Evidence map›Paper›PMID 40913639›Full record

Observational studyJournal of gastroenterology2025

Combination chemotherapy for older patients with unresectable biliary tract cancer: a prospective observational study using propensity-score matched analysis (JON2104-B).

Satoshi Kobayashi, Kohei Nakachi, Kouji Yamamoto, Makoto Ueno, Yuta Maruki, Kenji Ikezawa, Takeshi Terashima, Satoshi Shimizu, Kotoe Oshima, Kunihiro Tsuji and 31 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Journal of gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

41 authors.

Satoshi KobayashiDepartment of Gastroenterology, Kanagawa Cancer Center, 2-3-2, Nakao, Asahi-ku, Yokohama, 241-0815, Japan. kobayashi.0v70a@kanagawa-pho.jp.ORCID 0000-0002-2535-6586
Kohei NakachiDepartment of Medical Oncology, Tochigi Cancer Center, Utsunomiya, 320-0834, Japan.
Kouji YamamotoDepartment of Biostatistics, Yokohama City University School of Medicine, Yokohama, 236-0004, Japan.
Makoto UenoDepartment of Gastroenterology, Kanagawa Cancer Center, 2-3-2, Nakao, Asahi-ku, Yokohama, 241-0815, Japan.
Yuta MarukiDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, 104-0045, Japan.
Kenji IkezawaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, 541-8567, Japan.
Takeshi TerashimaDepartment of Gastroenterology, Kanazawa University Hospital, Kanazawa, 920-8641, Japan.
Satoshi ShimizuDepartment of Gastroenterology, Kanazawa University Hospital, Kita Adaci-Gun, 362-0806, Japan.
Kotoe OshimaDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shunto-gun, 411-8777, Japan.
Kunihiro TsujiDepartment of Gastroenterology, Ishikawa Prefectural Central Hospital, Kanazawa, 920-8530, Japan.
Yoshiharu MasakiDepartment of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan.
Hidetaka TsumuraDepartment of Gastroenterological Oncology, Hyogo Cancer Center, Akashi, 673-8558, Japan.
Taro ShibukiDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, 277-8577, Japan.
Masato OzakaHepato-Biliary-Pancreatic Medicine Department, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, 135-8550, Japan.
Naohiro OkanoDepartment of Medical Oncology, Kyorin University Faculty of Medicine, Mitaka, 181-8611, Japan.
Yukiyasu OkamuraDivision of Digestive Surgery, Department of Surgery, Nihon University School of Medicine, Tokyo, 173-8610, Japan.
Kumiko UmemotoDepartment of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, 216-8511, Japan.
Tatsunori SatohDepartment of Gastroenterology, Shizuoka General Hospital, Shizuoka, 420-8527, Japan.
Yasushi KojimaDepartment of Gastroenterology, National Center for Global Health and Medicine, Tokyo, 162-8655, Japan.
Kazuhiko ShiojiDepartment of Gastroenterology, Niigata Cancer Center Hospital, Niigata, 951-8566, Japan.
Hiroko NebikiDepartment of Gastroenterology, Osaka City General Hospital, Osaka, 534-0021, Japan.
Toshifumi DoiDepartment of Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, 602-8566, Japan.
Atsushi NaganumaDepartment of Gastroenterology, National Hospital Organization Takasaki General Medical Center, Takasaki, 370-0829, Japan.
Shigeki KataokaDepartment of Clinical Oncology, Graduate School of Medicine Faculty of Medicine, Kyoto University, Kyoto, 606-8507, Japan.
Emiri KitaDepartment of Gastroenterology, Chiba Cancer Center, Chiba, 260-8717, Japan.
Hiroyuki AsamaDepartment of Gastroenterology, Fukushima Medical University, Fukushima, 960-1295, Japan.
Kaoru TsuchiyaDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Musashino, 180-0023, Japan.
Michiaki UnnoDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai, 980-8574, Japan.
Reiko AshidaSecond Department of Internal Medicine, Wakayama Medical University, Wakayama, 641-8509, Japan.
Kazuyuki MatsumotoDepartment of Gastroenterology, Okayama University Graduate School of Medicine, Okayama, 700-8558, Japan.
Izumi OhnoDepartment of Gastroenterology, Chiba University Graduate School of Medicine, Chiba, 260-0856, Japan.
Takao ItoiDepartment of Gastroenterology, Tokyo Medical University, Tokyo, 160-0023, Japan.
Yuji NegoroDepartment of Oncologial Medicine, Kochi Health Sciences Center, Kochi, 781-8555, Japan.
Yasunari SakamotoDepartment of Gastroenterology and Hepatology, International University of Health and Welfare Atami Hospital, Atami, 413-0012, Japan.
Shiho ArimaDigestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, 890-0075, Japan.
Akinori AsagiDepartment of Gastroenterology, National Hospital Organization Shikoku Cancer Center, Matsuyama, 791-0280, Japan.
Hiroyuki OkuyamaDepartment of Medical Oncology, Kagawa University Hospital, Kita-Gun, 761-0793, Japan.
Yoshito KomatsuDepartment of Cancer Chemotherapy, Hokkaido University Hospital Cancer Center, Sapporo, 060-8648, Japan.
Noritoshi KobayashiDepartment of Oncology, School of Medicine Graduate School of Medicine, Yokohama City University, Yokohama, 236-0004, Japan.
Hiroaki NaganoDepartment of Gastroenterological, Breast and Endocrine Surgery, Yamaguchi University Graduate School of Medicine, Ube, 755-8505, Japan.
Junji FuruseDepartment of Gastroenterology, Kanagawa Cancer Center, 2-3-2, Nakao, Asahi-ku, Yokohama, 241-0815, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic chemotherapy with gemcitabine plus S-1 (GEM + S-1), GEM + CDDP plus S-1 (GEM + CDDP + S-1), or gemcitabine plus cisplatin (GEM + CDDP) is standard treatment for advanced biliary tract cancer (aBTC). We aimed to evaluate the efficacy and safety of combination chemotherapy in older patients with aBTC.

methodsThis multicenter prospective observational study (JON2104-B, UMIN000045156) included patients aged ≥ 70 years with aBTC. Inverse-probability weighting propensity-score analyses (IPW) were used to compare overall survival (OS) as the primary endpoint and progression-free survival (PFS) across treatment groups.

resultsThis study included 305 patients between August 2021 and January 2023. Of them, 75, 131, 26, 52, and 10 received GEM + CDDP + S-1, GEM + CDDP, GEM + S-1, gemcitabine, and S-1; their median ages were 74, 75, 77.5, 80, and 80 years, and approximately 24%, 16.8%, 23.1%, 9.6%, and 0% had G-8 scores of > 14, respectively. GEM + CDDP had a safety profile comparable to that of GEM + CDDP + S-1 but was more toxic than gemcitabine. Per IPW, the hazard ratio (HR) for GEM + CDDP + S-1 versus GEM + CDDP was 0.80 for OS (95% confidence interval [CI], 0.55-1.17) and 0.55 for PFS (95% CI 0.38-0.80). The HR for GEM + CDDP versus gemcitabine was 0.74 for OS (95% CI 0.42-1.29) and 0.79 for PFS (95% CI 0.42-1.49).

conclusionsGEM + CDDP + S-1 was associated with longer PFS without additional toxicity than GEM + CDDP for fit older patients. However, the OS for both were not statistically different. The efficacies of GEM + CDDP and gemcitabine for vulnerable older patients did not also differ significantly. These findings highlight the importance of vulnerability in patients with aBTC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiliary Tract NeoplasmsAgedAged, 80 and overCisplatinDeoxycytidineDrug CombinationsFemaleGemcitabineHumansMaleOxonic AcidProgression-Free SurvivalPropensity ScoreProspective StudiesTegafurCisplatinDeoxycytidineDrug CombinationsGemcitabineOxonic AcidS 1 (combination)TegafurBiliary tract cancerChemotherapyOlderSurvivalUnresectable

Identifiers

PMID40913639
PMCPMC12630146

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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.