Department of Radiology, Duke University Medical Center, Durham, North Carolina.
Division of Hematology and Oncology, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
J Nucl Med. 2018 Nov;59(11):1708-1713. doi: 10.2967/jnumed.117.202150. Epub 2018 May 18.
This retrospective analysis identifies predictors of survival in a cohort of patients with meta-iodobenzylguanidine (MIBG)-positive stage IV pulmonary and gastroenteropancreatic neuroendocrine tumor (P/GEP-NET) treated with I-MIBG therapy, to inform treatment selection and posttreatment monitoring. Survival, symptoms, imaging, and biochemical response were extracted via chart review from 211 P/GEP-NET patients treated with I-MIBG between 1991 and 2014. For patients with CT follow-up ( = 125), imaging response was assessed by RECIST 1.1 if images were available ( = 76) or by chart review of the radiology report if images could not be reviewed ( = 49). Kaplan-Meier analysis and Cox multivariate regression estimated survival and progression-free survival benefits predicted by initial imaging, biochemical response, and symptomatic response. All patients had stage IV disease at the time of treatment. Median survival was 29 mo from the time of treatment. Symptomatic response was seen in 71% of patients, with the median duration of symptomatic relief being 12 mo. Symptomatic response at the first follow-up predicted a survival benefit of 30 mo ( < 0.001). Biochemical response at the first clinical follow-up was seen in 34% of patients, with stability of laboratory values in 48%; response/stability versus progression extended survival by 40 mo ( < 0.03). Imaging response (20% of patients) or stability (60%) at the initial 3-mo follow-up imaging extended survival by 32 mo ( < 0.001). Additionally, multiple I-MIBG treatments were associated with 24 mo of additional survival ( < 0.05). Therapeutic I-MIBG for metastatic P/GEP-NETs appears to be an effective means of symptom palliation. Imaging, biochemical, and symptomatic follow-up help prognosticate expected survival after I-MIBG therapy. Multiple rounds of I-MIBG are associated with prolonged survival.
这项回顾性分析确定了接受碘代苄胍(MIBG)治疗的 IV 期肺和胃肠胰腺神经内分泌肿瘤(P/GEP-NET)患者队列的生存预测因素,为治疗选择和治疗后监测提供信息。通过对 1991 年至 2014 年间接受 I-MIBG 治疗的 211 名 P/GEP-NET 患者的图表审查,提取了生存、症状、影像学和生化反应数据。对于有 CT 随访的患者(n=125),如果有图像(n=76),则根据 RECIST 1.1 评估影像学反应,如果无法查看图像,则根据放射学报告的图表审查评估影像学反应(n=49)。Kaplan-Meier 分析和 Cox 多变量回归估计了初始影像学、生化反应和症状反应预测的生存和无进展生存获益。所有患者在治疗时均为 IV 期疾病。从治疗开始到中位生存时间为 29 个月。71%的患者出现症状缓解,症状缓解的中位持续时间为 12 个月。首次随访时的症状缓解预测生存获益为 30 个月(<0.001)。首次临床随访时生化反应见于 34%的患者,实验室值稳定见于 48%;反应/稳定与进展相比,延长了 40 个月的生存时间(<0.03)。初始 3 个月随访影像学上的影像学反应(20%的患者)或稳定(60%)延长了 32 个月的生存时间(<0.001)。此外,多次 I-MIBG 治疗与额外 24 个月的生存时间相关(<0.05)。 对于转移性 P/GEP-NET,治疗性 I-MIBG 似乎是一种有效的缓解症状的方法。影像学、生化和症状随访有助于预测 I-MIBG 治疗后的预期生存。多轮 I-MIBG 与延长生存时间相关。