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The effectiveness of nutritional interventions in malnutrition and cachexia

Published online by Cambridge University Press:  19 June 2015

Christine Baldwin*
Affiliation:
Division of Diabetes and Nutritional Sciences, King's College London, Franklin Wilkins Building, 150 Stamford Street, London SE1 9NH, UK
*
Corresponding author: C. Baldwin, email christine.baldwin@kcl.ac.uk
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Abstract

Cancer is a common diagnosis and leading cause of death worldwide. Amounts of weight loss vary but it is associated with considerable morbidity, poorer quality of life and reduced survival. Nutritional intervention has the potential to maximise response to treatment and improve functioning and quality of life. The aim of this paper was to review the evidence for oral nutritional interventions in the management of weight loss in patients with cancer. Comparison of studies of nutritional support interventions in people with cancer is complicated by variations in understanding of what constitutes a compromised nutritional status. There are similarities and differences between definitions of both malnutrition and cachexia and studies of oral nutritional interventions have failed to use standard criteria at study inclusion contributing to heterogeneity amongst studies. Meta-analysis of randomised controlled trials has suggested limited evidence of benefit to nutritional and clinical outcomes but some improvements to aspects of quality of life. The presence of cachexia in patients with cancer might explain the limited efficacy of simple oral nutritional interventions, which lack a component designed to address metabolic abnormalities associated with cachexia. Novel strategies combining nutritional support with therapeutic agents designed to down-regulate the metabolic aberrations have failed to demonstrate consistent benefits and the results of multimodal treatments combining several interventions are awaited. There is a need for intervention studies recruiting patients early in the disease course, which underlines the need for definitions which predict poor outcome and hence allow early recognition of vulnerable patients.

Type
Conference on ‘Nutrition and age-related muscle loss, sarcopenia and cachexia’
Copyright
Copyright © The Author 2015 

The most recent data indicate that worldwide there were about 14 million new cases of cancer diagnosed in 2012 and greater than 330 000 diagnoses being made in the UK in 2011( 1 , Reference Ferlay, Soerjomataram and Ervik 2 ). Cancer remains a leading cause of death worldwide and it is estimated that that 8·2 million people died from cancer in 2012 with about 162 000 deaths from cancer in the UK( 1 ). Despite the dismal nature of these data, more than half of people diagnosed with cancer will survive for 10 years or more;( 1 ) therefore efforts to maximise the ability of patients to respond to treatment and to achieve a good quality of life are paramount.

The morbidity experienced by people with cancer arises from the presence of disease and from the side-effects of treatment. The presence, number and intensity of symptoms are likely to account for a large amount of the suffering experienced by patients. Weight loss is a common symptom in people diagnosed with cancer. A pooled prevalence for any amount of weight loss of 46 (95 % CI 34, 59) % was reported by a systematic review of symptom prevalence in people with incurable cancer( Reference Teunissen, Wesker and Kruitwagen 3 ). Amounts of weight loss vary according to the site and stage of disease. A retrospective review of 3047 patients with different cancers entering clinical trials, reported a prevalence varying from 31 % to 87 % with the greatest amounts of weight loss found in patients with cancers of the upper gastrointestinal tract( Reference Dewys, Begg and Lavin 4 ). In a group of patients with advanced cancer and weight loss, 34 % reported concern about what weight loss meant for them( Reference Hopkinson, Wright and McDonald 5 ). In addition, pre-illness weight loss of as little as 5 % has been demonstrated to be associated with reduced survival( Reference Dewys, Begg and Lavin 4 , Reference Andreyev, Norman and Oates 6 ). Weight loss is also associated with more adverse reactions and poorer response to treatment as well as reduced quality of life compared with patients with no weight loss( Reference Arends, Bodoky and Bozzetti 7 ).

Taken together, these data provide a rationale for the use of strategies to limit and treat weight loss as part of care for people with cancer and indeed nutritional management is a widely accepted strategy recommended by a number of bodies( Reference Arends, Bodoky and Bozzetti 7 Reference Bauer, Ash and Davidson 9 ).

