From the Section of Hematology/Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA.
Section of Medical Oncology, Department of Medicine, Yale Cancer Center, Yale School of Medicine, New Haven, CT.
Pancreas. 2021 Jul 1;50(6):890-894. doi: 10.1097/MPA.0000000000001841.
Peptide receptor radionuclide therapy (PRRT) is a treatment option for somatostatin receptor-positive, unresectable or metastatic neuroendocrine tumors (NETs). Despite high disease control rates seen with PRRT, a subset of the NET population seems to have a short progression-free interval. We hypothesize that patients with NETs with rapid progression post-PRRT may have mixed low- and high-grade cell populations, and PRRT treats the lower-grade component, allowing the more aggressive high-grade component to progress.We report 7 patients with biopsy-proven NET who received PRRT with 177Lu-DOTATATE at the Stanford Cancer Center who had evidence of progressive disease (PD) on or within 6 months of therapy.All patients had primary pancreatic, metastatic, well-differentiated NET on diagnosis and were heavily pretreated before receiving PRRT. Two patients had PD while on PRRT; 5 had PD within 6 months of completing PRRT. The median time from the last cycle to PD was 3.2 months (range, 1.1-4.6 months). The median progression-free survival was 7.7 months (95% confidence interval, 5.7-9.8 months). Three patients had a repeat biopsy post-PRRT, 2 of which demonstrated higher disease grade compared with their initial pathology. Further evaluation in larger patient cohorts is warranted to elucidate predictive factors of PRRT response/nonresponse to enable better patient selection.
肽受体放射性核素治疗(PRRT)是治疗生长抑素受体阳性、不可切除或转移性神经内分泌肿瘤(NET)的一种选择。尽管 PRRT 可实现高疾病控制率,但一部分 NET 患者似乎存在较短的无进展间隔。我们假设 PRRT 后快速进展的 NET 患者可能具有混合的低级别和高级别细胞群体,PRRT 治疗低级别的成分,从而使更具侵袭性的高级别成分进展。我们报告了 7 名在斯坦福癌症中心接受 177Lu-DOTATATE 治疗的经活检证实的 NET 患者,这些患者在治疗期间或治疗后 6 个月内出现疾病进展(PD)的证据。所有患者在诊断时均患有原发性胰腺、转移性、分化良好的 NET,并在接受 PRRT 治疗前接受了大量预处理。2 名患者在 PRRT 期间出现 PD;5 名患者在完成 PRRT 后 6 个月内出现 PD。从最后一个周期到 PD 的中位时间为 3.2 个月(范围为 1.1-4.6 个月)。无进展生存期的中位数为 7.7 个月(95%置信区间为 5.7-9.8 个月)。3 名患者在 PRRT 后进行了重复活检,其中 2 名患者的疾病分级高于其初始病理学。需要在更大的患者队列中进一步评估,以阐明 PRRT 反应/无反应的预测因素,从而更好地选择患者。