Volume 77, Issue 4 pp. 416-425
INVITED POSITION PAPER
Open Access

Clinical Oncology Society of Australia: Position statement on cancer-related malnutrition and sarcopenia

Nicole Kiss PhD, AdvAPD

Corresponding Author

Nicole Kiss PhD, AdvAPD

Institute for Physical Activity and Nutrition, Deakin University, Geelong, Victoria, Australia

Allied Health, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

Correspondence

Dr Nicole Kiss, Institute for Physical Activity and Nutrition, Deakin University, 221 Burwood Highway, Burwood, VIC 3125, Australia.

Email: [email protected]

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Jenelle Loeliger MSc (Nutr & Diet), AdvAPD

Jenelle Loeliger MSc (Nutr & Diet), AdvAPD

Allied Health, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

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Merran Findlay MSc (Nutr & Diet), AdvAPD

Merran Findlay MSc (Nutr & Diet), AdvAPD

Cancer Services, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia

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Elizabeth Isenring PhD, AdvAPD

Elizabeth Isenring PhD, AdvAPD

Faculty of Health Sciences and Medicine, Bond University, Gold Coast, Queensland, Australia

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Brenton J. Baguley PhD, APD

Brenton J. Baguley PhD, APD

Institute for Physical Activity and Nutrition, Deakin University, Geelong, Victoria, Australia

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Anna Boltong PhD

Anna Boltong PhD

Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia

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Alexis Butler MBBS

Alexis Butler MBBS

GP Liaison, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

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Irene Deftereos BNutrDiet, APD

Irene Deftereos BNutrDiet, APD

Department of Surgery Western Health, University of Melbourne, Melbourne, Victoria, Australia

Department of Nutrition and Dietetics, Western Health, Melbourne, Victoria, Australia

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Michelle Eisenhuth MSc (Nutr & Diet), APD

Michelle Eisenhuth MSc (Nutr & Diet), APD

Nutrition and Dietetics Department, Nepean Hospital, Sydney, New South Wales, Australia

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Steve F. Fraser PhD

Steve F. Fraser PhD

Institute for Physical Activity and Nutrition, Deakin University, Geelong, Victoria, Australia

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Rebecca Fichera BHlthSc (Nutr & Diet), APD

Rebecca Fichera BHlthSc (Nutr & Diet), APD

Nutrition and Dietetics Departments, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

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Hayley Griffin PhD

Hayley Griffin PhD

Clinical Oncology Society of Australia, Sydney, New South Wales, Australia

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Sandi Hayes PhD

Sandi Hayes PhD

Menzies Health Institute Queensland, Griffith University, Brisbane, Queensland, Australia

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Emily Jeffery MDiet, APD

Emily Jeffery MDiet, APD

School of Public Health, Curtin University, Perth, Western Australia, Australia

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Catherine Johnson BNurs

Catherine Johnson BNurs

Gastrointestinal Cancer Service, Calvary Mater Newcastle, Newcastle, New South Wales, Australia

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Chris Lomma MBBS, FRACP

Chris Lomma MBBS, FRACP

Medical Oncology Department, Fiona Stanley Hospital, Perth, Western Australia, Australia

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Barbara van der Meij PhD

Barbara van der Meij PhD

Faculty of Health Sciences and Medicine, Bond University, Gold Coast, Queensland, Australia

Dietetics and Food Services, Mater Health, Brisbane, Queensland, Australia

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Carolyn McIntyre PhD

Carolyn McIntyre PhD

School of Medical and Health Science, Exercise Medicine Research Institute, Edith Cowan University, Perth, Western Australia, Australia

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Tracey Nicholls MN NPrac

Tracey Nicholls MN NPrac

Department of ENT Otolaryngology Head and Neck Surgery, Flinders Medical Centre, Adelaide, South Australia, Australia

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Lina Pugliano MBBS

Lina Pugliano MBBS

Medical Oncology, Northern Cancer Institute, Sydney, New South Wales, Australia

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Tina Skinner PhD

Tina Skinner PhD

School of Human Movement and Nutrition Sciences, University of Queensland, Brisbane, Queensland, Australia

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Jane Stewart BHlthSc (N&D) (Hons), APD

Jane Stewart BHlthSc (N&D) (Hons), APD

Allied Health, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

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Judy Bauer PhD, FDAA

Judy Bauer PhD, FDAA

School of Human Movement and Nutrition Sciences, University of Queensland, Brisbane, Queensland, Australia

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First published: 17 August 2020
Citations: 59
[Correction added on 24 August 2020, after first online publication: affiliation 3 has been amended and funding information section has been removed.]

