Evidence map›Paper›PMID 42426968›Full record

ArticleThe Journal of dermatology2026

Etoposide as Late-Line Therapy for Metastatic Extramammary Paget's Disease: A Case Series.

Takanobu Kan, Saito Ryo, Kayoko Nomoto, Hayato Mizuno, Daiki Matsubara, Takumi Sakamoto, Masaya Moriwaki, Akio Tanaka

Abstract readCase Reports
In one paragraph

Article in The Journal of dermatology, 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

8 authors.

Takanobu KanDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0003-4915-6498
Saito RyoDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-1927-8147
Kayoko NomotoDepartment of Dermatology, Miyoshi Central Hospital, Miyoshi, Japan.ORCID https://orcid.org/0009-0007-3046-311X
Hayato MizunoDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-8556-3408
Daiki MatsubaraDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-8744-7400
Takumi SakamotoDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0009-0008-9012-9030
Masaya MoriwakiDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-5616-8388
Akio TanakaDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-5354-7064

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extramammary Paget's disease (EMPD) is a rare cutaneous carcinoma that typically arises in apocrine gland-rich areas. Advanced or metastatic disease is associated with poor prognosis and limited therapeutic options. Due to its rarity, no standard chemotherapy regimen has been established. Agents such as docetaxel, cisplatin, and 5-fluorouracil have been used, but evidence supporting their efficacy remains limited. Etoposide has occasionally been reported to provide temporary benefit in advanced EMPD, although its effectiveness remains poorly characterized. We report a case series of three patients with metastatic EMPD treated with oral etoposide as third- or fourth-line therapy. They had experienced disease progression despite prior therapies, including docetaxel, S-1, and low-dose FP (5-fluorouracil and cisplatin) therapy. Oral etoposide was administered at 50 mg/day for 3-4 weeks followed by a 1-2 week rest period. Additional radiation therapy was provided for metastatic lesions in two patients. Two patients achieved a partial response on imaging, while one showed stable disease. Serum carcinoembryonic antigen levels decreased markedly in two evaluable patients, indicating a biological response. The average progression-free survival was 7.7 months. Adverse events included alopecia and neutropenia in one patient, both manageable. Although all patients eventually died from disease progression, etoposide provided disease control and symptomatic relief. These findings suggest that oral etoposide may represent a feasible and relatively well-tolerated late-line treatment option for metastatic EMPD.

Indexed as

Antineoplastic Agents, PhytogenicEtoposidePaget Disease, ExtramammarySkin NeoplasmsAdministration, OralAgedAlopeciaFemaleHumansMaleMiddle AgedNeutropeniaNon-Melanoma Skin NeoplasmsProgression-Free SurvivalAntineoplastic Agents, PhytogenicEtoposidechemotherapydocetaxelEMPDetoposide

Identifiers

PMID42426968
PMCPMC13555120

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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.