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A review of weight loss and sarcopenia in patients with head and neck cancer treated with chemoradiation

Cancers of the Head & Neck volume 1, Article number: 9 (2016) Cite this article

Abstract

Background

Concurrent chemotherapy and radiation (CTRT) improves disease-free survival in locally advanced head and neck cancer but is associated with numerous acute and chronic toxicities resulting in substantial alterations in body mass and composition. We aim to summarize the current evidence on body composition changes experienced by patients undergoing CTRT, examine the impact of these changes on clinical outcomes and address potential interventions aimed at mitigating the loss.

Main Body

Loss of 20 % of pre-CTRT weight predicts poorer treatment tolerance and 30-day mortality. While clinical practice focuses on body weight, emerging data indicates that CTRT causes profound adverse changes in lean body mass (sarcopenia). Higher prevalence of sarcopenia predicts poorer disease-free survival as well as overall survival, lower quality of life and functional performance. The magnitude of CTRT-induced sarcopenia is the equivalent to that observed in a decade of aging in a healthy adult. Alterations in body composition are only explained, in part, by decreased caloric intake; other significant predictors include body mass index, stage, and dysphagia. Lifestyle interventions aimed at preventing loss of whole-body and especially lean mass include nutritional counseling, nutritional supplements, dietary supplements and exercise training. Personalized nutritional counseling has been associated with improvement in quality of life, while the benefits of feeding tube placement are inconsistent. There are inconsistently reported benefits of resistance training in this population.

Conclusion

Patients with head and neck cancer undergoing CTRT therapy experience dramatic shifts in body composition, including sarcopenia, which can negatively impact clinical outcomes. Efforts to understand the magnitude, clinical importance and mechanisms of sarcopenia are needed to inform a more personalized approach to mitigating the body composition changes associated with CTRT.

Background

Head and neck squamous cell carcinoma (HNSCC) is a group of diseases arising from the upper aerodigestive tract including the oral cavity, pharynx and larynx. There are an estimated 59,000 cases of HNSCC diagnosed annually in the US, representing 3 % of all newly identified cancers [1, 2]. Despite remaining relatively consistent in overall incidence, the epidemiology of HNSCC has changed over the last three decades, most notably in Western countries [3]. Once considered a disease resulting mostly from chronic exposure to tobacco and alcohol, it is now recognized that there are other causative factors for HNSCC. One of the fastest growing subsets of patients are those diagnosed with HNSCC tumors arising from the oropharynx secondary to human papilloma-virus (HPV) [4]. Patients with HPV-positive tumors have a striking improvement in survival compared with patients with historical, HPV-negative tumors with 3-year survival of 82 % versus 57 %, respectively (p < 0.001) [5]. Patients with HPV-associated tumors also appear to have a lower risk of developing second primary malignancies, resulting in longer long-term survival [5, 6]. Changing epidemiology along with treatment advances have resulted in a rise in the number of survivors of HNSCC who are expected to live well beyond their cancer diagnosis and treatment. Efforts are underway to better understand the toxicities associated with treatment and implement strategies aimed at improving the long-term quality of life and survival in this emerging cohort of cancer survivors [7].

Main text

Approximately 70 % of patients with HNSCC will present with locally advanced disease and many will be treated with concurrent chemotherapy and radiation (CTRT). Concurrent chemotherapy and radiation is associated with significant in-field and systemic toxicities including mucositis, dysphagia, odynophagia, nausea, vomiting, anorexia, fatigue and dysgeusia resulting in difficulty eating [8–10]. Furthermore, many patients present with symptomatic tumors that lead to difficulty eating prior to the initiation of treatment, with most patients experiencing a loss of more than 5 % of pre-treatment body weight in the 6 months around CTRT [11–14]. In part, this has been exacerbated by a change in resting energy expenditure, which furthers the loss of lean body mass seen during and immediately after treatment [11, 15]. Predictors of excessive weight loss during treatment include higher weight at baseline, dysphagia at diagnosis, and higher stage tumors [16]. More specifically, a recent study from Denmark reported that patients with a body mass index (BMI) ≥ 25 are three times more likely to lose more than 5 % of baseline weight than patients with BMI < 25 (p < 0.0001) [12].

