Time to Castration Resistance Is an Independent Predictor of Castration-resistant Prostate Cancer Survival

被引:0
作者
Bournakis, Evangelos [1 ]
Efstathiou, Eleni [1 ,3 ]
Varkaris, Andreas [1 ]
Wen, Sijin [4 ]
Chrisofos, Michael [2 ]
Deliveliotis, Charalambos [2 ]
Alamanis, Christos [2 ]
Anastasiou, Ioannis [2 ]
Constantinides, Constantine [2 ]
Bamias, Aristotelis [1 ]
Dimopoulos, Meletios A. [1 ]
机构
[1] Kapodistrian Univ Athens, Oncol Dept Clin Therapeut, Sch Med, Alexandra Hosp, Athens 11528, Greece
[2] Kapodistrian Univ Athens, Dept Urol, Sch Med, Sismanogleio Hosp, Athens 11528, Greece
[3] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
Castrate-resistant prostate cancer; predictors of survival; time to castration resistance; chemotherapy; advanced prostate cancer; PROGNOSTIC FACTORS; ANTITUMOR-ACTIVITY; DOCETAXEL; MITOXANTRONE; ESTRAMUSTINE; PREDNISONE; THERAPY; DISEASE; EXTENT; BONE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Easily assessable clinical predictors of response to chemotherapy in advanced castration-resistant prostate cancer (CRPC) are few. The objective of this retrospective study was to search for and identify such candidate predictors of outcome. Patients and Methods: A retrospective analysis of clinical data of CRPC patients entered in the Clinical Therapeutics' departmental prostate cancer database from 1996-2009 was performed. Univariate and multivariate analyses for progression-free survival and overall survival included patients receiving both docetaxel- and non-docetaxel-containing regimens. Results: From 1996 until June 2009, 286 out of 313 patients in our database were treated with chemotherapy. Prostate-specific antigen (PSA) reduction > 30% correlated with improved survival irrespective of treatment. Beyond previously reported predictors, i.e. baseline PSA > 30 ng/dl, hemoglobin below 10 mg/dl, weight loss, poor performance status, elevated lactic dehydrogenase and alkaline phosphatase, and time to CRPC of less than or equal to two years was associated with a poor overall survival and shorter progression-free survival upon univariate analysis. Pain was associated with shorter survival. Multivariate analysis confirmed time to CRPC, lactate dehydrogenase and alkaline phosphatase as independent predictors of overall and progression-free survival. Conclusion: Time to castration resistance is an important predictor of outcome in CRPC. PSA reduction > 30% predicts survival improvement following chemotherapy for CRPC regardless of chemotherapy applied.
引用
收藏
页码:1475 / 1482
页数:8
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