Evidence map›Paper›PMID 40696299›Full record

ArticleBMC cancer2025

The clinical outcomes of adjuvant gemcitabine plus S-1 in resected pancreatic cancer: a single-center retrospective study.

Kuan-Yu Tseng, Yi-Ju Chen, Chiann-Yi Hsu, Yu-Hsuan Shih, Hsin-Chen Lin

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Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kuan-Yu TsengDivision of Medical Oncology, Department of Oncology, Taichung Veterans General Hospital, Taichung, Taiwan.
Yi-Ju ChenDivision of General Surgery, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
Chiann-Yi HsuBiostatistics Task Force, Taichung Veterans General Hospital, Taichung, Taiwan.
Yu-Hsuan ShihDivision of Medical Oncology, Department of Oncology, Taichung Veterans General Hospital, Taichung, Taiwan.
Hsin-Chen LinDivision of Medical Oncology, Department of Oncology, Taichung Veterans General Hospital, Taichung, Taiwan. jawlin15@hotmail.com.ORCID http://orcid.org/0000-0002-2780-520X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdjuvant chemotherapy is the standard form of care for resected pancreatic cancer (PC) patients. Its treatment regimens include monotherapy with gemcitabine or S-1 and combination therapy with gemcitabine plus capecitabine or modified FOLFIRINOX (fluorouracil, oxaliplatin, irinotecan, leucovorin). Whether the efficacy of the adjuvant gemcitabine plus S-1 (GS) combination is realized remains uncertain.

methodsThis single-institute, retrospective, real-world study included 122 patients with resected PC from the period January 2014 to July 2021. Amongst them, 73 patients received adjuvant chemotherapy, with 21 and 35 patients receiving gemcitabine monotherapy and GS combination adjuvant chemotherapy, respectively. The clinical characteristics, outcomes and toxicities of chemotherapy were compared between these two groups.

resultsThe disease-free survival (DFS) and overall survival (OS) for the patients who had received GS combination were 15.8 months and 31.2 months, respectively. Compared with gemcitabine monotherapy, there was a trend towards favorable DFS (10.7 months in gemcitabine monotherapy, p = 0.083), but no OS benefits (24 months, p = 0.517) with GS combination. However, for patients in an advanced disease condition (Stages II and III), the GS combination offered statistically significant longer DFS (14.9 vs. 8.8 months; p = 0.015) and OS (31.2 vs. 21.6 months; p = 0.036), when compared with gemcitabine monotherapy. The adverse effects were comparable between the two groups.

conclusionsIn our real-world study, use of the GS combination could be another option for resected PC patients, particularly for those who are in a more advanced (Stage II and III) disease condition.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDeoxycytidineOxonic AcidPancreatic NeoplasmsTegafurAdultAgedChemotherapy, AdjuvantDisease-Free SurvivalDrug CombinationsFemaleGemcitabineHumansMaleMiddle AgedRetrospective StudiesDeoxycytidineDrug CombinationsGemcitabineOxonic AcidS 1 (combination)TegafurAdjuvant chemotherapyDisease-free survivalGemcitabine plus S-1Overall survivalPancreatic cancer

Identifiers

PMID40696299
PMCPMC12284996

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.