Weight loss has been negatively associated with tumor control and survival outcomes in HNSCC [13]. For example, patients with early significant weight loss (defined as >20 % loss from baseline) are more likely to die from a treatment-related complication within 30 days of completing CTRT compared to those who do not (p = 0.029). In a secondary analysis from the phase III SAKK 10/94 trial of hyperfractionated radiation versus cisplatin and standard fraction radiation, Ghadjar and colleagues found that weight loss during treatment on either arm was common, but only weight loss experienced before treatment was associated with decreased time to treatment failure, disease free survival (DFS), and overall survival (OS) (p < 0.05 for all); weight loss occurring during treatment was not associated with survival outcomes [14]. The results from this study highlight two important aspects of weight loss and HNSCC. First, patients who are already losing weight at diagnosis are at a disadvantage and may be presenting with more aggressive disease at baseline. Second, while weight loss during treatment is common, it is not universally prognostic. One explanation for this discrepancy is that in some patients the weight loss is caused of decreased caloric intake, while in others weight loss is a manifestation of cachexia, or a syndrome of dysregulated catabolism and anabolism [17]. Historically, high-risk patients would have a percutaneous endoscopic gastrostomy (PEG) placed prior to starting treatment in order to prevent decreased caloric intake, but more recently there has been movement away from using feeding tubes due to concerns about delayed recovery of swallowing post-CTRT [18–20]. Interestingly, the placement of a PEG, or increased caloric intake alone, does not alleviate all the weight loss experienced during CTRT [12, 19, 21].

The weight loss experienced by patients with HNSCC undergoing CTRT is more specifically a change in body composition. Body weight or body mass is composed of fat, bone, water and lean body mass and the loss of lean body mass accounts for more than 70 % of weight lost during CTRT [15, 22]. Loss of lean body mass in cancer is mostly explained by sarcopenia, or loss of skeletal muscle [23]. Patients with HNSCC undergoing CTRT are often losing more than 5 % of their total muscle mass in less than 6 months time which is equivalent to the amount of muscle mass lost in the average, inactive adult over the course of a decade [24–26]. Skeletal muscle is the largest organ in the body and makes up approximately 50 % of total body weight and is essential for movement, strength, balance, body temperature regulation and respiration. Maintaining muscle mass involves a balance of protein breakdown (catabolism) and muscle synthesis (anabolism) and is tightly regulated through a network of external signaling pathways leading to intracellular gene transcription [22]. Lean body mass, mostly composed of muscle, can be measured using both validated direct and indirect methods. Examples of possible techniques include bioelectrical impedance (BIA), measurement of air displacement plethysmography, dual energy x-ray (DXA, and cross-sectional imaging on computed tomography (CT) or magnetic resonance imaging (MRI) [27].

Importantly, loss of lean body mass is associated with poorer treatment tolerance and worse cancer outcomes [28–30]. For example, in patients receiving systemic chemotherapy for colorectal cancer, loss of ≥ 9 % muscle mass during a 3 month period was independently predictive of lower survival at 6 months compared to patients who had < 9 % loss, 33 % versus 69 %, respectively, despite no difference in treatment modifications [31]. Similar associations have been described in patients with HNSCC. Grossberg and colleagues recently reported that in a cohort of 190 patients with HNSCC treated with definitive radiation, decreased overall survival was associated with baseline sarcopenia (Hazard Ratio (HR) 1.92, 95 % confidence interval [CI] 1.19–3.11) and post-radiation sarcopenia (HR 2.03, 95 % CI 1.02–4.24). However, in this analysis, weight loss alone, without associated loss of skeletal muscle, was not associated with worse clinical outcomes [32]. Further, when they evaluated by subsites, skeletal muscle depletion was associated with decreased survival in patients with non-oropharyngeal cancer (n = 51) but not in patients with oropharyngeal cancer (n = 139). This is a retrospective study and while causation cannot be gleaned, the results highlight that patients with more significant loss of skeletal muscle are experiencing poorer clinical outcomes. Further, it also highlights that patients with HNSCC are a heterogenous group and more research is necessary to understand what, and if any, relationship exists between change in body composition and oncologic outcomes. Emerging data suggests that patients with HPV-related oropharyngeal cancer, generally a healthier and younger population at diagnosis, are also experiencing significant alterations in body composition as a result of CTRT, but that this may not negatively impact the expected excellent clinical outcomes, at least not at early follow-up [33].

Sarcopenia is not only relevant for oncologic outcomes, but is predictive of worse survival in the general, non-cancer, and population as well. It is associated with numerous negative outcomes, including an impaired stress response, frailty, functional impairment, lower quality of life and decreased overall survival [34–37]. As such, acute sarcopenia, could then explain, at least in part, the dramatic drop in quality of life experienced by even the most functional patients at baseline who undergo CTRT for HNSCC [38]. In a large cross-sectional study in people over the age of 65, sarcopenia predicted for three times more functional impairment in females and two times more functional impairment in males compared to age- and sex-matched participants with normal lean body mass [39]. Further, a large portion of age-associated decline in cardiopulmonary fitness, measured by VO2peak, is also explained by sarcopenia [40]. Low cardiorespiratory fitness is an important precursor for premature mortality regardless of underlying cardiovascular risk factors [41]. Altogether, this highlights the need for studies to better understand the impact of sarcopenia sustained during CTRT and its impact on cardiorespiratory fitness and subsequent non-oncologic mortality in patients with HNSCC.

