inclusion criteria were limited to patients ≥18 years undergoing chemotherapy for malignancy with the ability to understand the questions, and the willingness to participate. All MNA were performed by the same scientist. Afterwards the patient was requested to complete the questionnaires while waiting for the appointment and was visited again by the researcher to collect the form subsequently. Patients were informed about the anonymity of the data and data protection laws were respected. The study was approved by the ethics commission of the University Hospital Jena (Number of the ethical vote: 2019–1585).

Outcome measures

Demographic and dietary information

Participant demographic data, including age, sex, height, current weight and weight before diagnosis, highest education, living situation was collected using a researcher-developed questionnaire filled in by the patient. Furthermore, the form included researcher-developed questions regarding the nutritional situation containing general information about diet habits in order to get an indication about the following: changes in nutrient intake before and after diagnosis, frequency of eating less following diagnosis to determine energy intake, information previously received about nutrition. In addition, it was asked if a nutrition counseling was performed to identify quality and source of knowledge and desire to involve in the nutritional situation as indication for compliance. Symptoms regarding nutritional intake to discover potentially influencing factors leading to reduced food intake have been obtained.

Quality of life

The European Organization for Research and Treatment of Cancer (EORTC QLQ-C30 version 3.0) questionnaire, which was developed specially for cancer patients and comprises 30 questions regarding quality of life, was also included. The 30 questions contained multi-item scales and single-item measures. It is composed of a global health status, five functional scales, three symptom scales and six symptom single items. Scores range from 0 to 100. For the global health status, a high score represents a high quality of life and for the functional scales a high score represents a high/ healthy level of functioning. For the symptom scales and items high scores represent a high level of symptoms/ problems [25].

Nutritional status

The long version of the Mini Nutritional Assessment in German was chosen as the third questionnaire. This questionnaire begins with six questions and produces a numerical score. Depending on the answer to these six questions, a further assessment consisting of 10 questions should be completed. These questions are completed if the total score of the answers to the first six questions add up to 11 points or more. The second section has a total of 16 points. Mid-arm circumference and calf circumference needs to be measured which was performed at the dominant arm on the same side of the body. A score of >23.5 indicates a well-nourished patient. A person is categorized as at risk for malnutrition when 17 to 23.5 points are reached and considered malnourished when less than 17 points are reached in the total assessment.

Statistical analysis

Data from the questionnaires were transferred into IBM SPSS Statistics 25. Results were computed as means and standard deviation for quantitative variables and frequencies and percentages for qualitative variables. Correlations were tested to compare quantitative variables by Chi-square and t-test (p-value < 0.05). Chi-square test was used for comparison of data in nominal scale to investigate a possible association between frequency of eating less/ change in dietary habits/ avoiding products/ receiving information/ taking vitamin supplements and existing symptoms in malnourished and not malnourished patients. Results of the EORTC QLQ-C30 were generated into scores within the range of 0 to 100. According to EORTC guidelines overall scores were calculated and compared to gender and MNA categories using t-test [25].

Results

Demographic data

One hundred and nine patients were interviewed and completed the questionnaire (70 females (64.2%), 39 (35.8%) males). The median age was 61 years (SD = 12.4 years) (see Table 1). Breast cancer and lymphoma/leukemia were the most common diagnoses with 25 patients (22.9%) each, followed by 22 gastrointestinal (20.2%) and 15 urogenital (13.8%) cancers. Ninety-one patients (83.5%) lived with their family or partner and only 11 lived alone (10.1%), three were in a nursing home (2.8%). Further demographic data are shown in Table 1.

Table 1.

Characteristics of study group (N = 109)

n (%)
Gender 109 (100)
Female 70 (64.2)
Male 39 (35.8)
Age 107 (98.2)
Minimum 32
Maximum 87
Median 61
≤ 40 years 9 (8.3)
41–50 years 11 (10.1)
51–60 years 30 (27.5)
61–70 years 32 (29.4)
71–80 years 20 (18.3)
≥ 81 years 5 (4.6)
Diagnosis (type of cancer) 106 (97.2)
Breast 25 (22.9)
Lymphomas/Leukemia 25 (22.9)
Gastrointestinal 22 (20.2)
Urological/Urogenital 15 (13.8)
Gynecological 7 (6.4)
Lung 6 (5.5)
Head and Neck 2 (1.8)
Other 4 (3.7)
Years from diagnosis 103 (94.5)
> 10 years ago 4 (3.7)
2 to 10 years ago (2007–2016) 22 (20.3)
Last year (2017) 44 (40.4)
Current year (2018) 5 (4.6)
Living situation 105 (96.3)
Alone 11 (10.1)
With partner 72 (66.1)
With family 19 (17.4)
Nursing home 3 (2.8)
Level of education 107 (98.2)
Primary school 14 (12.8)
Middle school leaving certificate (9th or 10th grade) 17 (15.6)
High school diploma 3 (2.8)
Vocational training 33 (30.3)
University degree 40 (36.7)
Physical activity 104 (95.4)
No 64 (58.7)
1-2x at least 30 min per week 23 (21.1)
3-4x at least 30 min per week 10 (9.2)
> 4x at least 30 min per week 7 (6.4)
Do you smoke? 105 (96.3)
Yes 12 (11)
No 93 (85.3)
How often do you drink alcohol? 103 (94.5)
Never 46 (42.2)
1x per month or less 25 (22.9)
2-3x per month 14 (12.8)
1-2x per week 12 (11)
3-4x per week 3 (2.8)
Every day 3 (2.8)

