Evidence map›Paper›PMID 39747638›Full record

ArticleScientific reports2025

A multicenter study on TROP2 as a potential targeted therapy for extramammary Paget disease in Japan.

Takamichi Ito, Yuka Tanaka, Dai Ogata, Haruto Nishida, Tatsushi Shiomi, Ryo Tanaka, Aya Kawaguchi, Azusa Miyashita, Satoshi Fukushima, Naoko Shojiguchi and 5 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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

15 authors.

Takamichi ItoDepartment of Dermatology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. ito.takamichi.657@m.kyushu-u.ac.jp.
Yuka TanakaDepartment of Dermatology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Dai OgataDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, 104-0045, Japan.
Haruto NishidaDepartment of Diagnostic Pathology, Faculty of Medicine, Oita University, Yufu, 879-5593, Japan.
Tatsushi ShiomiDepartment of Pathology, Kawasaki Medical School, Kurashiki, 701-0192, Japan.
Ryo TanakaDepartment of Dermatology, Kawasaki Medical School, Kurashiki, 701-0192, Japan.
Aya KawaguchiDepartment of Dermatology, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Azusa MiyashitaDepartment of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, 860-8556, Japan.
Satoshi FukushimaDepartment of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, 860-8556, Japan.
Naoko ShojiguchiDepartment of Pathology, Saitama Medical University International Medical Center, Saitama, 350-1298, Japan.
Hiroyuki GotoDepartment of Dermatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, 545-8585, Japan.
Yaei TogawaDepartment of Dermatology, Chiba University Hospital, Chiba, 260-8677, Japan.
Takahiro KiyoharaDepartment of Dermatology, Kansai Medical University Medical Center, Moriguchi, 570-8507, Japan.
Yoshinao OdaDepartment of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, 812-8582, Japan.
Takeshi NakaharaDepartment of Dermatology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extramammary Paget disease (EMPD) is a rare skin cancer that typically occurs in the anogenital area of older people. Since efficacy of treatments for metastatic or unresectable EMPD remains poor, development of a novel therapeutic approach is strongly desired. However, the lack of EMPD models has hampered investigation of EMPD. Here we investigated whether trophoblast cell surface antigen 2 (TROP2) could be a promising therapeutic target for EMPD. We retrospectively collected 108 samples from 54 patients with primary and metastatic EMPD from 10 Japanese institutions, and compared TROP2 expression between primary and metastatic lesions of each paired sample. In vitro assays were performed using a newly established EMPD cell line, KS-EMPD-1. TROP2 was strongly and homogeneously expressed in patient tissues, regardless of primary or metastatic lesions. The KS-EMPD-1 cells were treated with a TROP2-targeted antibody-drug conjugate (ADC), sacituzumab govitecan, and it significantly reduced cell viability in a dose-dependent manner compared with that of the cells treated with sacituzumab alone. Knockdown of TROP2 reduced cell viability and cell migration, and caused slight upregulation of the apoptosis-related factors, together with downregulation of the epithelial-to-mesenchymal transition-related factors. These findings suggest that a TROP2-targeted ADC may be a promising treatment option for unresectable EMPD.

Indexed as

Antigens, NeoplasmCell Adhesion MoleculesPaget Disease, ExtramammaryAgedAged, 80 and overAntibodies, Monoclonal, HumanizedCamptothecinCell Line, TumorCell SurvivalFemaleHumansImmunoconjugatesJapanMaleMiddle AgedMolecular Targeted TherapyAntibodies, Monoclonal, HumanizedAntigens, NeoplasmCamptothecinCell Adhesion MoleculesImmunoconjugatessacituzumab govitecanTACSTD2 protein, humanAntibody–drug conjugateExtramammary Paget diseaseSacituzumab govitecanTrophoblast cell surface antigen 2

Identifiers

PMID39747638
PMCPMC11697375

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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.