<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T13:45:08Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/219990" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/219990</identifier><datestamp>2026-03-20T08:15:53Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478916</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Salvage chemotherapy after progression on immunotherapy in recurrent/metastatic squamous cell head and neck carcinoma</dc:title>
   <dc:creator>Llop, Sandra</dc:creator>
   <dc:creator>Plana, Maria</dc:creator>
   <dc:creator>Tous, Sara</dc:creator>
   <dc:creator>Ferrando Díez, Angelica</dc:creator>
   <dc:creator>Brenes, Jesús</dc:creator>
   <dc:creator>Juarez, Marc</dc:creator>
   <dc:creator>Vidales Sepúlveda, Zara</dc:creator>
   <dc:creator>Vilajosana, Esther</dc:creator>
   <dc:creator>Linares, Isabel</dc:creator>
   <dc:creator>Arribas, Lorena</dc:creator>
   <dc:creator>Duch, Maria</dc:creator>
   <dc:creator>Fulla, Marta</dc:creator>
   <dc:creator>Brunet, Aina</dc:creator>
   <dc:creator>Lozano, Alicia</dc:creator>
   <dc:creator>Cirauqui, Beatriz</dc:creator>
   <dc:creator>Mesía, Ricard</dc:creator>
   <dc:creator>Oliva, Marc</dc:creator>
   <dc:subject>Quimioteràpia</dc:subject>
   <dc:subject>Immunoteràpia</dc:subject>
   <dc:subject>Càncer de pell</dc:subject>
   <dc:subject>Coll</dc:subject>
   <dc:subject>Cap</dc:subject>
   <dc:subject>Chemotherapy</dc:subject>
   <dc:subject>Immunotheraphy</dc:subject>
   <dc:subject>Skin cancer</dc:subject>
   <dc:subject>Neck</dc:subject>
   <dc:subject>Head</dc:subject>
   <dc:description>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&lt;0.001), and PFS2-I (HR=0.2; 95% CI 0.1-0.5; p&lt;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:description>
   <dc:date>2025-03-25T12:48:01Z</dc:date>
   <dc:date>2025-03-25T12:48:01Z</dc:date>
   <dc:date>2024-11-25</dc:date>
   <dc:date>2025-01-22T15:32:28Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>2234-943X</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/219990</dc:identifier>
   <dc:identifier>39655068</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.3389/fonc.2024.1458479</dc:relation>
   <dc:relation>Frontiers in Oncology, 2024, vol. 14</dc:relation>
   <dc:relation>https://doi.org/10.3389/fonc.2024.1458479</dc:relation>
   <dc:rights>cc-by (c) Llop, Sandra et al., 2024</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>9 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Frontiers Media SA</dc:publisher>
   <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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