Definition and recognition of malnutrition and cachexia

The timely management of patients with weight loss requires their early recognition as well as clear guidelines on the indicators that best identify patients most likely to benefit from nutritional treatment. An audit of the ability of healthcare professionals to recognise weight loss in patients with cancer demonstrated that the staff frequently failed to identify those that met the criteria as suggested by the Malnutrition Universal Screening Tool for being malnourished( Reference Baldwin, McGough and Norman 10 ). A survey of knowledge and practice of 337 oncologists in managing nutritional support suggested that 80 % were uncertain about identifying malnourished patients with lack of knowledge being identified as a barrier in 60 % of participants( Reference Spiro, Baldwin and Patterson 11 ). These studies underline the difficulties that staff face in meeting the nutritional needs of patients with weight loss and at least in part may result from variations in definitions but also overlap in understanding of the aetiology and clinical basis of observed weight loss. Guidelines and indicators for the identification of patients that are malnourished or at risk of malnutrition vary. The National Institute for Clinical Excellence in their guidance on the nutrition support of adults suggested malnutrition was defined as ‘a state in which a deficiency of energy, protein and other nutrients causes measurable adverse effects on body form, function or clinical outcome’( 12 ). National Institute for Clinical Excellence suggest that indicators based on low BMI (18·5 kg/m2) or unintentional weight loss (>10 %) or a combination of the two (BMI < 20 kg/m2 and weight loss >5 %) should be used to identify malnutrition. Other groups have suggested a classification of malnutrition, which is aetiology based and takes into consideration the disease and non-disease-related causes of malnutrition( Reference Jensen, Mirtallo and Compher 13 ). Operational cut-offs for use in practice are still in development, but have been suggested as including any two of insufficient energy intake, weight loss, loss of muscle, loss of subcutaneous fat, loss or gain of fluid or reduced function assessed by handgrip strength( Reference White, Guenter and Jensen 14 ).

The situation in patients with cancer may be further complicated by the existence of cachexia. Cancer cachexia was defined as an accelerated loss of skeletal muscle in the context of a chronic inflammatory response and was considered to be a syndrome consisting of combinations of anorexia, weight loss, metabolic alterations, an inflammatory state and anaemia( Reference Laviano, Meguid and Inui 15 ). This definition could be seen to make cachexia different from malnutrition but lacked operational cut-offs to guide recognition in practice. The concept of cachexia has received considerable attention recently and a number of groups have suggested definitions together with operational indicators as summarised in Table 1. The indicators considered to be indicative of the presence of cachexia were different with all definitions including weight loss and five of six including anorexia or a measure of food intake but the cut-offs suggested for each indicator varied. The most recent definition was the consensus view of an international group of experts and relies on combinations of weight loss together with low BMI or low appendicular skeletal muscle loss( Reference Fearon, Strasser and Anker 16 ). Notably there was disagreement about the inclusion of systemic inflammatory markers, which have been included by some expert groups but were absent in the consensus definition, although it was recognised that cachexia can exist with or without inflammation( Reference Fearon, Strasser and Anker 16 ). Importantly, cachexia is not a single event and has been recognised by many experts groups as representing a spectrum from pre-cachexia to refractory cachexia and death( Reference Fearon 17 ). The definition proposed by the expert panel has been widely recognised, but its predictive validity remains to be determined.

Table 1. Definitions of cachexia recently proposed by expert groups

CRP, C-Reactive Protein; FFM, fat free mass; kcal, kilocalories.

Cancer is primarily a disease of older people and in older people three primary categories of muscle loss in association with weight loss have been recognised; starvation, sarcopenia and cachexia( Reference Fearon and Thomas 18 ). In practical terms, the key question is whether all of these entities are similar and should therefore be managed in the same way or whether they are distinct entities, which may be related.

Which nutritional interventions?

In practice, the majority of patients identified as having weight loss and recognised for referral to a dietitian during the course of treatment for cancer will receive oral nutritional support interventions as a first line management strategy. Oral nutritional support consists of a range of options, including food-based interventions, which may include increased size of meals, the use of snacks to supplement intake from meals and fortification of food to increase their nutrient density, as well as the use of proprietary oral nutritional supplements( Reference Qureshi, Kellie, Darnley and Gandy 19 ). Oral nutritional support options may be provided directly to patients in any care settings, e.g. the provision of nourishing drinks and snacks in residential care or on hospital wards, or may be communicated to patients as dietary advice, to guide patients when at home. Dietary advice has the advantage of being able to be tailored to individual habits, as well as the social and psychological needs of the patient. Conversely, oral nutritional supplements require no preparation and are easy to take.

Each type of nutritional support is associated with different practical considerations. For example advising patients to increase their nutritional intake through the inclusion of additional snacks will allow a patient greater variety compared with a prescription for oral nutritional supplements, but requires the patient to be able to shop, cook and prepare food as well as needing to have sufficient money to buy additional snack items. In practice, patient-related aspects are taken into consideration during the dietetic assessment and many patients will receive a combination of oral nutritional support measures to improve their intake.

Assessment of effectiveness of nutritional interventions

Several societies and nutritional guideline bodies have supported the recommendation that patients with cancer and weight loss should receive nutritional support( Reference Arends, Bodoky and Bozzetti 7 , Reference Bauer, Ash and Davidson 9 , 12 ). The European Society for Clinical Nutrition and Metabolism suggest that ‘nutritional therapy should be started if under-nutrition already exists or if it is anticipated that the patient will be unable to eat for more than seven days. Enteral nutrition should also be started if an inadequate food intake (<60 % of estimated energy expenditure) is anticipated for more than 10 days’( Reference Arends, Bodoky and Bozzetti 7 ). This recommendation, like those of many of the other bodies, is based largely on expert opinion. To understand whether there is an evidence base to support this recommendation, it is necessary to examine the evidence for a benefit of nutritional interventions in people with cancer and weight loss. Before considering whether nutritional intervention resulted in benefits to patients it is necessary to consider which outcomes are most appropriate to assess the benefits of nutritional interventions.

An outcome has been defined as the quantifiable change in the health status of a patient between two or more timepoints( Reference Voss and Gallagher-Allred 20 ). Traditionally, outcomes have been defined in terms of mortality and morbidity and tended to focus on aspects that are of most concern to researchers. In the past 20 years, the assessment of outcomes has become a multidimensional concept that includes clinical outcomes (mortality and morbidity) as well as broader outcome measures such as quality of life, patient satisfaction, functionality and economic outcomes. Measurement of outcomes can take place at the individual level, organisational level through to the national and international levels and is a developing field with no single measure applicable to all situations( Reference Qureshi, Kellie, Darnley and Gandy 19 ). The use of Patient-Related Outcome Measures is being developed in some clinical situations and is likely to expand to cover different areas of healthcare( Reference Qureshi, Kellie, Darnley and Gandy 19 ).

Nutritional interventions are often assessed in terms of nutritional endpoints such as change in nutritional intake and their impact on nutritional status. It is equally valid to consider them in terms of their impact on clinical outcomes, functional endpoints and cost effectiveness. In 1995, The American Society for Clinical Oncology proposed guidelines for outcomes to be used in the assessment of treatment effects( 21 ). Outcomes were defined in two categories: those relating to the treatment (response to treatment, response duration and time to progression) and patient-related outcomes defined as survival, toxicity and quality of life. These guidelines were reconsidered recently and all working groups were in agreement that overall survival should remain the primary outcome for clinical trials but acknowledged the limitations of this outcome and the need to define clinically meaningful outcomes as well as to balance the risks and benefits of therapies( Reference Ellis, Bernstein and Voest 22 ). The European Society for Clinical Nutrition and Metabolism in its guidelines on the nutritional management of patients with cancer highlighted the therapeutic goal for cancer patients to be the improvement of function and outcome assessed by the prevention and treatment of undernutrition, enhancement of the anti-tumour effects, reduction of adverse effects of therapy and the improvement of quality of life( Reference Arends, Bodoky and Bozzetti 7 ).

Evidence for effectiveness in patients with cancer

The role of oral nutritional support in managing weight loss in patients with cancer has been examined in a recent systematic review( Reference Baldwin, Spiro and Ahern 23 ). Systematic searches of ten electronic databases identified thirteen randomised controlled trials of oral nutritional interventions in cancer patients who were malnourished or at risk of malnutrition, including 1414 participants. The trial were homogeneous for the interventions given in that all interventions comprised either dietary advice to increase nutritional intake, the provision of oral nutritional supplements or both given together. Included studies varied according to site and stage of tumour, the nature and intent of clinical treatment and the amount of information provided on the nutritional status of patients at baseline. Only four of the thirteen studies defined nutritional status as an inclusion criterion, using recent weight loss as a threshold. Although the inclusion of the remaining participants was justified on the basis of their being at nutritional risk, there was considerable heterogeneity both within and between studies with some studies, including both well-nourished and malnourished patients( Reference Baldwin, Spiro and Ahern 23 ). Despite the considerable attention being given to the definitions of malnutrition and cachexia, no study used a widely accepted definition for either malnutrition or cachexia to identify patients for inclusion into trials.

