Evidence map›Paper›PMID 41632323›Full record

ArticleCancer chemotherapy and pharmacology2026

Etoposide dosing challenges in a testicular cancer patient with hepatic impairment and drug-drug interactions-a case report.

Catharina J P Op 't Hoog, Loek A W de Jong, Joost Sijm, Minke Smits, Sasja F Mulder, Emmy Boerrigter

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In one paragraph

Article in Cancer chemotherapy and pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Catharina J P Op 't HoogDepartment of Pharmacy, Pharmacology & Toxicology, Radboud University Medical Center, P.O. box 9101, Nijmegen, 6525 GA, The Netherlands.
Loek A W de JongDepartment of Pharmacy, Pharmacology & Toxicology, Radboud University Medical Center, P.O. box 9101, Nijmegen, 6525 GA, The Netherlands.
Joost SijmDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, 6525 GA, The Netherlands.
Minke SmitsDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, 6525 GA, The Netherlands.
Sasja F MulderDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, 6525 GA, The Netherlands.
Emmy BoerrigterDepartment of Pharmacy, Pharmacology & Toxicology, Radboud University Medical Center, P.O. box 9101, Nijmegen, 6525 GA, The Netherlands. Emmy.Boerrigter@radboudumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEtoposide, together with cisplatin, is a cornerstone in the treatment of metastatic testicular cancer, but dosing can be challenging in patients with organ dysfunction and/or polypharmacy. We report a patient with cystic fibrosis, liver cirrhosis and preexisting pancytopenia grade 1, requiring multiple concomitant medications inhibiting CYP3A4 and P-gp, who presented with metastatic seminoma. METHOD AND 

resultsDue to potential drug-drug interactions and liver cirrhosis, the initial etoposide dose was reduced to 50% of standard. Monitoring of etoposide plasma concentrations showed that total exposure was not enhanced. The subsequent dose was increased to 100% and further adjusted based on tolerability. After a dose reduction from cycle 2 due to pancytopenia grade 4, the patient successfully completed the chemotherapy regimen and had a complete response on first evaluation.

conclusionThis case shows that monitoring of etoposide plasma concentrations can be beneficial in complex clinical scenarios involving organ dysfunction and/or potential drug-drug interactions. This is especially important in curative treatment to avoid under dosing. This case report highlights the challenges of dosing etoposide in a patient with cystic fibrosis and liver cirrhosis who is taking multiple drugs that may interact with etoposide. The patient should be monitored closely on how the treatment is tolerated and the dose should be adjusted accordingly.

Indexed as

EtoposideLiver CirrhosisSeminomaTesticular NeoplasmsAdultAntineoplastic Agents, PhytogenicAntineoplastic Combined Chemotherapy ProtocolsCystic FibrosisDose-Response Relationship, DrugDrug InteractionsHumansMaleAntineoplastic Agents, PhytogenicEtoposideCystic fibrosisDrug-drug interactionsEtoposideLiver cirrhosisSeminomaTesticular cancer

Identifiers

PMID41632323
PMCPMC12868044

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