The current strategies employed to combat metabolic derangements experienced by patients during CTRT generally focus on weight maintenance. Patients are encouraged to eat “as many calories as they can” and when food gets harder to swallow, supplementing it with either oral or parenteral nutrition via a PEG [42]. However, decreased caloric intake is probably only partially responsible for sarcopenia and simply increasing calories may not address loss of muscle mass. In a review of sarcopenia and cachexia in patients with all stages of HNSCC, Couch and colleagues describe the dysregulated metabolism and the resulting sarcopenia seen in patients with HNSCC, suggesting that nutrition alone is not enough to counteract the impact of body composition [21]. In spite of this, numerous studies have tried to optimize nutritional support in patients undergoing CTRT. Clinical trials have evaluated the benefit of individualized nutrition counseling, oral supplementation, and the right type and route of supplemental nutrition. In a systematic review on the effect of nutritional interventions on weight, quality of life and mortality in HNSCC patients treated with RT or CTRT, individualized dietary counseling was beneficial on quality of life, but the impact of tube feedings was not conclusive [43]. For example, in a prospective study of patients with HNSCC undergoing RT, Ravasco and colleagues found that nutritional counseling with regular foods was superior to only adding nutritional supplements in maintaining quality of life during and at 3 months post-RT, but the impact of these interventions on weight was not reported [44]. In a large retrospective review of patients on RTOG 90-03, investigators performed a secondary analysis of patients with HNSCC treated with four different radiation strategies, Rabinovitch and colleagues found that beginning nutritional supplementation before starting RT was a negative prognostic indicator for locoregional failure and death, HR 1.47, 95 % CI 1.21–1.79, p < .0001 and HR 1.41, 95 % CI 1.19–1.67, p < .0001, respectively [45]. Given the retrospective nature of this analysis, nutritional supplement was likely initiated pre-RT in patients who presented with weight loss at diagnosis. This suggests that patients with baseline weight loss have a worse clinical outcomes and not that nutritional supplement itself is having a negative impact on outcomes.

Integration of optimal nutritional support into clinical practice for HNSCC patients has been impeded due to the inconsistent methodology across studies, measuring various time points and outcomes. In response, a group of investigators published a review of the current state of the science on nutrition and malnutrition in HNSCC and provided a set of consensus criteria for implementation and definitions in studies on nutrition in this population [46].

There is growing interest in using pharmacologic supplements to combat cancer-related sarcopenia and cachexia, including amino acids, anabolic steroids, anti-inflammatory agents, and ghrelin-analogues, to counteract the deranged metabolism experienced by cancer patients. Most research in this space has been completed in patients with metastatic disease, often non-small cell lung cancer [44]. One agent of interest in HNSCC patients is eicosapentaenoic acid (EPA), which is an alpha-3-omega fatty acid found in fish oil. In vitro, EPA has been shown to mitigate the lipolysis and inflammatory underpinnings of cachexia [47, 48]. Patients with HNSCC undergoing primary surgical approach did show short-term benefit in loss of muscle mass with EPA, but longer-term follow is needed [49]. A Cochrane review on the use of EPA in cancer cachexia was completed in 2007 and recommended against regular use of EPA [50]. An alternative approach recently explored is anamorelin, an oral ghrelin mimetic. Ghrelin is a ligand for the growth hormone secretagogue receptor and leads to release of growth hormone. There have been two large phase III, double blind placebo-controlled trials of anamorelin in patients with cachexia resulting from unresectable lung cancer. The two studies included a combination of more 900 patients and reported improvement in body weight and anorexia with anamorelin but no improvement in overall survival or strength [51]. Hopefully, pharmacologic interventions will follow a better understanding of the exact mechanism of sarcopenia in patients with HNSCC undergoing CTRT.