Abstract

This position statement describes the recommendations of the Clinical Oncology Society of Australia (COSA) regarding management of cancer-related malnutrition and sarcopenia. A multidisciplinary working group completed a review of the literature, focused on evidence-based guidelines, systematic reviews and meta-analyses, to develop recommendations for the position statement. National consultation of the position statement content was undertaken through COSA members. All people with cancer should be screened for malnutrition and sarcopenia in all health settings at diagnosis and as the clinical situation changes throughout treatment and recovery. People identified as “at risk” of malnutrition or with a high-risk cancer diagnosis or treatment plan should have a comprehensive nutrition assessment; people identified as “at risk” of sarcopenia should have a comprehensive evaluation of muscle status using a combination of assessments for muscle mass, muscle strength and function. All people with cancer-related malnutrition and sarcopenia should have access to the core components of treatment, including medical nutrition therapy, targeted exercise prescription and physical and psychological symptom management. Treatment for cancer-related malnutrition and sarcopenia should be individualised, in collaboration with the multidisciplinary team (MDT), and tailored to meet needs at each stage of cancer treatment. Health services should ensure a broad range of health care professionals across the MDT have the skills and confidence to recognise malnutrition and sarcopenia to facilitate timely referrals and treatment. The position statement is expected to provide guidance at a national level to improve the multidisciplinary management of cancer-related malnutrition and sarcopenia.

1 BACKGROUND

Malnutrition is characterised by loss of weight, loss of muscle and loss of subcutaneous body fat.1 Cancer-related malnutrition can occur due to the presence of the cancer itself, the effect of cancer treatment on the consumption or absorption of nutrients, or patients undertaking “restrictive” cancer diets.2 Research over several decades has shown cancer-related malnutrition is associated with serious adverse consequences, including reduced survival and ability to complete treatment, poorer quality of life and higher costs to the health care system.3-7 It is a common condition, occurring in 30% to 40% of people with cancer, yet it is under-recognised and under-treated.7 Australian studies have found that almost 50% of people with cancer-related malnutrition are not under the care of a dietitian.8 Malnutrition can occur in people with any cancer diagnosis, although certain cancers, including head and neck, gastrointestinal and lung cancers, have up to a 4-fold increased risk of malnutrition compared to breast cancer.9 Malnutrition can occur in people of any body mass index (BMI) category, including those classified as overweight or obese.10, 11 However, with the rising incidence of obesity in Australia the identification of malnutrition and underlying muscle loss is becoming more complex and concurrently under-diagnosis is likely to rise.

Sarcopenia is characterised by loss of skeletal muscle mass and strength with an impact on physical performance, and is a key component of cancer-related malnutrition.12, 13 This is reflected in recent international definitions of malnutrition where the assessment of muscle mass is a criterion for the diagnosis of malnutrition.14, 15 Sarcopenia associated with ageing is known as primary sarcopenia, as opposed to secondary sarcopenia which is associated with disease (including cancer), sedentary lifestyle or inadequate nutrition.12 Research in cancer-related sarcopenia has largely focused on the presence of low muscle mass rather than the presence of both low muscle mass and low muscle function (strength or performance).16-18 Similar to malnutrition, low muscle mass can occur across all BMI categories.16 Cancer-related sarcopenia is associated with similar adverse consequences to cancer-related malnutrition and is also a common condition occurring in up to 60% of people with cancer, depending on cancer type.18-20 Furthermore, sarcopenic obesity, a unique phenotype where low muscle mass and obesity occur simultaneously, is independently associated with reduced survival and increased complications in multiple cancer diagnoses and treatment modalities.21

Loss of muscle mass in cancer-related malnutrition and sarcopenia may simply be related to reduced nutritional intake.2 Alternatively, muscle loss may develop as a result of tumour-related metabolic alterations or the presence of systemic inflammation.2 This is particularly evident in cancer cachexia, a multifactorial syndrome with a complex underlying pathology.22 While there are similarities across these conditions, it is generally accepted that weight and muscle loss occurring in cancer cachexia cannot be reversed by conventional nutrition intervention.23

