Department of Nuclear Medicine, University Hospital Bonn, Bonn, Germany.
Department of Internal Medicine 3, University Hospital Bonn, Bonn, Germany.
Clin Cancer Res. 2018 Oct 1;24(19):4672-4679. doi: 10.1158/1078-0432.CCR-18-0947. Epub 2018 Jun 27.
Although somatostatin analogues (SSA) and peptide receptor radionuclide therapy (PRRT) are validated therapies in patients with advanced gastroenteropancreatic neuroendocrine tumors (GEP-NET), it remains unclear whether SSA combined with PRRT or as maintenance therapy can provide prolonged survival compared with patients treated with PRRT alone. In this retrospective study, we aimed to investigate whether there is a survival benefit to adding SSA to PRRT as a combination therapy and/or maintenance therapy. The investigation included 168 patients with unresectable GEP-NETs treated at the University Hospital Bonn, Bonn, Germany. The patients were divided into two main groups: PRRT monotherapy ( = 81, group 1) and PRRT plus SSA ( = 87, group 2) as combined therapy with PRRT and/or as maintenance therapy after PRRT. Data for overall survival (OS) were available from 168 patients, of whom 160 had data for progression-free survival (PFS). The median PFS was 27 months in group 1 versus 48 months in group 2 ( = 0.012). The median OS rates were 47 months in group 1 and 91 months in group 2 ( < 0.001). The death-event rates were lower in group 2 (26%) than in group 1 (63%). SSA as a combination therapy with PRRT and/or as a maintenance therapy showed a clinical benefit rate (objective response or stable disease) of 95%, which was significantly higher than group 1 (79%). SSA as a combination therapy and/or maintenance therapy may play a significant role in tumor control in patients with GEP-NET who underwent a PRRT. .
虽然生长抑素类似物(SSA)和肽受体放射性核素治疗(PRRT)是晚期胃肠胰神经内分泌肿瘤(GEP-NET)患者的有效治疗方法,但尚不清楚 SSA 联合 PRRT 或作为维持治疗是否比单独接受 PRRT 治疗的患者提供更长的生存时间。在这项回顾性研究中,我们旨在研究将 SSA 添加到 PRRT 中作为联合治疗和/或维持治疗是否具有生存益处。该研究纳入了德国波恩大学医院治疗的 168 例不可切除的 GEP-NET 患者。患者分为两组:PRRT 单药治疗(n = 81,组 1)和 PRRT 联合 SSA 治疗(n = 87,组 2),作为 PRRT 的联合治疗和/或 PRRT 后维持治疗。总生存期(OS)数据可从 168 例患者中获得,其中 160 例患者有无进展生存期(PFS)数据。组 1 的中位 PFS 为 27 个月,组 2 为 48 个月(= 0.012)。组 1 的中位 OS 率为 47 个月,组 2 为 91 个月(<0.001)。组 2 的死亡事件率(26%)低于组 1(63%)。SSA 作为 PRRT 的联合治疗和/或维持治疗显示临床获益率(客观缓解或疾病稳定)为 95%,明显高于组 1(79%)。SSA 作为联合治疗和/或维持治疗可能在接受 PRRT 的 GEP-NET 患者的肿瘤控制中发挥重要作用。