Seventy-nine patients (72.4%) reported having had a change of weight after diagnosis. Sixty-five patients (59.6%) lost weight (mean 10 kg) while 14 reported having gained weight (12.8%; mean 6.6 kg) (Table 2). There were no significant correlations in terms of demographic data (gender, age, cancer entity, year of diagnosis or level of education). Significantly more patients with weight loss reported having changed their nutrition habits after diagnosis (p = 0.039).

Table 2.

Body weight changes and amount of loss/gain in kilograms (N = 96)

n (%)
Weight change 96 (88.1)
No weight change 17 (15.6)
Weight loss 65 (59.6)
Weight gain 14 (12.8)
Weight loss after diagnosis 65 (59.6)
Mean [IQR] 10 [4–14]
≤ 5 kg 27 (24.8)
6-10 kg 16 (14.7)
11-15 kg 8 (7.3)
16-20 kg 6 (5.5)
21-25 kg 4 (3.7)
> 25 kg 4 (3.7)
Weight gain after diagnosis 14 (12.8)
Mean [IQR] 6.6 [3–8.5]
≥ 5 kg 7 (6.4)
6-10 kg 5 (4.6)
> 11 kg 2 (1.8)

BMI varied slightly among the distribution of the different BMI classes in the whole collective. In total 41 patients had a change in weight after diagnosis resulting in a shift of their BMI. Whereas 35 lost weight resulting in a lower BMI and only 6 had a gain of weight resulting in higher BMI, respectively.

The MNA screening and consecutive full MNA were completed by 85 patients (78.0%). In total, the assessment revealed 34 patients at risk of malnutrition (31.2%) and 5 were considered to be malnourished (4.6%). 46 patients (42.2%) had a normal nutritional status.

Reduced dietary intake

One hundred and three patients (94.5%) completed the data relevant to dietary intake. Twenty-seven patients (24.8%) reported eating less than before diagnosis at least once a week and 18 (16.5%) reported doing so every day.

Figure 1 shows the frequency of symptoms reported as reasons for eating less. The most frequent problems were loss of appetite (41 (37.6%)) followed by altered taste sensation (33 (30.3%)) and dry mouth (28 (25.7%)). Several symptoms correlated with eating less: nausea (p = 0.006, φ = 0.399), loss of appetite (p < 0.001, φ = 0.586), altered taste sensation (p < 0.001, φ = 0.469), stomach pain (p = 0.036, φ = 0.340), other pain (p = 0.004, φ = 0.408), no desire (p = 0.007, φ = 0.394), mourning/worries (p = 0.004, φ = 0.410) and flatulence/diarrhea (p = 0.013, φ = 0.375) (Fig. 1).

Fig. 1.

Fig. 1

Participants who reported frequency of symptoms as reasons for eating less (N = 109)

Dietary habits

Seventy-five patients (68.8%) reported that they did not adhere to a special diet whereas 30 patients (27.5%) reported special dietary patterns such as vegetarian, no dairy, low carbohydrate, or no sugar. Among these patients, 27 reported not having followed any special diets before diagnosis (24.8%; p < 0.001, φ = 0.372). A change in dietary habits was associated with several side effects of cancer therapy. Considerably more patients with loss of appetite (p = 0.028, φ = 0.220) and altered taste sensation (p = 0.035, φ = 0.211) reported having changed dietary habits. Significantly more patients with altered taste sensation reported adhering to a special diet (p = 0.006, φ = 0.268). Patients who reported having received information on nutrition significantly more often wanted to be more involved with their nutrition decisions in the near future (p = 0.049, φ = 0.283). Thirty-one patients (28.4%) additionally stated that there were some foods which they avoided since diagnosis. Avoiding some products was correlated to the following symptoms: altered taste sensations (p = 0.005, φ = 0.275), stomach pain (p = 0.004, φ = 0.197), no desire to eat (p = 0.001, φ = 0.320) and flatulence/diarrhea (p = 0.019 each, φ = 0.231). Thirty-two patients (29.4%) reported taking vitamin supplements. Significantly more patients with the symptoms of loss of appetite (p = 0.004, φ = 0.197), dry mouth (p = 0.016, φ = 0.238), stomach pain (p = 0.013, φ = 0.244), no desire (p = 0.014, φ = 0.243) and flatulence/diarrhea (p = 0.042, φ = 0.201) took vitamin supplements.

EORTC QLQ-C30

The EORTC QLQ-C30 global health status showed a mean score of 52.72 with no significant differences between male and female participants. Patients with risk of malnutrition or manifest malnutrition in the MNA showed lower global health status than those without risk (mean value 43.8 vs. 58.93; p = 0.001).

