The role of chemotherapy in metastatic prostate cancer

被引:6
作者
Riaz, Irbaz B. [1 ,2 ,3 ]
Sweeney, Christopher J. [1 ,2 ]
机构
[1] Harvard Med Sch, Lank Ctr Genitourinary Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Brigham & Women Hosp, Harvard Med, Boston, MA USA
[3] Mayo Clin, Div Med Oncol, Dept Internal Med, Phoenix, AZ USA
关键词
cabazitaxel; chemotherapy; docetaxel; prostate cancer; PHASE-III TRIAL; ANDROGEN-DEPRIVATION THERAPY; QUALITY-OF-LIFE; MITOXANTRONE PLUS PREDNISONE; ABIRATERONE ACETATE; OPEN-LABEL; 1ST-LINE THERAPY; DOCETAXEL; MULTICENTER; OUTCOMES;
D O I
10.1097/MOU.0000000000000985
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 of review To summarize the role of chemotherapy and offer some guidance regarding the selection of chemotherapy in mPC. Recent findings Patients with mHSPC have varied prognoses with testosterone suppression alone (androgen deprivation therapy, ADT) and differential responses to docetaxel with ADT. Patients with de novo and metachronous high-volume disease have a robust survival benefit with the addition of docetaxel to hormonal therapies. Patients with synchronous low-volume disease have a more modest survival benefit from docetaxel and there is no evidence of survival benefit with docetaxel in patients with metachronous low-volume disease. Integration of biomarkers may refine treatment selection regardless of volume of disease. Docetaxel and cabazitaxel also impart an OS benefit in patients with metastatic castration-resistant prostate cancer (mCRPC). The choice of chemotherapy in mCRPC depends on treatment received in mHSPC setting. Docetaxel remains the first line chemotherapy in castration-resistant patients who have not received it in mHSPC followed by cabazitaxel, otherwise cabazitaxel can be deployed without docetaxel retreatment. Chemotherapy is a key class of therapy for selected patients with mHSPC and mCRPC.
引用
收藏
页码:292 / 301
页数:10
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