Evidence from national and international guidelines strongly supports the identification and treatment of cancer-related malnutrition and sarcopenia prior to, during and post-treatment in order to improve outcomes for people with cancer.3, 6, 24, 25 Despite this, considerable variation in screening, diagnosis and intervention occurs across Australian health care settings. Barriers to improving care largely include inadequate time and services and varying perception of responsibility for identification and treatment.26 Nevertheless, international studies demonstrate failure to improve care has a considerable financial burden that is likely to translate to a similar impact on the Australian health care system.27, 28

This document outlines the position of Clinical Oncology Society of Australia (COSA) on the role of health professionals and health services in recognising and treating patients with cancer-related malnutrition and sarcopenia, with a focus on practice tips to support implementation of optimal management. It is intended for use by clinicians and health services to advocate for the resources and services required to support optimal management of cancer-related malnutrition and sarcopenia. Malnutrition and muscle loss also occur in adolescents and young adults with cancer, however this document is intended to address the management of these conditions in adults.

2 METHODS

A multidisciplinary expert working group of dietitians, exercise physiologists, nurses, medical oncologists and general practitioners was convened to develop the position statement. A comprehensive literature review of PubMed and Conchrane databases from 1 July 2013 to 3 June 2019 was undertaken by the working group using search terms from the European Society of Clinical Nutrition and Metabolism (ESPEN) guidelines on nutrition in cancer patients.3 This was to capture literature not included in the ESPEN guidelines, for which the literature search was conducted up to 30 June 2013. A focus was placed on using evidence-based guidelines, systematic reviews and meta-analyses identified from the literature search to inform the recommendations. Consensus of the working group was used where evidence was limited. Subsequent national consultation was undertaken with COSA members and key stakeholders, with relevant feedback incorporated into the position statement.

3 RECOMMENDATIONS

Table 1 summarises COSA's position on cancer-related malnutrition and sarcopenia. Table 2 contains suggestions for the implementation of recommendations into health services. A pathway for the management of cancer-related malnutrition and sarcopenia, applicable across all health settings, is outlined in Figure 1.

TABLE 1. Clinical Oncology Society of Australia position on cancer-related malnutrition and sarcopenia
All people with cancer should be screened for malnutrition and sarcopenia in all health settings at diagnosis and as the clinical situation changes throughout treatment and recovery.
All people with cancer identified as being “at risk” of malnutrition following screening or with a cancer diagnosis or treatment plan known to lead to high risk of malnutrition should have comprehensive nutrition assessment using a tool validated in the oncology population.
All people with cancer identified as being “at risk” of sarcopenia following appropriate screening should have a comprehensive evaluation of muscle status using a combination of assessments for muscle mass, muscle strength and function.
All people with cancer-related malnutrition and sarcopenia should have access to the core components of treatment including medical nutrition therapy, targeted exercise prescription and physical activity advice, and physical and psychological symptom management.
Treatment for cancer-related malnutrition and sarcopenia should be individualised, in collaboration with the multidisciplinary team (MDT), and tailored to meet needs at each stage of cancer treatment.
Health services should ensure a broad range of health care professionals across the MDT have the skills and confidence to recognise malnutrition and sarcopenia to facilitate timely referrals and treatment.
TABLE 2. Tips for implementing recommendations into practice
Identification
Consider incorporating screening for malnutrition and sarcopenia into existing multidisciplinary and/or supportive care screening processes or patient-reported outcomes to aid ease of completion and compliance, reduce the need for additional resources and to support the initiation of appropriate assessment and care.
Screening should focus on early identification using a systematised model of care or pathway that defines the tools to be used, who will conduct screening, the timing and frequency of screening, and pathways for treatment referrals appropriate to the setting.
Assessment
Malnutrition assessment should be incorporated into the appropriate nutrition care policy directives with local governance, management committees and performance review processes embedded to support successful and sustainable implementation.
A measure of muscle mass should be a component of assessment of malnutrition and sarcopenia and incorporated into routine clinical practice.
Identification of barriers and enablers to malnutrition and sarcopenia assessment at individual, team and system levels is the first step to facilitate adherence to evidence-based nutrition care recommendations and policies.
Treatment
Models of care to treat malnutrition and sarcopenia should provide consistent information regarding cancer-related malnutrition and sarcopenia across disciplines and throughout phases of treatment to ensure reinforcement of a clear treatment plan.
Consider the use of a care pathway, or similar process, developed by MDT members and people with cancer to support implementation of optimal care for cancer-related malnutrition and sarcopenia.
Multidisciplinary care
Engage consumers in the development and evaluation of MDT services across the continuum of care.
Utilise a framework, for example team mental model, to develop and refine MDT services to optimise the success of the team, and importantly clinical and patient-reported outcome and experience measures.
Details are in the caption following the image
Pathway for the management of cancer-related malnutrition and sarcopenia within acute, community and primary care health services