Another intervention with the potential to counteract the negative effects of CTRT on body composition is exercise. Exercise has emerged as a promising component of cancer care and has been shown to improve clinical and survival outcomes [52–54]. In a large systematic review and meta-analysis, Speck and colleagues reported favorable changes of exercise on body composition, cardiopulmonary fitness, muscular fitness, psychological well-being, flexibility and quality of life for cancer patients both during and after treatment. While this study included 82 trials, few of the included studies focused on patients with HNSCC [55]. Of those that did, the majority used a progressive resistance training program to improve muscle quantity, quality and function. As sarcopenia and impaired physical functioning remain primary concerns for these patients, this becomes clinically important. Indeed, randomized studies from both breast and prostate cancer patients have shown that resistance training can increase lean muscle mass compared to the control (i.e., sedentary) group [52, 54, 56, 57]. This contrasts to aerobic (or endurance) exercise training, which primarily focuses on improving one’s peak oxygen consumption (VO2peak) – another independent predictor of survival in both oncologic and non-oncologic populations alike. Together, aerobic and resistance exercise training, are complementary to both the cardiovascular and musculoskeletal system.

Against this background, exercise is increasingly being explored as a potential method to combat the negative impact of HNSCC and its treatment on patients. A prior cross-sectional study demonstrated that HNSCC patients get less than the recommended level of activity at all time points; specifically, only 30.5 % are active at baseline, falling to only 8.5 % of patients at the end of treatment [58]. This demonstrates the great potential for exercise to improve outcomes in this currently inactive group. There is good data available on the benefit of therapeutic exercises for shoulder dysfunction or trismus resulting from fibrosis following treatment, but the systemic impacts of exercise in HNSCC are less well understood. We performed a review and summarized the data from studies on progressive resistance training in patients treated for locally advanced HNSCC (Table 1). There was considerable heterogeneity in the study methodology, differing in the type and timing of exercise intervention, as well as the outcomes measured. Regardless, it is clear from the control arms, when available, that there is a negative impact of no intervention [59, 60]. Much like the limitations of current literature in nutritional interventions for HNSCC, there is a need to standardize research in exercise interventions including the type, timing, frequency and duration of studied regimens. Only then can the results from one study be compared to the next and provide measurable, reproducible and generalizable interventions that are relevant to clinical practice.

Table 1 Prospective Studies on resistance training in patients with head and neck cancer
Full size table

Conclusions

HNSCC survivors remain at a substantial risk for long-term disability and early mortality despite achieving initial tumor control [58, 61]. Younger patients are now presenting with HNSCC due to the epidemic of HPV-related oropharyngeal cancer and have an expected better overall prognosis. As these patients live longer past diagnosis, maintaining quality of life and long-term survival is paramount. Longitudinal studies are required to measure the rates of recovery of weight and lean body mass and then in turn, discover new strategies to assist patients as they try to return to baseline functional capacity after aggressive CTRT therapy. Patients with HNSCC are unique in the challenges they face, and the applicability of studies performed in other cancer populations may not be directly relevant to these patients; standardized nutritional and exercise interventions are needed for HNSCC.

Abbreviations

CI, confidence interval; CTRT, concurrent chemotherapy and radiation; DFS, disease free survival; HNSCC, head and neck squamous cell carcinoma; HPV, human papillomavirus; HR, hazards ratio; OS, Overall survival; PEG, percutaneous endoscopic gastrostomy; RT, radiation

References

  1. 1.

    Siegel R, Miller K, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;64(1):5–29. doi:10.3322/caac.21254.

    Article  Google Scholar 

  2. 2.

    Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61(2):69–90. doi:10.3322/caac.20107.

    Article  PubMed  Google Scholar 

  3. 3.

    Chaturvedi A, Anderson W, Lortet-Tieulent J, Curado M, Ferlay J, Franceschi S, et al. Worldwide trends in incidence rates for oral cavity and oropharyngeal cancers. J Clin Oncol. 2013;31(36):4550–9. doi:10.1200/JCO.2013.50.3870.

    Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Simard EP, Torre LA, Jemal A. International trends in head and neck cancer incidence rates: differences by country, sex and anatomic site. Oral Oncol. 2014;50(5):387–403. doi:10.1016/j.oraloncology.2014.01.016.

    Article  PubMed  Google Scholar 

  5. 5.

    Ang K, Harris J, Wheeler R, Weber R, Rosenthal D, Nguyen-Tan P, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010;363(1):24–35. doi:10.1056/NEJMoa0912217.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Licitra L, Perrone F, Bossi P, Suardi S, Mariani L, Artusi R, et al. High-risk human papillomavirus affects prognosis in patients with surgically treated oropharyngeal squamous cell carcinoma. J Clin Oncol. 2006;24(36):5630–6. doi:10.1200/JCO.2005.04.6136.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Ringash J. Survivorship and quality of life in head and neck cancer. J Clin Oncol. 2015;33(29):3322–7. doi:10.1200/jco.2015.61.4115.

    Article  PubMed  Google Scholar 

  8. 8.

