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dc.contributor.author藤井, 昭男ja
dc.contributor.author安野, 博彦ja
dc.contributor.author川井田, 徳之ja
dc.contributor.author中村, 一朗ja
dc.contributor.alternativeFUJII, Akioen
dc.contributor.alternativeYASUNO, Hirohikoen
dc.contributor.alternativeKAWAIDA, Tokuyukien
dc.contributor.alternativeNAKAMURA, Ichiroen
dc.date.accessioned2010-06-02T02:13:59Z-
dc.date.available2010-06-02T02:13:59Z-
dc.date.issued1986-11-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/118955-
dc.description.abstract1984年6月から1年間の新鮮stage D前立腺癌11例に対し, Honvan 300 mg/day分3, Estracyt 4 cap/day分2, Prostal 100 mg/day分2の連日経口投与とCPM 1 g/m2/3 W (700~1, 500 mg/body)の大量間歇投与の併用療法を行った.1)自験例11例の臨床効果については, NPCP効果判定基準でHonvan群5例中1例にPR, 4例にstable, Estracyt群3例中3例, Prostal群3例中1例にstableが得られ, 残りのProstal群2例は1例がprogression例, 1例がdrop out例であった.stable以上を有効とすると効果判定可能症例10例中9例が有効となった.2)本療法の有効持続期間は5~16ヵ月, 平均9.9ヵ月で, 有効症例においては著明な自覚症状と全身症状の改善が得られた.3)副作用については, 悪心, 嘔吐あるいは食欲不振などの胃腸症状が9例に, 白血球減少が3例に, 血小板減少が1例に認められた.1例に黄疸の出現とGOT・GPTの上昇が見られたが, 外来通院治療にて完治し, 再度Estracyt・CPM併用治療の継続が可能であったja
dc.description.abstractEleven patients with newly diagnosed stage D prostate cancer between June, 1984 and June, 1985, were administered 300 mg/day of Honvan in 3 divided portions, 4 capsules/day of Estracyt in 2 divided portions, or 100 mg/day of Prostal in 2 divided portions was administered orally, concomitantly with large-dose intermittent treatment of 1 g/m2/3 weeks of cyclophosphamide. According to the NPCP criteria, of the 5 cases given Honvan 1 case was PR and 4 cases were stable: all 3 cases given Estracyt were stable: and in 3 cases given Prostal, 1 case was stable, 1 case had progression and 1 case dropped out. The response duration of this combination therapy was 3 to 16 months (average: 9.9 months), and obvious improvements in the subjective symptoms and performance status were noted in the cases that responded to the treatment. As for side effects, gastrointestinal symptoms were observed in 9 cases, leucopenia in 3 cases, and thrombocytopenia in 1 case. All these cases, however, were slight and transient. In 1 case, jaundice and an elevation in GOT and GPT were detected, but these changes were also temporary.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.subjectCanceren
dc.subjectProstateen
dc.subjectChemotherapyen
dc.subject.ndc494.9-
dc.title新鮮stage D前立腺癌に対するhormone・cyclophosphamide併用療法 第1報ja
dc.title.alternativeTreatment of stage D prostate cancer patients with hormones in combination with cyclophosphamideen
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume32-
dc.identifier.issue11-
dc.identifier.spage1713-
dc.identifier.epage1717-
dc.textversionpublisher-
dc.sortkey16-
dc.address兵庫県立成人病センターja
dc.address兵庫県立成人病センターja
dc.address兵庫県立成人病センターja
dc.address兵庫県立成人病センターja
dc.address.alternativethe Hyogo Medical Centerfor Adults, Department of Urologyen
dc.address.alternativethe Hyogo Medical Centerfor Adults, Department of Urologyen
dc.address.alternativethe Hyogo Medical Centerfor Adults, Department of Urologyen
dc.address.alternativethe Hyogo Medical Centerfor Adults, Department of Urologyen
dc.identifier.pmid2435128-
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.32 No.11

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