- Research article
- Open Access
Unfavorable impact of cancer cachexia on activity of daily living and need for inpatient care in elderly patients with advanced non-small-cell lung cancer in Japan: a prospective longitudinal observational study
BMC Cancer volume 17, Article number: 800 (2017)
Cancer cachexia in elderly patients may substantially impact physical function and medical dependency. The aim of this study was to estimate the impact of cachexia on activity of daily living (ADL), length of hospital stay, and inpatient medical costs among elderly patients with advanced non-small-cell lung cancer (NSCLC) receiving chemotherapy.
Thirty patients aged ≥70 years with advanced NSCLC (stage III-IV) scheduled to receive first-line chemotherapy were prospectively enrolled between January 2013 and November 2014. ADL was assessed using the Barthel index. The disability-free survival time (DFS) was calculated as the time between the date of study entry and the date of onset of a disabling event, which was defined as a 10-point decrease in the Barthel index from that at baseline. The mean cumulative function of the length of hospital stay and inpatient medical costs (¥, Japanese yen) was calculated.
The study patients comprised 11 women and 19 men, with a median age of 74 (range, 70–82) years. Cachexia was diagnosed in 19 (63%) patients. Cachectic patients had a shorter DFS (7.5 vs. 17.1 months, p < 0.05). During the first year from study entry, cachectic patients had longer cumulative lengths of hospital stay (80.7 vs. 38.5 days/person, p < 0.05), more frequent unplanned hospital visits or hospitalizations (4.2 vs. 1.7 times/person, p < 0.05), and higher inpatient medical costs (¥3.5 vs. ¥2.1 million/person, p < 0.05) than non-cachectic patients.
Elderly NSCLC patients with cachexia showed higher risks for disability, prolonged hospitalizations, and higher inpatient medical costs while receiving chemotherapy than patients without cachexia. Our results might indicate that there is a potential need for an early intervention to minimize progression to or development of cachexia, improve functional prognosis, and reduce healthcare resource burden in this population.
Trial registration number: UMIN000009768. Name of registry: UMIN (University hospital Medical Information Network). Date of registration: 14 January 2013. Date of enrolment of the first participant to the trial: 23 January 2013.
The number of elderly people living with advanced lung cancer is increasing worldwide, owing to the aging population and progress in cancer treatments . In Japan, 65% of lung cancer morbidity cases and 73% of lung cancer-related deaths were attributed to elderly individuals aged ≥70 years in 2012 . Patients with lung cancer, especially the elderly population, often develop dependency in activities of daily living (ADLs) during treatment [3, 4]. In addition, the financial burden of elderly lung cancer patients is growing. In Japan, about half (52%, ¥222 billion) of the annual national costs for tracheal, bronchus, and lung cancers are attributed to elderly individuals aged ≥70 years, and the majority of these funds (75%, ¥166 billion) are used for their inpatient care . Thus, the socioeconomic impact of elderly lung cancer patients is serious and cannot be ignored.
Cancer cachexia is a multifactorial syndrome characterized by a significant reduction in body weight associated with reduced muscle and adipose tissue mass . Cancer cachexia is frequently observed in advanced lung cancer patients not only in the terminal phase of the disease, but also in the early phase of cancer diagnosis [6, 7]. We have previously reported that approximately half of all patients with newly diagnosed advanced non-small-cell lung cancer (NSCLC) had cachexia and skeletal muscle mass depletion at the time of diagnosis. The skeletal muscle mass further decreases during subsequent chemotherapies along with loss of physical function . Standard treatment for cancer cachexia has not been established. However, a number of pharmacological agents [9,10,11] and multimodal care approaches  are currently being assessed in clinical trials. Patients with cancer cachexia have poor physical function  and are at high risk for disabilities, prolonged hospitalizations, and in-hospital death . As a result, patients with cancer cachexia are less likely to tolerate cancer treatment  and have poorer quality of life and prognosis [8, 16]. Recently, the presence of cancer cachexia was reported to have a substantial socioeconomic impact on cancer care [14, 17]. Thus, effective management of cancer cachexia may decrease medical dependency and the need for inpatient care. However, there is currently limited information about the socioeconomic impact of cachexia in elderly patients living with advanced NSCLC who are receiving palliative chemotherapy.
Accordingly, this study aimed to estimate the impact of cachexia on ADL, length of hospital stay, and inpatient medical costs among elderly patients with advanced NSCLC receiving chemotherapy.
