Abstract
Background
Patients with early stage (I–IIIA) nonsmall cell lung cancer (NSCLC) are typically treated via surgery, often accompanied by (neo-)adjuvant therapy. These interventions impose a significant burden on patients and potentially impact their physical functioning (PF). The impact on PF remains uncertain and existing evidence has not yet been systematically outlined.
Objective
This scoping review aimed to synthesise evidence concerning the effects of lung surgery, with or without (neo-)adjuvant therapy, on the PF of patients with NSCLC.
Methods
PubMed, Web of Science and Cochrane databases were systematically searched from inception until 1 July 2023. A comprehensive framework based on the International Classification of Functioning, Disability, and Health was used to define various aspects of PF. Longitudinal studies, reporting PF prior to and after NSCLC treatment, and cross-sectional studies reporting PF after treatment were included.
Results
85 included studies assessed the effects of surgery with (n=7) or without (n=78) (neo-) adjuvant therapy on body function (n=29), activity (n=67) and/or participation (n=15). 98% of reported outcomes within the longitudinal studies indicate a decline in PF, with 52% demonstrating significant deteriorations, with follow-up times ranging from immediately post-operative up to 1 year after treatment. Cross-sectional studies show impaired PF in 71% of reported outcomes.
Conclusion
PF of patients with NSCLC tends to deteriorate following lung surgery, irrespective of additional (neo-)adjuvant therapy. While the negative impact of lung surgery on ICF categories of “body function” and “activity” have been described to some depth, insights into the impact on “participation” are lacking.
Shareable abstract
The physical functioning of patients with NSCLC tends to deteriorate after lung surgery. While the impact on ICF categories of “body function” and “activity” have been described to some depth, insights into the impact on “participation” are lacking. https://bit.ly/4hIoppV
Introduction
Lung cancer is the leading cause of cancer-related death worldwide, both in men and women [1–3]. According to the World Health Organization, lung cancer accounts for 2.2 million new cases annually, representing 11.7% of all cancer cases, and 1.8 million deaths, representing approximately one-fifth of all cancer-related deaths [1, 3, 4]. Nonsmall cell lung cancer (NSCLC) is the most common subtype of lung cancer, comprising approximately 85% of all cases [5]. A significant proportion of these patients (39%) are diagnosed with early-stage NSCLC (I–IIIA) [5]. Surgery is the preferred treatment option for early-stage NSCLC in fit patients without contraindications in lung function and cardiac health, and with tumours deemed resectable in terms of pulmonary and cardiac functionality [5]. While surgery carries risks inherent to any surgical procedure, advances in surgical techniques and perioperative care have significantly improved outcomes, allowing patients to experience extended survival and improved quality of life post-surgery [6]. Often, surgical interventions are accompanied by (neo-)adjuvant therapy such as chemotherapy, radiotherapy and/or immunotherapy [7].
Surgery with or without (neo-)adjuvant therapy is likely to have a negative impact on physical functioning (PF), including exercise capacity and activities of daily living [8]. However, the precise impact of different treatment strategies on different dimensions of PF has not yet been systematically summarised. This information is crucial to design optimal nonpharmacological strategies (e.g., pulmonary rehabilitation) to counteract these complications. Theoretical models such as the International Classification of Functioning, Disability, and Health (ICF) [9] offer a valuable framework to investigate and describe the impact of cancer treatment on the entire spectrum of PF. This classification comprises three categories of health condition, as follows: 1) bodily function or structure (impairment); 2) activities (limitation); and 3) participation (restriction).
Hence, this scoping review aims to systematically summarise the existing scientific literature investigating the impact of lung surgery, with or without (neo-)adjuvant therapy, on different aspects of PF in patients with NSCLC, utilising the ICF framework as a guiding structure.
Methods
This review followed the updated methodological framework to conduct scoping reviews proposed by Peters et al. [10] and is reported according to the Preferred Reporting Items for Systematic reviews and Meta-analyses extension for Scoping Reviews (PRISMA-ScR) checklist guidelines [11].
Selection criteria
Studies were included if they met the following criteria: 1) involved patients diagnosed with NSCLC, who underwent surgery with or without (neo-)adjuvant therapy (chemo-, radio- and/or immunotherapy); 2) included at least one type of PF assessment at baseline and after NSCLC treatment or solely after treatment, with long-term follow-up periods allowed; 3) were randomised controlled trials (including a control group receiving standard care, these data were used in the current work), observational studies or case series (with a sample size greater than 10); and 4) were published in English.
Search strategy and screening
Two researchers (S.H. and E.A.) conducted a systematic electronic literature search of the PubMed, Web of Science and Cochrane databases from inception until 1 July 2023. The comprehensive search strategy is presented in table S1. Identified references were managed using EndNote X9, an electronic library, where duplicates were identified and removed. Further screening of articles was conducted using Covidence®, an online systematic review software (Veritas Health Innovation, Melbourne, Australia; available at www.covidence.org), by four researchers (S.H., E.A., D.C. and K.Q.). The screening of titles and abstracts followed a conservative approach, excluding only studies that clearly did not meet the criteria. Full-text screening was independently conducted by two researchers (S.H. and E.A.) and any discrepancies were resolved through consensus-based discussion. Authors of studies were contacted via e-mail if no full text was available.
Data extraction
A customised data collection tool in Covidence® and a data extraction table in Microsoft® Excel (Microsoft, Redmond, Washington, USA) were developed to extract the most relevant information from the included studies and facilitate their subsequent analysis and interpretation. S.H. and E.A. conducted the data extraction. A structured table in the supplementary material (table S2) includes details such as author information, publication year, country, study design, sample size, baseline characteristics (age, sex, type and stage of NSCLC, and treatment specifics), assessments of PF (tools used and timing; in cases of multiple post-treatment assessments, only the first assessment was extracted and described) and primary results. Authors of studies where no statistical analysis of the relevant data was presented in the results were contacted via e-mail.
Representation of results
The results are organised according to the ICF classification, treatment type and timing of assessment. First, results are presented in accordance with the subclassification of ICF [9, 12]. Various measures pertaining to body function, activity and participation relevant for patients with NSCLC were incorporated. Second, studies were categorised based on treatment type into “surgery” or “surgery with (neo-)adjuvant treatment”. Studies where more than 30% of the included sample received both surgery and (neo-)adjuvant therapy are classified under “surgery with (neo-)adjuvant therapy”. Further, results are categorised based on timing of assessment into “before versus after treatment” or “after treatment”. After treatment, impairments or limitations are defined if outcomes are lower than 80% of their predicted values or if the study defined the outcome as impaired. A comprehensive overview of the used classifications is included in table S3. Lastly, a subgroup analysis based on treatment type was performed. Studies were categorised as either minimally invasive (video-assisted thoracic surgery (VATS) or robotic-assisted thoracoscopic surgery (RATS)), or invasive procedures (traditional thoracotomy), with studies that combine both approaches excluded from the analysis. A summary of this analysis is provided in the supplementary material (figures S1 and S2).
