Department of Radiation Oncology, University of Miami, Miami, Florida.
Department of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts.
JAMA Netw Open. 2023 Nov 1;6(11):e2340787. doi: 10.1001/jamanetworkopen.2023.40787.
Patients with high-grade prostate cancer with low levels of prostate-specific antigen (PSA; <4 ng/mL) are at high risk of mortality, necessitating an improved treatment paradigm.
To assess for these patients whether adding docetaxel to standard of care (SOC) treatment is associated with decreased prostate cancer-specific mortality (PCSM) and all-cause mortality (ACM).
PubMed search from 2000 to 2022.
Five prospective randomized clinical trials (RCTs) performed in the US, France, and the United Kingdom evaluating SOC treatment with radiotherapy and androgen deprivation therapy (ADT) or with radical prostatectomy vs SOC plus docetaxel.
Individual data were included from patients with nonmetastatic prostate cancer, a PSA level of less than 4 ng/mL, and a Gleason score of 8 to 10. Patients initiated treatment between February 21, 2006, and December 31, 2015 (median follow-up, 7.1 [IQR, 5.4-9.9] years). Data were analyzed on December 16, 2022.
Hazard ratio (HR) of ACM and subdistribution HR (sHR) of PCSM adjusted for performance status (1 vs 0 or good health), Gleason score (9 or 10 vs 8), tumor category (T3-T4 vs T1-T2 or TX), and duration of ADT (2 years vs 4-6 months).
From a cohort of 2184 patients, 145 patients (6.6%) in 4 RCTs were eligible (median age, 63 [IQR, 46-67] years). Thirty-one patients died, and of these deaths, 22 were due to prostate cancer. Performance status was 0 for 139 patients (95.9%) and 1 for 6 patients (4.1%). A reduced but nonsignificant risk of ACM (HR, 0.51 [95% CI, 0.24-1.09]) and PCSM (sHR, 0.42 [95% CI, 0.17-1.02]) was associated with patients randomized to SOC plus docetaxel compared with SOC. The risk reduction in ACM (HR, 0.46 [95% CI, 0.21-1.02]) was more pronounced among patients with a performance status of 0 and was significant for PCSM (sHR, 0.30 [95% CI, 0.11-0.86]).
Adding docetaxel to SOC treatment for patients who are in otherwise good health with a PSA level of less than 4 ng/mL and a Gleason score of 8 to 10 was associated with a significant reduction in PCSM and therefore has the potential to improve prognosis.
前列腺特异性抗原(PSA;<4ng/mL)水平较低的高级别前列腺癌患者死亡率较高,需要改进治疗方案。
评估对于这些患者,在标准治疗(SOC)基础上添加多西他赛是否会降低前列腺癌特异性死亡率(PCSM)和全因死亡率(ACM)。
2000 年至 2022 年 PubMed 检索。
在美国、法国和英国进行的五项评估 SOC 治疗联合放疗和雄激素剥夺治疗(ADT)或根治性前列腺切除术与 SOC 加多西他赛的前瞻性随机临床试验(RCT)。
纳入了非转移性前列腺癌、PSA 水平<4ng/mL 和 Gleason 评分 8 至 10 的患者的个体数据。患者于 2006 年 2 月 21 日至 2015 年 12 月 31 日(中位随访时间,7.1[IQR,5.4-9.9]年)开始治疗。数据分析于 2022 年 12 月 16 日进行。
ACM 的风险比(HR)和 PCSM 的亚分布 HR(sHR),调整了表现状态(1 与 0 或健康良好)、Gleason 评分(9 或 10 与 8)、肿瘤类别(T3-T4 与 T1-T2 或 TX)和 ADT 持续时间(2 年与 4-6 个月)。
从 2184 名患者的队列中,4 项 RCT 中有 145 名(6.6%)患者符合条件(中位年龄 63[IQR,46-67]岁)。31 名患者死亡,其中 22 名死于前列腺癌。139 名患者表现状态为 0(95.9%),6 名患者为 1(4.1%)。与 SOC 相比,SOC 加多西他赛治疗的患者 ACM(HR,0.51[95%CI,0.24-1.09])和 PCSM(sHR,0.42[95%CI,0.17-1.02])的风险降低,但无统计学意义。在表现状态为 0 的患者中,ACM(HR,0.46[95%CI,0.21-1.02])的风险降低更为明显,并且对 PCSM 具有统计学意义(sHR,0.30[95%CI,0.11-0.86])。
对于 PSA 水平<4ng/mL 和 Gleason 评分 8 至 10 的健康状况良好的患者,在 SOC 治疗的基础上添加多西他赛与 PCSM 显著降低相关,因此有可能改善预后。