This prospective longitudinal observational study was designed to estimate the impact of cachexia on ADL, length of hospital stay, and inpatient medical costs among elderly patients with advanced NSCLC receiving chemotherapy. The study was performed at the Shizuoka Cancer Center, Japan, from January 2013 to April 2016. The Shizuoka Cancer Center is a 615-bed prefectural hospital designated as an advanced treatment hospital by the Japanese Ministry of Health, Labour and Welfare. The eligibility criteria were as follows: (1) histologically and/or cytologically proven stage III or IV NSCLC including postoperative recurrence; (2) age ≥ 70 years, with scheduled first-line systemic chemotherapy; (3) no previous systemic chemotherapy or thoracic radiotherapy (adjuvant chemotherapy was not counted as prior chemotherapy); (4) Eastern Cooperative Oncology Group performance status of 0–2; (5) ability to ambulate, read, and respond to questions without assistance; and (6) expected survival of >12 weeks. Patients were excluded if they had a severe psychiatric disorder, active infectious disease, unstable cardiac disease, or untreated symptomatic brain or bone metastases that prevented safe assessment.
All patients provided written informed consent. The study was approved by the institutional review board and registered on the clinical trials site of the University Hospital Medical Information Network Clinical Trials Registry in Japan (registration number: UMIN000009768).
Patient enrollment and timing of data collection
The first patient was enrolled on January 23, 2013, and the last on November 7, 2013. The study period for each patient was defined as the time between the date of study entry to the date of the last visit or the cutoff date (April 30, 2016). Baseline study assessments were performed by the attending physicians, physiotherapists, and national registered dietitians during the time between study entry and initiation of the first chemotherapy session.
Body weight (kg) was measured to the nearest 0.1 kg and the body mass index (BMI; kg/m2) was subsequently calculated. The registered dietitians (T.A. and H.S.) assessed nutritional status using the full version of the Mini Nutritional Assessment (full MNA®) . The incremental shuttle-walking test was conducted according to the recent guidelines  and original protocol described by Singh et al. . The 10-m course was established in the corridor of our hospital. Walking speed was dictated by a timed signal played on a CD recorder provided by the manufacturer (Japanese version, produced by the Graduate School of Biomedical Sciences, Nagasaki University, Japan, 2000). All patients were subjected to the test once under standardized conditions and were carefully observed during the test, so that they would not exceed their exercise limit. The maximal walking distance was described as incremental shuttle-walking distance. Hand-grip strength was measured using a grip strength dynamometer (GRIP-D, Takei Scientific Instruments Co., LTD, Niigata, Japan). One trial was performed for each hand, and the result from the strongest hand was used for the analysis. Lumbar skeletal muscle mass was measured by analyzing electronically stored computed tomography (CT) images using SYNAPSE VINCENT version 3 (FUJIFILM Medical Systems, Japan). The CT images were obtained with or without contrast enhancement at 5-mm slice thickness. The third lumbar vertebra (L3) was chosen as the standard landmark, and 2 consecutive CT images extending from L3 to the iliac crest were chosen to measure the cross-sectional area of the skeletal muscle that was identified based on Hounsfield unit thresholds of −29 to +150. The sum of the cross-sectional areas (cm2) of the muscles in the L3 region was computed for each image. The mean value of 2 images was normalized for height in meters squared and reported as the lumbar skeletal muscle index (cm2/m2) . The disease stage was determined according to the TNM classification, and the best response to chemotherapy was evaluated according to the Response Evaluation Criteria in Solid Tumors.
Diagnosis of muscle depletion, malnutrition, and cancer cachexia
Muscle depletion was defined based on lumbar skeletal muscle index cutoffs of <43.0 cm2/m2 for men with a BMI <25.0 kg/m2, <53.0 cm2/m2 for men with a BMI ≥25.0 kg/m2, and <41.0 cm2/m2 for women . Malnutrition or at risk of malnutrition was defined based on a full MNA® score < 17 points . Cancer cachexia was defined as unintentional weight loss of >5% during the preceding 6 months or >2% in patients with a BMI <20 kg/m2, or the presence of muscle depletion according to the consensus criteria . The patient’s weight 6 months before study entry was obtained by interviewing the patient and their family members at study entry.
Assessment of activity of daily living
For the assessment of ADL, the Barthel index was estimated by the attending physician or physiotherapists at each hospital visit. The disability-free survival (DFS) duration was calculated as the time between study enrollment and the date of onset of the disabling event. A disabling event was defined as a decrease in the Barthel index from the baseline value by >10 points. The event was confirmed as a true event if the condition persisted for >2 weeks from the initial report. In confirmed events, the dates of the initial reports were used as the event dates in the analysis.