Results
Search results
The initial literature search yielded a total of 12 867 records, which was reduced to 12 229 after elimination of duplicates. Among these, 11 795 records were excluded during the title and abstract screening phase. Subsequently, 434 remaining articles underwent full-text screening, resulting in the inclusion of 85 articles for this scoping review. The screening process is visually depicted in the flowchart (figure 1).
FIGURE 1.
Flowchart of the search results.
General characteristics
The 85 included studies, conducted between 1987 and 2023, assessed the effects of surgery with (n=7) or without (n=78) (neo-)adjuvant therapy on body function (n=32), activity (n=67) and/or participation (n=16) in patients with NSCLC.
ICF classification
Various measures pertaining to body function, activity and participation were identified. An overview can be found in figure 2. A comprehensive summary of the measurement tools used, along with the number of studies included and their corresponding sample sizes, is provided in table S4.
FIGURE 2.
Flowchart of the International Classification of Functioning, Disability, and Health (ICF) classification and outcome measures. 5STS: 5-sit-to-stand test; 6MWD: 6-min walk distance; 6MWT: 6-min walk test; BIA: bioelectrical impedance analysis; BMI: body mass index; CPET: cardiopulmonary exercise testing; CST: chair stand test; CT: computed tomography; DEXA: dual-energy X-ray absorptiometry; ECOG: Eastern Cooperative Oncology Group performance status; HGS: hand grip strength; ISWT: incremental shuttle walk test; KPS: Karnofsky performance status; LIPA: light-intensity physical activity; MM: muscle mass; MEP: maximal expiratory pressure; MIP: maximal inspiratory pressure; MVPA: moderate-to-vigorous physical activity; QMF: quadriceps muscle force; SRT: stair run test; TUG: timed up-and-go test; UULEX: Upper-Body Ultraportable Exercise; VʹO2max: maximal oxygen uptake; Wmax: maximal work rate.
An overview of the findings for different PF components can be found in figure 3 (before- versus after-treatment measurement) and figure 4 (only after-treatment measurement). For a detailed outline of the general characteristics of the included studies, please refer to table S2. The subgroup analysis based on treatment type can be found in figures S1 and S2.
FIGURE 3.
Physical functioning components before versus after treatment. Note: the fractions give the number of significant deteriorations divided by the total. BW: body weight; Kgf: kilogram-force; rep: repetition
FIGURE 4.
Physical functioning components after treatment. Note: the fractions give the number of impaired outcomes divided by the total. rep: repetition.
Body function
Components of PF measurements that were included in the ICF category “body function” (n=29) are body composition (n=10), peripheral muscle function (n=14) and respiratory muscle function (n=9).
Surgery
Before versus after treatment
20 studies focused on body function outcomes, with follow-up ranging from post-operative day 2 up to 1 year post-surgery. Most research is available on peripheral muscle function (n=9) [13–21] and respiratory muscle function (n=8) [16, 17, 22–27]. All studies investigating quadriceps muscle function (n=8) [13–20] found a deterioration (of which five statistically significant [16–20]), ranging from −1.6% to −27.0%. Of the three studies investigating handgrip strength [18–20], two studies concluded a statistically significant deterioration overall [18, 20] and one study only demonstrated a significant deterioration in the group with a high risk of developing postoperative pulmonary complications [19]. Bicep muscle strength [21] and upper limb endurance [19] were only investigated in one study, concluding a statistically significant deterioration for both measurements. For maximal inspiratory pressure (n=8) [16, 17, 22–27], all studies showed a deterioration, ranging from −1.2% to −29.3%. Of these, two studies were statistically significant [17, 27] and two studies only showed a significant deterioration in the conventional posterolateral thoracotomy group [16] and the wedge resection group [26]. For maximal expiratory pressure (n=8) [16, 17, 22–27], seven studies showed a deterioration [16, 17, 22–25, 27], ranging from −2.9 to −21.0%. Of these, two were statistically significant [17, 27] and one study only showed a significant deterioration in the conventional posterolateral thoracotomy group [16]. Within research on body composition (n=5) [28–32], thoracic muscle mass was only investigated in one study, concluding a statistically significant deterioration [29]. Lumbar muscle mass was investigated in two studies, both concluding a deterioration (without specified p-value) [30, 31]. Two studies investigated body weight [28, 32], both concluding an increase of which one is statistically significant [28].
In summary, 91% (32/35 results) of the results indicate a deterioration of body function outcomes, with 49% (17/35 results) demonstrating significant deteriorations. 9% (3/35 results) found an improvement.
After treatment
Six studies focused on body function outcomes, ranging from post-operative day 1 up to 1 year after surgery. Within body composition (n=2) [32, 33], body mass index is investigated in those two studies [32, 33], of which one study found an impairment [32]. Within peripheral muscle function (n=3) [34–36], quadriceps muscle function is investigated in three studies [34–36], of which one study found an impairment [36]. Handgrip strength is investigated in one study and found no impairment [34]. Within respiratory muscle function (n=1) [37], maximal inspiratory pressure and maximal expiratory pressure were only investigated in one study [37], concluding an impairments in both.
In summary, 50% (4/8) of the results found an impairment of body function outcomes after surgery.
Surgery with (neo-)adjuvant therapy
Before versus after treatment
Two studies focused on body function outcomes, ranging from post-operative day 1 up to 4–6 weeks after treatment, with research on body composition (n=2) [38, 39] and peripheral muscle function (n=1) [38]. Body mass index is only investigated in one study, concluding a deterioration (without a specified p-value) [39]. One study focused on muscle cross-sectional area and quadriceps muscle function and reported a statistically significant deterioration in both outcomes [38].
In summary, 100% (3/3 results) of the results indicate a deterioration of body function outcomes, with 67% (2/3 results) demonstrating significant deteriorations.
After treatment
One study focused on body function outcomes, 4–6 weeks after treatment, in body composition and peripheral muscle function (n=1) [40]. This study found no impairment in lean mass, quadriceps muscle function and handgrip strength.
Activity
Components of PF measurements that were included in the ICF category “activity” (n=67) are functional exercise capacity (n=46) and maximal exercise capacity (n=27).
Surgery
Before versus after treatment
52 studies focused on activity outcomes, ranging from post-operative day 1 up to 1 year after surgery. Most research is available on functional exercise capacity (n=35) [13–15, 17–21, 24, 25, 27, 41–64]. For the 6-min walked distance (n=28) [13, 15, 17, 18, 20, 21, 24, 25, 27, 41–59], all studies showed a deterioration when comparing post- to pre-measurements, of which eight were statistically significant [13, 15, 17, 18, 20, 21, 27, 59], ranging from −1.9% to −34.1%. The four studies investigating time of the stair-climb test [58, 62–64] all found a deterioration, of which two were statistically significant [58, 64]. Two studies investigated the repetitions of the 30-s chair–stand test, and showed both a statistically significant deterioration [21, 61]. Two studies investigated the walked distance of the incremental shuttle walk test and both showed a deterioration [14, 60], of which one is statistically significant [60]. Results of the timed up-and-go and five-repetitions sit-to-stand tests were only investigated in two [20, 61] and one [19] studies, respectively, all concluding a statistically significant deterioration.
