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TREATMENT OF ADVANCED UROGENITAL TRACT CANCERS WITH CIS-DIAMMINEDICHLOROPLATINUM

机译:CIS-双二叶铂治疗高级泌尿生殖道癌

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摘要

A total of 23 patients with urogenital tract cancers ... 17 non-seminomatous testicular cancers, 4 urinary bladder cancers, 1 renal pelvic cancer, and 1 penile cancer were treated with CDDP only or three-drug combination consisting of CDDP, vinblastine, and bleomycin. On the CDDP single therapy, platinum was given in a dosage of 25 mg/body as 2-hour intravenous infusion for 5 consecutive days in a week for 3 weeks. This treatment unit was repeated for 3 times. On the CDDP combination therapy, platinum was given in the same manner as the therapy with single CDDP, and vinblastine was given on the first and second days of 5 consecutive days in a week in a dosage of 10 mg/body for 3 weeks for 4 courses and then given as a single injection in a dosage of 10 mg/body for 4 weeks. This treatment was applied on and off for 2 years. Bleomycin was given weekly for 12 weeks in a dosage of 30 mg/body by intravenous injection. Three disseminated testicular cancers and one renal pelvic cancer were treated with CDDP. The therapy with CDDP single was not so effective for testicular cancers but a tumor regression was observed endoscopically in renal pelvic cancer. Fourteen disseminated testicular cancers, 4 urinary bladder cancers, and 1 penile cancer were treated with CDDP, vinblastine, and bleomycin given in combination. Two of the 14 testicular cancers (14%) achieved complete response and 5 of the 14 (36%) achieved partial response. But the 3-drug combination therapy was not so effective for urinary bladder cancer and penile cancer. On the toxicity of CDDP, the CDDP caused moderate to severe nausea and vomiting in almost of all patients during 5 days of treatment. None of these patients treated with CDDP showed nephrotoxity and ototoxity. But in the CDDP combination therapy, the most serious side effect is the myelosuppression due to vinblastine. Leukopenia (below 1,000/mm3) was observed in 5 of 19 patients. We believe the CDDP-combination therapy represents. a great advance in the management of patients with disseminated testicular cancer.
机译:总共23例泌尿生殖道癌症... 17例非精原细胞性睾丸癌,4例膀胱癌,1例肾盂癌和1例阴茎癌仅接受CDDP或CDDP,长春碱和三药联合治疗博来霉素。在CDDP单一疗法中,铂以25毫克/人的剂量作为2小时静脉输注的方式给药,每周连续5天,持续3周。将该处理单元重复3次。在CDDP联合疗法中,以与单一CDDP疗法相同的方式给予铂,并在每周连续5天的第一天和第二天给予长春碱,剂量为10 mg /人,持续3周,共4次疗程,然后以10毫克/人的剂量单次注射,持续4周。连续治疗该治疗2年。静脉注射博莱霉素,每周一次,剂量为30 mg /人,持续12周。 CDDP治疗了3例散布的睾丸癌和1例肾盂癌。 CDDP Single疗法对睾丸癌的疗效不佳,但在内镜下观察到肾盂癌的肿瘤消退。联合应用CDDP,长春碱和博来霉素治疗14例弥漫性睾丸癌,4例膀胱癌和1例阴茎癌。 14种睾丸癌中的2种(14%)达到完全缓解,14种睾丸癌中的5种(36%)实现部分缓解。但是,三药联合治疗对膀胱癌和阴茎癌的疗效不佳。关于CDDP的毒性,在治疗5天之内,几乎所有患者中CDDP都会引起中度至重度恶心和呕吐。这些用CDDP治疗的患者均未显示肾毒性和耳毒性。但是在CDDP联合疗法中,最严重的副作用是长春碱引起的骨髓抑制。在19例患者中有5例观察到白细胞减少(低于1,000 / mm3)。我们相信CDDP联合疗法代表了这一点。在弥散性睾丸癌患者管理方面取得了巨大进步。

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