Department of Radiation Oncology, Hannover Medical School, Hannover, Germany.
Department of Urology and Urologic Oncology, Hannover Medical School, Hannover, Germany.
Int J Radiat Oncol Biol Phys. 2019 Jan 1;103(1):95-104. doi: 10.1016/j.ijrobp.2018.08.066. Epub 2018 Sep 7.
To determine the patterns of progression after Ga prostate-specific membrane antigen (PSMA)-ligand positron emission tomography (PET)/computed tomography (CT)-guided radiation therapy (RT) for recurrent oligometastatic prostate cancer (PCa).
One hundred and eight patients with increased prostate-specific antigen levels, who received Ga-PSMA-ligand PET/CT-guided RT for recurrent oligometastatic disease after primary therapy for PCa were included. The biochemical progression-free survival and distant disease-free survival after PSMA-ligand PET/CT-guided RT were determined. The patterns of progression were determined using renewed Ga-PSMA-ligand PET/CT in patients with biochemical progression and compared with the clinical target volume of the Ga-PSMA-ligand PET/CT-guided RT. The frequency of infield and outfield relapses was recorded.
A total of 97.2% (105 of 108) of patients showed a decrease in prostate-specific antigen levels after RT and were classified as biochemical responders. After the median follow-up of 18 months, 43.5% (47 of 108) of the patients experienced biochemical progression, resulting in an estimated biochemical progression-free survival of 16 months. Renewed Ga-PSMA-ligand PET/CT allowed localization of recurrent disease in 91.7% (33 of 36) of patients. Analysis of the patterns of progression resulted in a cumulative infield relapse rate of 12.1% (4 of 33) and a cumulative outfield relapse rate of 87.9% (29 of 33). The resultant median disease-free survival was 11 months. In terms of the pattern of progression, we observed a shift in the pattern of metastases toward skeletal involvement and distant lymph node metastases. Of these patients, 45.5% (15 of 33) were treated with further RT to delay initiation or escalation of systemic therapies.
PSMA-ligand PET/CT-guided RT for relapsed PCa with limited tumor burden allowed individualization of treatment approaches, provided effective local control, and resulted in considerably prolonged biochemical progression-free survival. As indicated by the PSMA-ligand PET/CT-based patterns of progression, repeated PET/CT-guided RT may represent a treatment option in well-selected patients with relapse after RT for oligometastatic disease.
确定 Ga 前列腺特异性膜抗原(PSMA)-配体正电子发射断层扫描(PET)/计算机断层扫描(CT)引导放疗(RT)治疗复发性寡转移前列腺癌(PCa)后的进展模式。
本研究纳入了 108 例因 PCa 接受初始治疗后出现前列腺特异性抗原水平升高、接受 Ga-PSMA 配体 PET/CT 引导 RT 治疗复发性寡转移疾病的患者。评估 PSMA 配体 PET/CT 引导 RT 后患者的生化无进展生存期和远处无病生存期。在生化进展的患者中使用更新的 Ga-PSMA 配体 PET/CT 确定进展模式,并与 Ga-PSMA 配体 PET/CT 引导 RT 的临床靶区进行比较。记录场内和场外复发的频率。
97.2%(105/108)的患者在 RT 后前列腺特异性抗原水平下降,被归类为生化缓解者。中位随访 18 个月后,43.5%(47/108)的患者出现生化进展,估计生化无进展生存期为 16 个月。更新的 Ga-PSMA 配体 PET/CT 可在 91.7%(33/36)的患者中定位复发性疾病。进展模式分析显示,累计场内复发率为 12.1%(4/33),累计场外复发率为 87.9%(29/33)。中位无病生存期为 11 个月。就进展模式而言,我们观察到转移模式向骨骼受累和远处淋巴结转移转移。在这些患者中,45.5%(15/33)接受了进一步的 RT 治疗,以延迟或升级全身治疗的开始。
对于复发性前列腺癌,Ga PSMA 配体 PET/CT 引导 RT 可使肿瘤负荷有限的患者个体化治疗,提供有效的局部控制,并显著延长生化无进展生存期。基于 PSMA 配体 PET/CT 的进展模式,对于 RT 治疗寡转移疾病后复发的精选患者,重复 PET/CT 引导 RT 可能是一种治疗选择。