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神经内分泌肿瘤患者在接受 177Lu-DOTATATE 治疗后病情迅速进展。

Rapid Progression After 177Lu-DOTATATE in Patients With Neuroendocrine Tumors.

机构信息

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.

出版信息

Pancreas. 2021 Jul 1;50(6):890-894. doi: 10.1097/MPA.0000000000001841.

Abstract

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.

摘要

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。

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