Mean values of all five functional scales are shown in Table 3. There were no significant differences between male and female participants. The MNA revealed patients with risk of malnutrition and malnourished patients had significantly lower scores for all functional scales (p values shown in Table 3). Symptom scales are shown in Table 3. Fatigue (51.89) scored highest and nausea and vomiting scored lowest of all symptom items (11.9). Significant differences between male and female participants were only seen with regard to financial difficulties (27.03 vs. 15.00; p = 0.048). Patients with risk of malnutrition scored significantly higher for all symptoms except dyspnea and diarrhea comparing the MNA groups. Additionally, financial difficulties and nausea/vomiting were not significantly correlated with nutrition risk (p-values shown in Table 3).

Table 3.

Differences in EORTC QLQ-C30 scores of global health status, functional scales, symptom scales and measures between patients with and without malnutrition regarding the MNA (N = 91)

Mean
independent of nutritional status
MNA:
Risk of malnutrition/ malnourished
MNA:
Normal nutritional status
p-value
Global health status 52.7 43.80 58.93 0.001
Role functioning 51.7 40.95 63.95 0.003
Social functioning 57.1 47.75 70.54 0.002
Physical functioning 67.2 58.92 77.73 <0.001
Emotional functioning 68.7 61.62 77.50 0.004
Cognitive Functioning 78.2 70.72 87.70 0.001
Fatigue 51.9 61.59 41.80 0.002
Appetite loss 35 53.51 18.18 <0.001
Insomnia 34.2 45.61 27.41 0.01
Pain 34.7 44.74 18.22 <0.001
Dyspnoea 31.7 35.14 24.24 0.115
Financial difficulties 19.6 24.56 15.50 0.159
Constipation 17.6 21.93 6.35 0.007
Diarrhea 15.1 16.22 12.40 0.496
Nausea and vomiting 11.9 14.91 7.20 0.058

Information

In total, only 19 patients (17.4%) reported having received nutrition counseling. Significantly more men (12 (11.5%)) than women (7 (6.7%)) received counseling (p = 0.04, φ = 0.284). However, there were no statistically significant differences regarding weight loss, BMI or MNA category between patients who received and patients who did not receive nutrition counseling. Seventy-eight patients (71.6%) received nutrition information about nutrition and cancer. Twenty-four patients (22%) reported not to have received any information at all. Mostly the oncologist provided this information (30 (27.5%)). Only 17 patients (15.6%) got information from a nutritionist. Forty-one patients (37.6%) intended to focus on nutrition in the near future and 29 took this into consideration (26.6%). Significantly more patients with nutrition associated impact symptoms such loss of appetite (p = 0.002, φ = 0.38), altered taste sensation (p = 0.034, φ = 0.29), dry mouth (p = 0.046, φ = 0.279) and flatulence/diarrhea (p = 0.004, φ = 0.36) reported interest in nutrition. Patients who received no information on nutrition were significantly more often at risk of malnutrition (p = 0.008, φ = 0.292) (see Fig. 2).

Fig. 2.

Fig. 2

Source of information about nutrition regarding the type of cancer (N = 109)

Mini nutritional assessment

There were no significant correlations between the groups of the MNA classification and the demographic data. Patients in the MNA risk group significantly reported more weight loss (p = 0.003, φ = 0.383). Significantly more patients with risk of malnutrition also reported having changed their nutritional habits after diagnosis (18 (47.4%) vs. 8 (18.2%); p = 0.005, φ = 0.313). In the group with risk of malnutrition significantly more patients took vitamin supplements as in the group with no risk (16 (42.1%) vs. 9 (20%) (p = 0.029), φ = 0.240).

Discussion

The aim of this study was to assess the prevalence of malnutrition in cancer patients in an outpatient setting and to analyze factors associated with malnutrition and impact on quality of life. Our data show that there is still a high number of patients dealing with malnutrition and that malnutrition could be connected to reduced food intake due to nutrition associated impact symptoms. Additionally, we could confirm a high correlation to a poorer quality of life.

Overall, prevalence of suspected and manifested malnutrition was 45.9% among our patients. These results are higher than those reported by Calderon et al. [26] who revealed 36.4% of affected patients undergoing cancer surgery and initiated adjuvant chemotherapy using the Malnutrition Screening Tool (MST). Considering the prevalence of malnutrition at time of cancer diagnosis in outpatients settings, Alvaro Sanz et al. [27] reported 21.4% of patients being affected who were diagnosed with solid tumors from early diagnosis to advanced stages with begin of chemotherapy using Nutriscore to identify nutritional risk. Whereas another larger study using the MNA to assess malnutrition recorded prevalence of 43% in patients at first medical oncology visit [28]. However, the large range must be interpreted carefully. One reason for these differences are the miscellaneous populations and various tools used to determine the nutritional condition of cancer patients [22, 29].