Assessment of healthcare resource utilization
The medical claims data, including the numbers of outpatient visits and hospitalizations, lengths of hospital stay, healthcare resource utilization items, and medical costs, were obtained from the electronic medical records of our hospital. For patients who received medical care at another hospital, medical claims data was obtained through the institutional coordination office of local clinics and hospitals. Inpatient medical costs were estimated by certified medical accountants. In this study, the medical costs refer to the actual revenue that the hospital was paid from the health insurance funds of the Japanese health care system. Medical costs for home care were not included. In the healthcare utilization analysis, visits (or hospitalizations) for supportive care were defined as all visits (or hospitalizations) that involved physician medical examinations, except for visits (or hospitalizations) for chemotherapy or radiotherapy. Outpatient visits for regular radiological/blood tests without a physician examination or visits for non-medical reasons were not included.
The overall survival (OS) and DFS rates were estimated using the Kaplan-Meier method. OS was censored at the date of the last visit for patients whose deaths could not be confirmed. DFS was censored at the date of the last visit for patients whose disabling event could not be confirmed. To compare categorical variables, chi-square or Fisher’s exact tests were used. Continuous measures were compared using the Wilcoxon rank-sum test. For all analyses, p-values <0.05 were considered significant. We used a mean cumulative function for recurrent event analysis  of the cumulative length of hospital stay and medical costs related to cancer care, as previously described [25, 26]. Exploratory subset analyses for patients without epidermal growth factor receptor (EGFR) gene mutation were performed. All statistical analyses were performed using JMP version 12.0 for Windows (SAS Institute Inc., USA).
Thirty-one patients were screened and 30 patients were enrolled into this study, with a median age of 74 years (range, 70–82 years). Seven patients (23.3%) had activating EGFR gene mutation. Cancer cachexia was diagnosed in 19 (63.3%) patients (Table 1). Cachectic patients were older (76 vs. 73 years, p < 0.05), had a larger weight loss in the past 6 months (−9.4 vs. −0.1%, p < 0.05), and had a higher incidence of malnutrition or were more frequently at risk for malnutrition (73.7 vs. 27.3%, p < 0.05). Cachectic men had poorer physical function than non-cachectic men in regard to the incremental shuttle-walking distance (283.4 vs. 413.8 m, p < 0.05) and hand-grip strength (29.5 vs. 39.3 kg, p < 0.05). There was no statistical difference in physical function between cachectic and non-cachectic women.
Cancer treatment during the study period
All patients received first-line chemotherapy within 1 week after the baseline assessment. All patients initially received a standard dose of chemotherapy with a standard schedule. The chemotherapy regimens included single-agent chemotherapy (docetaxel or vinorelbine) in 10 patients, platinum-based chemotherapy (carboplatin + paclitaxel, or cisplatin + pemetrexed, gemcitabine, or vinorelbine) in 14, and gefitinib in 6 patients with epidermal growth factor receptor gene mutations. An objective tumor response was seen in 12 patients (40.0%). There was no statistical difference in the response rate between cachectic and non-cachectic patients (42.1% vs. 36.4%, p = 0.75). During the study period (January 23, 2013 to April 30, 2016), 18 patients (60.0%) received second or higher lines of chemotherapy, including docetaxel, erlotinib, pemetrexed, gemcitabine, carboplatin + pemetrexed, S-1, or investigational drugs. There was no statistical difference in the proportion of patients receiving second or higher lines of chemotherapy between cachectic and non-cachectic patients. Eighteen patients (60.0%) received palliative radiotherapy during the study period, including cranial radiation (n = 10, 33.3%), bone radiation (n = 6, 20.0%), and thoracic radiation (n = 2, 6.7%). None of our patients received immunotherapy or molecular targeted treatment other than gefitinib or erlotinib during the study period. One patient was transferred to another hospital for personal reasons 19.4 weeks after study entry and continued chemotherapy. Three patients were transferred to another hospital for palliative care. Three patients received gamma knife surgery at another hospital during the study period. A total of 29 patients were eligible for the analysis of length of hospital stay and medical costs (Fig. 1). None of our patients received anti-cachexia treatment such as megestrol acetate, eicosapentaenoic acid, or multimodal intervention specific for cancer cachexia.
