Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

114P - Cadonilimab plus chemotherapy as first-line (1L) treatment for metastatic gastric (G) or gastroesophageal junction adenocarcinoma (GEJA) with PD-L1 CPS=5: Updated results from a real-world study

Date

12 Dec 2024

Session

Poster Display session

Presenters

Qi Xu

Citation

Annals of Oncology (2024) 24 (suppl_1): 1-20. 10.1016/iotech/iotech100744

Authors

Q. Xu, L. Zhang, J. Li, P. Zeng, X. Yuan, D. Zhao, Q. Wei

Author affiliations

  • Cancer Hospital of the University of Chinese Academy of Sciences/ Zhejiang Cancer Hospital, Hangzhou/CN

Resources

This content is available to ESMO members and event participants.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.