In contrast to other recent studies we could not show a higher risk of malnutrition for older patients. Still our results appear to be similar to the data of Zhang et al. who assessed the MNA for older patients undergoing outpatient cancer care and categorized 31.0% at risk for malnutrition [30]. We could confirm the high prevalence with 35.7% in our patients who are 65 or older. Therefore, more attention should be paid to elderly patients who are at a high risk of malnutrition.

We could not detect any differences regarding gender and malnutrition. Alvaro Sanz et al. showed that significantly more males were at risk for malnutrition [27, 31]. However, that study included of a large proportion of patients with breast cancer, who do not present the same nutritional risk as patients with other types of tumors.

We found that patients with risk of, or manifest malnutrition, according to the MNA also showed lower values for the global health status. Likewise, those patients have significantly lower functionality scores and a higher symptom burden. Considering side effects of cancer therapies, we have found loss of appetite to be the most frequent symptom associated with a decrease in food intake. This was consistent with results to several previous studies [28, 3236]. Other symptoms often reported as reasons for diminished food intake were altered taste sensation and dry mouth [37], these are frequent side effects of several cancer therapies and so far, no truly effective supportive treatment exists. Further symptoms that seemed to increase the likelihood of reduced food intake are nausea and flatulence/diarrhea which likewise can be induced by radiation therapy or cancer drugs [38, 39]. In contrast, frequent nausea [40] is not associated with a higher risk for malnutrition but associated with a reduced QoL which is in accordance with the findings of Najafi et al. [41]. Interestingly, diarrhea did not show a significant association with malnutrition risk, while constipation was a symptom highly related for the risk of malnutrition. Still a study with patients surviving 2 years after gastric cancer resection showed an association between body weight loss and diarrhea [42].

Several short- and long-term health impacts are associated with malnutrition. Complications such as greater likelihood of length of reduced QoL [11], hospital stay [31, 43, 44] and costs [45] and other complications like postoperative complications [46], decreased response to treatment [47] and lower 90-day survival rate [44] and increased mortality [3] are connected to malnutrition.

Our data show that changes in nutrition habits are associated with loss of weight as well as different side effects such as alteration of taste or loss of appetite. This might be due to patients trying to react to nutrition problems [48]. It may also help physicians to identify patients at risk for malnutrition by routinely assessing side effects of cancer therapy [49]. On the other hand, our data might also point to an increased risk of malnutrition and side effects of cancer treatment resulting from nutritional changes, a hypothesis which should be assessed in further studies.

Several working groups were able to show that counseling by a trained dietitian is a cost effective method to reduce malnutrition [5053]. Kufeldt et al. showed that individual nutritional support teams should treat patients identified as at risk for malnutrition. Patients should be identified and treated as early as possible which includes outpatient arrangements prior to (elective) treatment [54]. Tanaka et al. showed that nutritional counseling by a dietitian including information and education, combined with oral supplements and appropriate antiemetic treatment can prevent weight loss during chemotherapy [55]. Patients should receive individual nutrition advice adapted to their current situation, diagnosis, therapy strategies, prognosis, as well as sociocultural habits. In total, our data showed that less than a fifth of the patients got a nutritional counseling. Considering that nearly a half was at risk of malnutrition, this is a disturbing result pointing to an important deficit in the health care system. Maschke et al. reported that many cancer patients still lack the access to high quality nutrition therapy [15]. In contrast, patients are highly interested in the topic and more than half of our patients wanted to focus on nutrition. Patients with symptoms associated with eating are highly motivated which most probably would increase the impact of (early) nutritional counseling. In fact, our results indicate that systematic screening and early integration of nutritional management in clinical practice is indispensable for cancer patients independently of tumors entity. Furthermore, it may be valuable for all demographic subgroups. According to our findings, the medical care of malnutrition should include management of symptoms and side effects with the goal to stabilize and improve patients’ nutritional condition. This includes nutritional counseling and provision of proper information regarding questions concerning eating habits. This will not only help to reduce the risk of malnutrition, but at the same time may influence quality of life.

This study confirmed the high prevalence of malnutrition in cancer patients and its negative impact on quality of life. Furthermore, certain nutrition impact symptoms may indicate patients at risk even when a valid screening tool is not utilized. Despite the increasing data on malnutrition and its consequences on quality of life and prognosis [56] there still is a high prevalence of malnutrition and most patients do not get timely or sufficient support. Efforts to integrate nutritional screening and assessment into routine clinical practice for all cancer patients must be combined with a proper dietary consulting. Moreover, early information on nutrition should be offered independently of the current nutritional condition and patients should be encouraged to get involved in their nutritional matters and to closely cooperate with physicians and dietitians.

Author contributions

MSP: study design, interviews of the patients and collection of the data, analysis of data, writing of the manuscript. CD: co-worker in the statistical analysis. VM: supervision of the manuscript, corresponding author. MH: co-worker on the manuscript. NE: supervision of the study design. TE: supervision of the study design and the interviews. JH: supervision of the whole concept, study conduct and manuscript.