Follow-up period and overall survival
Among the 30 patients, 28 (93.3%) died at the cutoff date. The median follow-up period was 10.7 (95% confidence interval, 7.9–21.6) months. There was no significant difference in OS between cachectic and non-cachectic patients (p = 0.0960, Fig. 2a). In the exploratory analysis for patients without EGFR mutation, there was also no significant difference in OS between cachectic and non-cachectic patients (p = 0.2055).
Disabling events and disability-free survival
Among the 30 patients, 27 (90.0%) were disabled at the cutoff date. Disabling events often affected multiple ADLs simultaneously. Frequently observed combinations of initial disabling events per the Barthel index included stair climbing (27 events, 100%), morbidity (26 events, 96.3%), bathing (24 events, 88.9%), toilet use (15 events, 55.6%), and transfer (11 events, 40.7%). Cachectic patients at baseline had a significantly shorter DFS than non-cachectic patients (7.5 vs. 17.1 months, p < 0.05, Fig. 2b). Additionally, cachectic patients had a longer post-disability survival than non-cachectic patients (2.5 vs. 0.7 months, p < 0.05, Fig. 3). In the exploratory analysis for patients without EGFR mutation, cachectic patients tended to have shorter DFS (6.8 vs. 10.3 months, p = 0.1078) and longer post-disability survival (2.6 vs. 0.6 months, p = 0.0541) than non-cachectic patients without statistical significance.
Healthcare resource utilization
During the first year since study entry, we recorded 525 outpatient visits and 144 hospitalizations for the 29 patients. There were 42 unplanned outpatient visits (8.0% of all outpatient visits), including 14 visits (2.7%) to the emergency room. The reasons for the unplanned visits included anorexia or dehydration (17 visits, 41%), infection or febrile disease (9 visits, 21%), constipation or diarrhea (5 visits, 12%), respiratory symptoms (5 visits, 12%), and others (6 visits, 14%). There were 30 emergency hospitalizations (20.8% of all hospitalizations). The reasons for emergency hospitalizations included anorexia or dehydration (7 hospitalizations, 23%), respiratory symptoms (6 hospitalizations, 20%), infection or febrile disease (5 hospitalizations, 17%), urgent radiotherapy (4 hospitalizations, 13%), end-of-life care (3 hospitalizations, 10%), and others (5 hospitalizations, 17%). Hospitalization for non-medical reasons (e.g. social hospitalization) was not observed.
Length of hospital stay and medical cost for cachectic patients
In the comparison of socioeconomic parameters during the first year of study entry, cachectic patients had a longer cumulative length of hospital stay (80.7 vs. 38.5 days/person, p < 0.05, Table 2), more frequent unplanned outpatient visits or emergency hospitalizations (4.2 vs. 1.7 times/person, p < 0.05, Table 2), and higher cumulative medical costs (¥5.0 vs. ¥3.3 million/person, p < 0.05, Table 2). In the exploratory analysis for patients without EGFR mutation, cachectic patients had a longer cumulative length of hospital stay (109.3 vs. 45.9 days/person, p < 0.05), more frequent unplanned outpatient visits or emergency hospitalizations (5.5 vs. 2.0 times/person, p < 0.05), and higher cumulative medical costs (¥5.3 vs. ¥3.3 million/person, p < 0.05). The differences in medical costs between the two groups were mainly attributed to the inpatient care (¥3.5 vs. 2.1 million, p < 0.05) and supportive care (¥1.2 vs. 0.4 million, p < 0.05), while the costs for outpatient care (¥1.5 vs. 1.3 million) and anticancer treatments, including radiotherapy (¥0.5 vs. 0.2 million) and chemotherapy (¥2.0 vs. 2.2 million), were similar between the groups (Table 2). The curves of cumulative hospital days (Fig. 4a) and inpatient medical costs (Fig. 4b) in cachectic and non-cachectic patients separated at 6 months and continued to diverge over the available follow-up period, with the length of hospitalization being 42.2 and 104.3 days (Fig. 4c) and in inpatient medical costs ¥1.5 and ¥4.2 million (Fig. 4d) at 12 and 24 months, respectively.
To our knowledge, this is the first prospective longitudinal observational study to evaluate the impact of cachexia on functional prognosis and socioeconomic parameters in elderly patients with advanced NSCLC. First, we found that cachectic patients tended to have lower muscle mass, muscle strength, and walking capacity than non-cachectic patients, especially the men. Second, in regards to functional prognosis, cachectic patients were found to be disabled earlier and have a longer duration of disability in their life time than non-cachectic patients. Third, from a socioeconomic view, cachectic patients required longer hospital stays and higher inpatient medical costs than non-cachectic patients, mainly due to the increased needs for supportive care rather than anti-cancer treatment.
