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Durvalumab therapy following chemoradiation compared with a historical cohort treated with chemoradiation alone in patients with stage III non–small cell lung cancer: A real-world multicentre study

Authors :
Victor Cohen
Chloé Charbonneau
Rui Kitadai
Lena Cvetkovic
Penelope A. Bradbury
Normand Blais
Julie Malo
Marie Florescu
Félix Blanc-Durand
S. Lau
Wiam Belkaid
Natasha B. Leighl
Arielle Elkrief
Adrian G. Sacher
Corentin Richard
Kevin Jao
Suzanne Kazandjian
Geoffrey Liu
Mustapha Tehfe
Taiki Hakozaki
Frances A. Shepherd
Jason Agulnik
Nathalie Daaboul
Benjamin Shieh
S. Owen
Houda Bahig
Nicolas Marcoux
Meriem Messaoudene
Bertrand Routy
Antoine Desilets
Source :
European Journal of Cancer. 142:83-91
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

The PACIFIC trial demonstrated that durvalumab therapy following chemoradiation (CRT) was associated with improved overall survival (OS) in patients with stage III non-small cell lung cancer (NSCLC). It is unclear whether the results obtained as part of randomised controlled trials are a reflection of real-world (RW) data. Several questions remain unanswered with regard to RW durvalumab use, such as optimal time to durvalumab initiation, incidence of pneumonitis and response in PD-L1 subgroups.In this multicentre retrospective analysis, 147 patients with stage III NSCLC treated with CRT followed by durvalumab were compared with a historical cohort of 121 patients treated with CRT alone. Survival curves were estimated using the Kaplan-Meier method and compared with the log-rank test in univariate analysis. Multivariate analysis was performed to evaluate the effect of standard prognostic factors for durvalumab use.Median OS was not reached in the durvalumab group, compared with 26.9 months in the historical group (hazard ratio [HR]: 0.56, 95% confidence interval [CI]: 0.37-0.85, p = 0.001). In the durvalumab group, our data suggest improved 12-month OS in patients with PD-L1 expression ≥50% (100% vs 86%, HR: 0.25, 95% CI: 0.11-0.58, p = 0.007). There was no difference in OS between patients with a PD-L1 expression of 1-49% and patients with PD-L1 expression1%. Delay in durvalumab initiation beyond 42 days did not impact OS. Incidence of pneumonitis was similar in the durvalumab and historical groups. In the durvalumab group, patients who experienced any-grade pneumonitis had a lower 12-month OS than patients without pneumonitis (85% vs 95%, respectively; HR: 3.3, 95% CI: 1.2-9.0, p = 0.006).This multicentre analysis suggests that PD-L1 expression ≥50% was associated with favourable OS in patients with stage III NSCLC treated with durvalumab after CRT, whereas the presence of pneumonitis represented a negative prognostic factor.

Details

ISSN :
09598049
Volume :
142
Database :
OpenAIRE
Journal :
European Journal of Cancer
Accession number :
edsair.doi.dedup.....ad538c6bbaa6f6714ec331bfd6f5eb7a