Research on maximal exercise capacity (n=21) all found a deterioration. For maximal oxygen consumption (n=19) [20, 22, 26, 40, 62–76], 12 studies showed a statistically significant deterioration [22, 40, 64, 68–76] and one study only demonstrated a significant deterioration in the group with nonwedge resection [26] ranging from −11.9% to −30.0%. For maximal work rate (n=11) [16, 22, 26, 64, 66–70, 72, 77], nine studies showed a statistically significant deterioration [16, 22, 26, 64, 68–70, 72, 77], ranging from −12.4% to −27.0%.
In summary, 100% (69/69 results) of the results indicate a deterioration of activity outcomes, with 55% (38/69 results) demonstrating significant deteriorations.
After treatment
Nine studies focused on activity outcomes, ranging from post-operative day 1 up to 1 year after surgery. Within functional exercise capacity (n=8) [32, 34–36, 39, 78–80], five studies investigated 6-min walked distance [34, 35, 78–80], of which three found an impairment [34, 35, 80]. All other studies reported results that were impaired in time of timed up and go (n=1) [32], gait (n=1) [36] and balance (n=1) [36]. Within maximal exercise capacity (n=4) [34, 35, 78, 81], all studies reported impaired results in maximal oxygen consumption (n=4) [34, 35, 78, 81] and maximal work rate (n=3) [34, 35, 78]. In summary, 87% (13/15 results) of the results found an impairment in activity outcomes.
Surgery with (neo-)adjuvant therapy
Before versus after treatment
Four studies focused on activity outcomes, from post-operative day 1 up to 8–10 weeks after surgery. Within functional exercise capacity (n=2) [82, 83], two studies investigating 6-min walked distance found both a deterioration [82, 83], of which one was statistically significant [83]. Within maximal exercise capacity (n=2) [39, 84], maximal oxygen consumption (n=2) [39, 84] and maximal work rate (n=1) [84] all showed a deterioration (without a specified p-value).
In summary, 100% (5/5 results) of the results indicate a deterioration of body function outcomes, with 20% (1/5 results) demonstrating a significant deterioration.
After treatment
One study focused on activity outcomes, 4–6 weeks post-treatment, in functional exercise capacity (n=1) [39]. This study found no impairment in the number of steps in the stair run test and repetitions of the 30-s chair–stand test.
Participation
Components of PF measurements that were included in the ICF category “participation” (n=15) are performance status (n=4) and objectively measured physical activity (n=11).
Surgery
Before versus after treatment
Seven studies focused on participation outcomes, from post-operative day 5 up to 2 months post-surgery. Objectively measured physical activity is investigated in five studies [14, 85–88]. Light-intensity physical activity is investigated in two studies, both showing a deterioration [87, 88], of which one is statistically significant [87]. Moderate-to-vigorous-intensity physical activity is only investigated in one study, concluding a statistically significant deterioration [87]. For total activity (n=3) [14, 87, 88], all studies found a deterioration, of which two were statistically significant [87, 88]. Sedentary time is only investigated in one study, showing a statistically nonsignificant deterioration [88]. Research on daily total steps (n=2) [85, 86], time of aerobic activity (n=1) [85] and daily walked distance (n=1) [85] all concluded a deterioration, without a specified p-value.
Within research on performance status (n=2) [27, 33], Karnofsky performance status and Eastern Cooperative Oncology Group (ECOG) score were both investigated in only one study, concluding a statistically significant deterioration [27] and a deterioration without a specified p-value [33] respectively.
In summary, 100% (13/13) of the results indicate a deterioration of participation outcomes, with 38% (5/13 results) demonstrating significant deteriorations.
After treatment
Seven studies focused on participation outcomes, ranging from post-operative day 1 up to 3 months post-treatment. Within research on objectively measured physical activity (n=5) [89–93], a limitation was found in moderate-to-vigorous physical activity (n=4) [89–92], total activity (n=1) [89] and sedentary time (n=4) [89–92]. Of the five studies investigating daily total steps [89–93], four studies showed a low physical activity [89, 91–93]. Light-intensity physical activity is investigated in four studies [89–92], of which three found a limitation [89, 90, 92].
Within research on performance status (n=2) [32, 33], Karnofsky performance status and ECOG were both investigated in one study, showing an impairment [32] and no impairment [33].
In summary, 85% (17/20) of the results found an impairment of participation outcomes.
Surgery with (neo-)adjuvant therapy
Before versus after treatment
One study focused on participation outcomes, 1 month post-treatment, in objectively measured physical activity [82]. This study found a statistically significant deterioration in light-intensity physical activity, moderate-to-vigorous-intensity physical activity, total activity and sedentary behaviour.
After treatment
No studies focusing on participation outcomes were found.
Discussion
This scoping review summarises the scientific literature investigating the impact of lung surgery with or without (neo-)adjuvant therapy on PF in patients with NSCLC.
The PF of patients with NSCLC tends to deteriorate following lung surgery, whether or not (neo-) adjuvant treatment is administered. The vast majority of studies showed a decline in many of the reported outcomes, across several ICF domains, from immediately post-operative up to 1 year after treatment.
Body weight is the only component showing a significant increase following surgery. However, this increase might be a sign of the development of oedema [28]. Weight gain due to oedema is a known complication of major surgical procedures, with an incidence rate as high as 40% [28]. However, with the recent advances in endoscopic instruments and operative techniques, lung resection surgery has become less invasive and oedema is less likely to occur [28].
The timing of assessment varied substantially among the different papers. As time emerges as a crucial factor, an attempt was made to standardise the timing of assessment by selecting and representing the earliest measurement moment from each paper. While there is likely spontaneous recovery over time, uncertainty remains regarding the extent of this recovery [18]. For instance, Edvardsen et al. [39] noted an improvement in lean mass, handgrip strength, stair climb test and 30-s chair–stand test 25–27 weeks after lung surgery, compared to pre-surgery values.
In addition to the substantial variation in assessment timing, most studies focus on assessments that fall within one single subcategory of the ICF classification, complicating the assessment of the overall impact of surgery with or without (neo-)adjuvant treatment on total PF. Within assessments classified under the subcategory “body function”, a differentiation can be made between body composition and muscle function. While body composition results remain unclear, both peripheral muscle function and respiratory muscle function demonstrate a decline following surgery with or without (neo-)adjuvant therapy. Assessments categorised in the subcategory of “activity” are predominant indicating a consistent negative impact of surgery with or without (neo-)adjuvant treatment on functional and maximal exercise capacity. There is a notable absence of objectively measured physical activity, falling under the subcategory of “participation”. This gap hinders our ability to gain insight into the impact of treatment on the daily activities of patients and their involvement in life situations.
Similarly, only few studies have examined objectively measured physical activity levels after breast cancer surgery, concluding significantly decreased physical activity post-surgery [94]. Interestingly, based on self-report, patients with breast cancer had significantly lower total physical activity levels in the year prior to surgery compared to a reference population [95]. In addition, about 25% of colorectal cancer patients managed to increase their physical activity levels from diagnosis to 6 months post-surgery [96].