Cancer cachexia is a hypercatabolic condition that cannot be simply reversed by energy supplementation . A previous study reported that two-thirds of incurable chemotherapy-naïve NSCLC patients experienced weight loss at the time of diagnosis  and a majority of them met the recent diagnostic criteria for cancer cachexia , as reported in our previous study . High incidences of malnutrition and sarcopenia have been reported in advanced lung cancer patients [22, 27]. Regarding physical function in patients with advanced NSCLC, cachectic patients had worse physical function at baseline and the rate of decline in physical function was more rapid than that in non-cachectic patients during the course of cancer treatment .
Arthur et al. [14, 28] recently reported that the presence of cachexia was strongly associated with higher risks for major loss of function (i.e. disability) and increased inpatient costs, not only in the general population but also in cancer patients. Among the 5 most common cancer types associated with cachexia, namely lung cancer, pancreatic cancer, esophageal cancer, stomach cancer, and Kaposi’s sarcoma, cachectic lung cancer patients are at the highest risk for major loss of function. Consistently, our study showed that cachectic patients were more likely to be disabled during their course of cancer treatment. The possible reasons for the increased susceptibility to disabling events in cachectic patients might include older age and higher incidence of malnutrition and muscle depletion in this subset of patients, as these conditions have been reported to be associated with functional impairment and disability [29,30,31].
There is currently limited information on the socioeconomic impact of cancer cachexia, including medical costs and use of healthcare resources . Cachectic lung cancer patients have been reported to require longer lengths of hospital stay, which in turn leads to a higher financial burden . Our data fully support this previous finding. In addition, our analysis provided more detailed information about the breakdown of healthcare resource utilization items. Most differences in medical costs between cachectic and non-cachectic patients could be attributed to the requirements for inpatient palliative care. Conversely, there were few differences in the costs associated with out-patient care and active cancer treatments between the groups.
Our study has several limitations. First, this study involved a small sample size that included only Japanese patients treated at a single institution. Second, our study population was heterogeneous in regard to the treatment regimens received. Additionally, there was a difference in age between the cachectic and non-cachectic groups. However, exploratory analyses for patients without EGFR mutation showed small impact on the results and age also had little impact on the comparison of endpoints (data not shown). Third, this study lacks a measurement of quality of life that may be important to estimate the net impact of cancer cachexia in comparison with the medical costs. Finally, the health insurance system in Japan differs from that of other countries or regions. Moreover, the medical environment and standard of care are rapidly changing with advances in medicine. Thus, our results are not directly transferable to other populations in different medical situations. However, we believe that increased medical dependency and needs for supportive care in cachectic patients might be important features of cancer cachexia that can be shared in different medical situations.
For optimal management of cancer cachexia, a multimodal treatment approach including medication, exercise, and nutritional intervention are reported to be essential [6, 32]. However, there are currently no pharmacotherapies that are specifically approved for the treatment of cancer cachexia. A number of investigational agents are now in clinical development, including ghrelin and ghrelin mimetics [10, 11], selective androgen receptor modulators , and anti-inflammatory agents . In addition, there is limited evidence for non-pharmacological treatments including nutrition and exercise intervention for patients with advanced cancer . Recently, Solheim TS et al.  reported the results of a randomized phase II study comparing a multimodal intervention (exercise, nutritional intervention, and anti-inflammatories) versus standard cancer care in patients with advanced NSCLC and pancreatic cancer (Pre-MENAC study, Clinical Trials Registry No. NCT01419145). They showed that the intervention was feasible and was associated with statistically significant weight gain. However, there was no significant improvement in muscle mass or physical activity. The MENAC study, a phase III randomized, open-label trial of this multimodal intervention plus standard care vs. standard care alone to prevent cachexia in advanced cancer patients undergoing chemotherapy, is now underway (Clinical Trials Registry No. NCT02330926).
Based on the results of our study, we are currently conducting a prospective multicenter feasibility study of early exercise and nutritional intervention for elderly patients with advanced NSCLC and pancreatic cancer in Japan (Clinical Trials Registry No. UMIN000023207). We hypothesize that early non-pharmacological supportive care might maintain physical function and hence reduce medical dependency and costs in elderly patients with advanced cancer at high risk for cachexia.
