Durvalumab after radiotherapy in patients with unresectable stage III non-small-cell lung cancer ineligible for chemotherapy: the DUART phase II nonrandomized controlled study

The safety profile of durvalumab after radiotherapy was consistent with PACIFIC (durvalumab after chemoradiotherapy). Efficacy across cohorts was encouraging. Some patients may achieve or maintain molecular remission with durvalumab even after palliative radiotherapy. Durvalumab following radiotherapy may be a potential treatment option in a frailer, older, chemotherapy-ineligible population.

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Publication Details

Journal
ESMO Open
Published
2025-08-21
DOI
https://doi.org/10.1016/j.esmoop.2025.105560
Citations
4
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
4.18

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article

Durvalumab after radiotherapy in patients with unresectable stage III non-small-cell lung cancer ineligible for chemotherapy: the DUART phase II nonrandomized controlled study

I. Toledano, G. Wetherill, I. Diaz Perez, K. Foroutanpour et al.
4 citations
ESMO Open
Cancer Immunotherapy and Biomarkers
4.18
article

Durvalumab after radiotherapy in patients with unresectable stage III non-small-cell lung cancer ineligible for chemotherapy: the DUART phase II nonrandomized controlled study

I. Toledano, G. Wetherill, I. Diaz Perez, K. Foroutanpour, Francesco Agustoni, Andrea Riccardo Filippi, Paolo Borghetti, Sylvie Van Hulst, Robert Mróz, D. Cortinovis, Chiara Bennati, Rafał Dziadziuszko, Giuseppe Tonini, Angelo Delmonte, Sergiusz Nawrocki, Nefeli Georgoulia, Carlo Genova, Zhen Zhu, Diane Kowalski, Jean-Baptiste Paoli, M.R. García Campelo
article en
4 citations

Abstract

The safety profile of durvalumab after radiotherapy was consistent with PACIFIC (durvalumab after chemoradiotherapy). Efficacy across cohorts was encouraging. Some patients may achieve or maintain molecular remission with durvalumab even after palliative radiotherapy. Durvalumab following radiotherapy may be a potential treatment option in a frailer, older, chemotherapy-ineligible population.

ESMO OpenVol. 10(9)
AstraZeneca (United Kingdom) (GB), Medical University of Białystok (PL), Università Campus Bio-Medico (IT), University of Pavia (IT), Ospedale "Santa Maria delle Croci" di Ravenna (IT), Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IT), Hôpital privé Clairval (FR), Azienda Ospedaliera San Gerardo (IT), Clinique Clémentville (FR), Campus Bio Medico University Hospital (IT), Ospedale Policlinico San Martino (IT), AstraZeneca (United States) (US), The Maria Sklodowska-Curie National Research Institute of Oncology (PL), Policlinico San Matteo Fondazione (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), University of Warmia and Mazury in Olsztyn (PL), Université de Nîmes (FR), University of Milano-Bicocca (IT), Gdańsk Medical University (PL), University of Brescia (IT)
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, GlaxoSmithKline, Sanofi, Gilead Sciences, Teva Pharmaceutical Industries, Regeneron Pharmaceuticals, Les Laboratories Pierre Fabre, BeiGene, Ministero della Salute, PharmaMar, Ipsen, Genentech, Cilag
Good health and well-being
Openalex Percentile: Top 5%
Cancer Immunotherapy and Biomarkers
4.18
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