Additionally, few studies in this review investigate the potential additional impact of (neo-)adjuvant therapies on the PF of patients, as the majority of studies recruited patients undergoing surgery without (neo-)adjuvant therapy. However, adjuvant treatment has been recommended for patients in order to minimise the chance of postoperative recurrence and adjuvant chemotherapy has been associated with better overall survival [97]. The potential added burden of adjuvant treatment on PF requires further insight to guide physicians in making informed decisions regarding adjuvant therapies. In other cancer populations, the extent of change in PF varies depending on the treatment modalities used for (neo-)adjuvant therapy [98]. However, more high-quality studies are needed to further understand the impact of (neo-)adjuvant therapies [99].
A key limitation of this review is its broad and generic scope. First, several factors likely influence the impact of surgical procedures on PF, including the degree of surgery (pneumonectomy, lobectomy, segmentectomy and atypical resection), the extent of resection, time since the resection, age and comorbidities. A subgroup analysis was conducted based on the type of surgery (minimally invasive VATS or RATS), or more invasive (traditional thoracotomy), showing a similar impact on PF. In many results, statistical data is unavailable because these analyses were not performed in the original studies. It is also important to note that 98% of the findings point to a deterioration in PF, though not all are statistically significant. Therefore, the lack of statistical analyses or significance levels means this subgroup analysis does not alter the conclusions of the manuscript, as no additional details on the magnitude or significance of this deterioration can be provided. Further subanalyses could not be performed, largely due to the absence of detailed subgroup analyses and the heterogeneity of the included patient populations
Certain limitations also persist regarding the role of time since surgery. Time frames used to assess outcomes varied significantly across studies, with some assessing outcomes days post-surgery, while others spanned weeks, months or even up to a year. An attempt was made to standardise timing by selecting the earliest measurement moment from each paper, but the substantial heterogeneity and lack of detailed subsample data prevented a more detailed analysis based on time frames.
Recommendations for clinical practice and future research
The impact of lung surgery, with or without (neo-)adjuvant therapy, on PF in patients with NSCLC is a complex interplay of surgical and medical interventions. While these treatments significantly improve survival rates, they also pose challenges to physical well-being. In light of these challenges, there is a clear need for focus on nonmedical treatment of these patients. This scoping review reveals that 98% of the results demonstrate a decline over time and 71% show an impairment compared to reference values in PF following surgery, with or without (neo-)adjuvant therapy. This finding underscores the need for comprehensive rehabilitation strategies to optimise patient outcomes [100]. Pulmonary rehabilitation is imperative and plays a crucial role in restoring and maintaining PF [100]. Effective rehabilitation strategies are vital to mitigate the impact of surgery and (neo-)adjuvant therapy, enabling patients to regain and maintain optimal PF throughout their cancer journey [101]. Tailored rehabilitation plans should be designed to address the unique needs of each patient, considering the extent of surgery, the type of (neo-)adjuvant therapy and individual health status, as PF among NSCLC survivors is influenced by these factors.
Future research should focus on insights into the impact of lung surgery on the ICF subcategory “participation” and the additional impact of (neo-)adjuvant therapies on PF.
Methodological considerations
A thorough systematic search and screening was performed, and the most well-established guideline for the conductance of scoping reviews (PRISMA-ScR) was followed. Nevertheless, several concepts have been used to define PF and numerous tools were designed to assess the different aspects of this comprehensive measure. To ensure clarity, this work followed a previously published assessment framework for PF [12].
The literature on this topic is markedly heterogeneous. The lack of detailed characteristics of the studied population is a challenge. Often, results are not presented separated when (neo-)adjuvant therapy is used, making it difficult to distinguish the specific effects of surgery and the effects of (neo-)adjuvant therapy on PF. As a result, there are only few findings available in this category “surgery with (neo-)adjuvant therapy”. Also, there is no continuity in the timing of assessment, making comparisons of results challenging. There is a lack of consensus on outcome measures and measurement tools used for assessing PF. Therefore, to structure the results, they are organised according to the ICF classification and in case of multiple post-treatment assessments, only the earliest assessment has been extracted and described. However, as a consequence, the analysis of the effects of different NSCLC treatments on PF was found to be challenging due to this diversity. All these aspects have hampered results synthesis and the draw of more definitive conclusions.
Several of the included studies are randomised controlled trials, providing data for a control group receiving standard care. However, this setup posed challenges in relevant data extraction, as these studies primarily focused on within-group results. Furthermore, sample size is low in many studies.
Conclusion
The PF of patients with NSCLC tends to deteriorate following lung surgery, whether or not (neo-)adjuvant treatment is administered, from immediately post-operative up to 1 year after treatment. While the negative impact of lung surgery on ICF categories of “body function” and “activity” have been described to some depth, insights into the impact on the “participation” subcategory are lacking.
Footnotes
Provenance: Submitted article, peer reviewed.
Conflict of interest: All authors have nothing to disclose.
Supplementary material
Please note: supplementary material is not edited by the Editorial Office, and is uploaded as it has been supplied by the author.
Supplementary table S1-S4 ERR-0156-2024.SUPPLEMENT (1MB, pdf)
Supplementary figures S1 and S2 ERR-0156-2024.SUPPLEMENT2 (122.9KB, pdf)
References
