Journal of Clinical Oncology · 1998 · 146 citations · 19 references
MedicineOncologyPharmacotherapyChemotherapyGenitourinary OncologyMetastasisCancer ImmunotherapyCombination ChemotherapyGenitourinary Cancer PharmacotherapyImmunotherapy For Genitourinary CancersMalignant NeoplasmsTesticular CancerAnticancer ChemotherapyChemotherapy Dose IntensityGerm Cell Tumor ChemotherapyGranulocyte Colony-stimulating Factor AdministrationGranulocyte Colony-stimulating Factor MobilizationGranulocyte-macrophage Colony-stimulating Factor MobilizationMultiagent ChemotherapyTesticular Cancer Chemotherapy
PURPOSE: To determine the effect of r-metHu granulocyte colony-stimulating factor (G-CSF) on the proportion of patients with metastatic poor-prognosis malignant germ cell tumors who receive full dose-intensity combination chemotherapy. PATIENTS AND METHODS: In a phase III study patients received six cycles of BEP/EP (etoposide, and cisplatin, plus or minus bleomycin) or six cycles of BOP/VIP-B (bleomycin, vincristine, cisplatin/etoposide, ifosfamide, cisplatin, bleomycin). A subset were secondarily randomized to receive or not receive filgrastim. Filgrastim 5 microg/kg/day was administered subcutaneously on days 3 through 9 after each BOP and on days 6 through 19 after each VIP, BEP, or EP cycle. RESULTS: Eighty-five percent of 120 eligible patients randomized to filgrastim received at least six chemotherapy cycles compared with 70% of 130 patients randomized to not receive filgrastim (VCP = .003). Patients in the filgrastim-arm achieved significantly higher dose-intensities. Neutropenic fever occurred in 25 of 128 filgrastim-patients and in 38 of 129 non-filgrastim-patients (P = .052). Twelve and three toxic deaths occurred in the non-filgrastim- and filgrastim-arms, respectively. Nine of the 12 toxic deaths and all of the three toxic deaths were associated with febrile grade 4 neutropenia. Failure-free and overall survival were similar in both arms. CONCLUSION: During combination chemotherapy in patients with malignant germ cell tumors, the routine use of filgrastim significantly improved the delivery of the planned treatment schedule without effect on failure-free or overall survival. The use of filgrastim was associated with a clinically important reduction in the number of toxic deaths, confined to the experimental intensified-chemotherapy schedule. This study does not support the routine use of filgrastim during standard chemotherapy with BEP.
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Janice Gabrilove, Ann A. Jakubowski, Howard I. Scher et al. · New England Journal of Medicine · 1988 · 953 citations
Treatment of testicular cancer: a new and improved model.
Lawrence H. Einhorn · Journal of Clinical Oncology · 1990 · 517 citations
Medicine, Oncology, Chemotherapy +9