Funding

Open Access funding enabled and organized by Projekt DEAL. There was no funding for this study.

Availability of data and material

Data may be obtained from the corresponding author.

Compliance with ethical standards

Conflicts of interest

The authors declare no conflict of interest.

Ethics approval

The study was approved by the ethics commission of the University Hospital Jena.

Consent to participate

All patients consented to participate (see “Patients and methods”).

Consent for publication

All patients consented to publication of anonymous data.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.White JV, Guenter P, Jensen G, Malone A, Schofield M, Academy Malnutrition Work G et al. Consensus statement: academy of nutrition and dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition) JPEN J Parenter Enteral Nutr. 2012;36(3):275–283. doi: 10.1177/0148607112440285. [DOI] [PubMed] [Google Scholar]
  • 2.Cederholm T, Bosaeus I, Barazzoni R, Bauer J, Van Gossum A, Klek S, et al. Diagnostic criteria for malnutrition - An ESPEN consensus statement. Clin Nutr. 2015;34(3):335–340. doi: 10.1016/j.clnu.2015.03.001. [DOI] [PubMed] [Google Scholar]
  • 3.Soderstrom L, Rosenblad A, Thors Adolfsson E, Bergkvist L. Malnutrition is associated with increased mortality in older adults regardless of the cause of death. Br J Nutr. 2017;117(4):532–540. doi: 10.1017/S0007114517000435. [DOI] [PubMed] [Google Scholar]
  • 4.Martin L, Senesse P, Gioulbasanis I, Antoun S, Bozzetti F, Deans C, et al. Diagnostic criteria for the classification of cancer-associated weight loss. J Clin Oncol. 2015;33(1):90–99. doi: 10.1200/JCO.2014.56.1894. [DOI] [PubMed] [Google Scholar]
  • 5.Bourdel-Marchasson I, Diallo A, Bellera C, Blanc-Bisson C, Durrieu J, Germain C, et al. One-year mortality in older patients with Cancer: development and external validation of an MNA-based prognostic score. PLoS One. 2016;11(2):e0148523. doi: 10.1371/journal.pone.0148523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Ozola Zalite I, Zykus R, Francisco Gonzalez M, Saygili F, Pukitis A, Gaujoux S, et al. Influence of cachexia and sarcopenia on survival in pancreatic ductal adenocarcinoma: a systematic review. Pancreatology. 2015;15(1):19–24. doi: 10.1016/j.pan.2014.11.006. [DOI] [PubMed] [Google Scholar]
  • 7.Shachar SS, Williams GR, Muss HB, Nishijima TF. Prognostic value of sarcopenia in adults with solid tumours: a meta-analysis and systematic review. Eur J Cancer. 2016;57:58–67. doi: 10.1016/j.ejca.2015.12.030. [DOI] [PubMed] [Google Scholar]
  • 8.Levolger S, van Vugt JL, de Bruin RW, JN IJ. Systematic review of sarcopenia in patients operated on for gastrointestinal and hepatopancreatobiliary malignancies. Br J Surg. 2015;102(12):1448–1458. doi: 10.1002/bjs.9893. [DOI] [PubMed] [Google Scholar]
  • 9.Andreyev HJN, Norman AR, Oates J, Cunningham D. Why do patients with weight loss have a worse outcome when undergoing chemotherapy for gastrointestinal malignancies? Eur J Cancer. 1998;34(4):503–9. 10.1016/S0959-8049(97)10090-9. [DOI] [PubMed]
  • 10.Arends J, Bachmann P, Baracos V, Barthelemy N, Bertz H, Bozzetti F, et al. ESPEN guidelines on nutrition in cancer patients. Clin Nutr. 2017;36(1):11–48. doi: 10.1016/j.clnu.2016.07.015. [DOI] [PubMed] [Google Scholar]
  • 11.Lis CG, Gupta D, Lammersfeld CA, Markman M, Vashi PG. Role of nutritional status in predicting quality of life outcomes in cancer--a systematic review of the epidemiological literature. Nutr J. 2012;11:27. doi: 10.1186/1475-2891-11-27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Norman K, Stobaus N, Zocher D, Bosy-Westphal A, Szramek A, Scheufele R, et al. Cutoff percentiles of bioelectrical phase angle predict functionality, quality of life, and mortality in patients with cancer. Am J Clin Nutr. 2010;92(3):612–619. doi: 10.3945/ajcn.2010.29215. [DOI] [PubMed] [Google Scholar]
  • 13.Nourissat A, Vasson MP, Merrouche Y, Bouteloup C, Goutte M, Mille D, et al. Relationship between nutritional status and quality of life in patients with cancer. Eur J Cancer. 2008;44(9):1238–1242. doi: 10.1016/j.ejca.2008.04.006. [DOI] [PubMed] [Google Scholar]