- 1.Noone A-M, Cronin KA, Altekruse SF, et al. Cancer incidence and survival trends by subtype using data from the surveillance epidemiology and end results program, 1992–2013. Cancer Epidemiol Biomark Prevent 2017; 26: 632–641. doi: 10.1158/1055-9965.EPI-16-0520 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018; 68: 394–424. doi: 10.3322/caac.21492 [DOI] [PubMed] [Google Scholar]
- 3.Ferlay J, Colombet M, Soerjomataram I, et al. Cancer statistics for the year 2020: an overview. Int J Cancer 2021; 149: 778–789. doi: 10.1002/ijc.33588 [DOI] [PubMed] [Google Scholar]
- 4.Sung H, Ferlay J, Siegel RL, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71: 209–249. doi: 10.3322/caac.21660 [DOI] [PubMed] [Google Scholar]
- 5.Godoy LA, Chen J, Ma W, et al. Emerging precision neoadjuvant systemic therapy for patients with resectable non-small cell lung cancer: current status and perspectives. Biomark Res 2023; 11: 7. doi: 10.1186/s40364-022-00444-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Kidane B, Bott M, Spicer J, et al. The American Association for Thoracic Surgery (AATS) 2023 expert consensus document: staging and multidisciplinary management of patients with early-stage non-small cell lung cancer. J Thorac Cardiovasc Surg 2023; 166: 637–654. doi: 10.1016/j.jtcvs.2023.04.039 [DOI] [PubMed] [Google Scholar]
- 7.Hopstaken JS, de Ruiter JC, Damhuis RAM, et al. Stage I non-small cell lung cancer: treatment modalities, Dutch daily practice and future perspectives. Cancer Treat Res Commun 2021; 28: 100404. doi: 10.1016/j.ctarc.2021.100404 [DOI] [PubMed] [Google Scholar]
- 8.Lemjabbar-Alaoui H, Hassan OU, Yang YW, et al. Lung cancer: biology and treatment options. Biochim Biophys Acta 2015; 1856: 189–210. doi: 10.1016/j.bbcan.2015.08.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Vargus-Adams, JN, Majnemer A. International Classification of Functioning, Disability and Health (ICF) as a framework for change: revolutionizing rehabilitation. J Child Neurol 2014; 29: 1030–1035. doi: 10.1177/0883073814533595. [DOI] [PubMed] [Google Scholar]
- 10.Peters MD, Marnie C, Tricco AC, et al. Updated methodological guidance for the conduct of scoping reviews. JBI Evid Synth 2020; 18: 2119–2126. doi: 10.11124/JBIES-20-00167 [DOI] [PubMed] [Google Scholar]
- 11.Tricco AC, Lillie E, Zarin W, et al. PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med 2018; 169: 467–473. doi: 10.7326/M18-0850 [DOI] [PubMed] [Google Scholar]
- 12.Caspersen CJ, Powell KE, Christenson GM. Physical activity, exercise, and physical fitness: definitions and distinctions for health-related research. Public Health Rep 1985; 100: 126–131. [PMC free article] [PubMed] [Google Scholar]
- 13.Arbane G, Tropman D, Jackson D, et al. Evaluation of an early exercise intervention after thoracotomy for non-small cell lung cancer (NSCLC), effects on quality of life, muscle strength and exercise tolerance: randomised controlled trial. Lung Cancer 2011; 71: 229–234. doi: 10.1016/j.lungcan.2010.04.025 [DOI] [PubMed] [Google Scholar]
- 14.Arbane G, Douiri A, Hart N, et al. Effect of postoperative physical training on activity after curative surgery for non-small cell lung cancer: a multicentre randomised controlled trial. Physiotherapy 2014; 100: 100–107. doi: 10.1016/j.physio.2013.12.002 [DOI] [PubMed] [Google Scholar]
- 15.Iwai K, Komada R, Ohshio Y, et al. Evaluation of predictive factors related to the presence or absence of supplemental oxygen therapy and comparison of physical functions after video-assisted thoracic surgery. Nagoya J Med Sci 2021; 83: 801–810. doi: 10.18999/nagjms.83.4.801 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Ziyade S, Baskent A, Tanju S, et al. Isokinetic muscle strength after thoracotomy: standard vs. muscle-sparing posterolateral thoracotomy. Thorac Cardiovasc Surg 2010; 58: 295–298. doi: 10.1055/s-0030-1249829 [DOI] [PubMed] [Google Scholar]
- 17.Maruyama R, Tanaka J, Kitagawa D, et al. Physical assessment immediately after lobectomy via miniposterolateral thoracotomy assisted by videothoracoscopy for non-small cell lung cancer. Surg Today 2011; 41: 908–913. doi: 10.1007/s00595-010-4372-3 [DOI] [PubMed] [Google Scholar]
- 18.Oikawa M, Hanada M, Nagura H, et al. Factors influencing functional exercise capacity after lung resection for non–small cell lung cancer. Integr Cancer Ther 2020; 19: 153473542092338. doi: 10.1177/1534735420923389 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Rodríguez-Torres J, Cabrera-Martos I, López-López L, et al. Reduced exercise capacity and self-perceived health status in high-risk patients undergoing lung resection. World J Crit Care Med 2021; 10: 232–243. doi: 10.5492/wjccm.v10.i5.23 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Anami K, Horie J, Hirayama Y, et al. Changes in exercise tolerance and quality of life are unrelated in lung cancer survivors who undergo video-assisted thoracic surgery. J Phys Ther Sci 2018; 30: 467–473. doi: 10.1589/jpts.30.467 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Sebio García R, Yáñez-Brage MI, Giménez Moolhuyzen E, et al. Preoperative exercise training prevents functional decline after lung resection surgery: a randomized, single-blind controlled trial. Clin Rehabil 2017; 31: 1057–1067. doi: 10.1177/0269215516684179 [DOI] [PubMed] [Google Scholar]
- 22.Messaggi-Sartor M, Marco E, Martínez-Téllez E, et al. Combined aerobic exercise and high-intensity respiratory muscle training in patients surgically treated for non-small cell lung cancer: a pilot randomized clinical trial. Eur J Phys Rehabil Med 2019; 55: 113–122. doi: 10.23736/S1973-9087.18.05156-0 [DOI] [PubMed] [Google Scholar]
- 23.Nomori H, Horio H, Suemasu K. Comparison of short-term versus long-term epidural analgesia after limited thoracotomy with special reference to pain score, pulmonary function, and respiratory muscle strength. Surg Today 2001; 31: 191–195. doi: 10.1007/s005950170167 [DOI] [PubMed] [Google Scholar]
- 24.Nomori H, Horio H, Naruke T, et al. What is the advantage of a thoracoscopic lobectomy over a limited thoracotomy procedure for lung cancer surgery? Ann Thorac Surg 2001; 72: 879–884. doi: 10.1016/S0003-4975(01)02891-0 [DOI] [PubMed] [Google Scholar]
- 25.Brocki BC, Westerdahl E, Langer D, et al. Decrease in pulmonary function and oxygenation after lung resection. ERJ Open Res 2018; 4: 00055-2017. doi: 10.1183/23120541.00055-2017 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Huang CY, Hsieh MS, Wu YK, et al. Chronic obstructive pulmonary disease assessment test for the measurement of deterioration and recovery of health status of patients undergoing lung surgery. Thorac Cancer 2022; 13: 613–623. doi: 10.1111/1759-7714.14306 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Araújo AS, Nogueira IC, Gomes Neto A, et al. The impact of lung cancer resection surgery on fibrinogen and C-reactive protein and their relationship with patients outcomes: a prospective follow up study. Cancer Biomark 2016; 16: 47–53. doi: 10.3233/CBM-150539 [DOI] [PubMed] [Google Scholar]
