Morris Michael J, Molina Arturo, Small Eric J, de Bono Johann S, Logothetis Christopher J, Fizazi Karim, de Souza Paul, Kantoff Philip W, Higano Celestia S, Li Jinhui, Kheoh Thian, Larson Steven M, Matheny Shannon L, Naini Vahid, Burzykowski Tomasz, Griffin Thomas W, Scher Howard I, Ryan Charles J
Michael J. Morris, Steven M. Larson, and Howard I. Scher, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY; Arturo Molina, Thian Kheoh, Shannon L. Matheny, Vahid Naini, and Thomas W. Griffin, Janssen Research & Development, Los Angeles; Eric J. Small and Charles J. Ryan, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA; Johann S. de Bono, Institute for Cancer Research and Royal Marsden Hospital, Sutton, United Kingdom; Christopher J. Logothetis, MD Anderson Cancer Center, Houston, TX; Karim Fizazi, Institut Gustave Roussy, University of Paris Sud, Villejuif, France; Paul de Souza, University of Western Sydney School of Medicine, Ingham Institute, Liverpool, New South Wales, Australia; Philip W. Kantoff, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA; Celestia S. Higano, University of Washington, Seattle, WA; Jinhui Li, Janssen Research & Development, Raritan, NJ; and Tomasz Burzykowski, International Drug Development Institute, Louvain-la-Neuve, Belgium.
J Clin Oncol. 2015 Apr 20;33(12):1356-63. doi: 10.1200/JCO.2014.55.3875. Epub 2015 Jan 26.
Progression-free survival (PFS) in metastatic castration-resistant prostate cancer (mCRPC) trials has been inconsistently defined and poorly associated with overall survival (OS). A reproducible quantitative definition of radiographic PFS (rPFS) was tested for association with a coprimary end point of OS in a randomized trial of abiraterone in patients with mCRPC.
rPFS was defined as ≥ two new lesions on an 8-week bone scan plus two additional lesions on a confirmatory scan, ≥ two new confirmed lesions on any scan ≥ 12 weeks after random assignment, and/or progression in nodes or viscera on cross-sectional imaging, or death. rPFS was assessed by independent review at 15% of deaths and by investigator review at 15% and 40% of deaths. rPFS and OS association was evaluated by Spearman's correlation.
A total of 1,088 patients were randomly assigned to abiraterone plus prednisone or prednisone alone. At first interim analysis, the hazard ratio (HR) by independent review was 0.43 (95% CI, 0.35 to 0.52; P < .001; abiraterone plus prednisone: median rPFS, not estimable; prednisone: median rPFS, 8.3 months). Similar HRs were obtained by investigator review at the first two interim analyses (HR, 0.49; 95% CI, 0.41 to 0.60; P < .001 and HR, 0.53; 95% CI, 0.45 to 0.62; P < .001, respectively), validating the imaging data assay used. Spearman's correlation coefficient between rPFS and OS was 0.72.
rPFS was highly consistent and highly associated with OS, providing initial prospective evidence on further developing rPFS as an intermediate end point in mCRPC trials.
转移性去势抵抗性前列腺癌(mCRPC)试验中的无进展生存期(PFS)定义不一致,且与总生存期(OS)的相关性较差。在一项阿比特龙治疗mCRPC患者的随机试验中,对影像学无进展生存期(rPFS)的可重复定量定义进行了测试,以评估其与OS这一共同主要终点的相关性。
rPFS定义为:8周骨扫描出现≥2个新病灶,且确认扫描出现另外2个病灶;随机分组后≥12周的任何扫描出现≥2个新的确诊病灶;和/或横断面成像显示淋巴结或内脏进展,或死亡。在15%的死亡病例时由独立审查评估rPFS,在15%和40%的死亡病例时由研究者审查评估rPFS。通过Spearman相关性评估rPFS与OS的关联。
共有1088例患者被随机分配至阿比特龙加泼尼松组或单独泼尼松组。在首次中期分析时,独立审查得出的风险比(HR)为0.43(95%CI,0.35至0.52;P<.001;阿比特龙加泼尼松组:中位rPFS,无法估计;泼尼松组:中位rPFS,8.3个月)。在前两次中期分析时,研究者审查得出了相似的HR(分别为HR,0.49;95%CI,0.41至0.60;P<.001和HR,0.53;95%CI,0.45至0.62;P<.001),验证了所使用的影像数据分析方法。rPFS与OS之间的Spearman相关系数为0.72。
rPFS高度一致且与OS高度相关,为在mCRPC试验中进一步将rPFS发展为中间终点提供了初步的前瞻性证据。