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dc.contributor.author関根, 英明ja
dc.contributor.author福井, 巌ja
dc.contributor.author山田, 拓己ja
dc.contributor.author竹内, 信一ja
dc.contributor.author立花, 祐一ja
dc.contributor.author横川, 正之ja
dc.contributor.alternativeSEKINE, Hideakien
dc.contributor.alternativeFUKUI, Iwaoen
dc.contributor.alternativeYAMADA, Takumien
dc.contributor.alternativeTAKEUCHI, Shinichien
dc.contributor.alternativeTACHIBANA, Yuuichien
dc.contributor.alternativeYOKOKAWA, Masayukien
dc.date.accessioned2010-06-02T01:39:45Z-
dc.date.available2010-06-02T01:39:45Z-
dc.date.issued1984-08-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/118245-
dc.description.abstract進行性尿路上皮癌18例に対しBLM, vinca alkaloidとDDPの3剤によるBVP療法をおこない, 完全寛解3例, 有効6例, 不変6例, 進行3例の成績を得, response rateは50%であった.効果は1~2コース終了後にみることが多く, とくにリンパ節転移に有効と考えた.2年以上生存例は4例あり, 2年生存率は, 寛解群が有意に良好な結果であった.副作用は, 消化器症状, 骨髄抑制, 腎毒性などを認めたが, すべて可逆性で重篤なものはなかった.vinca alkaloidとしては, vinblastineに劣らぬ抗腫瘍効果を認め, しかも副作用の軽微なvincristineを第1選択とすべきであろうja
dc.description.abstractSince October 1979, 18 patients with metastatic urothelial cancer have been treated with combination chemotherapy of bleomycin (5-10 mg/day administered on days 1 to 7), vinca alkaloid (vinblastine 5-10 mg/day or vincristine 1 mg/sqm on days 8 and 9) and CDDP (60 mg/sqm on day 10). CR was achieved in 3 of the 18 patients and PR in 6 patients. Over-all, the response rate was 50%. Among 3 patients who achieved CR, 2 patients are still free of disease for 31 months and for 28 months, and the other is alive with cancer for 26 months. The 2-year survival rate was 58% in responders (CR + PR) and 0% in nonresponders. (p less than 0.005). In many cases, the response was observed after the first or second course of BVP therapy, and there was a relatively good response in patients with lymphnode metastasis alone. The treatment was tolerated well and common toxic effects were nausea, vomiting of moderate to severe degree (100%), myelosuppression (50%) and mild nephrotoxicity (22%). As to the choice of vinca alkaloids, vincristine seemed to be the treatment of choice because it was less toxic than vinblastine and was almost equally effective.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.subjectUrothelial canceren
dc.subjectCombination chemotherapyen
dc.subjectBleomycinen
dc.subjectVinca alkaloidsen
dc.subjectCisplatinen
dc.subject.ndc494.9-
dc.title進行性尿路上皮癌に対するBVP療法ja
dc.title.alternativeCombination chemotherapy with bleomycin, vinca alkaloid and cisplatin (BVP) for advanced urothelial canceren
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume30-
dc.identifier.issue8-
dc.identifier.spage1095-
dc.identifier.epage1099-
dc.textversionpublisher-
dc.sortkey14-
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address東京医科歯科大学泌尿器科学教室ja
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Tokyo Medicaland Dental Universityen
dc.identifier.pmid6083719-
dcterms.accessRightsopen access-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.30 No.8

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