- 28.Cagini L, Capozzi R, Tassi V, et al. Fluid and electrolyte balance after major thoracic surgery by bioimpedance and endocrine evaluation. Eur J Cardiothorac Surg 2011; 40: e71–e76. doi: 10.1016/j.ejcts.2011.03.030 [DOI] [PubMed] [Google Scholar]
- 29.Takamori S, Toyokawa G, Okamoto T, et al. Clinical impact and risk factors for skeletal muscle loss after complete resection of early non-small cell lung cancer. Ann Surg Oncol 2018; 25: 1229–1236. doi: 10.1245/s10434-017-6328-y [DOI] [PubMed] [Google Scholar]
- 30.Nagata M, Ito H, Yoshida T, et al. Risk factors for progressive sarcopenia 6 months after complete resection of lung cancer: what can thoracic surgeons do against sarcopenia? J Thorac Dis 2020; 12: 307–318. doi: 10.21037/jtd.2020.01.44 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Choi J, Yang Z, Lee J, et al. Usefulness of pulmonary rehabilitation in non-small cell lung cancer patients based on pulmonary function tests and muscle analysis using computed tomography images. Cancer Res Treat 2022; 54: 793–802. doi: 10.4143/crt.2021.769 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Koczywas M, Williams AC, Cristea M, et al. Longitudinal changes in function, symptom burden, and quality of life in patients with early-stage lung cancer. Ann Surg Oncol 2013; 20: 1788–1797. doi: 10.1245/s10434-012-2741-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Irie M, Nakanishi R, Yasuda M, et al. Risk factors for short-term outcomes after thoracoscopic lobectomy for lung cancer. Eur Respir J 2016; 48: 495–503. doi: 10.1183/13993003.01939-2015 [DOI] [PubMed] [Google Scholar]
- 34.Cavalheri V, Jenkins S, Cecins N, et al. Impairments after curative intent treatment for non-small cell lung cancer: a comparison with age and gender-matched healthy controls. Respir Med 2015; 109: 1332–1339. doi: 10.1016/j.rmed.2015.08.015 [DOI] [PubMed] [Google Scholar]
- 35.Burtin C, Franssen FME, Vanfleteren LEGW, et al. Lower-limb muscle function is a determinant of exercise tolerance after lung resection surgery in patients with lung cancer. Respirology 2017; 22: 1185–1189. doi: 10.1111/resp.13041 [DOI] [PubMed] [Google Scholar]
- 36.Tough D, Dunning J, Robinson J, et al. Investigating balance, gait, and physical function in people who have undergone thoracic surgery for a diagnosis of lung cancer: a mixed-methods study. Chron Respir Dis 2021; 18: 14799731211052299. doi: 10.1177/14799731211052299 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Jeong J-H, Yoo W-G. Effect of caregiver education on pulmonary rehabilitation, respiratory muscle strength and dyspnea in lung cancer patients. J Phys Ther Sci 2015; 27: 1653–1654. doi: 10.1589/jpts.27.1653 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Salhi B, Huysse W, Van Maele G, et al. The effect of radical treatment and rehabilitation on muscle mass and strength: a randomized trial in stages I–III lung cancer patients. Lung Cancer 2014; 84: 56–61. doi: 10.1016/j.lungcan.2014.01.011 [DOI] [PubMed] [Google Scholar]
- 39.Edvardsen E, Holme I, Nordsletten L, et al. High-intensity training following lung cancer surgery: a randomised controlled trial. Thorax 2015; 70: 244–250. doi: 10.1136/thoraxjnl-2014-205944 [DOI] [PubMed] [Google Scholar]
- 40.Edvardsen E, Anderssen SA, Borchsenius F, et al. Reduction in cardiorespiratory fitness after lung resection is not related to the number of lung segments removed. BMJ Open Sport Exerc Med 2015; 1: e000032. doi: 10.1136/bmjsem-2015-000032 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Nomori H, Watanabe K, Ohtsuka T, et al. Six-minute walking and pulmonary function test outcomes during the early period after lung cancer surgery with special reference to patients with chronic obstructive pulmonary disease. Jpn J Thorac Cardiovasc Surg 2004; 52: 113–119. doi: 10.1007/s11748-004-0126-8 [DOI] [PubMed] [Google Scholar]
- 42.Nomori H, Ohtsuka T, Horio H, et al. Difference in the impairment of vital capacity and 6-minute walking after a lobectomy performed by thoracoscopic surgery, an anterior limited thoracotomy, an anteroaxillary thoracotomy, and a posterolateral thoracotomy. Surg Today 2003; 33: 7–12. doi: 10.1007/s005950300001 [DOI] [PubMed] [Google Scholar]
- 43.Nomori H, Horio H, Suemasu K. Early removal of chest drainage tubes and oxygen support after a lobectomy for lung cancer facilitates earlier recovery of the 6-minute walking distance. Surg Today 2001; 31: 395–399. doi: 10.1007/s005950170128 [DOI] [PubMed] [Google Scholar]
- 44.Chang NW, Lin KC, Lee SC, et al. Effects of an early postoperative walking exercise programme on health status in lung cancer patients recovering from lung lobectomy. J Clin Nurs 2014; 23: 3391–3402. doi: 10.1111/jocn.12584 [DOI] [PubMed] [Google Scholar]
- 45.Andreetti C, Menna C, Ibrahim M, et al. Postoperative pain control: videothoracoscopic versus conservative mini-thoracotomic approach. Eur J Cardiothorac Surg 2014; 46: 907–912. doi: 10.1093/ejcts/ezu092 [DOI] [PubMed] [Google Scholar]
- 46.D'Andrilli A, Maurizi G, Andreetti C, et al. Sleeve lobectomy versus standard lobectomy for lung cancer: functional and oncologic evaluation. Ann Thorac Surg 2016; 101: 1936–1942. doi: 10.1016/j.athoracsur.2015.11.057 [DOI] [PubMed] [Google Scholar]
- 47.Yang M, Zhong JD, Zhang JE, et al. Effect of the self-efficacy-enhancing active cycle of breathing technique on lung cancer patients with lung resection: a quasi-experimental trial. Eur J Oncol Nurs 2018; 34: 1–7. doi: 10.1016/j.ejon.2018.02.009 [DOI] [PubMed] [Google Scholar]
- 48.Liu Z, Qiu T, Pei L, et al. Two-week multimodal prehabilitation program improves perioperative functional capability in patients undergoing thoracoscopic lobectomy for lung cancer: a randomized controlled trial. Anesth Analg 2020; 131: 840–849. doi: 10.1213/ANE.0000000000004342 [DOI] [PubMed] [Google Scholar]
- 49.Li J, Davies M, Ye M, et al. Impact of an animation education program on promoting compliance with active respiratory rehabilitation in postsurgical lung cancer patients: a randomized clinical trial. Cancer Nurs 2021; 44: 106–115. doi: 10.1097/NCC.0000000000000758 [DOI] [PubMed] [Google Scholar]
- 50.Saito H, Shiraishi A, Nomori H, et al. Impact of age on the recovery of six-minute walking distance after lung cancer surgery: a retrospective cohort study. Gen Thorac Cardiovasc Surg 2020; 68: 150–157. doi: 10.1007/s11748-019-01191-7 [DOI] [PubMed] [Google Scholar]
- 51.Menna C, Poggi C, Andreetti C, et al. Does the length of uniportal video-assisted thoracoscopic lobectomy affect postoperative pain? Results of a randomized controlled trial. Thorac Cancer 2020; 11: 1765–1772. doi: 10.1111/1759-7714.13291 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Zou H, Qin Y, Gong F, et al. ABCDEF pulmonary rehabilitation program can improve the mid-term lung function of lung cancer patients after thoracoscopic surgery: a randomized controlled study. Geriatr Nurs 2022; 44: 76–83. doi: 10.1016/j.gerinurse.2021.12.021 [DOI] [PubMed] [Google Scholar]
- 53.Tenconi S, Mainini C, Rapicetta C, et al. Rehabilitation for lung cancer patients undergoing surgery: results of the PUREAIR randomized trial. Eur J Phys Rehabil Med 2021; 57: 1002–1011. doi: 10.23736/S1973-9087.21.06789-7 [DOI] [PubMed] [Google Scholar]
- 54.Chen X, Li C, Zeng L, et al. Comparative efficacy of different combinations of acapella, active cycle of breathing technique, and external diaphragmatic pacing in perioperative patients with lung cancer: a randomised controlled trial. BMC Cancer 2023; 23: 282. doi: 10.1186/s12885-023-10750-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Lu H-B, Ma RC, Yin YY, et al. Clinical indicators of effects of yoga breathing exercises on patients with lung cancer after surgical resection: a randomized controlled trial. Cancer Nurs 2024; 47: E151–E158. doi: 10.1097/NCC.0000000000001208 [DOI] [PubMed] [Google Scholar]
- 56.Stigt JA, Uil SM, van Riesen SJ, et al. A randomized controlled trial of postthoracotomy pulmonary rehabilitation in patients with resectable lung cancer. J Thorac Oncol 2013; 8: 214–221. doi: 10.1097/JTO.0b013e318279d52a [DOI] [PubMed] [Google Scholar]
- 57.Saad IAB, Botega NJ, Toro IFC. Predictors of quality-of-life improvement following pulmonary resection due to lung cancer. Sao Paulo Med J 2007; 125: 46–49. doi: 10.1590/S1516-31802007000100009 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Kubori Y, Matsuki R, Hotta A, et al. Comparison between stair-climbing test and six-minute walk test after lung resection using video-assisted thoracoscopic surgery lobectomy. J Phys Ther Sci 2017; 29: 902–904. doi: 10.1589/jpts.29.902 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Cesario A, Ferri L, Galetta D, et al. Post-operative respiratory rehabilitation after lung resection for non-small cell lung cancer. Lung Cancer 2007; 57: 175–180. doi: 10.1016/j.lungcan.2007.02.017 [DOI] [PubMed] [Google Scholar]
- 60.Win T, Groves AM, Ritchie AJ, et al. The effect of lung resection on pulmonary function and exercise capacity in lung cancer patients. Respir Care 2007; 52: 720–726. [PubMed] [Google Scholar]
- 61.Akezaki Y, Nakata E, Tominaga R, et al. Short-term impact of video-assisted thoracoscopic surgery on lung function, physical function, and quality of life. Healthcare (Basel) 2021; 9: 136. doi: 10.3390/healthcare9020136 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Ozeki N, Fukui T, Iwano S, et al. Factors associated with changes in the 12-m stair-climbing time after lung lobectomy. Gen Thorac Cardiovasc Surg 2021; 69: 282–289. doi: 10.1007/s11748-020-01458-4 [DOI] [PubMed] [Google Scholar]
- 63.Ozeki N, Iwano S, Nakamura S, et al. Chest three-dimensional-computed tomography imaging data analysis for the variation of exercise capacity after lung lobectomy. Clin Physiol Funct Imaging 2022; 42: 362–371. doi: 10.1111/cpf.12777 [DOI] [PubMed] [Google Scholar]
- 64.Brunelli A, Monteverde M, Salati M, et al. Stair-climbing test to evaluate maximum aerobic capacity early after lung resection. Ann Thorac Surg 2001; 72: 1705–1710. doi: 10.1016/S0003-4975(01)03100-9 [DOI] [PubMed] [Google Scholar]
- 65.Corris P, Ellis DA, Hawkins T, et al. Use of radionuclide scanning in the preoperative estimation of pulmonary function after pneumonectomy. Thorax 1987; 42: 285–291. doi: 10.1136/thx.42.4.285 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Van Mieghem W, Demedts M. Cardiopulmonary function after lobectomy or pneumonectomy for pulmonary neoplasm. Respir Med 1989; 83: 199–206. doi: 10.1016/S0954-6111(89)80032-0 [DOI] [PubMed] [Google Scholar]
- 67.Kushibe K, Kawaguchi T, Kimura M, et al. Changes in ventilatory capacity, exercise capacity, and pulmonary blood flow after lobectomy in patients with lung cancer–which lobectomy has the most loss in exercise capacity? Interact Cardiovasc Thorac Surg 2008; 7: 1011–1014. doi: 10.1510/icvts.2008.181255 [DOI] [PubMed] [Google Scholar]
- 68.Nezu K, Kushibe K, Tojo T, et al. Recovery and limitation of exercise capacity after lung resection for lung cancer. Chest 1998; 113: 1511–1516. doi: 10.1378/chest.113.6.1511 [DOI] [PubMed] [Google Scholar]
- 69.Karenovics W, Licker M, Ellenberger C, et al. Short-term preoperative exercise therapy does not improve long-term outcome after lung cancer surgery: a randomized controlled study. Eur J Cardiothorac Surg 2017; 52: 47–54. doi: 10.1093/ejcts/ezx030 [DOI] [PubMed] [Google Scholar]
- 70.Larsen KR, Svendsen UG, Milman N, et al. Cardiopulmonary function at rest and during exercise after resection for bronchial carcinoma. Ann Thorac Surg 1997; 64: 960–964. doi: 10.1016/S0003-4975(97)00635-8 [DOI] [PubMed] [Google Scholar]
- 71.Bobbio A, Chetta A, Carbognani P, et al. Changes in pulmonary function test and cardio-pulmonary exercise capacity in COPD patients after lobar pulmonary resection. Eur J Cardiothorac Surg 2005; 28: 754–758. doi: 10.1016/j.ejcts.2005.08.001 [DOI] [PubMed] [Google Scholar]
- 72.Wang J-S, Abboud RT, Wang L-M. Effect of lung resection on exercise capacity and on carbon monoxide diffusing capacity during exercise. Chest 2006; 129: 863–872. doi: 10.1378/chest.129.4.863 [DOI] [PubMed] [Google Scholar]
- 73.Nagamatsu Y, Iwasaki Y, Hayashida R, et al. Factors related to an early restoration of exercise capacity after major lung resection. Surg Today 2011; 41: 1228–1233. doi: 10.1007/s00595-010-4441-7 [DOI] [PubMed] [Google Scholar]
- 74.Nagamatsu Y, Maeshiro K, Kimura NY, et al. Long-term recovery of exercise capacity and pulmonary function after lobectomy. J Thorac Cardiovasc Surg 2007; 134: 1273–1278. doi: 10.1016/j.jtcvs.2007.06.025 [DOI] [PubMed] [Google Scholar]
- 75.Stefanelli F, Meoli I, Cobuccio R, et al. High-intensity training and cardiopulmonary exercise testing in patients with chronic obstructive pulmonary disease and non-small-cell lung cancer undergoing lobectomy. Eur J Cardiothorac Surg 2013; 44: e260–e265. doi: 10.1093/ejcts/ezt375 [DOI] [PubMed] [Google Scholar]
- 76.Bolliger CT, Wyser C, Roser H, et al. Lung scanning and exercise testing for the prediction of postoperative performance in lung resection candidates at increased risk for complications. Chest 1995; 108: 341–348. doi: 10.1378/chest.108.2.341 [DOI] [PubMed] [Google Scholar]
