Short-term efficacy and safety of recombinant human adenovirus type 5 combined with PD-1 immune checkpoint inhibitors and SOX regimen in neoadjuvant therapy of locally advanced gastric cancer: a retrospective study - Report - MDSpire
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Short-term efficacy and safety of recombinant human adenovirus type 5 combined with PD-1 immune checkpoint inhibitors and SOX regimen in neoadjuvant therapy of locally advanced gastric cancer: a retrospective study
Clinical Report: Evaluation of H101 with PD-1 Inhibitors in Gastric Cancer
Overview
This study evaluates the short-term efficacy and safety of recombinant human adenovirus type 5 (H101) combined with S-1 and oxaliplatin (SOXP regimen) in neoadjuvant treatment for locally advanced gastric cancer (LAGC). Results indicate an objective response rate (ORR) of 96% and a pathological complete response (pCR) rate of 40%, with manageable adverse events.
Background
Gastric cancer has a high incidence and mortality rate, particularly in China, where it accounts for a significant proportion of global cases. Current treatment strategies, including systemic chemotherapy, have shown limited efficacy.
Data Highlights
Response
Number of Patients
Complete Response (CR)
8 (32%)
Partial Response (PR)
16 (64%)
Stable Disease (SD)
1 (4%)
Pathological Complete Response (pCR)
10 (40%)
Objective Response Rate (ORR)
96%
Disease Control Rate (DCR)
100%
R0 Resection Rate
100%
Key Findings
32% of patients achieved a complete response (CR).
64% of patients achieved a partial response (PR).
The objective response rate (ORR) was 96%.
The pathological complete response (pCR) rate was 40%.
No grade 4 adverse events were observed, indicating manageable safety.
100% R0 resection rate was achieved post-treatment.
Clinical Implications
The combination of H101 with the SOXP regimen demonstrates a high response rate and favorable safety profile in patients with LAGC.
Conclusion
The study indicates that H101 combined with the SOXP regimen shows high efficacy and manageable safety in LAGC.