Characterizing cancer cachexia in the geriatric oncology population
Cancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevale...
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Published in | Journal of geriatric oncology Vol. 10; no. 3; pp. 415 - 419 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.05.2019
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Subjects | |
Online Access | Get full text |
ISSN | 1879-4068 1879-4076 1879-4076 |
DOI | 10.1016/j.jgo.2018.08.008 |
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Abstract | Cancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevalence utilizing standard definitions and evaluating associations with components of the geriatric assessment (GA) and survival.
Patients with cancer older than 65 years of age who underwent a GA and had baseline CT imaging were eligible in this cross-sectional study. Cancer cachexia was defined by the international consensus definition reported in 2011. Sarcopenia was measured using cross-sectional imaging and utilizing sex-specific cut-offs. Associations between cachexia, sarcopenia, and weight loss with survival and GA domains were explored.
Mean age of 100 subjects was 79.9 years (66–95) and 65% met criteria for cancer cachexia. Cachexia was associated with impairment in instrumental activities of daily living (IADL) (p = .017); no significant association was found between sarcopenia or weight loss and IADL impairment. Cachexia was significantly associated with poorer survival (median 1.0 vs 2.1 years, p = .011).
Cancer cachexia as defined by the international consensus definition is prevalent in older adults with cancer and is associated with functional impairment and decreased survival. Larger prospective studies are needed to further describe cancer cachexia in this population. |
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AbstractList | Cancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevalence utilizing standard definitions and evaluating associations with components of the geriatric assessment (GA) and survival.
Patients with cancer older than 65 years of age who underwent a GA and had baseline CT imaging were eligible in this cross-sectional study. Cancer cachexia was defined by the international consensus definition reported in 2011. Sarcopenia was measured using cross-sectional imaging and utilizing sex-specific cut-offs. Associations between cachexia, sarcopenia, and weight loss with survival and GA domains were explored.
Mean age of 100 subjects was 79.9 years (66-95) and 65% met criteria for cancer cachexia. Cachexia was associated with impairment in instrumental activities of daily living (IADL) (p = .017); no significant association was found between sarcopenia or weight loss and IADL impairment. Cachexia was significantly associated with poorer survival (median 1.0 vs 2.1 years, p = .011).
Cancer cachexia as defined by the international consensus definition is prevalent in older adults with cancer and is associated with functional impairment and decreased survival. Larger prospective studies are needed to further describe cancer cachexia in this population. ABSTRACTObjectivesCancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevalence utilizing standard definitions and evaluating associations with components of the geriatric assessment (GA) and survival. Materials and MethodsPatients with cancer older than 65 years of age who underwent a GA and had baseline CT imaging were eligible in this cross-sectional study. Cancer cachexia was defined by the international consensus definition reported in 2011. Sarcopenia was measured using cross-sectional imaging and utilizing sex-specific cut-offs. Associations between cachexia, sarcopenia, and weight loss with survival and GA domains were explored. ResultsMean age of 100 subjects was 79.9 years (66–95) and 65% met criteria for cancer cachexia. Cachexia was associated with impairment in instrumental activities of daily living (IADL) ( p = .017); no significant association was found between sarcopenia or weight loss and IADL impairment. Cachexia was significantly associated with poorer survival (median 1.0 vs 2.1 years, p = .011). ConclusionsCancer cachexia as defined by the international consensus definition is prevalent in older adults with cancer and is associated with functional impairment and decreased survival. Larger prospective studies are needed to further describe cancer cachexia in this population. Cancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevalence utilizing standard definitions and evaluating associations with components of the geriatric assessment (GA) and survival.OBJECTIVESCancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia remains poorly described in older adults with cancer. This study aims to characterize cancer cachexia in older adults by assessing its prevalence utilizing standard definitions and evaluating associations with components of the geriatric assessment (GA) and survival.Patients with cancer older than 65 years of age who underwent a GA and had baseline CT imaging were eligible in this cross-sectional study. Cancer cachexia was defined by the international consensus definition reported in 2011. Sarcopenia was measured using cross-sectional imaging and utilizing sex-specific cut-offs. Associations between cachexia, sarcopenia, and weight loss with survival and GA domains were explored.MATERIALS AND METHODSPatients with cancer older than 65 years of age who underwent a GA and had baseline CT imaging were eligible in this cross-sectional study. Cancer cachexia was defined by the international consensus definition reported in 2011. Sarcopenia was measured using cross-sectional imaging and utilizing sex-specific cut-offs. Associations between cachexia, sarcopenia, and weight loss with survival and GA domains were explored.Mean age of 100 subjects was 79.9 years (66-95) and 65% met criteria for cancer cachexia. Cachexia was associated with impairment in instrumental activities of daily living (IADL) (p = .017); no significant association was found between sarcopenia or weight loss and IADL impairment. Cachexia was significantly associated with poorer survival (median 1.0 vs 2.1 years, p = .011).RESULTSMean age of 100 subjects was 79.9 years (66-95) and 65% met criteria for cancer cachexia. Cachexia was associated with impairment in instrumental activities of daily living (IADL) (p = .017); no significant association was found between sarcopenia or weight loss and IADL impairment. Cachexia was significantly associated with poorer survival (median 1.0 vs 2.1 years, p = .011).Cancer cachexia as defined by the international consensus definition is prevalent in older adults with cancer and is associated with functional impairment and decreased survival. Larger prospective studies are needed to further describe cancer cachexia in this population.CONCLUSIONSCancer cachexia as defined by the international consensus definition is prevalent in older adults with cancer and is associated with functional impairment and decreased survival. Larger prospective studies are needed to further describe cancer cachexia in this population. |
Author | Pandya, Chintan Dunne, Richard F. Ramsdale, Erika Mohile, Supriya G. Loh, Kah Poh Mustian, Karen M. Culakova, Eva Hensley, Bradley Jatoi, Aminah Dale, William Roussel, Breton Gilles, Maxence Magnuson, Allison M. Fleming, Fergal J. Maggiore, Ronald J. |
AuthorAffiliation | d Mayo Clinic, Department of Oncology, Rochester, Minnesota c Department of Medicine, Brown University, Providence, RI b University of Rochester NCI Community Oncology Research Program (UR NCORP), Rochester, NY a Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY e City of Hope, Department of Supportive Care Medicine, Duarte, CA |
AuthorAffiliation_xml | – name: c Department of Medicine, Brown University, Providence, RI – name: b University of Rochester NCI Community Oncology Research Program (UR NCORP), Rochester, NY – name: e City of Hope, Department of Supportive Care Medicine, Duarte, CA – name: a Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY – name: d Mayo Clinic, Department of Oncology, Rochester, Minnesota |
Author_xml | – sequence: 1 givenname: Richard F. surname: Dunne fullname: Dunne, Richard F. email: richard_dunne@urmc.rochester.edu organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 2 givenname: Breton surname: Roussel fullname: Roussel, Breton organization: Department of Medicine, Brown University, Providence, RI, United States – sequence: 3 givenname: Eva surname: Culakova fullname: Culakova, Eva organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 4 givenname: Chintan surname: Pandya fullname: Pandya, Chintan organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 5 givenname: Fergal J. surname: Fleming fullname: Fleming, Fergal J. organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 6 givenname: Bradley surname: Hensley fullname: Hensley, Bradley organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 7 givenname: Allison M. surname: Magnuson fullname: Magnuson, Allison M. organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 8 givenname: Kah Poh orcidid: 0000-0002-6978-0418 surname: Loh fullname: Loh, Kah Poh organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 9 givenname: Maxence surname: Gilles fullname: Gilles, Maxence organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 10 givenname: Erika surname: Ramsdale fullname: Ramsdale, Erika organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 11 givenname: Ronald J. surname: Maggiore fullname: Maggiore, Ronald J. organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 12 givenname: Aminah surname: Jatoi fullname: Jatoi, Aminah organization: Mayo Clinic, Department of Oncology, Rochester, MN, United States – sequence: 13 givenname: Karen M. surname: Mustian fullname: Mustian, Karen M. organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States – sequence: 14 givenname: William surname: Dale fullname: Dale, William organization: City of Hope, Department of Supportive Care Medicine, Duarte, CA, United States – sequence: 15 givenname: Supriya G. surname: Mohile fullname: Mohile, Supriya G. organization: Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States |
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Keywords | Sarcopenia Geriatric assessment Cachexia Functional impairment Geriatric oncology Weight loss |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Study concepts: RF Dunne, B Roussel, C Pandya, W Dale, SG Mohile, Study design: RF Dunne, B Roussel, C Pandya, A Magnuson, SG Mohile, Data acquisition: RF Dunne, B Roussel, FJ Fleming, B Hensley, M Gilles, Quality control of data and algorithms: RF Dunne, B Roussel, M Gilles, Data analysis and interpretation: RF Dunne, E Culakova, KP Loh, E Ramsdale, RJ, Maggiore, A Jatoi, KM Mustian, Statistical analysis: E Culakova, KP Loh, Manuscript preparation: RF Dunne, E Culakova, E Ramsdale, SG Mohile, Manuscript editing: RF Dunne, B Roussel, E Culakova, C Pandya, FJ Fleming, B Hensley, A Magnuson, KP Loh, M Gilles, E Ramsdale, RJ Maggiore, A Jatoi, KM Mustian, W Dale, SG Mohile, Manuscript review: RF Dunne, B Roussel, E Culakova, C Pandya, FJ Fleming, B, Hensley, A Magnuson, KP Loh, M Gilles, E Ramsdale, RJ Maggiore, A Jatoi, KM, Mustian, W Dale, SG Mohile Author Contributions |
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Snippet | Cancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival. Cancer cachexia... ABSTRACTObjectivesCancer cachexia, characterized by weight loss and sarcopenia, leads to a decline in physical function and is associated with poorer survival.... |
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StartPage | 415 |
SubjectTerms | Cachexia Functional impairment Geriatric assessment Geriatric oncology Hematology, Oncology, and Palliative Medicine Internal Medicine Sarcopenia Weight loss |
Title | Characterizing cancer cachexia in the geriatric oncology population |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S1879406818301243 https://www.clinicalkey.es/playcontent/1-s2.0-S1879406818301243 https://dx.doi.org/10.1016/j.jgo.2018.08.008 https://www.ncbi.nlm.nih.gov/pubmed/30196027 https://www.proquest.com/docview/2101916292 https://pubmed.ncbi.nlm.nih.gov/PMC6401352 |
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