Efficacy of docetaxel addition to next-generation androgen receptor-axis-targeted therapies and androgen deprivation therapy in metastatic hormone-sensitive prostate cancer: A tumor volume-specific analysis.

IF 1.8 3区 医学 Q3 UROLOGY & NEPHROLOGY
Wei Chen, Soichiro Yoshida, Noriyoshi Miura, Shohei Fukuda, Yuma Waseda, Hajime Tanaka, Yasuhisa Fujii
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引用次数: 0

Abstract

Background: The effectiveness of docetaxel in addition to next-generation androgen receptor-axis-targeted therapies and androgen deprivation therapy (ADT) for metastatic hormone-sensitive prostate cancer (mHSPC) remains unclear. We evaluated the efficacy of this combination through tumor volume-specific analysis.

Methods: Individual patient data were reconstructed from seven clinical trials focusing mHSPC (ARASENS, PEACE-1, TITAN, ENZAMET, ARCHES, STAMPEDE, and LATITUDE) through the Shiny method. Overall survival (OS), radiological progression-free survival (rPFS), and time to castration-resistant prostate cancer (CRPC) were analyzed in the overall cohort and tumor volume-specific (high/low) subgroups. Sensitivity analyses were performed based on treatment methods and metastasis onset.

Results: In 6931 cases, adding docetaxel to ARAT and ADT did not significantly improve OS (hazard ratio [HR] = 1.07, 95% confidence interval [CI]: 0.95-1.22, p = 0.27), rPFS (HR = 0.88, 95% CI: 0.73-1.05, p = 0.16), or time to CRPC (HR = 0.97, 95% CI: 0.80-1.18, p = 0.74). High-volume disease showed a non-significant trend toward improved OS with the triplet regimen. Low-volume disease showed a similar trend. Sensitivity analyses for second-generation androgen receptor inhibitors indicated potentially less advantageous OS with docetaxel addition, but no significant differences when stratified by tumor volume. Analyses of the docetaxel-naïve, abiraterone, and synchronous metastasis subgroups showed no statistically significant differences in OS compared with the overall population and volume-stratified cases.

Conclusions: Patients with mHSPC did not show significant improvement with docetaxel addition to ARAT-based regimens, regardless of tumor volume. Further research is needed to identify potential beneficiaries of this combination therapy.

多西紫杉醇联合新一代雄激素受体轴靶向治疗和雄激素剥夺治疗转移性激素敏感前列腺癌的疗效:肿瘤体积特异性分析
背景:多西紫杉醇联合下一代雄激素受体轴靶向治疗和雄激素剥夺治疗(ADT)治疗转移性激素敏感前列腺癌(mHSPC)的有效性尚不清楚。我们通过肿瘤体积特异性分析来评估这种联合疗法的疗效。方法:通过Shiny方法重建7项以mHSPC为重点的临床试验(ARASENS、PEACE-1、TITAN、ENZAMET、ARCHES、STAMPEDE和LATITUDE)的个体患者数据。在总体队列和肿瘤体积特异性(高/低)亚组中分析总生存期(OS)、放射学无进展生存期(rPFS)和发生去势抵抗性前列腺癌(CRPC)的时间。根据治疗方法和转移发生情况进行敏感性分析。结果:6931例患者中,多西他赛联合ARAT和ADT均未显著改善OS(风险比[HR] = 1.07, 95%可信区间[CI]: 0.95 ~ 1.22, p = 0.27)、rPFS (HR = 0.88, 95% CI: 0.73 ~ 1.05, p = 0.16)和CRPC时间(HR = 0.97, 95% CI: 0.80 ~ 1.18, p = 0.74)。高容量疾病在三联体方案中表现出改善OS的无显著趋势。小体积疾病表现出类似的趋势。第二代雄激素受体抑制剂的敏感性分析表明,多西紫杉醇加药可能对OS不利,但按肿瘤体积分层时无显著差异。docetaxel-naïve、阿比特龙和同步转移亚组的分析显示,与总体人群和体积分层病例相比,OS无统计学差异。结论:无论肿瘤体积大小,mHSPC患者在多西他赛加用arat方案后均未显示出显著改善。需要进一步的研究来确定这种联合治疗的潜在受益者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Urology
International Journal of Urology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
11.50%
发文量
340
审稿时长
3 months
期刊介绍: International Journal of Urology is the official English language journal of the Japanese Urological Association, publishing articles of scientific excellence in urology. Submissions of papers from all countries are considered for publication. All manuscripts are subject to peer review and are judged on the basis of their contribution of original data and ideas or interpretation.
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