HCG Oncology Hospitals, Number 8, P Kalinga Rao Road, Near-GEO Hotel, Sampangirama Nagar, Bangalore, Karnataka, India,
Eur J Nucl Med Mol Imaging. 2014 Jul;41(7):1319-26. doi: 10.1007/s00259-014-2710-1. Epub 2014 Feb 26.
The choice of an appropriate treatment option in patients with inoperable or metastatic neuroendocrine tumours (NETs) is limited, and approximately 50 % of patients have advanced NET at diagnosis, and 65 % die within 5 years. Treatment with (177)Lu-DOTATATE ((177)Lu-[DOTA(0),Tyr(3)] octreotate) is a promising new option in the treatment of metastatic NETs.
Patients with metastatic NET who underwent (177)Lu-DOTATATE during the period 2009 to 2013 were included in this retrospective study. Follow-up imaging studies including a (68)Ga-DOTANOC PET/CT scan and a posttherapy (177)Lu-DOTATATE scan were compared with baseline imaging to determine response to treatment. Progression-free survival (PFS) was calculated using the Kaplan-Meier method and Cox regression analysis was also done.
Ten patients (25 %) had a minimal response, 13 (32.5 %) had a partial response and 9 (22.5 %) had stable disease. Progressive disease was seen in 8 patients (20 %), including 6 patients who died during or after the treatment period. The estimated mean PFS in those who received one or two cycles of (177)Lu-DOTATATE was 8.3 months (95 % CI 6.2 to 10.3 months) compared to an estimated mean PFS of 45.6 months (95 % CI 40.9 to 50.2 months) in those who received more than two cycles of (177)Lu-DOTATATE (log-rank Mantel-Cox Χ (2) = 8.01, p = 0.005).
Our study showed that treatment with (177)Lu-DOTATATE should be considered in the management of NETs, considering the limited success of alternative treatment modalities. Treatment response and PFS is determined primarily by the dose delivered and best results are obtained when more than two cycles of (177)Lu-DOTATATE are given, with careful monitoring for possible side effects.
对于无法手术或转移性神经内分泌肿瘤(NET)患者,选择合适的治疗方案受到限制。大约 50%的患者在诊断时已处于 NET 晚期,65%的患者在 5 年内死亡。(177)Lu-DOTATATE((177)Lu-[DOTA(0),Tyr(3)]octreotate)治疗是转移性 NET 治疗的一种有前途的新选择。
本回顾性研究纳入了 2009 年至 2013 年间接受(177)Lu-DOTATATE 治疗的转移性 NET 患者。通过与基线成像比较,对后续的(68)Ga-DOTANOC PET/CT 扫描和治疗后(177)Lu-DOTATATE 扫描来确定治疗反应。采用 Kaplan-Meier 法计算无进展生存期(PFS),并进行 Cox 回归分析。
10 名患者(25%)有轻微反应,13 名患者(32.5%)有部分反应,9 名患者(22.5%)疾病稳定。8 名患者(20%)出现疾病进展,包括 6 名在治疗期间或之后死亡的患者。接受 1 或 2 个周期(177)Lu-DOTATATE 治疗的患者中位 PFS 估计为 8.3 个月(95%CI 6.2-10.3 个月),而接受超过 2 个周期(177)Lu-DOTATATE 治疗的患者中位 PFS 估计为 45.6 个月(95%CI 40.9-50.2 个月)(对数秩 Mantel-Cox Χ(2)= 8.01,p = 0.005)。
我们的研究表明,(177)Lu-DOTATATE 治疗应考虑用于 NET 的治疗管理,因为替代治疗方法的疗效有限。治疗反应和 PFS 主要由所给予的剂量决定,当给予超过 2 个周期的(177)Lu-DOTATATE 时,可获得最佳结果,并应仔细监测可能的副作用。