    Adelstein D, Li Y, Adams G, Wagner H, Kish J, Ensley J, et al. An intergroup phase III comparison of standard radiation therapy and two schedules of concurrent chemoradiotherapy in patients with unresectable squamous cell head and neck cancer. J Clin Oncol. 2003;21(1):92–8.

    Article  PubMed  Google Scholar 

  9. 9.

    Forastiere A, Goepfert H, Maor M, Pajak T, Weber R, Morrison W, et al. Concurrent chemotherapy and radiotherapy for organ preservation in advanced laryngeal cancer. N Engl J Med. 2003;349(22):2091–8. doi:10.1056/NEJMoa031317.

    CAS  Article  PubMed  Google Scholar 

  10. 10.

    List MA, Siston A, Haraf D, Schumm P, Kies M, Stenson K, et al. Quality of life and performance in advanced head and neck cancer patients on concomitant chemoradiotherapy: a prospective examination. J Clin Oncol. 1999;17(3):1020.

    CAS  PubMed  Google Scholar 

  11. 11.

    García-Peris P, Lozano MA, Velasco C, de La Cuerda C, Iriondo T, Bretón I, et al. Prospective study of resting energy expenditure changes in head and neck cancer patients treated with chemoradiotherapy measured by indirect calorimetry. Nutrition. 2005;21(11–12):1107–12. http://dx.doi.org/10.1016/j.nut.2005.03.006.

    Article  PubMed  Google Scholar 

  12. 12.

    Lonbro S, Petersen GB, Andersen JR, Johansen J. Prediction of critical weight loss during radiation treatment in head and neck cancer patients is dependent on BMI. Support Care Cancer. 2016;24(5):2101–9. doi:10.1007/s00520-015-2999-8.

    Article  PubMed  Google Scholar 

  13. 13.

    Mick R, Vokes EE, Weichselbaum RR, Panje WR. Prognostic factors in advanced head and neck cancer patients undergoing multimodality therapy. Otolaryngol Head Neck Surg. 1991;105(1):62–73.

    CAS  PubMed  Google Scholar 

  14. 14.

    Ghadjar P, Hayoz S, Zimmermann F, Bodis S, Kaul D, Badakhshi H, et al. Impact of weight loss on survival after chemoradiation for locally advanced head and neck Cancer: secondary results of a randomized phase III trial (SAKK 10/94). Radiat Oncol. 2015;10(1):21.

    Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Silver HJ, Dietrich MS, Murphy BA. Changes in body mass, energy balance, physical function, and inflammatory state in patients with locally advanced head and neck cancer treated with concurrent chemoradiation after low-dose induction chemotherapy. Head Neck. 2007;29(10):893–900. doi:10.1002/hed.20607.

    Article  PubMed  Google Scholar 

  16. 16.

    Nourissat A, Bairati I, Samson E, Fortin A, Gelinas M, Nabid A, et al. Predictors of weight loss during radiotherapy in patients with stage I or II head and neck cancer. Cancer. 2010;116(9):2275–83. doi:10.1002/cncr.25041.

    PubMed  Google Scholar 

  17. 17.

    Couch ME, Dittus K, Toth MJ, Willis MS, Guttridge DC, George JR, et al. Cancer cachexia update in head and neck cancer: pathophysiology and treatment. Head Neck. 2015;37(7):1057–72. doi:10.1002/hed.23696.

    Article  PubMed  Google Scholar 

  18. 18.

    Caudell JJ, Schaner PE, Meredith RF, Locher JL, Nabell LM, Carroll WR, et al. Factors associated with long-term dysphagia after definitive radiotherapy for locally advanced head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2009;73(2):410–5. http://dx.doi.org/10.1016/j.ijrobp.2008.04.048.

    Article  PubMed  Google Scholar 

  19. 19.

    Langmore S, Krisciunas GP, Miloro KV, Evans SR, Cheng DM. Does PEG use cause dysphagia in head and neck cancer patients? Dysphagia. 2011;27(2):251–9. doi:10.1007/s00455-011-9360-2.

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Mekhail TM, Adelstein DJ, Rybicki LA, Larto MA, Saxton JP, Lavertu P. Enteral nutrition during the treatment of head and neck carcinoma. Cancer. 2001;91(9):1785–90. doi:10.1002/1097-0142(20010501)91:9<1785::AID-CNCR1197>3.0.CO;2-1.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Couch M, Lai V, Cannon T, Guttridge D, Zanation A, George J et al. Cancer cachexia syndrome in head and neck cancer patients: part I. Diagnosis, impact on quality of life and survival, and treatment. Head Neck. 2007;29. doi:10.1002/hed.20447.

