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Clinical response of immunotherapy targeting programmed cell death receptor 1/programmed cell death ligand 1 in advanced signet-ring-cell gastric cancer.

코호트 1/5 보강
Future oncology (London, England) 📖 저널 OA 90.9% 2021: 0/1 OA 2022: 1/2 OA 2023: 0/2 OA 2024: 3/4 OA 2025: 67/67 OA 2026: 79/88 OA 2021~2026 2026 Vol.22(3) p. 327-337
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
230 patients, with objective response rate (ORR) achieving 43.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] The findings suggest that GSRCC is associated with resistance to immunotherapy in advanced GC. Furthermore, peritoneal metastasis is significantly associated with poor prognosis in GSRCC patients.

Liang J, Chen X, Liang H, Zhao L, Yu J

📝 환자 설명용 한 줄

[BACKGROUND] The clinical benefit of PD-1/PD-L1-based immunotherapy in gastric signet ring cell carcinoma (GSRCC) remains unclear.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 95% CI 1.52-5.53
  • 연구 설계 cohort study

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↓ .bib ↓ .ris
APA Liang J, Chen X, et al. (2026). Clinical response of immunotherapy targeting programmed cell death receptor 1/programmed cell death ligand 1 in advanced signet-ring-cell gastric cancer.. Future oncology (London, England), 22(3), 327-337. https://doi.org/10.1080/14796694.2025.2612083
MLA Liang J, et al.. "Clinical response of immunotherapy targeting programmed cell death receptor 1/programmed cell death ligand 1 in advanced signet-ring-cell gastric cancer.." Future oncology (London, England), vol. 22, no. 3, 2026, pp. 327-337.
PMID 41486864 ↗

Abstract

[BACKGROUND] The clinical benefit of PD-1/PD-L1-based immunotherapy in gastric signet ring cell carcinoma (GSRCC) remains unclear. This study evaluated the efficacy of first-line immunotherapy in advanced GSRCC.

[METHODS] This single-center retrospective cohort study assessed the clinical response of patients with advanced GC diagnosed from November 2019 to January 2025 after receiving first-line immunotherapy combined with chemotherapy and/or target therapy, concurrently comparing therapeutic outcomes in GSRCC and non-GSRCC cohorts.

[RESULTS] This study included 230 patients, with objective response rate (ORR) achieving 43.9%. Among the 150 non-GSRCC patients, the ORR was 50.7%, compared to 31.3% in the 80 GSRCC patients. Non-GSRCC patients had longer median progression-free survival (PFS: 10.0 vs 7.9 months;  = 0.002) and overall survival (OS: 17.4 vs 15.3 months;  = 0.039). Peritoneal metastasis was independently associated with rapid progression and poor survival (HR 2.63, 95% CI 1.52-5.53;  = 0.001). Among GSRCC patients, those with peritoneal metastasis had significantly shorter PFS (6.6 vs 13.6 months;  < 0.001) and OS (11.0 vs 19.4 months;  = 0.001).

[CONCLUSIONS] The findings suggest that GSRCC is associated with resistance to immunotherapy in advanced GC. Furthermore, peritoneal metastasis is significantly associated with poor prognosis in GSRCC patients.

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