- 77.Pelletier C, Lapointe L, LeBlanc P. Effects of lung resection on pulmonary function and exercise capacity. Thorax 1990; 45: 497–502. doi: 10.1136/thx.45.7.497 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Cavalheri V, Jenkins S, Cecins N, et al. Comparison of the six-minute walk test with a cycle-based cardiopulmonary exercise test in people following curative intent treatment for non-small cell lung cancer. Chron Respir Dis 2016; 13: 118–127. doi: 10.1177/1479972316631137 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 79.Brocki BC, Andreasen J, Nielsen LR, et al. Short and long-term effects of supervised versus unsupervised exercise training on health-related quality of life and functional outcomes following lung cancer surgery–a randomized controlled trial. Lung Cancer 2014; 83: 102–108. doi: 10.1016/j.lungcan.2013.10.015 [DOI] [PubMed] [Google Scholar]
- 80.Şahin H, Naz İ, Aksel N, et al. Outcomes of pulmonary rehabilitation after lung resection in patients with lung cancer. Turk Gogus Kalp Damar Cerrahisi Derg 2022; 30: 227–234. doi: 10.5606/tgkdc.dergisi.2022.21595 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Brunelli A, Monteverde M, Borri A, et al. Predicted versus observed maximum oxygen consumption early after lung resection. Ann Thorac Surg 2003; 76: 376–380. doi: 10.1016/S0003-4975(03)00352-7 [DOI] [PubMed] [Google Scholar]
- 82.Timmerman JJ, Dekker-van Weering MGHM, Wouters MWJMM, et al. Physical behavior and associations with health outcomes in operable NSCLC patients: a prospective study. Lung Cancer 2018; 119: 91–98. doi: 10.1016/j.lungcan.2018.03.006 [DOI] [PubMed] [Google Scholar]
- 83.Granger CL, Parry SM, Edbrooke L, et al. Deterioration in physical activity and function differs according to treatment type in non-small cell lung cancer–future directions for physiotherapy management. Physiotherapy 2016; 102: 256–263. doi: 10.1016/j.physio.2015.10.007 [DOI] [PubMed] [Google Scholar]
- 84.Smulders SA, Smeenk FW, Janssen-Heijnen ML, et al. Actual and predicted postoperative changes in lung function after pneumonectomy: a retrospective analysis. Chest 2004; 125: 1735–1741. doi: 10.1378/chest.125.5.1735 [DOI] [PubMed] [Google Scholar]
- 85.Novoa N, Varela G, Jiménez MF, et al. Influence of major pulmonary resection on postoperative daily ambulatory activity of the patients. Interact Cardiovasc Thorac Surg 2009; 9: 934–938. doi: 10.1510/icvts.2009.212332 [DOI] [PubMed] [Google Scholar]
- 86.Kaplan SJ, Trottman PA, Porteous GH, et al. Functional recovery after lung resection: a before and after prospective cohort study of activity. Ann Thorac Surg 2019; 107: 209–216. doi: 10.1016/j.athoracsur.2018.07.050 [DOI] [PubMed] [Google Scholar]
- 87.Huang L, Kehlet H, Petersen R. Functional recovery after discharge in enhanced recovery video-assisted thoracoscopic lobectomy: a pilot prospective cohort study. Anaesthesia 2022; 77: 555–561. doi: 10.1111/anae.15682 [DOI] [PubMed] [Google Scholar]
- 88.Maeda K, Higashimoto Y, Honda N, et al. Effect of a postoperative outpatient pulmonary rehabilitation program on physical activity in patients who underwent pulmonary resection for lung cancer. Geriatr Gerontol Int 2016; 16: 550–555. doi: 10.1111/ggi.12505 [DOI] [PubMed] [Google Scholar]
- 89.Finet M, Bellicha A, Sage E, et al. Comprehensive assessment of postoperative mobility during the first days after mini-invasive lung surgery: a prospective observational study. J Clin Anesth 2023; 86: 111048. doi: 10.1016/j.jclinane.2022.111048 [DOI] [PubMed] [Google Scholar]
- 90.Cavalheri V, Jenkins S, Cecins N, et al. Patterns of sedentary behaviour and physical activity in people following curative intent treatment for non-small cell lung cancer. Chron Respir Dis 2016; 13: 82–85. doi: 10.1177/1479972315616931 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.D'Silva A, Bebb G, Boyle T, et al. Demographic and clinical correlates of accelerometer assessed physical activity and sedentary time in lung cancer survivors. Psychooncology 2018; 27: 1042–1049. doi: 10.1002/pon.4608 [DOI] [PubMed] [Google Scholar]
- 92.Jonsson M, Ahlsson A, Vidlund M, et al. In-hospital physiotherapy and physical recovery 3 months after lung cancer surgery: a randomized controlled trial. Integr Cancer Ther 2019; 18: 1534735419876346. doi: 10.1177/1534735419876346 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 93.Jonsson M, Ahlsson A, Vidlund M, et al. In-hospital physiotherapy improves physical activity level after lung cancer surgery: a randomized controlled trial. Physiotherapy 2019; 105: 434–441. doi: 10.1016/j.physio.2018.11.001 [DOI] [PubMed] [Google Scholar]
- 94.Harrison CA, Parks RM, Cheung KL. The impact of breast cancer surgery on functional status in older women – a systematic review of the literature. Eur J Surg Oncol 2021; 47: 1891–1899. doi: 10.1016/j.ejso.2021.04.010 [DOI] [PubMed] [Google Scholar]
- 95.De Groef A, Demeyer H, de Kinkelder C, et al. Physical activity levels of breast cancer patients before diagnosis compared to a reference population: a cross-sectional comparative study. Clin Breast Cancer 2022; 22: e708–e717. doi: 10.1016/j.clbc.2021.12.006 [DOI] [PubMed] [Google Scholar]
- 96.van Zutphen M, Winkels RM, van Duijnhoven FJ, et al. An increase in physical activity after colorectal cancer surgery is associated with improved recovery of physical functioning: a prospective cohort study. BMC Cancer 2017; 17: 74. doi: 10.1186/s12885-017-3066-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 97.Bradbury P, Sivajohanathan D, Chan A, et al. Postoperative adjuvant systemic therapy in completely resected non-small-cell lung cancer: a systematic review. Clin Lung Cancer 2017; 18: 259–273.e8. doi: 10.1016/j.cllc.2016.07.002 [DOI] [PubMed] [Google Scholar]
- 98.Grusdat NP, Tolkmitt M, Schnabel J, et al. Routine cancer treatments and their impact on physical function, symptoms of cancer-related fatigue, anxiety, and depression. Support Care Cancer 2022; 30: 3733–3744. doi: 10.1007/s00520-021-06787-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Xu XY, Jiang XM, Xu Q, et al. Skeletal muscle change during neoadjuvant therapy and its impact on prognosis in patients with gastrointestinal cancers: a systematic review and meta-analysis. Front Oncol 2022; 12: 892935. doi: 10.3389/fonc.2022.892935 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 100.Holland AE, Cox NS, Houchen-Wolloff L, et al. Defining modern pulmonary rehabilitation. An official American Thoracic Society workshop report. Ann Am Thorac Soc 2021; 18: e12–e29. doi: 10.1513/AnnalsATS.202102-146ST [DOI] [PMC free article] [PubMed] [Google Scholar]
- 101.Langer D. Addressing the changing rehabilitation needs of patients undergoing thoracic surgery. Chron Respir Dis 2021; 18: 1479973121994783. doi: 10.1177/1479973121994783 [DOI] [PMC free article] [PubMed] [Google Scholar]
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