VAB-6 combination chemotherapy in patients with stage II, III testicular tumor

Between 1983 and 1985, six patients with advanced testicular cancer were treated with 3 cycles of vinblastine, actinomycin D, bleomycin, cyclophosphamide and cisplatinum (VAB-6 combination chemotherapy without maintenance). The histology of the primary tumor was seminoma in one patient and nonsemino...

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Veröffentlicht in:Hinyokika kiyo. Acta urologica Japonica. - 1962. - 32(1986), 12 vom: 30. Dez., Seite 1849-58
1. Verfasser: Hida, S (VerfasserIn)
Weitere Verfasser: Kawakita, M, Takenawa, J, Fukuzawa, S, Okuno, H, Yamauchi, T, Oishi, K, Nishio, Y, Takeuchi, H, Okada, K
Format: Aufsatz
Sprache:Japanese
Veröffentlicht: 1986
Zugriff auf das übergeordnete Werk:Hinyokika kiyo. Acta urologica Japonica
Schlagworte:English Abstract Journal Article Bleomycin 11056-06-7 Chlorambucil 18D0SL7309 Dactinomycin 1CC1JFE158 Vinblastine 5V9KLZ54CY mehr... Doxorubicin 80168379AG Cyclophosphamide 8N3DW7272P Cisplatin Q20Q21Q62J
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245 1 0 |a VAB-6 combination chemotherapy in patients with stage II, III testicular tumor 
264 1 |c 1986 
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520 |a Between 1983 and 1985, six patients with advanced testicular cancer were treated with 3 cycles of vinblastine, actinomycin D, bleomycin, cyclophosphamide and cisplatinum (VAB-6 combination chemotherapy without maintenance). The histology of the primary tumor was seminoma in one patient and nonseminomatous germ cell testicular tumor (NSGCTT) in 5. Five men with stage III or bulky stage II diseases received no prior chemotherapy but one had received another chemotherapy without cisplatinum. Two patients showed a complete response to chemotherapy. Three were partial responders free of disease after a debulking operation and additional chemotherapy. The other patient who had NSGCTT had recurrence 5 months after the last induction chemotherapy and received additional chemotherapy (PVeBV regimen). Median follow-up was 16 months (range 2 to 28 months) and all patients are alive with no evidence of disease. Severe myelosuppression and serious renal toxicity were not experienced. Marked, but transient elevation of serum transaminase were observed in all patients. These data suggest that this protocol is highly effective and minimally toxic in the treatment of disseminated testicular tumor 
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650 4 |a Journal Article 
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650 7 |a Cyclophosphamide  |2 NLM 
650 7 |a 8N3DW7272P  |2 NLM 
650 7 |a Cisplatin  |2 NLM 
650 7 |a Q20Q21Q62J  |2 NLM 
700 1 |a Kawakita, M  |e verfasserin  |4 aut 
700 1 |a Takenawa, J  |e verfasserin  |4 aut 
700 1 |a Fukuzawa, S  |e verfasserin  |4 aut 
700 1 |a Okuno, H  |e verfasserin  |4 aut 
700 1 |a Yamauchi, T  |e verfasserin  |4 aut 
700 1 |a Oishi, K  |e verfasserin  |4 aut 
700 1 |a Nishio, Y  |e verfasserin  |4 aut 
700 1 |a Takeuchi, H  |e verfasserin  |4 aut 
700 1 |a Okada, K  |e verfasserin  |4 aut 
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