Glenn Heller, Martin Fleisher, and Howard I. Scher, Memorial Sloan Kettering Cancer Center; Howard I. Scher, Weill Cornell Medical College, New York, NY; Robert McCormack, Janssen Research & Development, Raritan, NJ; Thian Kheoh and Arturo Molina, Janssen Research & Development, Los Angeles; Dana T. Aftab, Exelixis, South San Francisco; Mohammad Hirmand, Medivation, San Francisco, CA; Matthew R. Smith, Massachusetts General Hospital, Boston; Ana Limon, Takeda Oncology, Cambridge, MA; Robert Dreicer, University of Virginia Medical School, Charlottesville, VA; Fred Saad, University of Montreal, Montreal, Quebec, Canada; Ronald de Wit, Erasmus Medical Center, Rotterdam, the Netherlands; Karim Fizazi, Institut Gustave Roussy, Villejuif, and University of Paris Sud, Orsay, France; and Johann S. de Bono, The Institute of Cancer Research, and The Royal Marsden Hospital, Sutton, Surrey, United Kingdom.
J Clin Oncol. 2018 Feb 20;36(6):572-580. doi: 10.1200/JCO.2017.75.2998. Epub 2017 Dec 22.
Purpose Measures of response that are clinically meaningful and occur early are an unmet need in metastatic castration-resistant prostate cancer clinical research and practice. We explored, using individual patient data, week 13 circulating tumor cell (CTC) and prostate-specific antigen (PSA) response end points in five prospective randomized phase III trials that enrolled a total of 6,081 patients-COU-AA-301, AFFIRM, ELM-PC-5, ELM-PC-4, and COMET-1- ClinicalTrials.Gov identifiers: NCT00638690, NCT00974311, NCT01193257, NCT01193244, and NCT01605227, respectively. Methods Eight response end points were explored. CTC nonzero at baseline and 0 at 13 weeks (CTC0); CTC conversion (≥ 5 CTCs at baseline, ≤ 4 at 13 weeks-the US Food and Drug Administration cleared response measure); a 30%, 50%, and 70% decrease in CTC count; and a 30%, 50%, and 70% decrease in PSA level. Patients missing week-13 values were considered nonresponders. The discriminatory strength of each end point with respect to overall survival in each trial was assessed using the weighted c-index. Results Of the eight response end points, CTC0 and CTC conversion had the highest weighted c-indices, with smaller standard deviations. For CTC0, the mean (standard deviation) was 0.81 (0.04); for CTC conversion, 0.79 (0.03); for 30% decrease in CTC count, 0.72 (0.06); for 50% decrease in CTC count, 0.72 (0.06); for 70% decrease in CTC count, 0.73 (0.05); for 30% decrease in PSA level, 0.71 (0.03); for 50% decrease in PSA level, 0.72 (0.06); and for 70% decrease in PSA level, 0.74 (0.05). Seventy-five percent of eligible patients could be evaluated with the CTC0 end point, compared with 51% with the CTC conversion end point. Conclusion The CTC0 and CTC conversion end points had the highest discriminatory power for overall survival. Both are robust and meaningful response end points for early-phase metastatic castration-resistant prostate cancer clinical trials. CTC0 is applicable to a significantly higher percentage of patients than CTC conversion.
在转移性去势抵抗性前列腺癌的临床研究和实践中,具有临床意义且早期发生的反应测量是未满足的需求。我们使用个体患者数据,探索了五项前瞻性随机 III 期试验中第 13 周的循环肿瘤细胞(CTC)和前列腺特异性抗原(PSA)反应终点,这些试验共纳入了 6081 名患者-COU-AA-301、AFFIRM、ELM-PC-5、ELM-PC-4 和 COMET-1-ClinicalTrials.gov 标识符:NCT00638690、NCT00974311、NCT01193257、NCT01193244 和 NCT01605227。
探索了 8 种反应终点。基线时 CTC 非零且第 13 周时 CTC0(CTC 为零);CTC 转换(基线时 CTC≥5,第 13 周时 CTC≤4-美国食品和药物管理局批准的反应测量);CTC 计数减少 30%、50%和 70%;PSA 水平降低 30%、50%和 70%。第 13 周缺失值的患者被视为无反应者。使用加权 c 指数评估每个试验中每个终点与总生存期的鉴别强度。
在 8 种反应终点中,CTC0 和 CTC 转换具有最高的加权 c 指数,且标准差较小。对于 CTC0,平均值(标准差)为 0.81(0.04);对于 CTC 转换,0.79(0.03);对于 CTC 计数减少 30%,0.72(0.06);对于 CTC 计数减少 50%,0.72(0.06);对于 CTC 计数减少 70%,0.73(0.05);对于 PSA 水平降低 30%,0.71(0.03);对于 PSA 水平降低 50%,0.72(0.06);对于 PSA 水平降低 70%,0.74(0.05)。有 75%的合格患者可以用 CTC0 终点进行评估,而用 CTC 转换终点进行评估的患者比例为 51%。
CTC0 和 CTC 转换终点对总生存期具有最高的鉴别能力。两者都是转移性去势抵抗性前列腺癌早期临床试验中稳健且有意义的反应终点。CTC0 比 CTC 转换适用于更高比例的患者。