Nutritional intake and nutritional status

Data were available on energy intake from ten of the thirteen studies and all reported significant improvements to energy intake. Meta-analysis was only possible on data for this outcome from four studies and the results were too heterogeneous to draw conclusions about the size of any overall effect( Reference Baldwin, Spiro and Ahern 23 ). Data were available on change in body weight from eight of the thirteen studies (twelve comparisons). The meta-analysis of all studies combined suggested a significant benefit of intervention on body weight, but again the heterogeneity between studies was high (I 2 = 76 %, P < 0·0001). The analysis was repeated with data from three studies that contributed the most heterogeneity removed and there was no difference in body weight between groups (mean difference 0·31 (95 % CI −0·60, +1·21) kg, P = 0·50; Table 2).

Table 2. Effectiveness of oral nutritional interventions in the management of weight loss in patients with cancer: findings of a systematic review and meta-analysis (based on the meta-analyses and results presented in( Reference Baldwin, Spiro and Ahern 23 ))

RR, relative risk; MD, mean difference; CI, confidence intervals.

* meta-analysis not undertaken, data previously unpublished.

Effects on outcomes of cancer treatment

Studies included in the meta-analysis assessed three different aspects of treatment outcome; effects on response to treatment, effects on treatment interruptions and effects on treatment toxicity. These data were analysed after completion and publication of the meta-analysis and are therefore reported according to the original studies. Six studies examined the efficacy of nutritional interventions in terms of response to anti-tumour treatment and there were no differences between groups in any study( Reference Arnold and Richter 24 Reference Ovesen, Allingstrup and Hannibal 28 , Reference Elkort, Baker and Vitale 31 ). Four studies assessed the effects of nutritional interventions on treatment interruptions and there were no statistically significant differences between groups, although two studies( Reference Macia, Moran and Santos 29 , Reference Nayel, El-Ghoneimy and El-Haddad 30 ) reported more days of treatment interruptions in patients receiving routine care than in those receiving intervention. Seven studies assessed the efficacy of nutritional interventions in reducing treatment toxicity. Two studies reported no difference between groups( Reference Arnold and Richter 24 , Reference Elkort, Baker and Vitale 31 ), five studies( Reference Evans, Nixon and Daly 25 , Reference Macia, Moran and Santos 29 , Reference Nayel, El-Ghoneimy and El-Haddad 30 , Reference Ravasco, Monteiro-Grillo and Vidal 32 , Reference Ravasco, Monteiro-Grillo and Marques Vidal 33 ) suggested fewer toxicities in patients receiving nutritional intervention compared with routine care, with two studies reporting significantly fewer symptoms at the end of treatment in groups receiving food-based or supplement-based nutritional support( Reference Ravasco, Monteiro-Grillo and Vidal 32 , Reference Ravasco, Monteiro-Grillo and Marques Vidal 33 ).

Effects on mortality

Data were available for meta-analysis from eleven of the thirteen studies on mortality and there were no significant differences between groups and no heterogeneity (relative risk 1·06 (95 % CI 0·92, 1·22), P = 0·43; Table 2).

Effects on patient-centred outcomes

Seven of the thirteen studies reported data on quality of life, of which five included data collected using the European Organisation for Research and Treatment of Cancer-core30 instrument that could be included in a meta-analysis. Data on each of the fifteen scales within the questionnaire were analysed separately and after adjustment for heterogeneity in some analyses, significantly greater benefits to emotional functioning, dyspnoea, loss of appetite and global quality of life were observed in patients receiving oral nutritional interventions compared with routine care. The improvements in quality of life noted were consistent with both small and large differences in scores( Reference King 34 ) and are likely to be clinically meaningful. The European Organisation for Research and Treatment of Cancer is a generic instrument and it is difficult to assess whether all of the issues relevant to patients have been accounted for with this instrument. There are many tumour-specific versions of the European Organisation for Research and Treatment of Cancer, which have not been used in the present study and it is possible that the other benefits from receiving nutritional interventions were experienced by patients but not identified by these analyses.