  22. 22.

    Lenk K, Schuler G, Adams V. Skeletal muscle wasting in cachexia and sarcopenia: molecular pathophysiology and impact of exercise training. J Cachexia Sarcopenia Muscle. 2010;1. doi:10.1007/s13539-010-0007-1.

  23. 23.

    Carmeli E, Coleman R, Reznick AZ. The biochemistry of aging muscle. Exp Gerontol. 2002;37(4):477–89. http://dx.doi.org/10.1016/S0531-5565(01)00220-0.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Doherty TJ. Invited Review: aging and sarcopenia. J Appl Physiol. 2003;95(4):1717–27. doi:10.1152/japplphysiol.00347.2003.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Tzankoff SP, Norris AH. Effect of muscle mass decrease on age-related BMR changes. J Appl Physiol. 1977;43(6):1001–6.

    CAS  PubMed  Google Scholar 

  26. 26.

    Forbes GB, Reina JC. Adult lean body mass declines with age: some longitudinal observations. Metabolism. 1970;19(9):653–63.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Mijnarends DM, Meijers JM, Halfens RJ, ter Borg S, Luiking YC, Verlaan S, et al. Validity and reliability of tools to measure muscle mass, strength, and physical performance in community-dwelling older people: a systematic review. J Am Med Dir Assoc. 2013;14(3):170–8. doi:10.1016/j.jamda.2012.10.009.

    Article  PubMed  Google Scholar 

  28. 28.

    Prado CMM, Baracos VE, McCargar LJ, Reiman T, Mourtzakis M, Tonkin K, et al. Sarcopenia as a determinant of chemotherapy toxicity and time to tumor progression in metastatic breast cancer patients receiving capecitabine treatment. Clin Cancer Res. 2009;15(8):2920–6. doi:10.1158/1078-0432.ccr-08-2242.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    McMillan DC, Watson WS, Preston T, McArdle CS. Lean body mass changes in cancer patients with weight loss. Clin Nutr. 2000;19(6):403–6. http://dx.doi.org/10.1054/clnu.2000.0136.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Kadar L, Albertsson M, Areberg J, Landberg T, Mattsson S. The prognostic value of body protein in patients with lung cancer. Ann N Y Acad Sci. 2000;904:584–91.

    CAS  Article  PubMed  Google Scholar 

  31. 31.

    Blauwhoff-Buskermolen S, Versteeg KS, de van der Schueren MA, den Braver NR, Berkhof J, Langius JA, et al. Loss of muscle mass during chemotherapy is predictive for poor survival of patients with metastatic colorectal cancer. J Clin Oncol. 2016;34(12):1339–44.

    Article  PubMed  Google Scholar 

  32. 32.

    Grossberg AJ, Chamchod S, Fuller CD, Mohamed AS, Heukelom J, Eichelberger H, et al. Association of body composition with survival and locoregional control of radiotherapy-treated head and neck squamous cell carcinoma. JAMA Oncol. 2016;2(6):782–9. doi:10.1001/jamaoncol.2015.6339.

    Article  PubMed  Google Scholar 

  33. 33.

    Baxi SS Jones L, Eaton A, Gandelman S, Halpenny D, Jackson J, et al. Changes in body composition and prognostic importance of sarcopenia in patients receiving CTRT for oropharyngeal cancer. J Clin Oncol. 2016;34(supplement):abstr 6077.

    Google Scholar 

  34. 34.

    Collins J, Noble S, Chester J, Coles B, Byrne A. The assessment and impact of sarcopenia in lung cancer: a systematic review. BMJ Open. 2014;46. doi:10.1136/bmjopen-2013-003697.

  35. 35.

    Pereira CT, Barrow RE, Sterns AM, Hawkins HK, Kimbrough CW, Jeschke MG, et al. Age-dependent differences in survival after severe burns: a unicentric review of 1,674 patients and 179 autopsies over 15 years. J Am Coll Surg. 2006;202(3):536–48. doi:10.1016/j.jamcollsurg.2005.11.002.

    Article  PubMed  Google Scholar 

  36. 36.

    Evans WJ. What is sarcopenia? J Gerontol A Biol Sci Med Sci. 1995;50(Spec No):5–8.

    Article  PubMed  Google Scholar 

  37. 37.

    Fulster S, Tacke M, Sandek A, Ebner N, Tschope C, Doehner W, et al. Muscle wasting in patients with chronic heart failure: results from the studies investigating co-morbidities aggravating heart failure (SICA-HF). Eur Heart J. 2013;34(7):512–9. doi:10.1093/eurheartj/ehs381.

