The clinical significance of hyperthermic intraperitoneal chemotherapy combined with PD-1 inhibitor and systemic chemotherapy for advanced gastric cancer patients with peritoneal metastasis: a single-center retrospective study.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
HIPEC combined with PD-1 inhibitor and systemic chemotherapy as first-line treatment (Nov 2021-Jun 2024)
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
All adverse events were manageable. [CONCLUSION] HIPEC combined with PD-1 inhibitor and systemic chemotherapy demonstrated encouraging survival and ascites control with an acceptable safety profile in GC patients with PM.
[BACKGROUND] Peritoneal metastasis (PM) in gastric cancer (GC) correlates with a poor prognosis.
- HR 2.804
APA
Ren M, Xie J, et al. (2025). The clinical significance of hyperthermic intraperitoneal chemotherapy combined with PD-1 inhibitor and systemic chemotherapy for advanced gastric cancer patients with peritoneal metastasis: a single-center retrospective study.. Frontiers in oncology, 15, 1728724. https://doi.org/10.3389/fonc.2025.1728724
MLA
Ren M, et al.. "The clinical significance of hyperthermic intraperitoneal chemotherapy combined with PD-1 inhibitor and systemic chemotherapy for advanced gastric cancer patients with peritoneal metastasis: a single-center retrospective study.." Frontiers in oncology, vol. 15, 2025, pp. 1728724.
PMID
41602425 ↗
Abstract 한글 요약
[BACKGROUND] Peritoneal metastasis (PM) in gastric cancer (GC) correlates with a poor prognosis. PD-1 inhibitor has significantly transformed the treatment landscape for GC, but data on the combination of HIPEC with PD-1 inhibitor and systemic chemotherapy are limited. This study evaluated the efficacy and safety of this triplet therapy as first-line treatment for GC with PM.
[METHODS] This was a retrospective, single-center study that included 34 advanced GC patients with PM. All patients received HIPEC combined with PD-1 inhibitor and systemic chemotherapy as first-line treatment (Nov 2021-Jun 2024). Primary endpoints were progression-free survival (PFS) and the duration of ascites control. Secondary endpoints were overall survival (OS) and adverse events (AEs).
[RESULTS] Median PFS was 7.8 months (range: 0.8-20.8), median OS was 14.3 months (range: 1.7-23.9). Patients diagnosed with moderate amount of ascites had significantly poorer PFS than with none or small amount of ascites (HR = 2.804, = 0.0197). Univariable Cox regression analysis showed that age ≤ 60 years was associated with ascites progression (HR = 4.266, = 0.02) and death (HR = 2.732, = 0.04). Additionally, univariable Cox regression analysis showed that age ≤ 60 years (HR = 5.762, = 0.001) and moderate amount of ascites (HR = 2.923, = 0.027) were potential risk factors for disease progression. The most common adverse events were anemia, hypokalemia, thrombocytopenia and leukopenia. All adverse events were manageable.
[CONCLUSION] HIPEC combined with PD-1 inhibitor and systemic chemotherapy demonstrated encouraging survival and ascites control with an acceptable safety profile in GC patients with PM.
[METHODS] This was a retrospective, single-center study that included 34 advanced GC patients with PM. All patients received HIPEC combined with PD-1 inhibitor and systemic chemotherapy as first-line treatment (Nov 2021-Jun 2024). Primary endpoints were progression-free survival (PFS) and the duration of ascites control. Secondary endpoints were overall survival (OS) and adverse events (AEs).
[RESULTS] Median PFS was 7.8 months (range: 0.8-20.8), median OS was 14.3 months (range: 1.7-23.9). Patients diagnosed with moderate amount of ascites had significantly poorer PFS than with none or small amount of ascites (HR = 2.804, = 0.0197). Univariable Cox regression analysis showed that age ≤ 60 years was associated with ascites progression (HR = 4.266, = 0.02) and death (HR = 2.732, = 0.04). Additionally, univariable Cox regression analysis showed that age ≤ 60 years (HR = 5.762, = 0.001) and moderate amount of ascites (HR = 2.923, = 0.027) were potential risk factors for disease progression. The most common adverse events were anemia, hypokalemia, thrombocytopenia and leukopenia. All adverse events were manageable.
[CONCLUSION] HIPEC combined with PD-1 inhibitor and systemic chemotherapy demonstrated encouraging survival and ascites control with an acceptable safety profile in GC patients with PM.
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