Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/219990
Title: Salvage chemotherapy after progression on immunotherapy in recurrent/metastatic squamous cell head and neck carcinoma
Author: Llop, Sandra
Plana, Maria
Tous, Sara
Ferrando Díez, Angelica
Brenes, Jesús
Juarez, Marc
Vidales, Zara
Vilajosana, Esther
Linares, Isabel
Arribas, Lorena
Duch, Maria
Fulla, Marta
Brunet, Aina
Lozano, Alicia
Cirauqui, Beatriz
Mesía, Ricard
Oliva, Marc
Keywords: Quimioteràpia
Immunoteràpia
Càncer de pell
Coll
Cap
Chemotherapy
Immunotheraphy
Skin cancer
Neck
Head
Issue Date: 25-Nov-2024
Publisher: Frontiers Media SA
Abstract: Objectives Anti-PD-(L)1 agents changed the landscape of recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) treatment. Previous studies showed improved response rates to salvage chemotherapy (SCT) after progression to anti-PD-(L)1 agents. This study aims to evaluate the outcomes of SCT and to identify predictors of response and survival in patients with R/M HNSCC. Materials and methods Retrospective cohort analysis of 63 R/M patients treated with SCT after antiPD-(L1)-based therapy between January 2015 and August 2022. The overall response rate (ORR) was evaluated. Progression-free survival (PFS) and overall survival (OS) were estimated with Kaplan-Meier method. Progression-free survival 2 was calculated from anti-PD-(L)1-therapy start until progression to SCT (PFS2-I). Logistic regression and Cox regression analyses were performed to identify predictors of outcome. Results A total of 63 patients were included: 76% were men, and median age was 60 years. PD-L1 status was available in 68% (61% positive). Up to 71% received SCT as third line or beyond. ORR to SCT was 49% with higher rates in PD-L1 positive tumors, 71% vs. 18% (p=0.001), and cetuximab-containing regimens, 68% vs. 39% (p=0.026). PD-L1 status was the only predictor of ORR in the adjusted model (OR=8.6, 95% CI 1.7-43.0). OS and PFS were 9.3 months (95% CI, 6.5-12.3) and 4.1 months (95% CI, 3.0-5.8) respectively. PFS2-I was 8.6 months (95% CI, 6.6-10.5). In the multivariate analysis, PD-L1 was the only independent factor for OS (HR=0.3; 95% CI, 0.1-0.7), PFS (HR=0.2; 95% CI, 0.1-0.5; p<0.001), and PFS2-I (HR=0.2; 95% CI 0.1-0.5; p<0.001). Conclusion PDL1 status appeared as a strong predictor of response of efficacy for SCT after anti-PD-(L)1 agents. Patients receiving cetuximab-containing regimens trended towards greater benefit. This highlights the importance of treatment sequencing and personalized treatment strategies.
Note: Reproducció del document publicat a: https://doi.org/10.3389/fonc.2024.1458479
It is part of: Frontiers in Oncology, 2024, vol. 14
URI: https://hdl.handle.net/2445/219990
Related resource: https://doi.org/10.3389/fonc.2024.1458479
ISSN: 2234-943X
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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