3.1 Identifying cancer-related malnutrition and sarcopenia

  1. All people with cancer should be screened for malnutrition in all health settings at diagnosis and repeated as the clinical situation changes, using a screening tool that is valid and reliable in the setting in which it is intended for use.
  2. All people with cancer should be screened for sarcopenia at diagnosis and repeated as the clinical situation changes, using the validated screening tool SARC-F or SARC-F in combination with calf circumference.

Cancer-related malnutrition and sarcopenia are under-recognised and therefore under-treated conditions. Neither malnutrition nor sarcopenia should be associated exclusively with being underweight, as these conditions can be present at any body weight or BMI category including obesity.18, 29 Timely and accurate identification of malnutrition and sarcopenia in all clinical practice settings is essential to support the initiation of optimal multidisciplinary care for people with these conditions, and a subsequent reduction in disability, mortality and health care costs.3, 7, 30 This identification process, commonly known as screening, enables recognition of people with cancer as “at risk” or “not at risk” of these conditions.

Screening for malnutrition should be undertaken on all people with cancer at diagnosis, and repeated as clinically indicated throughout each modality of treatment (eg, surgery, radiation therapy, chemotherapy), post-treatment and surveillance.3, 24, 25 Where limited resources restrict the ability to screen all patients, resources should be devoted to ensuring those at highest risk are screened (Table 3). Malnutrition screening should be undertaken using a malnutrition screening tool validated in the setting in which it is intended for use.6, 24 A number of malnutrition screening tools have been shown to be valid and reliable for identifying malnutrition in people with cancer including the Malnutrition Screening Tool (MST), Malnutrition Universal Screening Tool (MUST), Malnutrition Screening Tool for Cancer Patients (MSTC) and the Patient-Generated Subjective Global Assessment Short Form (PG-SGA SF).3 The MST and MUST are most commonly used in Australia and can be self-administered or completed by any health professional.31, 32 Screening for malnutrition can be bypassed for people with a cancer diagnosis or treatment plan known to lead to high risk of malnutrition, for example, radiation therapy with or without chemotherapy to the gastrointestinal tract or head and neck area.6, 25 All people with cancer identified as being “at risk” of malnutrition following screening, or with a diagnosis or treatment plan that places them at high risk of malnutrition, should be referred to an accredited practising dietitian for a comprehensive nutritional assessment and initiation of appropriate treatment.3, 6, 24

TABLE 3. Factors indicative of high risk of malnutrition in people with cancer
Cancer diagnosis Treatment Other
Head and neck Radiation therapy to oral cavity or gastrointestinal tract Advanced stage disease
Upper or lower gastrointestinal Chemotherapy, immunotherapy or targeted therapy with risk of gastrointestinal toxicity Older age (>65 years)
Thoracic Stem cell transplant
Acute leukaemia (myeloid and lymphoid) Surgery to the oral cavity or gastrointestinal tract
Steroid use with treatment

Screening for sarcopenia should be completed in all people with cancer at diagnosis and as clinically indicated throughout each modality of treatment (eg, surgery, radiation therapy, chemotherapy), post-treatment and surveillance. The SARC-F is a sarcopenia screening tool that has been well studied and validated in older adults.33 The SARC-F has recently been validated for use in people with cancer, either alone or in combination with measurement of calf circumference for greater sensitivity.34 All people identified as “at risk” of sarcopenia should be referred to an accredited practising dietitian and exercise specialist that is, accredited exercise physiologist and/or physiotherapist, experienced in the cancer setting and with knowledge of body composition science, for assessment of muscle strength, muscle mass and physical performance and initiation of appropriate treatment.