Cachectic elderly patients with advanced NSCLC were more frequently disabled, required prolonged hospitalizations, and were associated with higher medical costs while receiving chemotherapy. Our results suggest that there is a potential need for early multimodal intervention with exercise and nutrition for elderly patients with advanced lung cancer to maintain functional independence and reduce medical dependency during chemotherapy. Further randomized control study is needed to determine the optimal treatment regimen for cancer cachexia and its impact on functional prognosis.
activity of daily living
body mass index
non-small cell lung cancer
Miller KD, Siegel RL, Lin CC, Mariotto AB, Kramer JL, Rowland JH, Stein KD, Alteri R, Jemal A. Cancer treatment and survivorship statistics, 2016. CA Cancer J Clin. 2016;66:271–89.
Hori M, Matsuda T, Shibata A, Katanoda K, Sobue T, Nishimoto H. Cancer incidence and incidence rates in Japan in 2009: a study of 32 population-based cancer registries for the monitoring of cancer incidence in Japan (MCIJ) project. Jpn J Clin Oncol. 2015;45:884–91.
Global Burden of Disease Cancer Collaboration, Fitzmaurice C, Dicker D, Pain A, Hamavid H, Moradi-Lakeh M, MF MI, et al. The Global Burden of Cancer 2013. JAMA Oncol. 2015;1:505–27.
Tsilidis KK, Papadimitriou N, Capothanassi D, Bamia C, Benetou V, Jenab M, Freisling H, Kee F, Nelen A, O'Doherty MG, Scott A, Soerjomataram I, Tjønneland A, May AM, Ramón Quirós J, Pettersson-Kymmer U, Brenner H, Schöttker B, Ordóñez-Mena JM, Karina Dieffenbach A, Eriksson S, Bøgeberg Mathiesen E, Njølstad I, Siganos G, Wilsgaard T, Boffetta P, Trichopoulos D, Trichopoulou A. Burden of Cancer in a Large Consortium of Prospective Cohorts in Europe. J Natl Cancer Inst. 2016;108(10). https://academic.oup.com/jnci/article/108/10/djw127/2412485.
Ministry of Health, Labour and Welfare. Estimates of National Medical Care Expenditure, Summary for 2015, http://www.mhlw.go.jp/toukei/saikin/hw/k-iryohi/13/index.html. Accessed 10 Apr 2017.
Fearon K, Strasser F, Anker SD, Bosaeus I, Bruera E, Fainsinger RL, Jatoi A, Loprinzi C, MacDonald N, Mantovani G, Davis M, Muscaritoli M, Ottery F, Radbruch L, Ravasco P, Walsh D, Wilcock A, Kaasa S, Baracos VE. Definition and classification of cancer cachexia: an international consensus. Lancet Oncol. 2011;12:489–95.
Dewys WD, Begg C, Lavin PT, Band PR, Bennett JM, Bertino JR, Cohen MH, Douglass HO, Engstrom PF, Ezdinli EZ, Horton J, Johnson GJ, Moertel CG, Oken MM, Perlia C, Rosenbaum C, Silverstein MN, Skeel RT, Sponzo RW, Tormey DC. Prognostic effect of weight loss prior to chemotherapy in cancer patients. Eastern cooperative oncology group. Am J Med. 1980;69:491–7.
Kimura M, Naito T, Kenmotsu H, Taira T, Wakuda K, Oyakawa T, Hisamatsu Y, Tokito T, Imai H, Akamatsu H, Ono A, Kaira K, Murakami H, Endo M, Mori K, Takahashi T, Yamamoto N. Prognostic impact of cancer cachexia in patients with advanced non-small cell lung cancer. Support Care Cancer. 2015;23:1699–708.
Crawford J, Prado CM, Johnston MA, Gralla RJ, Taylor RP, Hancock ML, Dalton JT. Study design and rationale for the phase 3 clinical development program of Enobosarm, a selective androgen receptor modulator, for the prevention and treatment of muscle wasting in cancer patients (POWER trials). Curr Oncol Rep. 2016;18:37.
Temel JS, Abernethy AP, Currow DC, Friend J, Duus EM, Yan Y, Fearon KC. Anamorelin in patients with non-small-cell lung cancer and cachexia (ROMANA 1 and ROMANA 2): results from two randomised, double-blind, phase 3 trials. Lancet Oncol. 2016;17:519–31.
Takayama K, Katakami N, Yokoyama T, Atagi S, Yoshimori K, Kagamu H, Saito H, Takiguchi Y, Aoe K, Koyama A, Komura N, Eguchi K. Anamorelin (ONO-7643) in Japanese patients with non-small cell lung cancer and cachexia: results of a randomized phase 2 trial. Support Care Cancer. 2016;24:3495–505.
