Durvalumab after radiotherapy in patients with unresectable stage III non-small-cell lung cancer ineligible for chemotherapy: the DUART phase II nonrandomized controlled study
Year: 2025
Type: article
Study design: Clinical Trial
Abstract: BACKGROUND: Currently, patients with unresectable stage III non-small-cell lung cancer (NSCLC) ineligible for chemotherapy receive radiotherapy alone, with unsatisfactory results. DUART was a phase II single-arm trial of durvalumab in patients without progression after radiotherapy for unresectable stage III NSCLC. PATIENTS AND METHODS: Patients were enrolled into parallel cohorts per radiotherapy dose (A: definitive; B: palliative) and received durvalumab (1500 mg every 4 weeks for up to 12 months). The primary endpoint was incidence of grade 3/4 possibly related adverse events (PRAEs) within 6 months of durvalumab initiation. Secondary endpoints included objective response rate, progression-free survival (PFS), and overall survival (OS). Exploratory circulating tumor (ctDNA) analyses utilized a targeted methylation assay (GRAIL, Inc.). RESULTS: As of 06 December 2023, 102 patients received durvalumab (cohort A: 53; cohort B: 49); 18.8%/73.3%/7.9% had Eastern Cooperative Oncology Group performance status 0/1/2 and median age was 79.0 years. Overall, 9.8% [95% confidence interval (CI) 4.8% to 17.3%] had grade 3/4 PRAEs within 6 months of durvalumab initiation. Median PFS (investigator assessed) was 9.2 months, with a 12-month landmark rate of 39.6%. Median OS was 21.1 months and the 12-month landmark rate was 64.7%. Patients who were ctDNA positive at cycle 1 or 7 had shorter PFS versus patients who were ctDNA negative at the same time point. CONCLUSIONS: 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.
Source: ESMO Open
Institutions: University of Milan, Fondazione IRCCS Istituto Nazionale dei Tumori, Complexo Hospitalario Universitario A Coruña, Hôpital privé Clairval, The Maria Sklodowska-Curie National Research Institute of Oncology, Ospedale "Santa Maria delle Croci" di Ravenna, Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia, University of Brescia, University of Milano-Bicocca, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Ospedale Policlinico San Martino, University of Genoa, Centre Hospitalier Universitaire de Nîmes, Medical University of Białystok, University of Warmia and Mazury in Olsztyn, Clinique Clémentville, Università Campus Bio-Medico, Campus Bio Medico University Hospital, University of Pavia, Policlinico San Matteo Fondazione, AstraZeneca (United Kingdom), AstraZeneca (United States), Gdańsk Medical University
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,910
OpenAlex ID: W4413367030
