The association between geriatric assessment, muscle measures, and treatment-related toxicity in older adults with cancer: An Israeli prospective study.


Journal

Journal of geriatric oncology
ISSN: 1879-4076
Titre abrégé: J Geriatr Oncol
Pays: Netherlands
ID NLM: 101534770

Informations de publication

Date de publication:
11 2022
Historique:
received: 12 05 2022
revised: 11 07 2022
accepted: 11 08 2022
pubmed: 22 8 2022
medline: 24 11 2022
entrez: 21 8 2022
Statut: ppublish

Résumé

We investigated the associations among frailty, as determined via the comprehensive geriatric assessment (CGA), muscle measures (i.e., sarcopenia), and treatment-related toxicity in older adults with cancer in Israel. This prospective cohort study enrolled patients ≥65 years with newly-diagnosed stage IV lung, breast, or genitourinary cancer. Patients were enrolled and completed CGA before their first line of systemic therapy (chemotherapy, biologic therapy, immunologic therapy, or a combination thereof). CGA was used to classify patients as robust, pre-frail, or frail, and routine pre-treatment computed tomography (CT) images were used to quantify skeletal muscle index (SMI) and skeletal muscle density (SMD) at L3 cross-section. Two sarcopenia definitions were used: i. for women SMI <41 cm In total, 51 patients were included in the analysis. The median (interquartile range) age was 72 (68-76) years, 30 (59%) were male, and 26 (51%) had lung cancer. CGA data were available for 48 patients: fifteen (31%), thirteen (27%), and twenty (42%) were defined as robust, pre-frail, and frail, respectively. Overall, 33 (65%) were sarcopenic by the first aforementioned definition, and sixteen (31%) by the second. No statistically significant associations were identified between frailty and having at least one AE grade ≥ 2, or between frailty and sarcopenia. Statistically significant associations were found between having sarcopenia (the second definition) and having at least one AE grade ≥ 2 (P = 0.0217). The corresponding odds ratio (95% CI) was 4.2 (1.2-15.0), P = 0.026. Our findings suggests that sarcopenia is significantly associated with treatment-related toxicity. Further studies with larger sample sizes are warranted.

Identifiants

pubmed: 35989184
pii: S1879-4068(22)00198-9
doi: 10.1016/j.jgo.2022.08.007
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1203-1207

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no conflict of interest.

Auteurs

Shlomit S Shachar (SS)

Division of Oncology, Sourasky- Tel Aviv Medical Center, Tel Aviv, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: shlomitss@tlvmc.gov.il.

Gil Bar-Sela (G)

Emek Medical Center, Department of Oncology, Afula, Israel; Technion Rappaport Faculty of Medicine, Haifa, Israel.

Avivit Peer (A)

Technion Rappaport Faculty of Medicine, Haifa, Israel; Ramban Health Care Campus, Haifa, Israel.

Mor Tal Moskovitz (MT)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.

Avital Bareket-Samish (A)

BioInsight Ltd., Binyamina, Israel.

Jessica Epstein (J)

Division of Oncology, Sourasky- Tel Aviv Medical Center, Tel Aviv, Israel.

Mira Wollner (M)

Ramban Health Care Campus, Haifa, Israel.

Itamar Shafran (I)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Amit Boukal (A)

Technion Rappaport Faculty of Medicine, Haifa, Israel.

Grant R Williams (GR)

Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham, AL, USA.

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