Gresswell Steven, Wegner Rodney E, Werts Day, Miller Ralph, Fuhrer Russell
Division of Radiation Oncology, Allegheny General Hospital, Pittsburgh, Pennsylvania.
Division of Urology, Allegheny General Hospital, Pittsburgh, Pennsylvania.
Adv Radiat Oncol. 2016 Aug 18;1(4):317-324. doi: 10.1016/j.adro.2016.08.005. eCollection 2016 Oct-Dec.
A phase 2 protocol was designed and implemented to assess the toxicity and efficacy of hypofractionated image guided intensity modulated radiation therapy (IG-IMRT) combined with low-dose rate Pd prostate seed implant for treatment of localized intermediate- and high-risk adenocarcinoma of the prostate.
This is a report of an interim analysis on 24 patients enrolled on an institutional review board-approved phase 2 single-institution study of patients with intermediate- and high-risk adenocarcinoma of the prostate. The median pretreatment prostate-specific antigen level was 8.15 ng/mL. The median Gleason score was 4 + 3 = 7 (range, 3 + 4 = 7 - 4 + 4 = 8), and the median T stage was T2a. Of the 24 patients, 4 (17%) were high-risk patients as defined by the National Comprehensive Cancer Network criteria, version 2016. The treatment consisted of 2465 cGy in 493 cGy/fraction of IG-IMRT to the prostate and seminal vesicles. This was followed by a Pd transperineal prostate implant boost (prescribed dose to 90% of the prostate volume of 100 Gy) using intraoperative planning. Five patients received neoadjuvant, concurrent, and adjuvant androgen deprivation therapy.
The median follow-up was 18 months (range, 1-42 months). The median nadir prostate-specific antigen was 0.5 ng/mL and time to nadir was 16 months. There was 1 biochemical failure associated with distant metastatic disease without local failure. Toxicity (acute or late) higher than grade 3 was not observed. There was a single instance of late grade 3 genitourinary toxicity secondary to hematuria 2 years and 7 months after radiation treatment. There were no other grade 3 gastrointestinal or genitourinary toxicities.
Early results on the toxicity and efficacy of the combination of hypofractionated IG-IMRT and low-dose-rate brachytherapy boost are favorable. Longer follow-up is needed to confirm safety and effectiveness.
设计并实施一项2期试验方案,以评估大分割影像引导调强放射治疗(IG-IMRT)联合低剂量率钯前列腺籽源植入治疗局限性中高危前列腺腺癌的毒性和疗效。
这是一份关于24例患者的中期分析报告,这些患者参加了一项经机构审查委员会批准的2期单机构研究,该研究针对中高危前列腺腺癌患者。治疗前前列腺特异性抗原水平的中位数为8.15 ng/mL。Gleason评分中位数为4 + 3 = 7(范围为3 + 4 = 7 - 4 + 4 = 8),T分期中位数为T2a。在这24例患者中,根据2016年版美国国立综合癌症网络标准,4例(17%)为高危患者。治疗包括对前列腺和精囊进行IG-IMRT,每次分割剂量493 cGy,总剂量2465 cGy。随后使用术中计划进行经会阴钯前列腺植入物补充照射(规定剂量为前列腺体积的90%,100 Gy)。5例患者接受了新辅助、同步和辅助雄激素剥夺治疗。
中位随访时间为18个月(范围1 - 42个月)。前列腺特异性抗原最低点的中位数为0.5 ng/mL,达到最低点的时间为16个月。有1例生化复发与远处转移疾病相关,无局部复发。未观察到高于3级的毒性(急性或晚期)。放疗后2年7个月有1例因血尿继发的晚期3级泌尿生殖系统毒性。无其他3级胃肠道或泌尿生殖系统毒性。
大分割IG-IMRT联合低剂量率近距离放疗补充照射的毒性和疗效的早期结果良好。需要更长时间的随访来确认安全性和有效性。