Evidence map›Paper›PMID 41125910›Full record

ArticleCancer chemotherapy and pharmacology2025

Substitution of ifosfamide for cyclophosphamide in the TI-CE regimen: pharmacology and dose justification in a patient with refractory metastatic germ-cell tumor post-nephrectomy-A case report.

Lotte M G Hulskotte, Loek A W de Jong, Alwin D R Huitema, Joost Sijm, Ingrid Desar, Minke Smits, Nielka P van Erp

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Article in Cancer chemotherapy and pharmacology, 2025. 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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5 · Who and what money

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7 authors.

Lotte M G HulskotteDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.
Loek A W de JongDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.
Alwin D R HuitemaDepartment of Pharmacy and Pharmacology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Joost SijmDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ingrid DesarDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Minke SmitsDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Nielka P van ErpDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands. Nielka.vanerp@radboudumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-dose chemotherapy (HDCT) combined with autologous stem cell transplantation (ASCT) rescue is an effective treatment option for relapsed or refractory germ-cell tumors. The TI-CE regimen, consisting of paclitaxel and ifosfamide for stem cell mobilization followed by high dose carboplatin and etoposide with ASCT rescue, is frequently used in the treatment of refractory disease. This regimen is challenging in patients who have undergone unilateral nephrectomy, since potential nephrotoxicity of ifosfamide poses a serious risk for permanent damage of the preserved kidney. Currently, the literature lacks data on the substitution of ifosfamide in the TI-CE regimen for an alternative chemotherapeutic agent with equivalent potency while being less nephrotoxic. CASE PRESENTATION: We present a case of a patient with refractory progressive metastatic germ-cell tumor who underwent nephrectomy and was successfully treated with a modified chemo-mobilization strategy. In the TI-CE protocol, ifosfamide was replaced for cyclophosphamide (TC-CE), resulting in a sufficient stem cell harvest through a single apheresis session. Post chemo-mobilization, LDH and hCG + hCGβ levels were normalized. Renal function remained stable throughout the course of treatment. Two months after HDCT, the patient showed a complete metabolic response, with no detectable tumor remnants. Currently, one year post-therapy, there are no signs of disease recurrence.

conclusionAn effective and potentially less nephrotoxic chemo-mobilization regimen, using paclitaxel and cyclophosphamide (TC-CE), was administered to a patient with refractory metastatic germ-cell tumor who underwent HDCT followed by ASCT rescue after unilateral nephrectomy. Cyclophosphamide demonstrated to be a viable substitute for ifosfamide within the TI-CE regimen.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCyclophosphamideIfosfamideNeoplasms, Germ Cell and EmbryonalTesticular NeoplasmsAdultCarboplatinEtoposideHumansMaleNephrectomyPaclitaxelTransplantation, AutologousCarboplatinCyclophosphamideEtoposideIfosfamidePaclitaxelASCTCase reportGerm-cell tumorNephrectomyTI-CE regimen

Identifiers

PMID41125910
PMCPMC12546300

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