Quality of life is not the same as patient satisfaction and many other patient-related outcomes are relevant to consider in the context of examining the efficacy of oral nutritional interventions in patients with cancer and weight loss, but have not been reported in studies. One study included in the review reported higher levels of patient satisfaction with both the nutrition services provided and perceived health benefits in participants receiving nutritional intervention compared with participants receiving routine care( Reference Isenring, Capra and Bauer 35 ).

Cost-effectiveness

The cost utility of providing oral nutritional interventions to patients with cancer and weight loss was examined using original data from two studies, mapping data collected using the European Organisation for Research and Treatment of Cancer-core30 instrument onto the EuroQol-5D( Reference Baldwin, Spiro and McGough 36 , Reference Uster, Ruefenacht and Ruehlin 37 ). There was no difference in Quality of Life Years gained between the intervention and control groups in either study. The costs of providing nutritional intervention (estimated from the cost of dietitian time and the cost of oral nutritional supplements) were higher in those receiving oral nutritional interventions, suggesting that usual care may be a more cost-effective approach (M Manzorou, PW Emery, P McCrone and C Baldwin, unpublished results). This analysis is preliminary, based on data only from two studies and not derived from a full cost-effectiveness analysis and should be interpreted with caution.

Overall the findings of this recent meta-analysis suggest that oral nutritional interventions have no effect on survival and that the effect on body weight and energy intake is inconsistent but that statistically significant improvements in some aspects of quality of life may be achieved. In addition, there is a small amount of evidence suggesting that nutritional interventions are associated with greater patient satisfaction and that in some patients reductions in treatment toxicity may be experienced. The data on cost-effectiveness are too preliminary to determine any potential benefits.

The management of weight loss in the context of cachexia

The limited effectiveness of oral nutritional support strategies in managing weight loss in patients with cancer may in part be explained by the aetiology of the underlying condition. It has been suggested that the multifactorial nature of the problem is likely to require a multidimensional solution( Reference Fearon 17 , Reference Mantovani, Maccio and Madeddu 38 ). It is likely that successful strategies will need to address more than the food-related aspects of weight loss and combine strategies to improve nutritional intake with substances that will modulate the metabolic derangements associated with cachexia (Fig. 1). With this in mind a number of potential therapeutic strategies have been trialled and their progress to date is summarised in Table 3. Despite the relatively large number of agents trialled, both with and without additional nutrition, and either singly or in combination with one another, there remains no standard accepted treatment for the management of cancer cachexia available. Prostagens are currently the only approved drug for the management of cachexia but they have limited efficacy in clinical practice with their benefits being limited to gains in appetite and fat mass and heterogeneous effects on quality of life( Reference Macciò, Madeddu and Mantovani 39 ). The majority of reviews and recommendations now point to the potential of multimodal therapies( Reference Arends, Bodoky and Bozzetti 7 , Reference Macciò, Madeddu and Mantovani 39 , Reference Aapro, Arends and Bozzetti 40 ). Although some trials in this area have already demonstrated superiority to single- and dual-agent strategies, the tablet burden was large and understanding and acceptance by patients were limited( Reference Mantovani, Maccio and Madeddu 38 ). The findings of a multicentre trial, incorporating exercise with nutritional and pharmacological interventions, is awaited( Reference Aapro, Arends and Bozzetti 40 ).

Fig. 1. Diagram to illustrate the suggestion that strategies for the management of cachexia in patients with cancer should include interventions to manage anorexia in combination with strategies to modulate the metabolic changes. (( Reference Fearon 17 ) Reprinted from Clinical Nutrition (2012) 31, 577-582, Fearon KCH. THe 2011 ESPEN Arvin Wretlind lecture. Cancer cachexia: the potential impact of translational research on patient-focused outcomes, with permission from Elsevier).

Table 3. Summary of information on studies examining ‘novel’ agents with or without nutritional support in the management of weight loss in patients with cancer (based on( Reference Macciò, Madeddu and Mantovani 39 , Reference Aapro, Arends and Bozzetti 40 , Reference Dodson, Baracos and Jatoi 46 ))

COX, cyclo-oxygenase; QOL, quality of life; PS, performance status; GH, growth hormone; LBM, lean body mass.

