Cancer · 1992 · 108 citations · 30 references
MedicineOncologyPharmacologyChemotherapyHematologic OncologyMedical OncologyChemotherapy In Hematologic MalignanciesCombination ChemotherapyHigh-dose ChemotherapyMalignant NeoplasmsSupportive Care In CancerChemotherapy Response AssessmentComplete Response AssessmentGerm Cell Tumor ChemotherapyGerm Cell Tumor Salvage TherapyIfosfamide-based TherapyRefractory Germ Cell TumorsRelapsed Germ Cell TumorsSerum Tumor Markers
Therapy with high-dose carboplatin plus etoposide-based chemotherapy plus autologous bone marrow rescue (AUBMR) was administered to 29 patients with advanced germ cell tumors (GCT) refractory to cisplatin-based chemotherapy. Two groups of patients with refractory disease were treated. Sixteen patients had been identified as "poor risk" at diagnosis and had an inappropriately slow decline of serum tumor markers after two cycles of induction cisplatin-based therapy (Group A). In addition, 13 patients were treated who had never had a complete response (CR) or had relapses after ifosfamide-based salvage chemotherapy (Group B). Patients in Group A were treated with high-dose carboplatin etoposide, and patients in Group B received high-dose carboplatin, etoposide, and cyclophosphamide. Fifteen of 29 (52%) patients had a CR (9, Group A; 6, Group B). The patients in Group A had fewer hematologic toxic effects, and the median number of days from day 0 to a granulocyte count greater than 0.5/microliters was 16 and to a platelet count of more than 50/microliters was 15, compared with 22 days and 23 days in Group B, respectively. There were fewer episodes of culture-positive sepsis in Group A (12%) compared with Group B (26%), and the only treatment-related death occurred in Group B. Therapy with high-dose carboplatin plus etoposide-based chemotherapy plus AUBMR is effective for patients with GCT refractory to regimens of cisplatin with or without ifosfamide. Early use of high-dose chemotherapy reduces hematologic toxic effects and allows patients to start treatment in a more predictable fashion after cytoreduction, rather than when the disease is progressing rapidly.
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VENOOCCLUSIVE DISEASE OF THE LIVER FOLLOWING BONE MARROW TRANSPLANTATION
Richard J. Jones, KAMTHORN S. K. LEE, William E. Beschorner et al. · Transplantation · 1987 · 914 citations
Medicine, Hematology, Surgery +14
Ellin Berman, Glenn Heller, J Santorsa et al. · Blood · 1991 · 369 citations · Full text
Medicine, Hematology, Oncology +11
Craig R. Nichols, Guido Tricot, Stephen D. Williams et al. · Journal of Clinical Oncology · 1989 · 351 citations
Medicine, Oncology, Pharmacology +15