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Ifosfamide in testicular cancer: the Indiana University experience

P J Loehrer1, S D Williams, L H Einhorn

  • 1Section of Hematology/Oncology, Indiana University School of Medicine, Indiana University Hospital, Indianapolis 46223.

Seminars in Oncology
|February 1, 1989
PubMed

Insights

Salvage chemotherapy with ifosfamide-containing regimens like VeIP and VIP shows curative potential for refractory germ cell tumors. This approach offers hope for patients previously unresponsive to standard cisplatin-based treatments.

Area of Science:

  • Oncology
  • Medical Chemotherapy

Background:

  • Metastatic germ cell tumors (GCTs) have seen improved systemic treatment outcomes.
  • A subset of GCT patients require salvage chemotherapy after initial treatment failure.
  • Pseudoprogression must be excluded before initiating salvage therapy.

Purpose of the Study:

  • To evaluate the efficacy of ifosfamide-based salvage chemotherapy regimens in refractory GCT patients.
  • To assess the curative potential of VeIP (vinblastine, ifosfamide, cisplatin) and VIP (etoposide, ifosfamide, cisplatin) regimens.

Main Methods:

  • A clinical trial was conducted involving 57 patients with GCTs previously treated with cisplatin, vinblastine, and etoposide.
  • Patients received either VeIP or VIP chemotherapy.
  • Response was assessed, including disease-free status achieved through chemotherapy alone or with subsequent surgical resection.

Main Results:

  • Twenty out of 57 patients achieved disease-free status (12 with chemotherapy alone, 8 with chemotherapy plus surgery).
  • Fifteen of these 20 patients remained recurrence-free for 18 to 53 months.
  • Seven patients achieved continuous remission for over two years.

Conclusions:

  • Ifosfamide combination chemotherapy demonstrates curative potential in heavily pretreated GCT patients.
  • Salvage therapy with VeIP and VIP regimens is effective for refractory germ cell tumors.
  • Further research is ongoing to explore ifosfamide's role in initial GCT therapy.

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