Cisplatin, bleomycin, and vinblastine combination therapy of testicular tumors: An analysis
β Scribed by D'aoust, Joan C. ;Prestayko, Archie W. ;Einhorn, Lawrence H. ;Comis, Robert L. ;Ginsberg, Sandra J. ;Archambault, W. A. T. ;Crooke, Stanley T.
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 542 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0098-1532
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β¦ Synopsis
A combination regimen consisting of cisplatin, bleomycin, and vinblastine was evaluated in 86 patients with metastatic testicular tumors. Prior therapy included surgical resection of primary tumor (84 patients), radiotheapy (21 patients), chemotherapy (33 patients). Thirteen patients received prior bleomycin and vincristine or vinblastine. Of 80 evaluable patients 51 achieved complete response (CR) and 26 achieved partial response (PR), for an overall response rate 96.5%. There was no significant difference in response rates or survival with respect to prior therapy, sites of metastatic lesions, and tumor histology. The median survival time was not reached in an observation period of 44+ months. Sixty patients were alive 11+--44+ months, and 57 of these were free of disease. Thirty-two of the 60 patients (53%) had a survival time greater than 20 months. Toxicities included nephrotoxicity (18 patients) leukopenia, (69 patients), thrombocytopenia (nine patients), and anemia (56 patients). Bleomycin-induced pulmonary toxicity was fatal in one patient. Other toxicities included nausea and vomiting, stomatitis, fever, alopecia, and neurological effects.
π SIMILAR VOLUMES
Sixty consecutive patients with Stage I11 or bulky Stage II nonseminatous germinal testis tumors were treated with cisplatin, vinblastine, bleomycin combination chemotherapy (PVB). One patient died of acute toxicity after the first course of therapy, 16 entered complete remission (CR) after two or t
## Abstract A 31βyearβold female developed multiple episodes of grand mal seizures after combination chemotherapy with cisplatin, vinblastine and bleomycin for germ cell ovarian cancer stage Ic. The clinicoradiologic feaβtures in this patient were consistent with posterior leukoencephalopathy, whic