851. Maintenance chemotherapy with daily oral etoposide following salvage therapy in patients with germ cell tumors.
- Author
-
Cooper MA and Einhorn LH
- Subjects
- Administration, Oral, Bone Marrow Transplantation, Combined Modality Therapy, Disease-Free Survival, Drug Administration Schedule, Etoposide adverse effects, Female, Follow-Up Studies, Hematologic Diseases chemically induced, Humans, Male, Remission Induction methods, Etoposide therapeutic use, Germinoma therapy, Mediastinal Neoplasms therapy, Ovarian Neoplasms therapy, Salvage Therapy
- Abstract
Purpose: To evaluate the role of maintenance daily oral etoposide (VP-16) chemotherapy for germ cell patients who had a response to salvage therapy., Patients and Methods: Thirty-seven patients were entered onto this trial, and 34 were fully assessable. This was as heavily pretreated patient population, with a median of two prior salvage regimens. The salvage treatment that immediately preceded oral VP-16 consisted of autologous bone marrow transplantation in 14 patients (41%), surgery in 10 (29%), and standard-dose salvage chemotherapy in 10 (29%). Daily oral VP-16 was administered at a dose of 50 mg/m2 for 21 consecutive days every 4 weeks for three cycles., Results: The major toxicity with daily oral VP-16 was leukopenia. Three patients had grade III and two grade IV leukopenia. Two of these patients had granulocytopenic fever. Other grade III toxicities included thrombocytopenia (n = 1) and mucositis (n = 2). Twenty-three patients started daily oral VP-16 while in complete remission (CR) following salvage therapy. Seventeen (74%) remain continuously disease-free, with a median follow-up time of 36 months (range, 26 to 49) from initiation of daily oral VP-16. Eleven patients started daily oral VP-16 while in partial remission (PR) following salvage therapy. Three of these 11 patients converted to CR, but all three subsequently relapsed., Conclusion: Maintenance oral VP-16 was well tolerated in this heavily treated patient population. Results in this poor-risk population were encouraging.
- Published
- 1995
- Full Text
- View/download PDF