A Systematic Review and a Meta-analysis of Randomized Controlled Trials' Control Groups in Metastatic Hormone-Sensitive Prostate Cancer (mHSPC)

被引:7
作者
Napoli, Giuseppe [1 ]
Arcangeli, Stefano [2 ]
Fionda, Bruno [3 ]
Munoz, Fernando [4 ]
Tebano, Umberto [1 ]
Durante, Emilia [5 ]
Tucci, Marcello [6 ]
Bortolus, Roberto [7 ]
Muraro, Marco [1 ]
Rinaldi, Giulia [1 ]
Luca, Nicoletta [1 ]
Fiorica, Francesco [1 ]
机构
[1] AULSS 9 Scaligera, Dept Radiat Oncol & Nucl Med, Verona, Italy
[2] Univ Milano Bicocca, Sch Med & Surg, Dept Radiat Oncol, Milan, Italy
[3] Fdn Policlin Univ Agostino Gemelli IRCCS, UOC Radioterapia Oncol, Rome, Italy
[4] Reg Hosp Aosta, Radiat Oncol Unit, Aosta, Italy
[5] AULSS 9 Scaligera, Dept Med Oncol, Verona, Italy
[6] Reg Hosp Aosta, Med Oncol Unit, Aosta, Italy
[7] NCI CRO Aviano, Dept Radiat Oncol, Aviano, Italy
关键词
mHSPC and ADT; Deprivation Therapy; Metastatic Hormone-Sensitive Prostate Cancer; ANDROGEN-DEPRIVATION THERAPY; ZOLEDRONIC ACID; SURVIVAL; DOCETAXEL; ARM;
D O I
10.1007/s11912-022-01323-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review Determining the risk for progression or survival after standard androgen deprivation treatment (ADT) in metastatic hormone-sensitive prostate cancer (mHSPC) is essential for stratifying patients according to expected outcomes in future studies of treatment combination. This systematic review and meta-analysis aims to estimate the progression-free survival (PFS) and overall survival (OS) probabilities in the control group of randomized controlled trials (RCTs) of different regimens of standard androgen deprivation treatment (ADT) in mHSPC and to identify possible predictors of outcomes. Recent Findings Studies reporting time-dependent outcomes (progression or death) after standard ADT treatment of mHSPC were searched in MEDLINE, CANCERLIT, the Cochrane Controlled Trials Register, and the Cochrane Library from inception through June 2021. Data on patient populations and outcomes were extracted from each study by three independent observers and combined using a distribution-free summary survival curve. Primary outcomes were actuarial probabilities of disease progression and survival. Fifteen studies met the inclusion criteria. The pooled estimate of the actuarial PFS rate was 35.2% at two years. The pooled actuarial OS rate was 62.5% at three years. Heterogeneity among studies was highly significant for all outcomes. By univariate meta-regression analyses, high-volume disease and the presence of visceral metastases were associated with shorter survival. Summary Our findings show that PFS and OS are highly variable in patients with mHSPC treated with ADT, providing a helpful benchmark for indirect comparisons of the benefits of the combination of chemotherapy and second-generation hormonotherapy.
引用
收藏
页码:1633 / 1644
页数:12
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