Solheim TS, Laird BJA, Balstad TR, Stene GB, Bye A, Johns N, Pettersen CH, Fallon M, Fayers P, Fearon K, Kaasa S. A Randomized phase II feasibility trial of a multimodal intervention for the management of cachexia in lung and pancreatic cancer. J Cachexia Sarcopenia Muscle 2017 Jun 14. doi:10.1002/jcsm.12201. [Epub ahead of print].
LeBlanc TW, Nipp RD, Rushing CN, Samsa GP, Locke SC, Kamal AH, Cella DF, Abernethy AP. Correlation between the international consensus definition of the cancer anorexia-cachexia syndrome (CACS) and patient-centered outcomes in advanced non-small cell lung cancer. J Pain Symptom Manag. 2015;49:680–9.
Arthur ST, Van Doren BA, Roy D, Noone JM, Zacherle E, Blanchette CM. Cachexia among US cancer patients. J Med Econ. 2016;19:874–80.
Ross PJ, Ashley S, Norton A, Priest K, Waters JS, Eisen T, Smith IE, O'Brien ME. Do patients with weight loss have a worse outcome when undergoing chemotherapy for lung cancers? Br J Cancer. 2004;90:1905–11.
Takayama K, Atagi S, Imamura F, Tanaka H, Minato K, Harada T, Katakami N, Yokoyama T, Yoshimori K, Takiguchi Y, Hataji O, Takeda Y, Aoe K, Kim YH, Yokota S, Tabeta H, Tomii K, Ohashi Y, Eguchi K, Watanabe K. Quality of life and survival survey of cancer cachexia in advanced non-small cell lung cancer patients-Japan nutrition and QOL survey in patients with advanced non-small cell lung cancer study. Support Care Cancer. 2016;24:3473–80.
Tarricone R, Ricca G, Nyanzi-Wakholi B, Medina-Lara A. Impact of cancer anorexia-cachexia syndrome on health-related quality of life and resource utilisation: a systematic review. Crit Rev Oncol Hematol. 2016;99:49–62.
Guigoz Y, Vellas B, Garry PJ. Assessing the nutritional status of the elderly: the mini nutritional assessment as part of the geriatric evaluation. Nutr Rev. 1996;54:S59–65.
Singh SJ, Puhan MA, Andrianopoulos V, Hernandes NA, Mitchell KE, Hill CJ, Lee AL, Camillo CA, Troosters T, Spruit MA, Carlin BW, Wanger J, Pepin V, Saey D, Pitta F, Kaminsky DA, McCormack MC, MacIntyre N, Culver BH, Sciurba FC, Revill SM, Delafosse V, Holland AE. An official systematic review of the European Respiratory Society/American Thoracic Society: measurement properties of field walking tests in chronic respiratory disease. Eur Respir J. 2014;44:1447–78.
Singh SJ, Morgan MD, Scott S, Walters D, Hardman AE. Development of a shuttle walking test of disability in patients with chronic airways obstruction. Thorax. 1992;47:1019–24.
Mourtzakis M, Prado CM, Lieffers JR, Reiman T, McCargar LJ, Baracos VEA. Practical and precise approach to quantification of body composition in cancer patients using computed tomography images acquired during routine care. Appl Physiol Nutr Metab. 2008;33:997–1006.
Martin L, Birdsell L, Macdonald N, Reiman T, Clandinin MT, McCargar LJ, Murphy R, Ghosh S, Sawyer MB, Baracos VE. Cancer cachexia in the age of obesity: skeletal muscle depletion is a powerful prognostic factor, independent of body mass index. J Clin Oncol. 2013;31:1539–47.
Vellas B, Guigoz Y, Garry PJ, Nourhashemi F, Bennahum D, Lauque S, Albarede JL. The mini nutritional assessment (MNA) and its use in grading the nutritional state of elderly patients. Nutrition. 1999;15:116–22.
Nelson W. Confidence limits for recurrence data - applied to cost or number of product repairs. Technometrics. 1995;37:147–57.
Humphries KH, Pu A, Gao M, Carere RG, Pilote L. Angina with "normal" coronary arteries: sex differences in outcomes. Am Heart J. 2008;155:375–81.
Smedira NG, Hoercher KJ, Lima B, Mountis MM, Starling RC, Thuita L, Schmuhl DM, Blackstone EH. Unplanned hospital readmissions after HeartMate II implantation: frequency, risk factors, and impact on resource use and survival. JACC Heart Fail. 2013;1:31–9.
