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Adjuvant durvalumab for esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy: a placebo-controlled, randomized, double-blind, phase II study.

Publication ,  Journal Article
Park, S; Sun, J-M; Choi, Y-L; Oh, D; Kim, HK; Lee, T; Chi, SA; Lee, S-H; Choi, YS; Jung, S-H; Ahn, M-J; Ahn, YC; Park, K; Shim, YM
Published in: ESMO Open
February 2022

BACKGROUND: We evaluated the efficacy of adjuvant durvalumab after neoadjuvant concurrent chemoradiotherapy (CCRT) in patients with esophageal squamous cell carcinoma (ESCC). PATIENTS AND METHODS: This randomized, double-blind, phase II study included patients with ESCC who underwent curative surgery after neoadjuvant CCRT. Patients were randomized to receive either durvalumab (20 mg/kg/i.v. every 4 weeks for 12 months) or placebo in a 1:1 ratio and were stratified by age and pathologic tumor stage. The primary endpoint was disease-free survival (DFS). RESULTS: Between March 2016 and June 2018, 86 patients were randomized to the durvalumab (n = 45) or placebo (n = 41) arm. The median follow-up duration was 38.7 months. There was no difference in DFS [hazard ratio (HR) 1.18, 95% confidence interval (CI) 0.62-2.27, P = 0.61] or overall survival (HR 1.08, 95% CI 0.52-2.24, P = 0.85) between the two arms. Subgroup analysis was performed for patients for whom the post-CCRT programmed death-ligand 1 (PD-L1) expression profile could be assessed (n = 54). In the PD-L1-positive group, based on tumor proportion score ≥1%, durvalumab was associated with longer overall survival compared with the placebo (36-month survival rate: 94% versus 64%; HR 0.42, 95% CI 0.10-1.76), while in the PD-L1-negative group, it was associated with shorter overall survival (42% versus 55%; HR 1.53, 95% CI 0.48-4.83), showing the tendency of interaction between post-CCRT PD-L1 status and adjuvant durvalumab therapy for overall survival (interaction P = 0.18). CONCLUSIONS: We failed to demonstrate that adjuvant durvalumab improved survival after neoadjuvant CCRT in patients with ESCC. However, post-CCRT PD-L1 expression could predict the survival of patients who receive adjuvant durvalumab after neoadjuvant CCRT, which needs to be validated.

Duke Scholars

Published In

ESMO Open

DOI

EISSN

2059-7029

Publication Date

February 2022

Volume

7

Issue

1

Start / End Page

100385

Location

England

Related Subject Headings

  • Neoadjuvant Therapy
  • Humans
  • Esophageal Squamous Cell Carcinoma
  • Esophageal Neoplasms
  • Antibodies, Monoclonal
  • 3211 Oncology and carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Park, S., Sun, J.-M., Choi, Y.-L., Oh, D., Kim, H. K., Lee, T., … Shim, Y. M. (2022). Adjuvant durvalumab for esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy: a placebo-controlled, randomized, double-blind, phase II study. ESMO Open, 7(1), 100385. https://doi.org/10.1016/j.esmoop.2022.100385
Park, S., J. -. M. Sun, Y. -. L. Choi, D. Oh, H. K. Kim, T. Lee, S. A. Chi, et al. “Adjuvant durvalumab for esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy: a placebo-controlled, randomized, double-blind, phase II study.ESMO Open 7, no. 1 (February 2022): 100385. https://doi.org/10.1016/j.esmoop.2022.100385.
Park, S., et al. “Adjuvant durvalumab for esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy: a placebo-controlled, randomized, double-blind, phase II study.ESMO Open, vol. 7, no. 1, Feb. 2022, p. 100385. Pubmed, doi:10.1016/j.esmoop.2022.100385.
Park S, Sun J-M, Choi Y-L, Oh D, Kim HK, Lee T, Chi SA, Lee S-H, Choi YS, Jung S-H, Ahn M-J, Ahn YC, Park K, Shim YM. Adjuvant durvalumab for esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy: a placebo-controlled, randomized, double-blind, phase II study. ESMO Open. 2022 Feb;7(1):100385.

Published In

ESMO Open

DOI

EISSN

2059-7029

Publication Date

February 2022

Volume

7

Issue

1

Start / End Page

100385

Location

England

Related Subject Headings

  • Neoadjuvant Therapy
  • Humans
  • Esophageal Squamous Cell Carcinoma
  • Esophageal Neoplasms
  • Antibodies, Monoclonal
  • 3211 Oncology and carcinogenesis