Evidence map›Paper›PMID 41743913›Full record

ArticleCase reports in oncological medicine2026

Sustained Drug-Drug Interaction Between Cyclosporine and Apalutamide in a Patient With Metastatic Hormone-Sensitive Prostate Cancer: A Case Report and Evaluation of CYP3A4 Induction via Pregnane X Receptor Activation by Apalutamide.

Yoshihisa Mimura, Takaomi Sanda, Rei Unno, Yuki Furukawa, Ryota Shizu, Kotona Motokatsu, Yuusuke Tashiro, Yoshihiko Tasaki, Yosuke Sugiyama, Tomoya Yasujima and 8 more

Abstract read
In one paragraph

Article in Case reports in oncological medicine, 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. 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

18 authors.

Yoshihisa MimuraDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Takaomi SandaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Rei UnnoDepartment of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.ORCID https://orcid.org/0000-0003-0584-3712
Yuki FurukawaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Ryota ShizuLaboratory of Molecular Toxicology, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Shizuoka, Japan, u-shizuoka-ken.ac.jp.
Kotona MotokatsuLaboratory of Molecular Toxicology, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Shizuoka, Japan, u-shizuoka-ken.ac.jp.
Yuusuke TashiroDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Yoshihiko TasakiDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Yosuke SugiyamaDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Tomoya YasujimaDepartment of Biopharmaceutics, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Aichi, Japan.
Taku NaikiDepartment of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.ORCID https://orcid.org/0000-0002-7638-6048
Yasuhiro HoritaDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Yuji HottaDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Hiroaki YuasaDepartment of Biopharmaceutics, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Aichi, Japan.
Kouichi YoshinariLaboratory of Molecular Toxicology, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Shizuoka, Japan, u-shizuoka-ken.ac.jp.
Takahiro YasuiDepartment of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.
Yoko Furukawa-HibiDepartment of Clinical Pharmaceutics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan, nagoya-cu.ac.jp.ORCID https://orcid.org/0000-0002-2126-5652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Apalutamide (Apa) is a key therapeutic agent for prostate cancer. Despite its efficacy, Apa is known to induce several drug-metabolizing enzymes including cytochrome P450 3A4 (CYP3A4), raising concerns about drug-drug interactions (DDIs). This study reports a rare case of a sustained DDI between Apa and cyclosporine (CsA)-a CYP3A4 substrate-in a patient with metastatic hormone-sensitive prostate cancer (mHSPC) and primary pure red cell aplasia (PRCA). We further investigated whether Apa could activate pregnane X receptor (PXR), a key nuclear receptor that regulates CYP3A4 expression. Methods: With informed consent, residual blood samples were used to measure serum Apa concentration. To assess the potential of Apa in activating PXR, a reporter gene assay and a CYP3A4 mRNA induction test were performed. Case Presentation: A 75-year-old man with mHSPC was treated with Apa and leuprorelin. He developed PRCA and was administered CsA (5 mg/kg/day) on Day 1. Despite a target trough concentration ( Conclusion: Apa induced CYP3A4 via the PXR pathway, leading to a sustained DDI with CsA. Careful monitoring is necessary when Apa is coadministered with CYP3A4 substrates.

Indexed as

apalutamidecyclosporinecytochrome P450 3A4drug–drug interactionspregnane X receptor

Identifiers

PMID41743913
PMCPMC12930205

What OpenQuestion holds

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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.