3.2 Assessing cancer-related malnutrition and sarcopenia

  1. All people with cancer identified as being “at risk” of malnutrition following screening or with a cancer diagnosis or treatment plan known to lead to high risk of malnutrition should have a comprehensive nutrition assessment using a tool validated in the oncology population.
  2. All people with cancer identified as being “at risk” of sarcopenia following appropriate screening should have a comprehensive evaluation of muscle status using a combination of assessments for muscle mass, muscle strength and function.
  3. Interpretation of diagnostic criteria for sarcopenia should be applied recognising that:

    1. Threshold values for assessing muscle mass, muscle strength and physical performance are variable.
    2. Care should be taken to determine the appropriate cut-off values in the population in which they are being applied.
    3. Most data regarding muscle strength and performance comes from older populations.
    4. The applicability of diagnostic criteria in different ethnicities is uncertain.

Nutrition assessment is recommended for all people with cancer identified as “at risk” of malnutrition following screening or with a cancer diagnosis or treatment plan known to lead to high risk of malnutrition for example, patients receiving radiation therapy to the oral cavity or gastrointestinal tract.6, 25 Nutrition assessment and malnutrition diagnosis should be completed by an appropriately trained health care professional such as an accredited practising dietitian or if not available, other allied health or medical professional. Nutrition assessment should be repeated as the clinical situation changes and incorporated into routine clinical consultations.3 Nutrition assessment should incorporate measures of involuntary weight loss, BMI, body composition, food intake and nutrient absorption, functional status and inflammation.3 The 2019 Global Leadership Initiative on Malnutrition (GLIM) has produced a consensus statement outlining the recommended assessment domains for a diagnosis of malnutrition including etiologic (reduced food intake or assimilation; inflammation) and phenotypic criteria (weight loss; low BMI; reduced muscle mass).15 The Patient-Generated Subjective Global Assessment (PG-SGA)35 and Subjective Global Assessment (SGA)36 are validated assessment tools that align with the GLIM criteria for diagnosing malnutrition and can be used to assess and diagnose malnutrition in people with cancer.6

Sarcopenia assessment is recommended for all people identified as “at risk” of sarcopenia following screening and is ideally performed at the time of cancer diagnosis and before an initial treatment plan is implemented. Reassessment should occur as the clinical situation changes and incorporated into routine clinical consultations during active treatment and then ongoing surveillance throughout the course of care. Sarcopenia assessment and diagnosis should be completed by an appropriately trained health care professional such as an accredited practising dietitian, accredited exercise physiologist, physiotherapist or other allied health or medical professional. Assessment should consider whether it is primary sarcopenia (age-related) or secondary sarcopenia (other causal factors).13 These causal factors may include: (a) Disease—secondary to a systemic disease especially where inflammation is present as in cancer; (b) Inactivity—sedentary lifestyle or disease-related immobility or disability; or (c) Malnutrition—as a result of inadequate energy or protein caused by anorexia, malabsorption, food insecurity or limited ability to eat.13

There is no global consensus on the diagnostic criteria for sarcopenia. Commonly used definitions include the European Working Group on Sarcopenia in Older People (EWGSOP) 112 and EWGSOP 2,13 and the Foundation for the National Institutes of Health (FNIH) Biomarkers Consortium Sarcopenia Project37 (Table 4). However, these definitions and cut-points have been developed based on research in older adults and have not been extensively researched in cancer populations. Most research in cancer has assessed sarcopenia based on low muscle mass alone from computed tomography images using cut-points prognostic for poor survival.40, 44 The various methods used for diagnosing sarcopenia are presented in Table 4. Selection of assessment method may depend on patient factors, access to the required technical resources and the purpose of testing. Clinicians and researchers should understand the strengths and limitations of the assessment method being applied and understand these are not interchangeable.12, 13 Ongoing research will contribute to identifying cut-points relative to patient population and ethnicity.

