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Physical function endpoints in cancer cachexia clinical trials: Systematic Review 1 of the cachexia endpoints series.
McDonald, James; Sayers, Judith; Anker, Stefan D; Arends, Jann; Balstad, Trude Rakel; Baracos, Vickie; Brown, Leo; Bye, Asta; Dajani, Olav; Dolan, Ross; Fallon, Marie T; Fraser, Eilidh; Griel, Christine; Grzyb, Aleksandra; Hjermstad, Marianne; Jamal-Hanjani, Mariam; Jakobsen, Gunnhild; Kaasa, Stein; McMillan, Donald; Maddocks, Matthew; Philips, Iain; Ottestad, Inger O; Reid, Kieran F; Sousa, Mariana S; Simpson, Melanie R; Vagnildhaug, Ola Magne; Skipworth, Richard J E; Solheim, Tora S; Laird, Barry J A.
Afiliación
  • McDonald J; Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
  • Sayers J; St Columba's Hospice, Edinburgh, UK.
  • Anker SD; Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
  • Arends J; St Columba's Hospice, Edinburgh, UK.
  • Balstad TR; Clinical Surgery, University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Baracos V; Department of Cardiology (CVK), Berlin Institute of Health Center for Regenerative Therapies (BCRT), and German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin, Berlin, Germany.
  • Brown L; Institute of Heart Diseases, Wroclaw Medical University, Wroclaw, Poland.
  • Bye A; German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Dajani O; Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
  • Dolan R; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU-Norwegian University of Science and Technology, Trondheim, Norway.
  • Fallon MT; Department of Clinical Medicine, Clinical Nutrition Research Group, UiT The Arctic University of Norway, Tromsø, Norway.
  • Fraser E; Division of Palliative Care Medicine, Department of Oncology, University of Alberta, Edmonton, AB, Canada.
  • Griel C; Clinical Surgery, University of Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Grzyb A; Regional Advisory Unit for Palliative Care, Department of Oncology, Oslo University Hospital/European Palliative Care Research Centre (PRC), and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Hjermstad M; Department of Nursing and Health Promotion, Faculty of Health Sciences, Oslo Metropolitan University, Oslo, Norway.
  • Jamal-Hanjani M; Regional Advisory Unit for Palliative Care, Department of Oncology, Oslo University Hospital/European Palliative Care Research Centre (PRC), and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Jakobsen G; Academic Unit of Surgery, University of Glasgow, Glasgow Royal Infirmary, Glasgow, UK.
  • Kaasa S; Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
  • McMillan D; Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
  • Maddocks M; Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
  • Philips I; Edinburgh Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
  • Ottestad IO; Regional Advisory Unit for Palliative Care, Department of Oncology, Oslo University Hospital/European Palliative Care Research Centre (PRC), and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Reid KF; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.
  • Sousa MS; Cancer Metastasis Laboratory, University College London Cancer Institute, London, UK.
  • Simpson MR; Department of Oncology, University College London Hospitals, London, UK.
  • Vagnildhaug OM; Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.
  • Skipworth RJE; Regional Advisory Unit for Palliative Care, Department of Oncology, Oslo University Hospital/European Palliative Care Research Centre (PRC), and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Solheim TS; Academic Unit of Surgery, University of Glasgow, Glasgow Royal Infirmary, Glasgow, UK.
  • Laird BJA; Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King's College London, London, UK.
J Cachexia Sarcopenia Muscle ; 14(5): 1932-1948, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37671529
ABSTRACT
In cancer cachexia trials, measures of physical function are commonly used as endpoints. For drug trials to obtain regulatory approval, efficacy in physical function endpoints may be needed alongside other measures. However, it is not clear which physical function endpoints should be used. The aim of this systematic review was to assess the frequency and diversity of physical function endpoints in cancer cachexia trials. Following a comprehensive electronic literature search of MEDLINE, Embase and Cochrane (1990-2021), records were retrieved. Eligible trials met the following criteria adults (≥18 years), controlled design, more than 40 participants, use of a cachexia intervention for more than 14 days and use of a physical function endpoint. Physical function measures were classified as an objective measure (hand grip strength [HGS], stair climb power [SCP], timed up and go [TUG] test, 6-min walking test [6MWT] and short physical performance battery [SPPB]), clinician assessment of function (Karnofsky Performance Status [KPS] or Eastern Cooperative Oncology Group-Performance Status [ECOG-PS]) or patient-reported outcomes (physical function subscale of the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaires [EORTC QLQ-C30 or C15]). Data extraction was performed using Covidence and followed PRISMA guidance (PROSPERO registration CRD42022276710). A total of 5975 potential studies were examined and 71 were eligible. Pharmacological interventions were assessed in 38 trials (54%). Of these, 11 (29%, n = 1184) examined megestrol and 5 (13%, n = 1928) examined anamorelin; nutritional interventions were assessed in 21 trials (30%); and exercise-based interventions were assessed in 6 trials (8%). The remaining six trials (8%) assessed multimodal interventions. Among the objective measures of physical function (assessed as primary or secondary endpoints), HGS was most commonly examined (33 trials, n = 5081) and demonstrated a statistically significant finding in 12 (36%) trials (n = 2091). The 6MWT was assessed in 12 trials (n = 1074) and was statistically significant in 4 (33%) trials (n = 403), whereas SCP, TUG and SPPB were each assessed in 3 trials. KPS was more commonly assessed than the newer ECOG-PS (16 vs. 9 trials), and patient-reported EORTC QLQ-C30 physical function was reported in 25 trials. HGS is the most commonly used physical function endpoint in cancer cachexia clinical trials. However, heterogeneity in study design, populations, intervention and endpoint selection make it difficult to comment on the optimal endpoint and how to measure this. We offer several recommendations/considerations to improve the design of future clinical trials in cancer cachexia.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Caquexia / Neoplasias Tipo de estudio: Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Caquexia / Neoplasias Tipo de estudio: Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido