Evidence map›Paper›PMID 40635151›Full record

ArticleMolecular cancer therapeutics2026

DS-3939a: A TA-MUC1-Directed Antibody-Drug Conjugate with Broad Antitumor Activity.

Kohei Takano, Mayuko Yukiura, Kazuki Takahashi, Michiko Kitamura, Hiroko Okuno, Yoshinobu Shiose, Kokichi Honda, Kazunori Oyama, Makiko Yamada, Wataru Obuchi and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05875168 (Phase 1/2, Open-label, Multicenter, First-in-Human Study of DS-3939a in Subjects With Advanced Solid Tumors), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT05875168 phase1 / phase2recruitingnot on this map

Phase 1/2, Open-label, Multicenter, First-in-Human Study of DS-3939a in Subjects With Advanced Solid Tumors

TypeinterventionalSponsorDaiichi SankyoRan2023 to 2027Enrolled590ConditionsAdvanced Solid Tumor, Metastatic Solid TumorArmsDS-3939a
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Predictive Biomarkers of Antibody-Drug Conjugate Efficacy for Solid Tumors: Current Challenges and the Potential Role of Quantitative Proteomics.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  4. Review
  5. Review
  6. 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

17 authors.

Kohei Takano *Daiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0002-3759-9972
Mayuko Yukiura *Daiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0000-3027-0691
Kazuki Takahashi *Daiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0000-3348-3860
Michiko KitamuraDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0008-9524-8098
Hiroko OkunoDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0003-4299-0233
Yoshinobu ShioseDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0007-6233-0733
Kokichi HondaDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0006-7442-641X
Kazunori OyamaDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0001-8198-3314
Makiko YamadaDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0007-0451-266X
Wataru ObuchiDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0008-3812-2413
Kazuyoshi KumagaiDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0003-4974-939X
Ken SakuraiDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0002-9143-8691
Riki GotoDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0009-0003-7392-9902
Akiko ZembutsuDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0002-7911-0573
Takashi KagariDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0003-2593-5120
Yuki AbeDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0002-5352-724X
Toshinori AgatsumaDaiichi Sankyo Co., Ltd., Tokyo, Japan.ORCID 0000-0001-7319-9442

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated mucin-1 (TA-MUC1) is a glycoform of the MUC1 protein that is aberrantly glycosylated and is primarily observed in cancer cells. TA-MUC1 is highly expressed in various human epithelial cancers, making it an attractive target for cancer therapies. In this study, we describe the development of DS-3939a, a novel TA-MUC1-targeting antibody-drug conjugate that utilizes the potent DNA topoisomerase I inhibitor DXd, and evaluation of its pharmacologic activity in preclinical in vitro and in vivo models. IHC of clinical tumor tissue microarrays of various cancer types exhibited positive staining for TA-MUC1 in a number of samples, with a particularly high positive rate in bladder, lung, and breast cancers. In vitro profiling of DS-3939a confirmed that it could specifically bind to TA-MUC1 and inhibit the growth of TA-MUC1-positive cancer cells by inducing DNA damage and apoptosis. DS-3939a also exhibited significant antitumor effects in multiple TA-MUC1-positive cell line-derived and patient-derived xenograft models. Moreover, DS-3939a elicited strong tumor regression in several xenograft models even following treatment with other cytotoxic antibody-drug conjugates, likely through its efficient payload delivery. Overall, these data provide evidence for the potential utility of DS-3939a for the treatment of TA-MUC1-expressing tumors and support the rationale for the ongoing phase I/II clinical study (NCT05875168).

Indexed as

Antineoplastic AgentsImmunoconjugatesMucin-1NeoplasmsAnimalsApoptosisCell Line, TumorCell ProliferationFemaleHumansMiceXenograft Model Antitumor AssaysAntineoplastic AgentsImmunoconjugatesMUC1 protein, humanMucin-1

Identifiers

PMID40635151
PMCPMC12757726

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Registered trials

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.