  • 14.Muscaritoli M, Molfino A, Scala F, Christoforidi K, Manneh-Vangramberen I, De Lorenzo F. Nutritional and metabolic derangements in Mediterranean cancer patients and survivors: the ECPC 2016 survey. J Cachexia Sarcopenia Muscle. 2019; 10.1002/jcsm.12420. [DOI] [PMC free article] [PubMed]
  • 15.Maschke J, Kruk U, Kastrati K, Kleeberg J, Buchholz D, Erickson N, et al. Nutritional care of cancer patients: a survey on patients’ needs and medical care in reality. Int J Clin Oncol. 2017;22(1):200–206. doi: 10.1007/s10147-016-1025-6. [DOI] [PubMed] [Google Scholar]
  • 16.Vetter ML, Herring SJ, Sood M, Shah NR, Kalet AL. What do resident physicians know about nutrition? An evaluation of attitudes, self-perceived proficiency and knowledge. J Am Coll Nutr. 2008;27(2):287–298. doi: 10.1080/07315724.2008.10719702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Wirth R, Smoliner C, Spamer C, Marburger C, Schreiber FS, Willschrei HP, et al. Do doctors know how much nutrition patients need--a survey from Germany? Eur J Clin Nutr. 2014;68(7):840–843. doi: 10.1038/ejcn.2014.94. [DOI] [PubMed] [Google Scholar]
  • 18.Janssen G, Pourhassan M, Lenzen-Grossimlinghaus R, Jager M, Schafer R, Spamer C, et al. The refeeding syndrome revisited: you can only diagnose what you know. Eur J Clin Nutr. 2019; 10.1038/s41430-019-0441-x. [DOI] [PubMed]
  • 19.Poulia KA, Klek S, Doundoulakis I, Bouras E, Karayiannis D, Baschali A, et al. The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria for malnutrition. Clin Nutr. 2017;36(4):1130–1135. doi: 10.1016/j.clnu.2016.07.014. [DOI] [PubMed] [Google Scholar]
  • 20.Isenring E, Cross G, Daniels L, Kellett E, Koczwara B. Validity of the malnutrition screening tool as an effective predictor of nutritional risk in oncology outpatients receiving chemotherapy. Support Care Cancer. 2006;14(11):1152–1156. doi: 10.1007/s00520-006-0070-5. [DOI] [PubMed] [Google Scholar]
  • 21.Castillo-Martinez L, Castro-Eguiluz D, Copca-Mendoza ET, Perez-Camargo DA, Reyes-Torres CA, Avila EA, et al. Nutritional assessment tools for the identification of malnutrition and nutritional risk associated with cancer treatment. Rev Invest Clin. 2018;70(3):121–125. doi: 10.24875/RIC.18002524. [DOI] [PubMed] [Google Scholar]
  • 22.Ye XJ, Ji YB, Ma BW, Huang DD, Chen WZ, Pan ZY, et al. Comparison of three common nutritional screening tools with the new European Society for Clinical Nutrition and Metabolism (ESPEN) criteria for malnutrition among patients with geriatric gastrointestinal cancer: a prospective study in China. BMJ Open. 2018;8(4):e019750. doi: 10.1136/bmjopen-2017-019750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Du H, Liu B, Xie Y, Liu J, Wei Y, Hu H, et al. Comparison of different methods for nutrition assessment in patients with tumors. Oncol Lett. 2017;14(1):165–170. doi: 10.3892/ol.2017.6154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Read JA, Crockett N, Volker DH, MacLennan P, Choy ST, Beale P, et al. Nutritional assessment in cancer: comparing the mini-nutritional assessment (MNA) with the scored patient-generated subjective global assessment (PGSGA) Nutr Cancer. 2005;53(1):51–56. doi: 10.1207/s15327914nc5301_6. [DOI] [PubMed] [Google Scholar]
  • 25.Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85(5):365–376. doi: 10.1093/jnci/85.5.365. [DOI] [PubMed] [Google Scholar]
  • 26.Calderon C, Carmona-Bayonas A, Beato C, Ghanem I, Hernandez R, Majem M, et al. Risk of malnutrition and emotional distress as factors affecting health-related quality of life in patients with resected cancer. Clin Transl Oncol. 2019;21(5):687–691. doi: 10.1007/s12094-018-1954-9. [DOI] [PubMed] [Google Scholar]
  • 27.Alvaro Sanz E, Garrido Siles M, Rey Fernandez L, Villatoro Roldan R, Rueda Dominguez A, Abiles J. Nutritional risk and malnutrition rates at diagnosis of cancer in patients treated in outpatient settings: early intervention protocol. Nutrition. 2019;57:148–153. doi: 10.1016/j.nut.2018.05.021. [DOI] [PubMed] [Google Scholar]
  • 28.Muscaritoli M, Lucia S, Farcomeni A, Lorusso V, Saracino V, Barone C, et al. Prevalence of malnutrition in patients at first medical oncology visit: the PreMiO study. Oncotarget. 2017;8(45):79884–79896. doi: 10.18632/oncotarget.20168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Araujo dos Santos C, de Oliveira Barbosa Rosa C, Queiroz Ribeiro A, Lanes Ribeiro Rde C. Patient-generated subjective global assessment and classic anthropometry: comparison between the methods in detection of malnutrition among elderly with cancer. Nutr Hosp. 2015;31(1):384–392. doi: 10.3305/nh.2015.31.1.7543. [DOI] [PubMed] [Google Scholar]
