Abstract 114P
Background
PD-1 inhibitors plus chemotherapy have been the standard 1L treatment for metastatic G/GEJA, but its efficacy remain poor in patients (pts) with low PD-L1 expression. A phase III study has demonstrated that cadonilimab, a PD-1/CTLA-4 bispecific antibody, showed encouraging activity and manageable safety in previously untreated pts with metastatic G/GEJA, even those with PD-L1 CPS<5. Currently, cadonilimab combined with XELOX as 1L treatment for metastatic G/GEJA was approved by NMPA. Here, we presented the updated efficacy and safety of the combination for metastatic G/GEJA with PD-L1 CPS≤5 in a real-world setting.
Methods
Untreated pts with metastatic G/GEJA and PD-L1 CPS≤5 who has received cadonilimab combined with chemotherapy (SOX, XELOX or FOLFOX) were included in this real-world study. Baseline characteristics, treatment patterns, and clinical outcomes, including objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS) and treatment-related adverse events (TRAEs) were analyzed.
Results
As of August 24, 2024, 31 pts were enrolled. At baseline, median age was 56.0 years (range: 25-75), 67.7% were ECOG PS 1/2 and 48.4% were PD-L1 CPS<1. 4 pts underwent surgical treatment under the guidance of MDT, including 3 with PD-L1 CPS<1. All pts were evaluable for safety and efficacy. 17 reached PR and 14 were SD. Overall ORR was 54.8% and DCR was 100.0%. Median PFS (mPFS) was 7.38 months (mo) (95% Cl: 5.55-9.21) and median OS (mOS) was 14.26 mo (95% Cl: 11.08-17.44). In the PD-L1 CPS<1 group, the ORR was 53.3% (8/15) and DCR was 100.0% (15/15), mPFS was 9.25 mo (95% Cl: 0.00-20.09) and mOS was 14.26 mo (95% Cl: 7.78-20.74). Pts with liver metastasis (25.8%, 8/31) had a higher ORR (8 PR, 100%) compared to the overall ORR (54.8%). TRAEs were observed in 67.7% pts, including 9.7% grade 3 TRAEs (neutropenia 6.5%, thrombocytopenia 3.2% and diabetes 3.2%). There were no grade 4/5 toxicities.
Conclusions
Cadonilimab plus chemotherapy continued to show a promising efficacy with manageable safety in the 1L treatment of metastatic G/GEJA pts with PD-L1 CPS≤5, particularly a high ORR in pts with liver metastasis.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
226P - Profiling of gastric adenocarcinomas from EU and LATAM countries identifies distinct tumor immune subgroups and a central role of the tumor microbiome in shaping the immune microenvironment
Presenter: Manuel Cabeza Segura
Session: Poster Display session
Resources:
Abstract
228P - Modulating mitochondrial dynamics in TAMs to enhance anti-tumor immunity
Presenter: Pu-ste Liu
Session: Poster Display session
Resources:
Abstract
229P - Investigation of the effects of long-noncoding RNA NRAV on interferon response in melanoma
Presenter: Kadir Durmus
Session: Poster Display session
Resources:
Abstract
230P - Deciphering the mechanism of immunosuppressive activity of acetaminophen in the context of cancer immunotherapy
Presenter: Jeanne Lena
Session: Poster Display session
Resources:
Abstract
231P - The impact of calcitriol and tacalcitol on the Th17 lymphocytes in breast cancer
Presenter: Beata Filip-Psurska
Session: Poster Display session
Resources:
Abstract