Baracos VE, Reiman T, Mourtzakis M, Gioulbasanis I, Antoun S. Body composition in patients with non-small cell lung cancer: a contemporary view of cancer cachexia with the use of computed tomography image analysis. Am J Clin Nutr. 2010;91:1133S–7S.
Arthur ST, Noone JM, Van Doren BA, Roy D, Blanchette CM. One-year prevalence, comorbidities and cost of cachexia-related inpatient admissions in the USA. Drugs Context. 2014;3:212265.
Janssen I, Heymsfield SB, Ross R. Low relative skeletal muscle mass (sarcopenia) in older persons is associated with functional impairment and physical disability. J Am Geriatr Soc. 2002;50:889–96.
Lee LC, Tsai AC. Mini-nutritional-assessment (MNA) without body mass index (BMI) predicts functional disability in elderly Taiwanese. Arch Gerontol Geriatr. 2012;54:e405–10.
Tanimoto Y, Watanabe M, Sun W, Hirota C, Sugiura Y, Kono R, Saito M, Kono K. Association between muscle mass and disability in performing instrumental activities of daily living (IADL) in community-dwelling elderly in Japan. Arch Gerontol Geriatr. 2012;54:e230–3.
Aapro M, Arends J, Bozzetti F, Fearon K, Grunberg SM, Herrstedt J, Hopkinson J, Jacquelin-Ravel N, Jatoi A, Kaasa S, Strasser F, ESMO (European School of Medical Oncology). Early recognition of malnutrition and cachexia in the cancer patient: a position paper of a European School of Oncology Task Force. Ann Oncol. 2014;25:1492–9.
Hong DS, Janku F, Naing A, Falchook GS, Piha-Paul S, Wheler JJ, Fu S, Tsimberidou AM, Stecher M, Mohanty P, Simard J, Kurzrock R. Xilonix, a novel true human antibody targeting the inflammatory cytokine interleukin-1 alpha, in non-small cell lung cancer. Investig New Drugs. 2015;33:621–31.
Arends J, Bachmann P, Baracos V, Barthelemy N, Bertz H, Bozzetti F, Fearon K, Hutterer E, Isenring E, Kaasa S, Krznaric Z, Laird B, Larsson M, Laviano A, Muhlebach S, Muscaritoli M, Oldervoll L, Ravasco P, Solheim T, Strasser F, De van der Schueren M, Preiser JC. ESPEN guidelines on nutrition in cancer patients. Clin Nutr. 2017;36:11–48.
We thank Ms. Mami Oba, a certified medical accountant at Shizuoka Cancer Center, for her instructions regarding medical costs.
This work was supported by the 35th grant-in-aid from the Japanese Foundation for the Multidisciplinary Treatment of Cancer in 2014. They have no role in designing of the study, collecting data, and analyzing data. They supported the interpretation of data in the annual research conference and research fund was used in writing the manuscript and proofreading.
Availability of data and materials
The datasets generated and analyzed during the current study are available from the corresponding author on reasonable request.
TN, the principal and corresponding author, designed the clinical trial and prepared the draft of manuscript. TOk, MK, HM, HK, HI, TOy, NY, AT, and TTak, the member of protocol committee, designed the clinical trial and revised the draft of the manuscript. ME, a diagnostic radiologist and the instructor of muscle mass analysis using computed tomography. TA and HS, the registered dietitian, collected nutritional data and revised the draft of the manuscript. TOh, YM, and TI, the physiotherapist, collected physical function data and revised the draft of the manuscript. SO, TTair, AO, KW and KN, the oncologist, recruited the patients, collected clinical data, and revised the draft of the manuscript. KO and KM, the biostatistician, designed the statistical methodology and analyzed the data. All authors have read and approved the manuscript.
Ethics approval and consent to participate
This clinical trial was approved by the institutional review board of Shizuoka Cancer Center (study number: T24–30–24-1-3) on January 11, 2013 and was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki. Written informed consent was obtained from all participants in this study.
Consent for publication
The authors declare that they have no competing interests.
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Cite this article
Naito, T., Okayama, T., Aoyama, T. et al. Unfavorable impact of cancer cachexia on activity of daily living and need for inpatient care in elderly patients with advanced non-small-cell lung cancer in Japan: a prospective longitudinal observational study. BMC Cancer 17, 800 (2017). https://doi.org/10.1186/s12885-017-3795-2
- Non-small-cell lung cancer
- Cancer cachexia
- Activity of daily living
- Length of hospital stay
- Medical cost