The Japanese Journal of Urology
Online ISSN : 1884-7110
Print ISSN : 0021-5287
ISSN-L : 0021-5287
Original Article
SALVAGE THERAPY FOR CASTRATION-REFRACTORY PROSTATE CANCER RESISTANT TO DOCETAXEL
Tatsuya TakayamaTakayuki SugiyamaHiroshi FuruseTakashi YajimaTakahisa SuzukiFumitake KaiMasao NagataAtsushi OtsukaYasuo IshiiSeiichiro Ozono
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2013 Volume 104 Issue 6 Pages 681-687

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Abstract

(Objectives) To evaluate the treatment for castration-refractory prostate cancer (CRPC) resistant to docetaxel (Materials and methods) Among 45 patients with CRPC treated with docetaxel (70-75 mg/m2) every 3 to 4 weeks at Hamamatsu University Hospital from January 2004 to July 2012, 19 patients underwent salvage treatments. We retrospectively analyzed the medical records of 14 patients except for 5 patients who were enrolled in clinical trials. (Results) The median age and serum prostate-specific antigen (PSA) level at starting salvage treatments was 71 years (range 45 to 79) and 241.1 ng/mL (range 3.06 to 1,643.0), respectively. All patients maintained castration status. Salvage treatments include DTX (30 mg/m2) +cisplatin (CDDP) (70 mg/m2) /carboplatin (Area under the curve=4), etoposide+CDDP, paclitaxel+CDDP, cyclophosphamide, S-1, tegaful-uracil. The reasons why 14 patients moved to salvage treatments after DTX were progressive disease in 12 patients and adverse events in 2. Eight patients had a PSA response, 3 patients>50% and 5 patients<50%. Six patients had a PSA progression. The median overall survival was 10.4 months (range 4.1 to 27.3). All patients died of cancer, 13 patients with prostate cancer and one patient with lung adenocarcinoma. Most adverse events were mild. Transitory grade 3 leukopenia was observed in 2 patients, and grade 3 anemia in 2. No grade 4 toxicities were noted. (Conclusions) All salvage treatments without grade 4 toxicities described in this study may be acceptable in the patients with CRPC progressing after docetaxel although the effect would be limited.

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© 2013 Japanese Urological Association
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