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ID 30759
JaLCDOI
フルテキストURL
著者
Kaku, Haruki Okayama University Kaken ID publons
Saika, Takashi Okayama University
Tsushima, Tomoyasu Medical Center of Okayama
Nagai, Atsushi Okayama University
Yokoyama, Teruhiko Okayama University
Abarzua, Fernando Okayama University
Ebara, Shin Okayama University
Manabe, Daisuke Okayama University
Nasu, Yasutomo Okayama University Kaken ID publons researchmap
Kumon, Hiromi Okayama University Kaken ID publons
抄録

We evaluated the efficiency and toxicity of estramustine phosphate (ECT), ifosfamide (IFM) and cisplatin (CDDP) combination chemotherapy in twenty-one patients with hormone-refractory prostate cancer (HRPC), for which there is currently no effective treatment. Patients received a daily dose of 560 mg ECT in combination with 1.2 g/m2 IFM on days 1 to 5 and 70 mg/m2 CDDP on day 1. This combination therapy was given every 3 to 4 weeks. An objective response of more than 50% reduction in prostate-specific antigen was observed in 9 of 18 patients (50%), and a more than 50% reduction in bi-dimensionally measurable soft-tissue lesions was observed in 2 of 7 patients (29%). The median duration of response among the cases showing partial response was 40 weeks, while the median duration of response of overall partial-response plus stable cases was 30 weeks. The median survival duration of all cases was 47 weeks. Toxicity was modest and acceptable. In conclusion, the ECT, IFM and CDDP combination chemotherapy regimen is a viable treatment option for HRPC. However, in comparison with our previous chemotherapy regimen of IFM and CDDP, no additional long-lasting effects resulting from the inclusion of ECT could be affirmed.

キーワード
hormone-refractory prostate cancer
chemotherapy
estramustine phosphate
ifosfamide
cisplatin
Amo Type
Article
出版物タイトル
Acta Medica Okayama
発行日
2006-02
60巻
1号
出版者
Okayama University Medical School
開始ページ
43
終了ページ
49
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT