Zhang Jingsong, Gallaher Jill, Cunningham Jessica J, Choi Jung W, Ionescu Filip, Chatwal Monica S, Jain Rohit, Kim Youngchul, Wang Liang, Brown Joel S, Anderson Alexander R, Gatenby Robert A
Department of Genitourinary Oncology, Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Department of Integrated Mathematical Oncology, Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Cancers (Basel). 2022 Oct 25;14(21):5225. doi: 10.3390/cancers14215225.
Background: We hypothesize that cancer survival can be improved through adapting treatment strategies to cancer evolutionary dynamics and conducted a phase 1b study in metastatic castration sensitive prostate cancer (mCSPC). Methods: Men with asymptomatic mCSPC were enrolled and proceeded with a treatment break after achieving > 75% PSA decline with LHRH analog plus an NHA. ADT was restarted at the time of PSA or radiographic progression and held again after achieving >50% PSA decline. This on-off cycling of ADT continued until on treatment imaging progression. Results: At data cut off in August 2022, only 2 of the 16 evaluable patients were off study due to imaging progression at 28 months from first dose of LHRH analog for mCSPC. Two additional patients showed PSA progression at 12.4 and 20.5 months and remain on trial. Since none of the 16 patients developed imaging progression at 12 months, the study succeeded in its primary objective of feasibility. The secondary endpoints of median time to PSA progression and median time to radiographic progression have not been reached at a median follow up of 26 months. Conclusions: It is feasible to use an individual’s PSA response and testosterone levels to guide intermittent ADT in mCSPC.
我们假设通过使治疗策略适应癌症进化动力学可以提高癌症生存率,并在转移性去势敏感性前列腺癌(mCSPC)中开展了一项1b期研究。方法:纳入无症状mCSPC男性患者,在使用促黄体生成素释放激素(LHRH)类似物加一种新型雄激素合成酶抑制剂(NHA)使前列腺特异性抗原(PSA)下降>75%后进行治疗中断。在PSA或影像学进展时重新开始雄激素剥夺治疗(ADT),在PSA下降>50%后再次中断。这种ADT的开关循环持续到治疗期间影像学进展。结果:在2022年8月数据截止时,16例可评估患者中只有2例因影像学进展在首次给予mCSPC的LHRH类似物后28个月退出研究。另外2例患者分别在12.4个月和20.5个月出现PSA进展,仍在试验中。由于16例患者中无一人在12个月时出现影像学进展,该研究成功实现了其可行性的主要目标。在中位随访26个月时,尚未达到PSA进展的中位时间和影像学进展的中位时间这些次要终点。结论:利用个体的PSA反应和睾酮水平来指导mCSPC的间歇性ADT是可行的。