Evidence map›Paper›PMID 42410894›Full record

ArticleCancer science2026

Phase II Trial of Nivolumab in Advanced Solid Tumors Based on Genomic Profiling: BELIEVE Trial (NCCH1901) Subcohort.

Masashi Kanai, Kuniko Sunami, Tatsunori Shimoi, Satoshi Nishiwaki, Ichiro Kinoshita, Tetsuhiro Yoshinami, Chigusa Morizane, Yusuke Sato, Toshio Kubo, Mamoru Ito and 7 more

Abstract read
In one paragraph

Article in Cancer science, 2026. 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

17 authors.

Masashi KanaiDepartment of Medical Oncology, Kyoto University Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6954-4474
Kuniko SunamiDepartment of Laboratory Medicine, National Cancer Center Hospital, Chuo, Japan.ORCID https://orcid.org/0000-0002-7137-5649
Tatsunori ShimoiDepartment of Medical Oncology, National Cancer Center Hospital, Chuo, Japan.
Satoshi NishiwakiDepartment of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
Ichiro KinoshitaDepartment of Medical Oncology, Hokkaido University Hospital, Sapporo, Japan.ORCID https://orcid.org/0000-0002-6694-8414
Tetsuhiro YoshinamiCenter for Cancer Genomics and Personalized Medicine, The University of Osaka Hospital, Suita, Japan.
Chigusa MorizaneDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yusuke SatoDepartment of Urology and Andrology, The University of Tokyo Hospital, Bunkyo-ku, Japan.
Toshio KuboCancer for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Mamoru ItoDepartment of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital, Fukuoka, Japan.
Hiroshi NishiharaCenter for Cancer Genomics, Keio University School of Medicine, Shinjuku-ku, Japan.
Toru MukoharaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-8573-418X
Hidekazu ShirotaDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.ORCID https://orcid.org/0000-0001-9154-9004
Ryo KoDivision of Thoracic Oncology, Shizuoka Cancer Center, Nagaizumi-cho, Japan.
Taro ShibataBiostatistics Division, Center for Research Administration and Support, National Cancer Center, Tokyo, Japan.
Manabu MutoDepartment of Medical Oncology, Kyoto University Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-3127-8203
Noboru YamamotoDepartment of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0787-2851

Funding

Health and Labour Sciences Research Grants 19EA1008Japan Agency for Medical Research and Development 20ck0106622h0001Ono Pharmaceutical
6 · The paper itself

Abstract

Comprehensive genomic profiling (CGP) tests can identify putative biomarkers for immune checkpoint inhibitors (ICIs), including tumor mutational burden (TMB); however, their clinical utility remains uncertain. In this study, the efficacy and safety of nivolumab treatment based on the CGP results were investigated using a subcohort from the BELIEVE trial (NCCH1901; jRCTs031190104). This trial aims to improve drug accessibility for patients with advanced solid tumors harboring actionable genetic variants through off-label drug administration. Patients for whom off-label nivolumab treatment was proposed based on CGP results were eligible. Nivolumab was administered until disease progression or unacceptable toxicity. The primary endpoint was the best objective response rate (ORR) in patients with measurable disease. Secondary endpoints included progression-free survival (PFS), overall survival (OS), disease control rate (DCR), and safety. Among 60 enrolled patients, 56 patients who received study treatment were included in the analysis. TMB-High was the most frequent biomarker prompting nivolumab treatment (47/56, 83.9%), followed by CD274 (PD-L1) amplification (6/56, 10.7%) and CDK12 inactivating variants (3/56, 5.4%). Among 50 patients with measurable disease, the ORR was 16.0% (95% confidence interval [CI], 7.2-29.1) and the DCR was 40.0% (95% CI, 26.4-54.8). Median PFS and OS were 2.7 months (95% CI, 2.2-4.3) and 7.2 months (95% CI, 4.4-9.0), respectively. Although a subset of patients achieved durable responses, nivolumab treatment guided by CGP results demonstrated limited efficacy. The predictive value of TMB-High may differ across tumor types, and integration with other clinicogenomic factors is warranted to improve its predictive accuracy.

Indexed as

biomarkersgenomic profilingimmune checkpoint inhibitorsmolecular tumor boardTMB

Identifiers

PMID42410894
PMCPMC13394981

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.