Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/219990
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dc.contributor.authorLlop, Sandra-
dc.contributor.authorPlana, Maria-
dc.contributor.authorTous, Sara-
dc.contributor.authorFerrando Díez, Angelica-
dc.contributor.authorBrenes, Jesús-
dc.contributor.authorJuarez, Marc-
dc.contributor.authorVidales, Zara-
dc.contributor.authorVilajosana, Esther-
dc.contributor.authorLinares, Isabel-
dc.contributor.authorArribas, Lorena-
dc.contributor.authorDuch, Maria-
dc.contributor.authorFulla, Marta-
dc.contributor.authorBrunet, Aina-
dc.contributor.authorLozano, Alicia-
dc.contributor.authorCirauqui, Beatriz-
dc.contributor.authorMesía, Ricard-
dc.contributor.authorOliva, Marc-
dc.date.accessioned2025-03-25T12:48:01Z-
dc.date.available2025-03-25T12:48:01Z-
dc.date.issued2024-11-25-
dc.identifier.issn2234-943X-
dc.identifier.urihttps://hdl.handle.net/2445/219990-
dc.description.abstractObjectives 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.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFrontiers Media SA-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fonc.2024.1458479-
dc.relation.ispartofFrontiers in Oncology, 2024, vol. 14-
dc.relation.urihttps://doi.org/10.3389/fonc.2024.1458479-
dc.rightscc-by (c) Llop, Sandra et al., 2024-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationQuimioteràpia-
dc.subject.classificationImmunoteràpia-
dc.subject.classificationCàncer de pell-
dc.subject.classificationColl-
dc.subject.classificationCap-
dc.subject.otherChemotherapy-
dc.subject.otherImmunotheraphy-
dc.subject.otherSkin cancer-
dc.subject.otherNeck-
dc.subject.otherHead-
dc.titleSalvage chemotherapy after progression on immunotherapy in recurrent/metastatic squamous cell head and neck carcinoma-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2025-01-22T15:32:28Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid39655068-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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