Summary and conclusions

Nutritional interventions in the management of weight loss in cancer continue to be recommended as the preferred strategy but their efficacy as a single modality intervention in terms of nutritional, clinical and patient-centred outcomes remains doubtful. Future management needs to take into consideration the likely aetiology of weight loss in people with cancer and will probably involve multiple strategies that target the nutritional deficit as well as the metabolic derangements associated with cachexia. It is also likely to be important to begin treatment for cachexia in the early stages of development of the syndrome. In order for this to happen, there needs to be a widely accepted definition of cachexia, validated to predict successful and meaningful outcomes, that can be used to identify those patients most likely to benefit from early intervention.

Acknowledgement

I would like to thank Professor Peter Emery for his assistance in proof reading this article.

Financial Support

None.

Conflicts of Interest

None.

Authorship

The author was solely responsible for all aspects of preparation of this paper.

References

1. Cancer Research UK (2015) Cancer Stats. http://www.cancerresearchuk.org/cancer-info/cancerstats/ accessed February 2015.Google Scholar
2. Ferlay, J, Soerjomataram, I, Ervik, M et al. (2013) GLOBOCAN 2012 v1. 0. Cancer incidence and mortality worldwide: IARC CancerBase. globocan.iarc.fr/ accessed January 2015Google Scholar
3. Teunissen, SCCM, Wesker, W, Kruitwagen, C et al. (2007) Symptom prevalence in patients with incurable cancer: a systematic review. J Pain Symptom Manage 34, 94104.CrossRefGoogle ScholarPubMed
4. Dewys, WD, Begg, C, Lavin, PT et al. (1980) Prognostic effect of weight loss prior tochemotherapy in cancer patients. Am J Med 69, 491497.CrossRefGoogle ScholarPubMed
5. Hopkinson, JB, Wright, DNM, McDonald, JW et al. (2006) The prevalence of concern about weight loss and change in eating habits in people with advanced cancer. J Pain Symptom Manage 32, 322331.CrossRefGoogle ScholarPubMed
6. Andreyev, HJN, Norman, AR, Oates, J et al. (1998) Why do patients with weight loss have a worse outcome when undergoing chemotherapy for gastrointestinal malignancies? Eur J Cancer 34, 503509.CrossRefGoogle ScholarPubMed
7. Arends, J, Bodoky, G, Bozzetti, F et al. (2006) ESPEN guidelines on enteral nutrition: non-surgical oncology. Clin Nutr 25, 245259.CrossRefGoogle ScholarPubMed
8. August, DA & Huhmann, MB (2009) ASPEN clinical guidelines: nutrition support therapy during adult anticancer treatment and in hematopoietic cell transplantation. J Parenter Enteral Nutr 33, 472500.CrossRefGoogle ScholarPubMed
9. Bauer, JD, Ash, S, Davidson, WL et al. (2006) Evidence based practice guidelines for the nutritional management of cancer cachexia. Nutr Diet 63, S3S32.CrossRefGoogle Scholar
10. Baldwin, C, McGough, C, Norman, AR et al. (2006) Failure of dietetic referral in patients with gastrointestinal cancer and weight loss. Eur J Cancer 42, 25042509.CrossRefGoogle ScholarPubMed
11. Spiro, A, Baldwin, C, Patterson, A et al. (2006) The views and practice of oncologists towards nutritional support in patients receiving chemotherapy. Br J Cancer 95, 431434.CrossRefGoogle ScholarPubMed
12. National Collaborating Centre for Acute Care (2006) Nutrition Support in Adults. Oral nutrition support, enteral tube feeding and parenteral nutrition. Available from http://www.rcseng.ac.uk Google Scholar
13. Jensen, GL, Mirtallo, J, Compher, C et al. (2010) Adult starvation and disease-related malnutrition a proposal for etiology-based diagnosis in the clinical practice setting from the international consensus guideline committee. J Parenter Enteral Nutr 34, 156159.CrossRefGoogle ScholarPubMed
14. White, JV, Guenter, P, Jensen, G et al. (2012) Consensus statement of The Academy of nutrition and dietetics/American society for parenteral and enteral nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition). J Acad Nutr Diet 112, 730738.CrossRefGoogle Scholar