TABLE 4. Appropriate methods for assessing sarcopenia12, 38, 39
Definition Low muscle strength Low muscle mass Poor muscle function
EWGSOP 1 (2010)—Low muscle mass + low muscle strength or low physical performance Grip strength: <30 kg men; <20 kg women ALM/height (m)2: <7.26 kg/m2 men; <5.50 kg/m2 women Gait speed:≤0.8 m/second (4 m walk) or SPPB Score ≤8 points
FNIH (2014)—Low muscle mass + low muscle strength Grip strength: <26 kg men; <16 kg women ALM/BMI: <0.789 kg/BMI men; <0.512 kg/BMI women NA
EWGSOP 2 (2019)—Low muscle strength + low muscle mass or low physical performance Grip strength: <27 kg men; <16 kg women or Chair Stands: >15 seconds five rises ALM/height (m)2: <7.00 kg/m2 men; <5.50 kg/m2 women or ALM: <20 kg men; <15 kg women Gait speed: ≤0.8 m/second (4 m walk) or SPPB Score ≤8 points or TUG ≥20 seconds or 400 m walk ≥6 minutes or non-completion. Only used to classify severity of sarcopenia.
Cancer-specific CT image analysis researchLow muscle mass NA SMI (SMA/height [m]2) at L3: <52.4 cm2/m2 (men)18; <38.5 cm2/m2 (women)18; or <43 cm2/m2 (men with BMI < 24.9)40; <53 cm2/m2 (men with BMI ≥ 25)40; <41 cm2/m2 (women of any BMI)40 NA
  • Notes: Muscle mass outputs produced automatically by BIA and BIS devices may be less accurate due potential to be affected by fluid shifts and a lack of transparency regarding the population-specific regression equations underpinning their outputs owing to their proprietary nature39, 41-43; however, some guidelines support use in clinical practice.
  • Abbreviations: ALM, appendicular lean mass; BMI, body mass index; CT, computed tomography; EWGSOP 1, European Working Group on Sarcopenia in Older People; EWGSOP 2, European Working Group on Sarcopenia in Older People updated definition; FNIH, Foundation for the National Institutes of Health Biomarkers Consortium Sarcopenia Project; SMA, skeletal muscle area determined from cross-sectional CT image at the third lumbar vertebrae; SMI, Skeletal Muscle Index; SPPB, short physical performance battery; TUG, timed up and go.13
  • a ALM can be assessed using dual energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), CT, raw bioelectrical impedance analysis (BIA) or bioelectrical impedance spectroscopy (BIS).
  • b Multiple cut-points for SMI at the third lumbar vertebrae are used in the literature, depending on population and ethnicity. These are suggested cut-points; however, clinicians are advised to research the most appropriate cut-point for their population.

3.3 Treating cancer-related malnutrition and sarcopenia

  1. All people with cancer-related malnutrition and sarcopenia should have access to the core components of treatment including individualised medical nutrition therapy, targeted exercise prescription and physical activity advice and physical and psychological symptom management.
  2. Treatment for cancer-related malnutrition and sarcopenia should be individualised, in collaboration with the multidisciplinary team (MDT), and tailored to consider multi-morbidities and meet needs at each stage of cancer treatment.

Treatment of cancer-related malnutrition and sarcopenia aims to provide adequate nutritional intake and participation in exercise in order to optimise body composition with a focus on preserving or improving lean mass and physical function, as well as assisting patients to complete cancer treatment.6, 25, 29 However, people with cancer commonly report unmet needs in regards to access and provision of nutrition and exercise advice for the management of their malnutrition or sarcopenia, and are seeking consistent care from health professionals across their treating team to address these needs.45-48

Medical nutrition therapy that considers symptoms, social situation and treatment plan, has been found to improve nutritional intake, weight and patient-reported physical function and reduce treatment breaks and unplanned hospital admissions.3, 6, 25 Sufficient nutritional intake of energy and protein is required to treat malnutrition, with evidence-based guidelines recommending between 105 and 125 kJ/kg/day and between 1.0 and 1.5 g/kg/day in protein.3 Preliminary data suggest that in fact a higher protein intake of 2.0 g/kg/day may be required to combat muscle loss; however, this is not yet supported by sufficient research.17 Specific recommendations regarding the use and timing of initiation of medical nutrition therapy, including enteral and parenteral nutrition, and Enhanced Recovery After Surgery protocols are available for some cancer types including head and neck and upper and lower gastrointestinal cancers.3, 6, 24, 25