    Article  PubMed  Google Scholar 

  38. 38.

    Sharma A, Méndez E, Yueh B, Lohavanichbutr P, Houck J, Doody DR, et al. Human papillomavirus–positive oral cavity and oropharyngeal cancer patients do not have better quality-of-life trajectories. Otolaryngol Head Neck Surg. 2012;146(5):739–45.

    Article  PubMed  PubMed Central  Google Scholar 

  39. 39.

    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(5):889–96.

    Article  PubMed  Google Scholar 

  40. 40.

    Fleg JL, Lakatta EG. Role of muscle loss in the age-associated reduction in VO2 max. J Appl Physiol. 1988;65(3):1147–51.

    CAS  PubMed  Google Scholar 

  41. 41.

    Blair SN, Kampert JB, Kohl HW, Barlow CE, Macera CA, Paffenbarger RS, et al. Influences of cardiorespiratory fitness and other precursors on cardiovascular disease and all-cause mortality in men and women. JAMA. 1996;276(3):205–10.

    CAS  Article  PubMed  Google Scholar 

  42. 42.

    Ravasco P, Monteiro-Grillo I, Vidal PM, Camilo ME. Nutritional deterioration in cancer: the role of disease and diet. Clin Oncol. 2003;15(8):443–50. doi:10.1016/S0936-6555(03)00155-9.

    CAS  Article  Google Scholar 

  43. 43.

    Langius JA, Zandbergen MC, Eerenstein SE, van Tulder MW, Leemans CR, Kramer MH, et al. Effect of nutritional interventions on nutritional status, quality of life and mortality in patients with head and neck cancer receiving (chemo)radiotherapy: a systematic review. Clin Nutr. 2013;32(5):671–8. doi:10.1016/j.clnu.2013.06.012.

    Article  PubMed  Google Scholar 

  44. 44.

    Ravasco P, Monteiro-Grillo I, Marques Vidal P, Camilo ME. Impact of nutrition on outcome: a prospective randomized controlled trial in patients with head and neck cancer undergoing radiotherapy. Head Neck. 2005;27(8):659–68. doi:10.1002/hed.20221.

    Article  PubMed  Google Scholar 

  45. 45.

    Rabinovitch R, Grant B, Berkey BA, Raben D, Ang KK, Fu KK, et al. Impact of nutrition support on treatment outcome in patients with locally advanced head and neck squamous cell cancer treated with definitive radiotherapy: a secondary analysis of RTOG trial 90-03. Head Neck. 2006;28(4):287–96. doi:10.1002/hed.20335.

    Article  PubMed  Google Scholar 

  46. 46.

    Dechaphunkul T, Martin L, Alberda C, Olson K, Baracos V, Gramlich L. Malnutrition assessment in patients with cancers of the head and neck: A call to action and consensus. Crit Rev Oncol Hematol. 2013;88(2):459–76. doi:10.1016/j.critrevonc.2013.06.003.

  47. 47.

    Wigmore SJ, Fearon KC, Maingay JP, Ross JA. Down-regulation of the acute-phase response in patients with pancreatic cancer cachexia receiving oral eicosapentaenoic acid is mediated via suppression of interleukin-6. Clin Sci. 1997;92(2):215–21.

    CAS  Article  PubMed  Google Scholar 

  48. 48.

    Price SA, Tisdale MJ. Mechanism of inhibition of a tumor lipid-mobilizing factor by eicosapentaenoic acid. Cancer Res. 1998;58(21):4827–31.

    CAS  PubMed  Google Scholar 

  49. 49.

    Weed HG, Ferguson ML, Gaff RL, Hustead DS, Nelson JL, Voss AC. Lean body mass gain in patients with head and neck squamous cell cancer treated perioperatively with a protein‐and energy‐dense nutritional supplement containing eicosapentaenoic acid. Head Neck. 2011;33(7):1027–33.

    Article  PubMed  Google Scholar 

  50. 50.

    Dewey A, Baughan C, Dean T, Higgins B, Johnson I. Eicosapentaenoic acid (EPA, an omega-3 fatty acid from fish oils) for the treatment of cancer cachexia. Cochrane Database Syst Rev. 2007(1):CD004597. doi:10.1002/14651858.CD004597.pub2.

  51. 51.

    Temel JS, Abernethy AP, Currow DC, Friend J, Duus EM, Yan Y, et al. 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(4):519–31. http://dx.doi.org/10.1016/S1470-2045(15)00558-6.

    CAS  Article  PubMed  Google Scholar 

  52. 52.