15. Laviano, A, Meguid, MM, Inui, A et al. (2005) Therapy insight: cancer anorexia–cachexia syndrome—when all you can eat is yourself. Nat Clin Pract Oncol 2, 158165.CrossRefGoogle ScholarPubMed
16. Fearon, K, Strasser, F, Anker, SD et al. (2011) Definition and classification of cancer cachexia: an international consensus. Lancet Oncol 12, 489495.CrossRefGoogle ScholarPubMed
17. Fearon, KCH (2012) The 2011 ESPEN Arvid Wretlind lecture: cancer cachexia: the potential impact of translational research on patient-focused outcomes. Clin Nutr 31, 577582.CrossRefGoogle ScholarPubMed
18. Fearon, KCH & Thomas, DR (2007) Loss of skeletal muscle mass in aging: examining the relationship of starvation, sarcopenia and cachexia. Clin Nutr 26, 389399.Google Scholar
19. Qureshi, N, Kellie, S, Darnley, I et al. (2014) Professional practice. In Manual of Dietetic Practice 5th ed., pp. 519 [Gandy, J editor]. Oxford: Wiley Blackwell.Google Scholar
20. Voss, AC & Gallagher-Allred, C (1996) The importance of outcomes research in documenting the benefit of nutrition intervention. Nutrition 12, 5960.CrossRefGoogle ScholarPubMed
21. American Society of Clinical Oncology (1996) Outcomes of cancer treatment for technology assessment and cancer treatment guidelines. J Clin Oncol 4, 671679.Google Scholar
22. Ellis, LM, Bernstein, DS, Voest, EE et al. (2014) American Society of Clinical Oncology perspective: raising the bar for clinical trials by defining clinically meaningful outcomes. J Clin Oncol 32, 12771280.CrossRefGoogle Scholar
23. Baldwin, C, Spiro, A, Ahern, R et al. (2012) Oral nutritional interventions in malnourished patients with cancer: a systematic review and meta-analysis. J Natl Cancer Inst 104, 371385.CrossRefGoogle Scholar
24. Arnold, C & Richter, MP (1989) The effect of oral nutritional supplements on head and neck cancer. Int J Radiat Oncol Biol Phys 16, 15951599.CrossRefGoogle ScholarPubMed
25. Evans, WK, Nixon, DW, Daly, JM et al. (1987) A randomized study of oral nutritional support versus ad lib nutritional intake during chemotherapy for advanced colorectal and non-small-cell lung cancer. J Clin Oncol 5, 113124.CrossRefGoogle ScholarPubMed
26. Moloney, M, Moriarty, M & Daly, L (1983) Controlled studies of nutritional intake in patients with malignant disease undergoing treatment. Hum Nutr Appl Nutr 37, 3035.Google ScholarPubMed
27. Ollenschlager, G, Thomas, W, Konkol, K et al. (1992) Nutritional behaviour and quality of life during oncological polychemotherapy: results of a prospective study on the efficacy of oral nutrition therapy in patients with acute leukaemia. Eur J Clin Invest 22, 546553.CrossRefGoogle ScholarPubMed
28. Ovesen, L, Allingstrup, L, Hannibal, J et al. (1993) Effect of dietary counseling on food intake, body weight, response rate, survival, and quality of life in cancer patients undergoing chemotherapy: a prospective, randomized study. J Clin Oncol 11, 20432049.CrossRefGoogle ScholarPubMed
29. Macia, E, Moran, J, Santos, J et al. (1990) Nutritional evaluation and dietetic care in cancer patients treated with radiotherapy: prospective study. Nutrition 7, 205209.Google Scholar
30. Nayel, H, El-Ghoneimy, E & El-Haddad, S (1991) Impact of nutritional supplementation on treatment delay and morbidity in patients with head and neck tumors treated with irradiation. Nutrition 8, 1318.Google Scholar
31. Elkort, RJ, Baker, FL, Vitale, JJ et al. (1981) Long-term nutritional support as an adjunct to chemotherapy for breast cancer. JPEN J Parenter Enteral Nutr 5, 385390.CrossRefGoogle ScholarPubMed
32. Ravasco, P, Monteiro-Grillo, I, Vidal, PM et al. (2005) Dietary counseling improves patient outcomes: a prospective, randomized, controlled trial in colorectal cancer patients undergoing radiotherapy. J Clin Oncol 23, 14311438.CrossRefGoogle ScholarPubMed
