
doi: 10.1159/000073364
pmid: 14586153
Ifosfamide has always had significant single-agent activity in patients with germ cell tumors. We first began studies of cisplatin + ifosfamide combination chemotherapy as salvage chemotherapy in 1982. The regimen of etoposide (VP-16) + ifosfamide + cisplatin (VIP) was initially utilized as third-line chemotherapy. Even in this refractory setting, we were able to cure a small cohort of patients. Ifosfamide-cisplatin combination chemotherapy then became a standard second-line chemotherapy program, and achieved a 25% cure rate. Subsequent phase III studies compared VIP to bleomycin + etoposide + cisplatin (BEP) as initial chemotherapy. Although the results of the ifosfamide-based regimen were slightly better, there was no statistically significant difference and BEP was less toxic. However, for individual patients with concern for bleomycin-induced pulmonary fibrosis, VIP remains an attractive first-line regimen.
Male, Salvage Therapy, Clinical Trials as Topic, Neoadjuvant Therapy, Treatment Outcome, Antineoplastic Combined Chemotherapy Protocols, Humans, Female, Germinoma, Ifosfamide, Antineoplastic Agents, Alkylating
Male, Salvage Therapy, Clinical Trials as Topic, Neoadjuvant Therapy, Treatment Outcome, Antineoplastic Combined Chemotherapy Protocols, Humans, Female, Germinoma, Ifosfamide, Antineoplastic Agents, Alkylating
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