Real-world outcomes with durvalumab after chemoradiotherapy in patients with unresectable stage III NSCLC: interim analysis of overall survival from PACIFIC-R.

Details

Serval ID
serval:BIB_8BA41A1F1CC3
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Real-world outcomes with durvalumab after chemoradiotherapy in patients with unresectable stage III NSCLC: interim analysis of overall survival from PACIFIC-R.
Journal
ESMO open
Author(s)
Filippi A.R., Bar J., Chouaid C., Christoph D.C., Field J.K., Fietkau R., Garassino M.C., Garrido P., Haakensen V.D., Kao S., Markman B., McDonald F., Mornex F., Moskovitz M., Peters S., Sibille A., Siva S., van den Heuvel M., Vercauter P., Anand S., Chander P., Licour M., de Lima A.R., Qiao Y., Girard N.
ISSN
2059-7029 (Electronic)
ISSN-L
2059-7029
Publication state
Published
Issued date
06/2024
Peer-reviewed
Oui
Volume
9
Number
6
Pages
103464
Language
english
Notes
Publication types: Journal Article ; Observational Study ; Multicenter Study
Publication Status: ppublish
Abstract
Based on the findings of the PACIFIC trial, consolidation durvalumab following platinum-based chemoradiotherapy (CRT) is a global standard of care for patients with unresectable, stage III non-small-cell lung cancer (NSCLC). An earlier analysis from the ongoing PACIFIC-R study (NCT03798535) demonstrated the effectiveness of this regimen in terms of progression-free survival (PFS). Here, we report the first planned overall survival (OS) analysis.
PACIFIC-R is an observational/non-interventional, retrospective study of patients with unresectable, stage III NSCLC who started durvalumab (10 mg/kg intravenously every 2 weeks) within an AstraZeneca-initiated early access program between September 2017 and December 2018. Primary endpoints are OS and investigator-assessed PFS, estimated using the Kaplan-Meier method.
By 30 November 2021, the full analysis set included 1154 participants from 10 countries (median follow-up in censored patients: 38.7 months). Median OS was not reached, and the 3-year OS rate was 63.2% (95% confidence interval 60.3% to 65.9%). Three-year OS rates were numerically higher among patients with programmed death-ligand 1 (PD-L1) expression on ≥1% versus <1% of tumor cells (TCs; 67.0% versus 54.4%) and patients who received concurrent CRT (cCRT) versus sequential CRT (sCRT) (64.8% versus 57.9%).
PACIFIC-R data continue to provide evidence for the effectiveness of consolidation durvalumab after CRT in a large, diverse, real-world population. Better outcomes were observed among patients with PD-L1 TCs ≥1% and patients who received cCRT. Nevertheless, encouraging outcomes were still observed among patients with TCs <1% and patients who received sCRT, supporting use of consolidation durvalumab in a broad population of patients with unresectable, stage III NSCLC.
Keywords
Humans, Carcinoma, Non-Small-Cell Lung/mortality, Carcinoma, Non-Small-Cell Lung/pathology, Carcinoma, Non-Small-Cell Lung/therapy, Carcinoma, Non-Small-Cell Lung/drug therapy, Female, Male, Lung Neoplasms/mortality, Lung Neoplasms/therapy, Lung Neoplasms/pathology, Lung Neoplasms/drug therapy, Middle Aged, Retrospective Studies, Aged, Chemoradiotherapy/methods, Antibodies, Monoclonal/therapeutic use, Antineoplastic Agents, Immunological/therapeutic use, Antineoplastic Agents, Immunological/pharmacology, Adult, Neoplasm Staging, Aged, 80 and over, PD-L1, durvalumab, immunotherapy, locally advanced NSCLC, real-world evidence
Pubmed
Web of science
Open Access
Yes
Create date
14/06/2024 14:16
Last modification date
26/07/2024 6:02
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