For medical nutrition therapy to be optimally effective, it needs to occur alongside exercise intervention.49 Exercise training provides the necessary support for nutrition intervention to improve (or prevent worsening) in body composition, specifically, preservation or increases in lean tissue, with or without changes in body weight.3, 50, 51 Resistance exercise is more effective than aerobic exercise at improving muscle mass and strength.52 However, aerobic exercise remains relevant as it also modulates muscle metabolism, insulin sensitivity and levels of inflammation in a way that could potentially aid in preservation of muscle mass and function.52 As such, in line with the most up to date Australian exercise prescription guidelines for people with cancer, individually prescribed multimodal exercise training (including targeted aerobic and resistance exercise) at moderate to high intensity, with emphasis on resistance exercise incorporating exercises for major muscle groups, is recommended.52

Although promising, evidence is variable for the use of anabolic or appetite stimulating agents, such as progestins, or non-steroidal anti-inflammatory agents, and their use should be evaluated on an individual basis by the MDT or disease protocol.3 Supportive care screening to identify unmet needs, including symptom management and psychosocial needs, is important for a holistic approach.

Interventions are most effective when commenced early, with a focus on prevention or the treatment of mild to moderate malnutrition and/or sarcopenia.22 However, despite the evidence for treatment of cancer-related malnutrition and sarcopenia, consistent and equitable access to care is lacking.3, 47, 48 The potential benefit to the health system through implementing evidence-based treatment of malnutrition and sarcopenia is significant, estimated to be the equivalent of AU$800 000 per 100 000 population.27, 53 Detailed recommendations regarding evidence-based treatment for people undergoing different treatment modalities and for specific cancer diagnoses can be found in the relevant evidence-based guidelines.3, 6, 24, 25, 52

3.4 Role of the multidisciplinary team

  1. Health services should ensure a broad range of health care professionals across the MDT have the skills and confidence to recognise malnutrition and sarcopenia to facilitate timely referrals and treatment.
  2. MDTs should work towards an individualised and coordinated approach to treating cancer-related malnutrition and sarcopenia.

A multidisciplinary approach to identifying and treating cancer-related malnutrition and sarcopenia is essential. Alongside medical nutrition therapy, interventions that have been shown to contribute to optimising nutritional status and body composition include exercise, management of treatment side effects through optimising medications and the management of anorexia and dysphagia.3, 25 Frameworks, such as the team mental model, have been found to optimise team processes and functioning.54 Multidisciplinary cancer prehabilitation and rehabilitation programs providing individualised care demonstrate capacity to improve nutritional status, muscle mass and strength, fatigue and performance status.55-58 These interventions require the specialist skills of various MDT members as part of a coordinated approach to individualised treatment of cancer-related malnutrition and sarcopenia and can be accessed through acute hospital services, community-based services or general practices.

Guidance regarding optimal practice at a national level is expected to improve the management of cancer-related malnutrition and sarcopenia across health sectors. Implementation of the position statement recommendations within health services will require the support and training of multidisciplinary health professionals, health service managers and policy makers. The position statement recommendations and pathway provide a framework for achieving optimal care.

ENDORSING AND SUPPORTING ORGANISATIONS

The COSA Position Statement on Cancer-Related Malnutrition and Sarcopenia is a stand-alone document, the content of which is not influenced by any other authority. The position statement is endorsed by Cancer Council Australia, Dietitians Australia, Cancer Nurses Society of Australia and the Australia New Zealand Society for Sarcopenia and Frailty Research. Supporting organisations include the Multinational Association of Supportive Care in Cancer, Beyond Five, Australian Physiotherapy Association, Australia New Zealand Head and Neck Society, Australasian Lung Cancer Trials Group, Pancare Foundation, Lung Foundation Australia, Australia New Zealand Society of Palliative Medicine, Exercise and Sports Science Australia, Australian Gastro-intestinal Trials Group, Australasian Leukaemia and Lymphoma Group and Australia New Zealand Children's Haematology and Oncology Group, Psycho-oncology Cooperative Research Group.

CONFLICT OF INTEREST

The authors declare no potential conflict of interest.

AUTHOR CONTRIBUTIONS

N. K., M. F., J. B., J. L., E. I. developed the structure for the position statement. All authors contributed to the literature review and drafting content, recommendations and implementation tips. N. K. drafted the manuscript and chaired the working group. All authors are in agreement with the manuscript and declare that the content has not been published elsewhere. N. K. is supported by a fellowship from the Victorian Cancer Agency. Cancer Council Queensland is to be acknowledged for S. H. fellowship support for contributions made during the fellowship funding period.

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