    Schmitz KH, Ahmed RL, Hannan PJ, Yee D. Safety and efficacy of weight training in recent breast cancer survivors to alter body composition, insulin, and insulin-like growth factor axis proteins. Cancer Epidemiol Biomark Prev. 2005;14. doi:10.1158/1055-9965.epi-04-0736.

  53. 53.

    Mock V, Pickett M, Ropka ME, Muscari Lin E, Stewart KJ, Rhodes VA et al. Fatigue and quality of life outcomes of exercise during cancer treatment. Cancer Pract. 2001;9. doi:10.1046/j.1523-5394.2001.009003119.x.

  54. 54.

    Courneya KS, Mackey JR, Bell GJ, Jones LW, Field CJ, Fairey AS. Randomized controlled trial of exercise training in postmenopausal breast cancer survivors: cardiopulmonary and quality of life outcomes. J Clin Oncol. 2003;21(9):1660–8.

    Article  PubMed  Google Scholar 

  55. 55.

    Speck RM, Courneya KS, Masse LC, Duval S, Schmitz KH. An update of controlled physical activity trials in cancer survivors: a systematic review and meta-analysis. J Cancer Surviv. 2010;4. doi:10.1007/s11764-009-0110-5.

  56. 56.

    Segal RJ, Reid RD, Courneya KS, Malone SC, Parliament MB, Scott CG, et al. Resistance exercise in men receiving androgen deprivation therapy for prostate cancer. J Clin Oncol. 2003;21(9):1653–9. doi:10.1200/JCO.2003.09.534.

    Article  PubMed  Google Scholar 

  57. 57.

    Galvão DA, Taaffe DR, Spry N, Joseph D, Newton RU. Combined resistance and aerobic exercise program reverses muscle loss in men undergoing androgen suppression therapy for prostate cancer without bone metastases: a randomized controlled trial. J Clin Oncol. 2010;28(2):340–7.

    Article  PubMed  Google Scholar 

  58. 58.

    Rogers L, Courneya K, Robbins KT, Malone J, Seiz A, Koch L, et al. Physical activity and quality of life in head and neck cancer survivors. Support Care Cancer. 2006;14(10):1012–9. doi:10.1007/s00520-006-0044-7.

    Article  PubMed  Google Scholar 

  59. 59.

    Samuel SR, Maiya GA, Babu AS, Vidyasagar MS. Effect of exercise training on functional capacity & quality of life in head & neck cancer patients receiving chemoradiotherapy. Indian J Med Res. 2013;137(3):515–20.

    PubMed  PubMed Central  Google Scholar 

  60. 60.

    Rogers LQ, Anton PM, Fogleman A, Hopkins–Price P, Verhulst S, Rao K, et al. Pilot, randomized trial of resistance exercise during radiation therapy for head and neck cancer. Head Neck. 2013;35(8):1178–88. doi:10.1002/hed.23118.

    Article  PubMed  Google Scholar 

  61. 61.

    Baxi SS, Pinheiro LC, Patil SM, Pfister DG, Oeffinger KC, Elkin EB. Causes of death in long-term survivors of head and neck cancer. Cancer. 2014;120(10):1507–13. doi:10.1002/cncr.28588.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We have no acknowledgements to report.

Funding

This work was also supported by a Cancer Center Support Grant from the National Cancer Institute to Memorial Sloan Kettering Cancer Center (award number P30 CA008748).

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Authors’ contributions

SB made substantial contributions to conception and design, drafted the manuscript and ensures the integrity of the work. ES made substantial contributions to conception and design, drafted parts of the manuscript and ensures the integrity of the work. LJ contributed to the conception and design and ensures the integrity of the work. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests however SSB does serve on an advisory board for AstraZeneca and Lilly Oncology and serves as a consultant for Bristol Myers Squibb.

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  1. Head and Neck Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, 300 East 66th Street, Rm 1459, New York, NY, 10065, USA

    Shrujal S. Baxi

  2. Department of Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Ave, New York, NY, 10065, USA

    Emily Schwitzer & Lee W. Jones

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  1. Shrujal S. Baxi
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  2. Emily Schwitzer
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Correspondence to Shrujal S. Baxi.

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Baxi, S.S., Schwitzer, E. & Jones, L.W. A review of weight loss and sarcopenia in patients with head and neck cancer treated with chemoradiation. Cancers Head Neck 1, 9 (2016). https://doi.org/10.1186/s41199-016-0010-0

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Keywords

  • Head and neck cancer
  • Sarcopenia
  • Chemoradiation
  • Quality of life
  • Cardiopulmonary fitness
  • Nutrition

Cancers of the Head & Neck

ISSN: 2059-7347

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