Tucci Marcello, Bertaglia Valentina, Vignani Francesca, Buttigliero Consuelo, Fiori Cristian, Porpiglia Francesco, Scagliotti Giorgio Vittorio, Di Maio Massimo
Division of Medical Oncology, Department of Oncology, University of Turin, San Luigi Gonzaga Hospital, Orbassano, Turin, Italy.
Division of Urology, Department of Oncology, University of Turin, San Luigi Gonzaga Hospital, Orbassano, Turin, Italy.
Eur Urol. 2016 Apr;69(4):563-573. doi: 10.1016/j.eururo.2015.09.013. Epub 2015 Sep 28.
Several randomized clinical trials (RCTs) have recently tested the early addition of docetaxel to androgen deprivation therapy (ADT) in hormone-sensitive metastatic prostate cancer (PCa).
To perform a systematic review and meta-analysis of RCTs evaluating the combination of docetaxel and ADT in hormone-sensitive metastatic PCa. The primary end point was overall survival (OS). Secondary end point was progression-free survival. Exploratory subgroup analysis according to high-volume versus low-volume disease was performed.
A systematic review of PubMed/Medline, Embase, and the proceedings of major international meetings was performed in June 2015 and updated in August 2015. Three trials were selected for inclusion.
Overall, 2951 patients were included in the three trials. Two trials enrolled only metastatic patients; in the third trial, 61% were metastatic. A total of 2262 patients (951 docetaxel and ADT; 1311 ADT alone) were metastatic. Most patients had a good performance status. In metastatic patients, the addition of docetaxel was associated with improved OS (hazard ratio [HR]: 0.73; 95% confidence interval [CI], 0.60-0.90; p=0.002), with nonsignificant heterogeneity among the three trials. Considering the whole study population (2951 patients), the addition of docetaxel was associated with a similar OS improvement (HR: 0.74; 95% CI, 0.61-0.91; p=0.003). Although with limited statistical power, no significant interaction was demonstrated between the addition of docetaxel and the high or low volume of disease (p=0.5). The addition of docetaxel was associated with improvement in progression-free survival (metastatic patients: HR: 0.63; 95% CI, 0.57-0.70; p<0.001).
This meta-analysis shows a significant OS benefit from concomitant administration of docetaxel and ADT in patients with metastatic hormone-sensitive PCa.
We synthesized the evidence available about the early administration of docetaxel in patients starting hormonal treatment for metastatic prostate cancer. Based on the results of this meta-analysis, we believe the combination of chemotherapy and hormonal treatment should be considered in fit patients.
近期多项随机临床试验(RCT)对在激素敏感性转移性前列腺癌(PCa)的雄激素剥夺治疗(ADT)中早期加用多西他赛进行了测试。
对评估多西他赛与ADT联合用于激素敏感性转移性PCa的RCT进行系统评价和荟萃分析。主要终点为总生存期(OS)。次要终点为无进展生存期。根据高肿瘤负荷与低肿瘤负荷疾病进行探索性亚组分析。
2015年6月对PubMed/Medline、Embase及主要国际会议论文集进行了系统评价,并于2015年8月更新。选择三项试验纳入分析。
总体而言,三项试验共纳入2951例患者。两项试验仅纳入转移性患者;在第三项试验中,61%为转移性患者。共有2262例患者(951例接受多西他赛与ADT联合治疗;1311例仅接受ADT治疗)为转移性患者。大多数患者的体能状态良好。在转移性患者中,加用多西他赛与OS改善相关(风险比[HR]:0.73;95%置信区间[CI],0.60 - 0.90;p = 0.002),三项试验间异质性无统计学意义。考虑整个研究人群(2951例患者),加用多西他赛与相似的OS改善相关(HR:0.74;95% CI,0.61 - 0.91;p = 0.003)。尽管统计学效力有限,但多西他赛的加用与高或低肿瘤负荷疾病之间未显示出显著交互作用(p = 0.5)。加用多西他赛与无进展生存期改善相关(转移性患者:HR:0.63;95% CI,0.57 - 0.70;p < 0.001)。
这项荟萃分析表明,在转移性激素敏感性PCa患者中,多西他赛与ADT联合应用可显著改善OS。
我们综合了关于在开始接受转移性前列腺癌激素治疗的患者中早期应用多西他赛的现有证据。基于这项荟萃分析的结果,我们认为适合的患者应考虑化疗与激素治疗联合应用。