Association of age with survival in older patients with cutaneous melanoma treated with immune checkpoint inhibitors.


Journal

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

Informations de publication

Date de publication:
09 2022
Historique:
received: 23 01 2022
revised: 15 04 2022
accepted: 16 05 2022
pubmed: 7 6 2022
medline: 21 9 2022
entrez: 6 6 2022
Statut: ppublish

Résumé

Several types of immune checkpoint inhibitors (ICIs) are approved to treat advanced melanoma, but their effectiveness has not been compared in older patients treated outside of a clinical trial. Moreover, evidence suggests that a patient's response to ICI therapy may vary by age and type of ICI. The purpose of this study was to compare survival by ICI type in older patients with melanoma and to investigate treatment effect modification by age. Using the SEER-Medicare database, we identified patients with cutaneous melanoma (2012-2015) treated with an ICI (CTLA-4, PD-1, or combination CTLA-4 + PD-1 inhibitors). Cox proportional hazards regression was used to estimate hazard ratios (HRs) with 95% confidence intervals (CI) for ICI types. We used an interaction term and stratified models to test for treatment effect modification by age. Of the 1435 patients included in our analysis, 790 (55.1%) received CTLA-4 inhibitors, 512 (35.7%) received PD-1 inhibitors, and 133 (9.3%) were treated with combination ICIs. Median survival ranged from 13.4 months (95%CI: 10.7-16.3) for CTLA-4 inhibitors to 23.5 months (95%CI: 16.2-30.0) for combination ICIs. In multivariable models, the risk of death was lower with PD-1 inhibitors compared to CTLA-4 inhibitors (HR = 0.78, 95%CI: 0.68-0.89). An age*ICI type interaction term was significant (p < 0.001), and survival gains were greater the older age group (≥80) compared to the younger group (65-79). In a population-based setting, we identified important differences in survival by ICI type in older patients with melanoma treated with ICIs, with prolonged survival associated with PD-1 inhibitors compared to CTLA-4 inhibitors.

Identifiants

pubmed: 35660090
pii: S1879-4068(22)00113-8
doi: 10.1016/j.jgo.2022.05.005
pii:
doi:

Substances chimiques

CTLA-4 Antigen 0
Immune Checkpoint Inhibitors 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1003-1010

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no potential conflicts of interest.

Auteurs

Ashley V Howell (AV)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA. Electronic address: ashleyvhowell@gmail.com.

Mulugeta Gebregziabher (M)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.

Bruce H Thiers (BH)

Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, SC, USA.

Evan M Graboyes (EM)

Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.

Chrystal M Paulos (CM)

Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.

John M Wrangle (JM)

Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.

Kelly J Hunt (KJ)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.

Kristin Wallace (K)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.

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Classifications MeSH