4.6 Article

Durvalumab After Sequential Chemoradiotherapy in Stage III, Unresectable NSCLC: The Phase 2 PACIFIC-6 Trial

Journal

JOURNAL OF THORACIC ONCOLOGY
Volume 17, Issue 12, Pages 1415-1427

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtho.2022.07.1148

Keywords

Durvalumab; Immunotherapy; Sequential che-moradiotherapy; Non-small-cell lung cancer; Locally advanced

Funding

  1. AstraZeneca
  2. National Institute for Health Research Manchester Biomedical Research Centre [NCT03693300]

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The study included 117 patients with advanced unresectable stage III NSCLC, showing that durvalumab after sequential CRT has a comparable safety profile to durvalumab after concurrent CRT and has promising preliminary efficacy in a frailer population.
Introduction: On the basis of the findings of the phase 3 PACIFIC trial (NCT02125461), durvalumab is standard of care for patients with stage III, unresectable NSCLC and no disease progression after concurrent chemoradiotherapy (cCRT). Many patients are considered unsuitable for cCRT owing to concerns with tolerability. The phase 2 PACIFIC-6 trial (NCT03693300) evaluates the safety and tolerability of durvalumab after sequential CRT (sCRT).Methods: Patients with stage III, unresectable NSCLC and no progression after platinum-based sCRT were enrolled to receive durvalumab (1500 mg intravenously) every 4 weeks for up to 24 months. The primary end point was the incidence of grade 3 or 4 adverse events possibly related to treatment occurring within 6 months. Secondary end points included investigator -assessed progression-free survival (PFS; Response Evaluation Criteria in Solid Tumors version 1.1) and overall survival.Results: Overall, 117 patients were enrolled (59.8% with performance status >0, 65.8% aged >65 y, and 37.6% with stage IIIA disease). Median treatment duration was 32.0 weeks; 37.6% of patients remained on treatment at data cutoff (July 15, 2021). Grade 3 or 4 AEs occurred in 18.8% of patients. Five patients had grade 3 or 4 possibly related adverse events within 6 months (incidence: 4.3%; 95% confidence interval: 1.4-9.7), including two pneumonitis cases. Two patients (1.7%) had grade 5 AEs of any cause. Survival data maturity was limited. Median PFS was 10.9 months (95% confidence interval: 7.3-15.6), and 12-month PFS and overall survival rates were 49.6% and 84.1%, respectively.Conclusions: Durvalumab after sCRT had a comparable safety profile with that observed with durvalumab after cCRT in PACIFIC and had encouraging preliminary efficacy in a frailer population. (c) 2022 International Association for the Study of Lung Can-cer. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).

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