Sowa-Staszczak Anna, Stefanska Agnieszka, Chrapczynski Pawel, Trofimiuk-Müldner Malgorzata, Szura Miroslaw, Hubalewska-Dydejczyk Alicja
Department of Endocrinology, University Hospital, Krakow, Poland.
Endocr J. 2017 Feb 27;64(2):171-177. doi: 10.1507/endocrj.EJ16-0219. Epub 2016 Nov 17.
A number of detected neuroendocrine neoplasms (NENs) has been on the increase due to our awareness of the NENs risk and the development of different imaging techniques. Therapy of NENs involves surgery, chemotherapy, "cold" somatostatin analogs (SSA), peptide receptor radionuclide therapy (PRRT) and kinase inhibitors in pancreatic NENs. The aim of this study is to assess the efficacy of SSA in combination with "hot" somatostatin analogs, and the survival rate of our patients with advanced NENs. Seventy nine patients with metastatic NEN and positive somatostatin receptor scintigraphy (SRS) were enrolled in the study. Every patient was supposed to receive a dose of 7.4 GBq/m PRRT in 4-5 cycles every 4-9 weeks. Response to the therapy was assessed according to Response Evaluation Criteria In Solid Tumors (RECIST). SSA were administered one month after the last cycle of PRRT and have been continued during the whole follow up period. Median observation time was 33 months (IQR 13.6-55.6), median time to progression was 28 months (IQR 12.1-39.2) and median time to event was 28 months (IQR 12.1-39.2). Overall survival for this group of patients was 60 months. PFS was 39 months and EFS was equal to 33 months. In our group of patients not many serious adverse events were observed. PRRT using radiolabelled somatostatin analogs followed by therapy with "cold" somatostatin analogs is a promising treatment option for patients with metastatic or inoperable somatostatin receptor-positive NENs with the possibility of survival prolongation.
由于我们对神经内分泌肿瘤(NENs)风险的认识提高以及不同成像技术的发展,已检测到的神经内分泌肿瘤数量一直在增加。NENs的治疗包括手术、化疗、“冷”生长抑素类似物(SSA)、肽受体放射性核素治疗(PRRT)以及胰腺NENs中的激酶抑制剂。本研究的目的是评估SSA与“热”生长抑素类似物联合使用的疗效,以及我们晚期NENs患者的生存率。79例转移性NEN且生长抑素受体闪烁显像(SRS)阳性的患者纳入本研究。每位患者每4 - 9周接受4 - 5个周期、剂量为7.4 GBq/m的PRRT。根据实体瘤疗效评价标准(RECIST)评估治疗反应。在PRRT的最后一个周期后1个月给予SSA,并在整个随访期间持续使用。中位观察时间为33个月(四分位间距13.6 - 55.6),中位进展时间为28个月(四分位间距12.1 - 39.2),中位事件发生时间为28个月(四分位间距12.1 - 39.2)。该组患者的总生存期为60个月。无进展生存期为39个月,无事件生存期为33个月。在我们的患者组中,未观察到许多严重不良事件。使用放射性标记生长抑素类似物的PRRT,随后用“冷”生长抑素类似物治疗,对于转移性或无法手术的生长抑素受体阳性NENs患者是一种有前景的治疗选择,有可能延长生存期。