  • 30.Zhang X, Sun M, McKoy JM, Bhulani NNA, Valero V, Barcenas CH, et al. Malnutrition in older patients with cancer: appraisal of the mini nutritional assessment, weight loss, and body mass index. J Geriatr Oncol. 2018;9(1):81–83. doi: 10.1016/j.jgo.2017.07.012. [DOI] [PubMed] [Google Scholar]
  • 31.Leandro-Merhi VA, Aquino JLB. Relationship between nutritional status and the clinical outcomes of patients with and without neoplasms according to multiple correspondence analysis. Arq Gastroenterol. 2017;54(2):148–155. doi: 10.1590/S0004-2803.201700000-05. [DOI] [PubMed] [Google Scholar]
  • 32.Gyan E, Raynard B, Durand JP. Lacau saint Guily J, Gouy S, Movschin ML et al. malnutrition in patients with Cancer: comparison of perceptions by patients, relatives, and physicians-results of the NutriCancer2012 study. JPEN J Parenter Enteral Nutr. 2018;42(1):255–260. doi: 10.1177/0148607116688881. [DOI] [PubMed] [Google Scholar]
  • 33.Lacau St Guily J, Bouvard E, Raynard B, Goldwasser F, Maget B, Prevost A, et al. NutriCancer: a French observational multicentre cross-sectional study of malnutrition in elderly patients with cancer. J Geriatr Oncol. 2018;9(1):74–80. doi: 10.1016/j.jgo.2017.08.003. [DOI] [PubMed] [Google Scholar]
  • 34.Uster A, Ruefenacht U, Ruehlin M, Pless M, Siano M, Haefner M, et al. Influence of a nutritional intervention on dietary intake and quality of life in cancer patients: a randomized controlled trial. Nutrition. 2013;29(11–12):1342–1349. doi: 10.1016/j.nut.2013.05.004. [DOI] [PubMed] [Google Scholar]
  • 35.Bozzetti F, Mariani L, Lo Vullo S, Amerio ML, Biffi R, Caccialanza R, et al. The nutritional risk in oncology: a study of 1,453 cancer outpatients. Support Care Cancer. 2012;20(8):1919–1928. doi: 10.1007/s00520-012-1387-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Tong H, Isenring E, Yates P. The prevalence of nutrition impact symptoms and their relationship to quality of life and clinical outcomes in medical oncology patients. Support Care Cancer. 2009;17(1):83–90. doi: 10.1007/s00520-008-0472-7. [DOI] [PubMed] [Google Scholar]
  • 37.Renken RJ, Gietema JA, Slart R, MGJ M, Lefrandt JD, et al. Changes in taste and smell function, dietary intake, food preference, and body composition in testicular cancer patients treated with cisplatin-based chemotherapy. Clin Nutr. 2017;36(6):1642–1648. doi: 10.1016/j.clnu.2016.10.013. [DOI] [PubMed] [Google Scholar]
  • 38.Khalid U, McGough C, Hackett C, Blake P, Harrington KJ, Khoo VS, et al. A modified inflammatory bowel disease questionnaire and the Vaizey incontinence questionnaire are more sensitive measures of acute gastrointestinal toxicity during pelvic radiotherapy than RTOG grading. Int J Radiat Oncol Biol Phys. 2006;64(5):1432–1441. doi: 10.1016/j.ijrobp.2005.10.007. [DOI] [PubMed] [Google Scholar]
  • 39.Gangadharan A, Choi SE, Hassan A, Ayoub NM, Durante G, Balwani S, et al. Protein calorie malnutrition, nutritional intervention and personalized cancer care. Oncotarget. 2017;8(14):24009–24030. doi: 10.18632/oncotarget.15103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Harder SL, Groenvold M, Herrstedt J, Johnsen AT. Nausea in advanced cancer: relationships between intensity, burden, and the need for help. Support Care Cancer. 2019;27(1):265–273. doi: 10.1007/s00520-018-4326-7. [DOI] [PubMed] [Google Scholar]
  • 41.Najafi S, Haghighat S, Raji Lahiji M, RazmPoosh E, Chamari M, Abdollahi R, et al. Randomized study of the effect of dietary counseling during adjuvant chemotherapy on chemotherapy induced nausea and vomiting, and quality of life in patients with breast Cancer. Nutr Cancer. 2018:1–10. 10.1080/01635581.2018.1527375. [DOI] [PubMed]
  • 42.Climent M, Munarriz M, Blazeby JM, Dorcaratto D, Ramon JM, Carrera MJ, et al. Weight loss and quality of life in patients surviving 2 years after gastric cancer resection. Eur J Surg Oncol. 2017;43(7):1337–1343. doi: 10.1016/j.ejso.2017.01.239. [DOI] [PubMed] [Google Scholar]
