PO.CL05.06 · 临床研究

Enhanced monocyte activation and T cell cytotoxicity underlie the benefit of neoadjuvant durvalumab plus gemcitabine-cisplatin (D+GP) in localized biliary tract cancer (BTC): Phase 2 DEBATE study

海报缩略图:Enhanced monocyte activation and T cell cytotoxicity underlie the benefit of neoadjuvant durvalumab plus gemcitabine-cisplatin (D+GP) in localized biliary tract cancer (BTC): Phase 2 DEBATE study
编号 6454 展板 2 时间 4/21 02:00–05:00 区域 Section 41 主讲 Changhoon Yoo, MD;PhD
分会场 Clinical Correlates of Immunotherapy
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作者与单位

Changhoon Yoo1, Hyung-Don Kim1, Chang Yeon Kim2, Joon Oh Park3, Hyehyun Jeong1, Kyu-Pyo Kim1, Jung Yong Hong4, Sang Hyun Shin4, Tae Jun Song1, Dongwook Oh1, Woohyung Lee1, Jae Hoon Lee1, Dae Wook Hwang1, Jeong Seok Lee5

1University of Ulsan College of Medicine, Seoul, Korea, Republic of,2Seoul National University College of Medicine, Seoul, Korea, Republic of,3Associate Professor, Dept. of Hem./Onc., Samsung Medical Center, Seoul, Korea, Republic of,4Samsung Medical Center, Seoul, Korea, Republic of,5Korea Advanced Institute of Science and Technology, Daejeon, Korea, Republic of

摘要 Abstract

Introduction: The prognosis of localized BTC remains poor despite surgery. The role of neoadjuvant therapy in BTC has not been well established. Methods: DEBATE is a multicenter, randomized, non-comparative phase 2 trial enrolling treatment-naïve patients (pts) with localized BTC. Pts were randomized (2:1) to receive 4 cycles of neoadjuvant D+GP or GP alone. Those undergoing surgery received 6 cycles of adjuvant durvalumab. The primary endpoint was the R0 resection rate. Biomarker analyses included single-cell RNA sequencing (scRNA-seq) of peripheral blood mononuclear cells (PBMCs), and plasma proteomics (baseline and cycle 1 day 8 [C1D8]). Results: A total of 45 pts were enrolled (D+GP, n=31; GP, n=14). Surgery was performed in 64.5% vs. 42.9%, and R0 resection rates were 48.4% vs. 42.9% in the D+GP and GP arms, respectively. In the D+GP group, the objective response rate was 38.7%, median PFS 19 months (1-sided 80% CI, 15-21), and OS 28 months (24-43), versus 14.3%, 6 months (3-11), and 30 months (23-44) in the GP group. Biomarker data were available in 98% (n=44). scRNA-seq showed a significant enrichment of classical monocytes with pro-inflammatory signatures in the D+GP group, especially among responders, along with increased CXCL10 expression in both scRNA-seq and plasma proteomics. Responders in the D+GP group also exhibited increased CD8+ T cell cytotoxicity, CD4+ Terminally differentiated effector memory T (TEMRA) cells, and IL12RB2 expression. TIGIT expression in CD4+ TEMRA cells decreased from baseline to C1D8 only in responders treated with D+GP. Conclusion: Neoadjuvant D+GP was feasible and demonstrated encouraging efficacy in localized BTC. Integrated biomarker analyses suggest that enhanced monocyte activation and T cell responses contribute to the added benefit of durvalumab. Current study provide the rationale of adding anti-TIGIT to D+GP in BTC (NCT04308174).
利益披露 Disclosure
C. Yoo, AstraZeneca ). Servier ). BMS ). MSD ). Boryung ). Servier ). Ipsen ). H. Kim, None.. C. Kim, None.. H. Jeong, None.. K. Kim, None.. J. Hong, None.. S. Shin, None.. T. Song, None.. D. Oh, None.. W. Lee, None.. J. Lee, None.. D. Hwang, None.. J. Lee, None.

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