Evidence map›Paper›PMID 41584602›Full record

ArticleFrontiers in oncology2025

Sequential salvage systemic therapy after immunotherapy in head and neck cancer: a real-world study.

Santiago Cabezas-Camarero, Salomé Merino-Menéndez, María Nieves Cabrera-Martín, Pablo Pérez-Alonso, Miguel J Sotelo, Pedro Pérez-Segura

Abstract read
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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Santiago Cabezas-CamareroDepartment of Medical Oncology, Instituto de Investigación Sanitaria San Carlos (IdISSC), Hospital Clínico Universitario San Carlos, Madrid, Spain.
Salomé Merino-MenéndezDepartment of Radiology, Instituto de Investigación Sanitaria San Carlos (IdISSC), Hospital Clínico Universitario San Carlos, Madrid, Spain.
María Nieves Cabrera-MartínDepartment of Nuclear Medicine, Instituto de Investigación Sanitaria San Carlos (IdISSC), Hospital Clínico Universitario San Carlos, Madrid, Spain.
Pablo Pérez-AlonsoDepartment of Pathology, Hospital Clínico Universitario San Carlos, Madrid, Spain.
Miguel J SoteloDepartment of Medical Oncology, Aliada Cancer Center, Lima, Peru.
Pedro Pérez-SeguraDepartment of Medical Oncology, Instituto de Investigación Sanitaria San Carlos (IdISSC), Hospital Clínico Universitario San Carlos, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In recurrent/metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN) there is no established standard therapy after progression to immune checkpoint inhibitors (ICI). Retrospective and limited prospective studies have suggested that salvage chemotherapy after ICI (SCAI) may outperform historical pre-ICI data. We evaluated cetuximab-based SCAI outcomes in a real-world setting. Methods: Objective response rate (ORR), median duration of response (DoR), and median best percentage change in target lesions (PCTL) by Response Evaluation Criteria In Solid Tumors version 1.1 (RECIST 1.1), and median progression-free survival (PFS) and overall survival (OS) with SCAI and with last chemotherapy before immunotherapy (LCBI) were assessed. Adverse events (AEs) by Common Terminology Criteria for Adverse Events (CTCAE) 5.0 were evaluated during SCAI, as well as treatment exposure to cetuximab-based therapy and to ICI across the whole R/M setting. Results: Among 80 patients, 96% and 100% received cetuximab-based first and second SCAI, respectively, primarily as weekly (90%-94%) regimens, as follows. First SCAI: ORR of 59% (41/70; 31 partial and 10 complete responses), PCTL of -57% (range, -30% to -100%), DoR of 9.4 months, and PFS and OS of 5.9 and 12.4 months, respectively; first-line OS of 24 months. Cetuximab-based exposure (256 days) significantly exceeded ICI exposure (168.5 days; p = 0.038). LCBI-treated (n = 22): ORR of 36% (LCBI) Conclusion: Cetuximab-based SCAI post-ICI showed high rates of response, which were durable and profound, and improved survival compared to historical data, with modest efficacy in re-sequenced patients. Time on cetuximab was significantly longer than on ICI. These results should be confirmed in a larger prospective study.

Indexed as

cetuximabhead and neck cancerimmune checkpoint inhibitorsrechallengesequential therapy

Identifiers

PMID41584602
PMCPMC12827138

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