Icon Cancer Centre, Richmond, VIC, Australia.
Department of Surgery, Monash University, Clayton, VIC, Australia.
Int J Cancer. 2020 Jan 1;146(1):161-168. doi: 10.1002/ijc.32509. Epub 2019 Jun 28.
Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospective, single institution study of men relapsing with up to five synchronous lesions following definitive local treatment for primary PCa. Our aim was to determine the proportion of patients not requiring treatment escalation following SBRT. In total, 199 patients were enrolled to receive fractionated SBRT (50 Gray in 10 fractions) to each visible lesion. Fourteen patients were castration resistant at enrolment. The proportion of patients not requiring treatment escalation 2 years following SBRT was 51.7% (95% CI: 44.1-59.3%). The median length of treatment escalation-free survival over the entire follow-up period was 27.1 months (95% CI; 21.8-29.4 months). Prior androgen deprivation therapy (ADT) predicted a significantly lower rate of freedom from treatment escalation at 2 years compared to no prior ADT (odds ratio = 0.21, 95% CI: 0.08-0.54, p = 0.001). There was no difference in the efficacy of SBRT when treating 4-5 vs. 1-3 initial lesions. A prostate-specific antigen (PSA) decline was induced in 75% of patients, with PSA readings falling to an undetectable level in six patients. No late grade three toxicities were observed. These interim results suggest that SBRT can be used to treat up to five synchronous PCa oligometastases to delay treatment escalation.
立体定向体部放疗(SBRT)可延迟寡转移前列腺癌(PCa)男性患者进展至全身治疗。然而,仍需要大型前瞻性研究来评估该方法在不同患者群体中的疗效。这是一项针对局部治疗初发 PCa 后复发最多 5 个同步转移灶的男性患者的前瞻性单机构研究的中期分析。我们的目的是确定 SBRT 后无需进行治疗升级的患者比例。共有 199 例患者接受了分次 SBRT(50Gy,10 次)治疗每个可见病灶。入组时有 14 例患者存在去势抵抗。SBRT 后 2 年无需治疗升级的患者比例为 51.7%(95%CI:44.1-59.3%)。整个随访期间无治疗升级的中位无进展生存时间为 27.1 个月(95%CI;21.8-29.4 个月)。与无先前 ADT 相比,先前接受雄激素剥夺治疗(ADT)显著降低了 2 年内免于治疗升级的比例(比值比=0.21,95%CI:0.08-0.54,p=0.001)。治疗 4-5 个与 1-3 个初始病灶的 SBRT 疗效无差异。75%的患者诱导了前列腺特异性抗原(PSA)下降,6 例患者的 PSA 读数降至无法检测水平。未观察到晚期 3 级毒性。这些中期结果表明,SBRT 可用于治疗多达 5 个同步的 PCa 寡转移灶,以延迟治疗升级。