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Durvalumab as consolidation therapy in post-concurrent chemoradiation (Ccrt) in unresectable stage iii non-small cell lung cancer patients: A multicenter observational study

  • Chin Chou Wang
  • , Li Chung Chiu
  • , Jia Shiuan Ju
  • , Yu Ching Lin
  • , Yueh Fu Fang
  • , Cheng Ta Yang
  • , Ping Chih Hsu*
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital
  • Chang Gung University
  • New Taipei Municipal Tucheng Hospital
  • Chang Gung University of Science and Technology

Research output: Contribution to journalJournal Article peer-review

26 Scopus citations

Abstract

Background: The experience of using consolidation durvalumab in post-concurrent chemoradiation (CCRT) unresectable stage III non-small cell lung cancer (NSCLC) is rare in real-world clinical practice, and the factors associated with its efficacy are also unclear. We sought to analyze the efficacy of consolidation durvalumab and the factors associated with its efficacy using a multicenter observational study. Methods: The data for 61 patients with post-CCR unresectable stage III NSCLC receiving consolidation durvalumab at the Chang Gung Memorial Hospitals in Linkou, Keelung, Chiayi, and Kaohsiung from November 2017 to March 2020 were analyzed. (3) Results: The median post-CCRT progression-free survival (PFS) and time to metastatic disease or death (TMDD) for consolidation durvalumab were 14.0 months and 16.7 months, respectively. In multiple variant factors analysis, we found that an epidermal growth factor receptor (EGFR) mutation was an independently unfavorable predictive factor for consolidation durvalumab therapy regarding PFS. The median post-CCRT PFS was 6.50 months for EGFR-mutated patients and 33.63 months for EGFR wild-type and unknown patients (HR = 10.47; 95% CI, 4.55–24.07; p < 0.001). Conclusions: Consolidation durvalumab is effective and safe for post-CCRT unresectable stage III NSCLC in clinical practice, but EGFR mutation is an unfavorable factor for consolidation durvalumab. Thus, searching for a better consolidation therapy for EGFR-mutated patients is warranted.

Original languageEnglish
Article number1122
JournalVaccines
Volume9
Issue number10
DOIs
StatePublished - 10 2021

Bibliographical note

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Concurrent chemoradiation (CCRT)
  • Durvalumab
  • Epidermal growth factor receptor (EGFR) mutation
  • Immune checkpoint inhibitors (ICIs)
  • Programmed death-ligand 1 (PD-L1)
  • Stage III non-small cell lung cancer (NSCLC)

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