Texas Oncology and Department of Medicine, Section of Medical Oncology, Baylor College of Medicine, Houston, Texas, USA.
Cancer. 2011 Sep 1;117(17):3963-71. doi: 10.1002/cncr.25982. Epub 2011 Mar 1.
In men with metastatic castration-resistant prostate cancer (CRPC), the association of measurable tumor responses with overall survival (OS) is unknown. The authors retrospectively evaluated the TAX327 phase 3 trial to study this relation.
Eligible patients for this analysis included those with World Health Organization (WHO)-defined measurable metastatic disease randomized to receive either docetaxel or mitoxantrone. OS was estimated by using the Kaplan-Meier method, and the prognostic relation of WHO-defined radiologic response with OS was performed by using Cox proportional hazards regression. Landmark analyses evaluated survival from baseline and at 2, 3, 4, and 6 months after baseline.
Four hundred twelve patients enrolled on the TAX327 trial had measurable tumors. Thirty-seven patients exhibited a complete or partial objective response (CR/PR, 9.0%), 116 had stable disease (SD, 28.2%), 99 had progressive disease (PD, 24%) and 160 (38.8%) did not have a after-baseline objective assessment. Partial responders demonstrated longer median OS (29.0 months) than patients with SD (22.1 months) or those with PD (10.8 months) or those who were not assessed (12.7 months). These results remained after landmark analysis. The authors found a significant association between ≥ 30% prostate-specific antigen (PSA) declines and radiologic response, with ≥ 30% PSA declines occurring in all patients with CR/PR, 79.8% of patients with SD, and 34.4% with PD. Radiologic response remained a significant but modest post-treatment prognostic factor for OS after adjusting for treatment, pain response, and ≥ 30% PSA decline (P = .009).
In men with metastatic CRPC and measurable disease receiving chemotherapy, objective tumor response was prognostic for OS and appeared to complement PSA assessment.
在转移性去势抵抗性前列腺癌(CRPC)患者中,可测量肿瘤反应与总生存期(OS)的关系尚不清楚。作者回顾性评估了 TAX327 期 3 试验,以研究这种关系。
本分析纳入了符合条件的患者,这些患者具有世界卫生组织(WHO)定义的可测量转移性疾病,随机接受多西他赛或米托蒽醌治疗。采用 Kaplan-Meier 法估计 OS,并采用 Cox 比例风险回归法对 WHO 定义的影像学反应与 OS 的预后关系进行分析。 landmark 分析评估了从基线和基线后 2、3、4 和 6 个月的生存情况。
TAX327 试验共纳入 412 例可测量肿瘤患者。37 例患者出现完全或部分客观缓解(CR/PR,9.0%),116 例患者疾病稳定(SD,28.2%),99 例患者疾病进展(PD,24%),160 例(38.8%)患者无基线后客观评估。部分缓解患者的中位 OS (29.0 个月)长于 SD 患者(22.1 个月)或 PD 患者(10.8 个月)或未评估患者(12.7 个月)。这些结果在 landmark 分析后仍然存在。作者发现,与 PSA 下降≥30%相比,≥30%PSA 下降与影像学反应之间存在显著相关性,CR/PR 患者的所有患者均发生≥30%PSA 下降,SD 患者的 79.8%和 PD 患者的 34.4%发生≥30%PSA 下降。调整治疗、疼痛反应和≥30%PSA 下降后,影像学反应仍然是 OS 的一个显著但适度的治疗后预后因素(P=0.009)。
在接受化疗的转移性 CRPC 且有可测量疾病的男性中,肿瘤客观缓解是 OS 的预后因素,并且似乎补充了 PSA 评估。