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Pembrolizumab plus chemotherapy following lack of response to nivolumab-based therapy in MSI-High/dMMR advanced gastric cancer: a case report.

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International cancer conference journal 📖 저널 OA 100% 2024: 3/3 OA 2025: 17/17 OA 2026: 20/20 OA 2024~2026 2026 Vol.15(2) p. 234-240 OA Gastric Cancer Management and Outcom
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PubMed DOI PMC OpenAlex 마지막 보강 2026-05-01

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유사 논문
P · Population 대상 환자/모집단
환자: advanced gastric cancer who initially show limited response to ICI-based therapy
I · Intervention 중재 / 시술
ramucirumab-based therapy, paclitaxel, and irinotecan
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
추출되지 않음
OpenAlex 토픽 · Gastric Cancer Management and Outcomes Genetic factors in colorectal cancer Cancer Immunotherapy and Biomarkers

Kawabata R, Hara H, Takeoka T, Yasuhara Y, Yoshihara T, Kitagawa A

📝 환자 설명용 한 줄

Microsatellite instability-high (MSI-H) or deficient mismatch repair (dMMR) gastric cancer is generally sensitive to immune checkpoint inhibitors (ICIs); however, the clinical role of re-administratio

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APA Ryohei Kawabata, Hisashi Hara, et al. (2026). Pembrolizumab plus chemotherapy following lack of response to nivolumab-based therapy in MSI-High/dMMR advanced gastric cancer: a case report.. International cancer conference journal, 15(2), 234-240. https://doi.org/10.1007/s13691-026-00847-5
MLA Ryohei Kawabata, et al.. "Pembrolizumab plus chemotherapy following lack of response to nivolumab-based therapy in MSI-High/dMMR advanced gastric cancer: a case report.." International cancer conference journal, vol. 15, no. 2, 2026, pp. 234-240.
PMID 41929547 ↗

Abstract

Microsatellite instability-high (MSI-H) or deficient mismatch repair (dMMR) gastric cancer is generally sensitive to immune checkpoint inhibitors (ICIs); however, the clinical role of re-administration of ICI plus chemotherapy after an initial lack of response remains unclear. We report a 76-year-old man with HER2-negative advanced gastric adenocarcinoma who exhibited no clear radiologic response and worsening gastric outlet obstruction after two cycles of first-line SOX (S-1 plus oxaliplatin) with nivolumab, necessitating gastrojejunostomy. He subsequently received ramucirumab-based therapy, paclitaxel, and irinotecan. Genomic profiling revealed MSI-H/dMMR with loss of MLH1 and PMS2 expression. Pembrolizumab combined with capecitabine and oxaliplatin (CAPOX) was initiated as fifth-line therapy, resulting in notable regression of hepatic and nodal metastases. This case underscores the clinical importance of early MSI/MMR and genomic testing and suggests that re-administration of ICI plus chemotherapy may be a therapeutic option for selected patients with advanced gastric cancer who initially show limited response to ICI-based therapy.

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