Prostate specific antigen working group guidelines on prostate specific antigen doubling time

被引:110
作者
Arlen, Philip M.
Bianco, Fernando [2 ]
Dahut, William L.
D'Amico, Anthony [3 ,4 ]
Figg, William D. [1 ]
Freedland, Stephen J. [5 ,6 ,9 ]
Gulley, James L.
Kantoff, Philip W. [3 ,4 ]
Kattan, Michael W. [7 ]
Lee, Andrew [8 ]
Regan, Meredith M. [3 ,4 ]
Sartor, Oliver [3 ,4 ]
机构
[1] NCI, Med Oncol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] George Washington Univ, Dept Urol, Washington, DC USA
[3] Harvard Univ, Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Harvard Univ, Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Duke Univ, Div Urol, Durham, NC USA
[6] Duke Univ, Duke Prostate Ctr, Dept Surg, Durham, NC USA
[7] Cleveland Clin, Cleveland, OH 44106 USA
[8] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[9] Duke Univ, Dept Pathol, Duke Prostate Ctr, Durham, NC USA
关键词
prostatic neoplasms; prostate-specific antigen; consensus; clinical trials as topic; biological markers;
D O I
10.1016/j.juro.2008.01.099
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Prostate specific antigen is a glycoprotein found almost exclusively in normal and neoplastic prostate cells. Prostate specific antigen doubling time, or the change in prostate specific antigen over time, has emerged as a useful predictive marker for assessing disease outcome in patients with prostate cancer. It is important to agree on definitions and values for the calculation of prostate specific antigen doubling time, and to develop a common approach to outcome analysis and reporting. Materials and Methods: In September 20,06 a conference was held at the National Cancer Institute in Bethesda, Maryland to define these parameters and develop guidelines for their use. Results: The Prostate Specific Antigen Working Group defined criteria regarding prostate specific antigen doubling time including the calculation of prostate specific antigen doubling time, evidence to support prostate specific antigen doubling time as a predictive factor in the setting of biochemical recurrence and the use of prostate specific antigen doubling time as a stratification factor in clinical trials. Conclusions: We propose that investigators calculate prostate specific antigen doubling time before enrolling patients in clinical studies and calculate it as an additional measurement of therapeutic activity. We believe we have developed practical guidelines for the calculation of prostate specific antigen doubling time and its use as a measurement of prognosis and outcome. Furthermore, the use of common standards for prostate specific antigen doubling time in clinical trials is important as we determine which treatments should progress to randomized trials in which "hard" end points such as survival will be used.
引用
收藏
页码:2181 / 2185
页数:5
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