Alkaline phosphatase in metastatic castration-resistant prostate cancer: reassessment of an older biomarker

被引:59
|
作者
Heinrich, Daniel [1 ]
Bruland, Oyvind [2 ]
Guise, Theresa A. [3 ]
Suzuki, Hiroyoshi [4 ]
Sartor, Oliver [5 ,6 ]
机构
[1] Akershus Univ Hosp, Dept Oncol, Sykehusveien 25, N-1478 Lorenskog, Norway
[2] Oslo Univ Hosp, Dept Oncol, Norwegian Radium Hosp, Ullernchausseen 70, N-0379 Oslo, Norway
[3] Indiana Univ Sch Med, Dept Med, 980 W Walnut St,Walther Hall,R3,Room C130, Indianapolis, IN 46202 USA
[4] Toho Univ, Dept Urol, Sakura Med Ctr, 564-1 Shimazu, Sakura, Chiba 2858741, Japan
[5] Tulane Canc Ctr, Dept Med, 1430 Tulane Ave,SL-42, New Orleans, LA 70112 USA
[6] Tulane Canc Ctr, Dept Urol, 1430 Tulane Ave,SL-42, New Orleans, LA 70112 USA
关键词
alkaline phosphatase; biomarker; bone metastases; castration-resistant prostate cancer; mechanism of action; prognostic marker; survival; BONE METASTASES; SIPULEUCEL-T; ABIRATERONE ACETATE; ANDROGEN RECEPTOR; PROGNOSTIC MODEL; DOUBLE-BLIND; 1ST-LINE CHEMOTHERAPY; RADIUM-223; DICHLORIDE; EXPLORATORY ANALYSIS; SKELETAL METASTASES;
D O I
10.2217/fon-2018-0087
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since most patients with metastatic castration-resistant prostate cancer (mCRPC) have bone metastases, it is important to understand the potential impact of therapies on prognostic biomarkers, such as ALP. Clinical studies involving mCRPC life-prolonging agents (i.e., sipuleucel-T, abiraterone, enzalutamide, docetaxel, cabazitaxel, and radium-223) have shown that baseline ALP level is prognostic for overall survival, and may be a better prognostic marker for overall survival than prostate-specific antigen in patients with bone-dominant mCRPC. Mechanism of action differences between therapies may partly explain ALP dynamics during treatment. ALP changes can be interpreted within the context of other parameters while monitoring disease activity to better understand the underlying pathology. This review evaluates the current role of ALP in mCRPC.
引用
收藏
页码:2543 / 2556
页数:14
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