Evidence map›Paper›PMID 41764635›Full record

ArticleJapanese journal of clinical oncology2026

Study protocol for a phase I investigator-initiated clinical trial of E7820 in Japanese patients with unresectable solid tumours: CIRCUS trial (NCCH2303).

Mao Okada, Jun Sato, Chikako Funasaka, Noboru Yamamoto, Tetsuya Sasaki, Masayuki Yokoyama, Akinobu Hamada, Toshihiko Doi, Hiroyuki Mano

Abstract readClinical Trial ProtocolMulticenter Study
In one paragraph

Article in Japanese journal of clinical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Mao OkadaDepartment of Experimental Therapeutics, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.ORCID 0000-0001-5476-483X
Jun SatoDepartment of Experimental Therapeutics, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Chikako FunasakaDepartment of Experimental Therapeutics, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0003-0585-4884
Noboru YamamotoDepartment of Experimental Therapeutics, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.ORCID 0000-0002-0787-2851
Tetsuya SasakiClinical Research Support Office, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Masayuki YokoyamaClinical Research Support Office, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Akinobu HamadaDivision of Molecular Pharmacology, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Toshihiko DoiDepartment of Experimental Therapeutics, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0003-2042-6829
Hiroyuki ManoDivision of Cellular Signaling, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.

Funding

Development of Anticancer Treatments for Rare and Refractory Cancers 20 pc0101051h0001Japan Agency for Medical Research and Development
6 · The paper itself

Abstract

E7820, a sulphonamide-type anticancer agent, was developed to inhibit angiogenesis by suppressing integrin α2 expression. Although early-phase trials outside Japan established 100 mg/day as the maximum tolerated dose in monotherapy, no objective responses were observed, and further development was not planned. Subsequent studies revealed that E7820 promotes DCAF15-mediated degradation of the splicing factor RBM39 and acts as a molecular glue, providing a novel mechanism and rationale for clinical evaluation. Preclinical screening using patient-derived xenograft models demonstrated antitumour activity in biliary tract and endometrial cancers and in tumours with homologous recombination repair gene alterations. Based on these findings, the CIRCUS trial, a multicentre investigator-initiated phase I study, was initiated to assess the safety, tolerability, and preliminary efficacy of E7820 in Japanese patients with unresectable solid tumours. If the proof of concept is demonstrated in biomarker-defined cohorts, E7820 may be repositioned for selected patients, providing insights into the development of previously intractable compounds.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsNeoplasmsSulfonamidesClinical Trials, Phase I as TopicEast Asian PeopleFemaleHumansIndolesJapanMaleMaximum Tolerated DoseRNA-Binding ProteinsAngiogenesis InhibitorsAntineoplastic AgentsIndolesN-(3-cyano-4-methyl-1H-indol-7-yl)-3-cyanobenzene-sulfonamideRNA-Binding ProteinsSulfonamidesE7820Japanphase IRNA splicing factorsxenograft model antitumor assays

Identifiers

PMID41764635
PMCPMC13237872

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Registered trials

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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.