Abstract 1032P
Background
EBV is associated with about 10% of gastric cancers. Preliminary data has indicated that patients(pts) with EBV-associated gastric cancer (EBVaGC) could benefit from immunotherapy. The purpose of this study is to evaluate safety and efficacy of sintilimab (anti-PD-1) plus IBI310 (anti-CTLA-4) for EBVaGC. The preliminary results of first-line (cohort B) and ≥ 2 line (cohort C) settings were reported. The study is still recruiting.
Methods
Adult pts with EBV+ (in situ hybridization, ISH), unresectable locally advanced or metastatic, histopathologically confirmed GC/GEJC (cohort B: pts with treatment-naïve; cohort C, pts who had failed at least one standard treatment regimen) were enrolled. Pts in both cohorts received sintilimab 3mg/kg (200mg for weight≥60kg)IV Q3W plus IBI310 1mg/kg IV Q6W combination regimen for 1-3 cycles, and sintilimab monotherapy maintenance thereafter until disease progression, unacceptable toxicity or for up to 24 months. The endpoints include ORR per RECIST v1.1 by investigator, other efficacy measures and safety profile in both cohorts.
Results
As of Feb 22, 2023, 49 pts were enrolled (28 in cohort B and 21 in cohort C). Any and grade ≥ 3 treatment-related adverse events (TRAEs) occurred in 38 (77.6%) and 10 (20.4%) pts, respectively. No TRAE leading to drug discontinuation or death. Any and grade ≥ 3 immune related adverse events (irAEs) occurred in 33 (67.3%) and 7 (14.3%) pts, respectively. In cohort B, for 26 efficacy evaluable pts, the confirmed ORR were 61.5% (95% CI, 40.6-79.8), and DCR was 80.8% (95% CI, 60.7-93.5). The median DoR was 8.3 months (95% CI, 4.0-15.1). With a median follow-up of 13.3 months, the median PFS and OS were 5.5 months (95% CI, 2.8-9.7) and 24.6 months (95% CI, 10.3-28.8), respectively. In cohort C, for 17 efficacy evaluable pts, the confirmed ORR was 47.1% (95% CI: 23.0-72.2) and the DCR was 76.5% (95% CI, 50.1-93.2). The median DoR was 5.6 months (95% CI, 1.4-NR). With a median follow-up of 21.1 months, the median PFS and OS were 5.4 months (95% CI, 1.3-8.4) and 12.8 months (95% CI, 4.1-NR), respectively.
Conclusions
Sintilimab in combination with IBI310 were well tolerated, and shown promising anti-tumor efficacy both in first-line and ≥ 2 line locally advanced or metastatic EBV-associated gastric cancer.
Clinical trial identification
NCT04202601.
Editorial acknowledgement
Lin Shen is the corresponding author.
Legal entity responsible for the study
Innovent Biologics Inc.
Funding
Innovent Biologics Inc.
Disclosure
Y. Zhang, Y. Luo, L. Li, H. Zhou: Personal, Emplyment: Innovent Biologics, Inc.. All other authors have declared no conflicts of interest.
Resources from the same session
1048P - Phase I/II Study of JK08, an IL-15 antibody fusion protein targeting CTLA-4, with unresectable locally advanced or metastatic cancer
Presenter: Nuria Kotecki
Session: Poster session 19
1049P - Phase Ib/II trial of envafolimab, a novel subcutaneous single-domain anti-PD-L1 monoclonal antibody, plus lenvatinib in patients with selected advanced solid tumors
Presenter: Tianshu Liu
Session: Poster session 19
1050P - Sensitization to immunotherapy through manipulation of tumor transcription by lurbinectedin
Presenter: Joan Russo-Cabrera
Session: Poster session 19
1051P - Intratumoral injection of LTX-315 in combination with pembrolizumab in patients with advanced melanoma refractory to prior PD-1/PD-L1 therapy: Interim results from the ATLAS-IT-05 trial
Presenter: Stephane Dalle
Session: Poster session 19
1052P - Phase-Ib trial of metformin combined with nivolumab for refractory/recurrent solid tumors
Presenter: Toshio Kubo
Session: Poster session 19
1053P - Tumor-restricted delivery of an immune-therapeutic payload by modified macrophages for the treatment of glioblastoma: The TEM-GBM STUDY (NCT03866109)
Presenter: Fabio Ciceri
Session: Poster session 19
1054P - A phase Ia study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of a modular CLDN18.2-targeting PG CAR-T therapy (IBI345) in patients with CLDN18.2+ solid tumors
Presenter: Songbing Qin
Session: Poster session 19
1055P - Safety and Activity of SmarT cells plus PD-1 blocking antibodies in patients with heavily pretreated solid cancers: An open-label and dose-escalation study
Presenter: Qin Liu
Session: Poster session 19
1056P - Efficacy of spartalizumab across multiple cancer types in patients with PD1-high mRNA expressing tumors (SOLTI-1904 ACROPOLI)
Presenter: Aleix Prat
Session: Poster session 19
1057P - Long-term follow-up of a phase II study of tislelizumab (TIS) monotherapy in patients (pts) with previously treated, locally advanced, unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) solid tumors
Presenter: Jian Li
Session: Poster session 19