33. Ravasco, P, Monteiro-Grillo, I, Marques Vidal, P et al. (2005) Impact of nutrition on outcome: a prospective randomized controlled trial in patients with head and neck cancer undergoing radiotherapy. Head Neck 27, 659668.CrossRefGoogle ScholarPubMed
34. King, MT (1996) The interpretation of scores from the EORTC quality of life questionnaire QLQ-C30. Qual Life Res 5, 555567.CrossRefGoogle ScholarPubMed
35. Isenring, E, Capra, S & Bauer, J (2004) Patient satisfaction is rated higher by radiation oncology outpatients receiving nutrition intervention compared with usual care. J Hum Nutr Diet 17, 145152.CrossRefGoogle ScholarPubMed
36. Baldwin, C, Spiro, A, McGough, C et al. (2011) Simple nutritional intervention in patients with advanced cancers of the gastrointestinal tract, non-small cell lung cancers or mesothelioma and weight loss receiving chemotherapy: a randomised controlled trial. J Hum Nutr Diet 24, 431440.CrossRefGoogle ScholarPubMed
37. Uster, A, Ruefenacht, U, Ruehlin, M et al. (2013) Influence of a nutritional intervention on dietary intake and quality of life in cancer patients: a randomized controlled trial. Nutrition 29, 13421349.CrossRefGoogle ScholarPubMed
38. Mantovani, G, Maccio, A, Madeddu, C et al. (2010) Randomized phase III clinical trial of five different arms of treatment in 332 patients with cancer cachexia. Oncologist 15, 200211.CrossRefGoogle ScholarPubMed
39. Macciò, A, Madeddu, C & Mantovani, G (2012) Current pharmacotherapy options for cancer anorexia and cachexia. Expert Opin Pharmacother 13, 24532472.CrossRefGoogle ScholarPubMed
40. Aapro, M, Arends, J, Bozzetti, F et al. (2014) Early recognition of malnutrition and cachexia in the cancer patient: a position paper of a European School of Oncology Task Force. Ann Oncol 25, 14921499.CrossRefGoogle Scholar
41. Fearon, KC, Voss, AC & Hustead, DS (2006) Definition of cancer cachexia: effect of weight loss, reduced food intake, and systemic inflammation on functional status and prognosis. Am J Clin Nutr 83, 13451350.CrossRefGoogle ScholarPubMed
42. Evans, WJ, Morley, JE, Argiles, J et al. (2008) Cachexia: a new definition. Clin Nutr 27, 793799.CrossRefGoogle ScholarPubMed
43. Bozzetti, F & Mariani, L (2009) Defining and classifying cancer cachexia: a proposal by the SCRINIO Working Group. JPEN J Parenter Enteral Nutr 33, 361367.CrossRefGoogle ScholarPubMed
44. Muscaritoli, M, Anker, SD, Argiles, J et al. (2010) Consensus definition of sarcopenia, cachexia and pre-cachexia: joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics”. Clin Nutr 29, 154159.CrossRefGoogle Scholar
45. Blum, D, Omlin, A, Fearon, K et al. (2010) Evolving classification systems for cancer cachexia: ready for clinical practice? Support Care Cancer 18, 273279.CrossRefGoogle ScholarPubMed
46. Dodson, S, Baracos, VE, Jatoi, A et al. (2011) Muscle wasting in cancer cachexia: clinical implications, diagnosis, and emerging treatment strategies. Annu Rev Med 62, 265279.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Definitions of cachexia recently proposed by expert groups

Figure 1

Table 2. Effectiveness of oral nutritional interventions in the management of weight loss in patients with cancer: findings of a systematic review and meta-analysis (based on the meta-analyses and results presented in(23))

Figure 2

Fig. 1. Diagram to illustrate the suggestion that strategies for the management of cachexia in patients with cancer should include interventions to manage anorexia in combination with strategies to modulate the metabolic changes. ((17) Reprinted from Clinical Nutrition (2012) 31, 577-582, Fearon KCH. THe 2011 ESPEN Arvin Wretlind lecture. Cancer cachexia: the potential impact of translational research on patient-focused outcomes, with permission from Elsevier).

Figure 3

Table 3. Summary of information on studies examining ‘novel’ agents with or without nutritional support in the management of weight loss in patients with cancer (based on(39,40,46))