  • 43.Thomas MN, Kufeldt J, Kisser U, Hornung HM, Hoffmann J, Andraschko M, et al. Effects of malnutrition on complication rates, length of hospital stay, and revenue in elective surgical patients in the G-DRG-system. Nutrition. 2016;32(2):249–254. doi: 10.1016/j.nut.2015.08.021. [DOI] [PubMed] [Google Scholar]
  • 44.Kang MC, Kim JH, Ryu SW, Moon JY, Park JH, Park JK, et al. Prevalence of malnutrition in hospitalized patients: a multicenter Cross-sectional study. J Korean Med Sci. 2018;33(2):e10. doi: 10.3346/jkms.2018.33.e10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Correia MI, Waitzberg DL. The impact of malnutrition on morbidity, mortality, length of hospital stay and costs evaluated through a multivariate model analysis. Clin Nutr. 2003;22(3):235–239. doi: 10.1016/S0261-5614(02)00215-7. [DOI] [PubMed] [Google Scholar]
  • 46.Nishiyama VKG, Albertini SM, Moraes C, Godoy MF, Netinho JG. Malnutrition and clinical outcomes in surgical patients with colorectal disease. Arq Gastroenterol. 2018;55(4):397–402. doi: 10.1590/S0004-2803.201800000-85. [DOI] [PubMed] [Google Scholar]
  • 47.Ovesen L, Hannibal J, Mortensen EL. The interrelationship of weight loss, dietary intake, and quality of life in ambulatory patients with cancer of the lung, breast, and ovary. Nutr Cancer. 1993;19(2):159–167. doi: 10.1080/01635589309514246. [DOI] [PubMed] [Google Scholar]
  • 48.Ghelfi F, Tieri M, Gori S, Nicolis F, Petrella MC, Filiberti A, et al. Do cancer patients change their diet in the e-health information era? A review of the literature and a survey as a proposal for the Italian population. Food Res Int. 2018;104:59–68. doi: 10.1016/j.foodres.2017.10.021. [DOI] [PubMed] [Google Scholar]
  • 49.Grace EM, Shaw C, Lalji A, Mohammed K, Andreyev HJN, Whelan K. Nutritional status, the development and persistence of malnutrition and dietary intake in oesophago-gastric cancer: a longitudinal cohort study. J Hum Nutr Diet. 2018;31(6):785–792. doi: 10.1111/jhn.12588. [DOI] [PubMed] [Google Scholar]
  • 50.Ravasco P, Monteiro-Grillo I, Camilo M. Individualized nutrition intervention is of major benefit to colorectal cancer patients: long-term follow-up of a randomized controlled trial of nutritional therapy. Am J Clin Nutr. 2012;96(6):1346–1353. doi: 10.3945/ajcn.111.018838. [DOI] [PubMed] [Google Scholar]
  • 51.Poulsen GM, Pedersen LL, Osterlind K, Baeksgaard L, Andersen JR. Randomized trial of the effects of individual nutritional counseling in cancer patients. Clin Nutr. 2014;33(5):749–753. doi: 10.1016/j.clnu.2013.10.019. [DOI] [PubMed] [Google Scholar]
  • 52.Baldwin C, Spiro A, Ahern R, Emery PW. Oral nutritional interventions in malnourished patients with cancer: a systematic review and meta-analysis. J Natl Cancer Inst. 2012;104(5):371–385. doi: 10.1093/jnci/djr556. [DOI] [PubMed] [Google Scholar]
  • 53.Cereda E, Cappello S, Colombo S, Klersy C, Imarisio I, Turri A, et al. Nutritional counseling with or without systematic use of oral nutritional supplements in head and neck cancer patients undergoing radiotherapy. Radiother Oncol. 2018;126(1):81–88. doi: 10.1016/j.radonc.2017.10.015. [DOI] [PubMed] [Google Scholar]
  • 54.Kufeldt J, Viehrig M, Schweikert D, Fritsche A, Bamberg M, Adolph M. Treatment of malnutrition decreases complication rates and shortens the length of hospital stays in a radiation oncology department. Strahlenther Onkol. 2018;194(11):1049–1059. doi: 10.1007/s00066-018-1360-9. [DOI] [PubMed] [Google Scholar]
  • 55.Tanaka N, Takeda K, Kawasaki Y, Yamane K, Teruya Y, Kodani M, et al. Early intensive nutrition intervention with dietary counseling and Oral nutrition supplement prevents weight loss in patients with advanced lung Cancer receiving chemotherapy: a clinical prospective study. Yonago Acta Med. 2018;61(4):204–212. doi: 10.33160/yam.2018.12.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Hiesmayr M, Schindler K, Pernicka E, Schuh C, Schoeniger-Hekele A, Bauer P, et al. Decreased food intake is a risk factor for mortality in hospitalised patients: the NutritionDay survey 2006. Clin Nutr. 2009;28(5):484–491. doi: 10.1016/j.clnu.2009.05.013. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data may be obtained from the corresponding author.


Articles from Medical Oncology (Northwood, London, England) are provided here courtesy of Springer

RESOURCES