Choong Ee Siang, Hruby George, Yang Jean, Kwong Carol, Patanjali Nitya
Department of Radiation Oncology, Chris O'Brien Lifehouse, Camperdown, Sydney, New South Wales, Australia.
Department of Radiation Oncology, Royal North Shore Hospital, St Leonards, Sydney, New South Wales, Australia.
Asia Pac J Clin Oncol. 2017 Oct;13(5):e356-e363. doi: 10.1111/ajco.12637. Epub 2016 Nov 10.
In prostate cancer, fiducial marker image-guided radiotherapy (FMIGRT) allows correction of setup errors and interfraction physiological motion resulting in improved accuracy of target and sparing of at risk organs. We aim to report outcomes and toxicities observed in patients treated with dose escalation to 78Gy with FMIGRT in our center.
Retrospective review of consecutive patients with histologically confirmed T1-4N0M0 localized prostate cancer treated with dose escalation to 78Gy with FMIGRT in our center. All patients had 3-D conformal radiotherapy. Duration of androgen deprivation therapy use was tailored to risk group. Toxicity was scored according to CTCAE.v04. Kaplan-Meier analysis was performed for freedom from biochemical failure (FFBF), prostate cancer-specific survival and overall survival.
Median follow-up was 48.6 months. Median duration of androgen deprivation therapy was 6 and 23 months in the intermediate- and high-risk group, respectively. FFBF at 5 years was 88.8%. FFBFs when stratified to risk groups were 100% for low risk, 88.9% for low-intermediate risk, 89.9% for high-intermediate risk and 85.4% for high risk, respectively. Acute severe toxicity (grade≥3) rate for both genitourinary (GU) and gastrointestinal (GI) was 1%. Late moderate-to-severe toxicity (grade≥2) rates for GU and GI were 15% and 17%, respectively, with severe (grade≥3) toxicity rate for GU and GI at 2% and 3%, respectively.
Dose escalation to 78Gy with FMIGRT in our series achieved good FFBF at 5 years with low acute and late toxicity rates. These results provide a good comparator cohort to our current use of image-guided intensity modulated radiotherapy.
在前列腺癌中,基准标记图像引导放射治疗(FMIGRT)可校正摆位误差和分次间生理运动,从而提高靶区精度并保护危及器官。我们旨在报告在本中心接受FMIGRT剂量递增至78Gy治疗的患者中观察到的结果和毒性。
回顾性分析本中心连续接受FMIGRT剂量递增至78Gy治疗的组织学确诊为T1-4N0M0局限性前列腺癌患者。所有患者均接受三维适形放疗。雄激素剥夺治疗的持续时间根据风险组进行调整。毒性按照CTCAE.v04评分。对无生化失败(FFBF)、前列腺癌特异性生存和总生存进行Kaplan-Meier分析。
中位随访时间为48.6个月。中危组和高危组雄激素剥夺治疗的中位持续时间分别为6个月和23个月。5年时的FFBF为88.8%。按风险组分层时,低危组、低中危组、高中危组和高危组的FFBF分别为100%、88.9%、89.9%和85.4%。泌尿生殖系统(GU)和胃肠道(GI)的急性重度毒性(≥3级)发生率均为1%。GU和GI的晚期中重度毒性(≥2级)发生率分别为15%和17%,GU和GI的重度(≥3级)毒性发生率分别为2%和3%。
在我们的系列研究中,FMIGRT剂量递增至78Gy在5年时实现了良好的FFBF,且急性和晚期毒性发生率较低。这些结果为我们目前使用的图像引导调强放疗提供了一个良好的对照队列。