Evidence map›Paper›PMID 40341952›Full record

ArticleCancer research communications2025

Microbiome Landscape and Association with Response to Immune Checkpoint Inhibitors in Advanced Solid Tumors: A SCRUM-Japan MONSTAR-SCREEN Study.

Kentaro Sawada, Riu Yamashita, Shunsuke A Sakai, Satoshi Horasawa, Ayumu Yoshikawa, Takao Fujisawa, Shigenori Kadowaki, Ken Kato, Makoto Ueno, Eiji Oki and 22 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
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

32 authors.

Kentaro Sawada *Department of Medical Oncology, Kushiro Rosai Hospital, Kushiro, Japan.ORCID 0000-0001-7952-2765
Riu Yamashita *Division of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.ORCID 0000-0003-0068-6949
Shunsuke A Sakai *Division of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.ORCID 0009-0002-3740-6795
Satoshi HorasawaTranslational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0009-0007-0501-067X
Ayumu YoshikawaDepartment of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0009-0005-3142-6164
Takao FujisawaHead and Neck Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0009-0002-3438-5757
Shigenori KadowakiDepartment of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.ORCID 0000-0001-9923-5309
Ken KatoDepartment of Head and Neck Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-1733-5072
Makoto UenoDepartment of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.ORCID 0000-0003-4480-0029
Eiji OkiDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.ORCID 0000-0002-9763-9366
Yoshito KomatsuDepartment of Cancer Center, Hokkaido University Hospital, Sapporo, Japan.ORCID 0000-0002-1570-6802
Tatsuyuki ChiyodaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-8214-2242
Yosuke HoritaDepartment of Medical Oncology, Saitama Medical University International Medical Center, Hidaka, Japan.ORCID 0000-0003-2352-2234
Hisateru YasuiDepartment of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Japan.ORCID 0000-0001-5563-5802
Tadamichi DendaDepartment of Gastroenterology, Chiba Cancer Center, Chiba, Japan.ORCID 0000-0003-2570-9692
Hironaga SatakeCancer Treatment Center, Kansai Medical University Hospital, Hirakata, Japan.ORCID 0000-0001-7629-6803
Taito EsakiDepartment of Gastrointestinal and Medical Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.ORCID 0000-0002-9169-8453
Taroh SatohDepartment of Frontier Science for Cancer and Chemotherapy, Graduate School of Medicine, Osaka University, Suita, Japan.ORCID 0000-0002-4615-2638
Naoki TakahashiDepartment of Gastroenterology, Saitama Cancer Center, Ina, Japan.ORCID 0000-0001-6377-9507
Kentaro YamazakiDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Nagaizumi, Japan.ORCID 0000-0001-6269-9345
Nobuhisa MatsuhashiDepartment of Gastroenterological Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0001-5993-9571
Tomohiro NishinaGastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Gifu, Japan.ORCID 0000-0002-4073-3757
Hiroyuki TakedaDepartment of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0002-2847-7105
Koushiro OhtsuboDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.ORCID 0000-0002-4490-4306
Takashi OhtaDepartment of Clinical Oncology, Kansai Rosai Hospital, Amagasaki, Japan.ORCID 0000-0002-1941-206X
Akihito TsujiDepartment of Clinical Oncology, Kagawa University Hospital, Amagasaki, Japan.ORCID 0000-0003-4034-1945
Masahiro GotoCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Takatsuki, Japan.ORCID 0000-0003-4279-8682
Takeshi KatoDepartment of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan.ORCID 0000-0001-5347-550X
Hideaki BandoTranslational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0001-5041-2765
Katsuya TsuchiharaDivision of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.ORCID 0000-0001-7507-2349
Yoshiaki NakamuraTranslational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0002-5241-6855
Takayuki YoshinoDepartment of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0002-0489-4756

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the gut microbiome is associated with cancer development and progression, little is known about the effects of the gut microbiome landscape and the efficacy of immune checkpoint inhibitors (ICI) across cancer types. We investigated the association between the microbiome, clinical features, and ICI efficacy across cancer types in a large nationwide screening project for solid tumors. Among 2,180 patients with advanced solid tumors enrolled in the SCRUM-Japan MONSTAR-SCREEN between October 2019 and September 2021, in the chemotherapy-naïve cohort (n = 817), a high prevalence of oral bacteria was observed in patients using proton pump inhibitors (PPI) and those with upper gastrointestinal cancers, particularly postoperative patients with gastric or pancreatic cancer. Among patients treated with ICIs (n = 333), a high abundance of sequence variants in the gut microbiome was not significantly associated with ICI efficacy across cancer types (HR = 0.94; 95% confidence interval, 0.73-1.21). However, high oral bacteria in feces significantly correlated with a shorter progression-free survival compared with low oral bacteria (median, 4.34 vs. 6.97 months; HR = 1.38; 95% confidence interval, 1.07-1.78). Notably, in patients using PPIs, a higher proportion of oral bacteria influenced progression-free survival outcomes of ICI treatment (median, 3.15 vs. 2.04 months; P = 0.08), unlike in PPI nonusers (median, 7.13 vs. 5.55 months; P = 0.74). This study of the gut microbiome has unveiled significant insights into its landscape and potential impact on ICI efficacy. It highlights that the abundance of oral bacteria in feces may play a critical role in diminishing ICI efficacy among patients using PPIs. SIGNIFICANCE: As part of the MONSTAR-SCREEN, a prospective nationwide project for patients with solid tumors, we found that although gut microbiome diversity does not consistently predict ICI efficacy across cancer types, a high level of oral bacteria in the gut is linked to reduced ICI effectiveness, especially in patients using PPIs. These findings highlight the potential clinical impact of microbiome variations on cancer treatment outcomes.

Indexed as

Gastrointestinal MicrobiomeImmune Checkpoint InhibitorsNeoplasmsAgedFecesFemaleHumansJapanMaleMiddle AgedProton Pump InhibitorsImmune Checkpoint InhibitorsProton Pump Inhibitors

Identifiers

PMID40341952
PMCPMC12107420

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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.