Department of Surgery, Division of Surgical Oncology, Endocrine Surgery Research Program, University of Chicago Medicine, IL.
Department of Surgery, Division of Surgical Oncology, Endocrine Surgery Research Program, University of Chicago Medicine, IL.
Surgery. 2021 Jan;169(1):162-167. doi: 10.1016/j.surg.2020.04.001. Epub 2020 May 20.
Peptide receptor radionuclide therapy is a targeted therapy used to treat unresectable somatostatin receptor-positive neuroendocrine tumors. The objective of this study was to evaluate response rates among neuroendocrine tumors of different primaries and identify factors relevant to future treatment strategies.
We retrospectively reviewed patients who received peptide receptor radionuclide therapy for neuroendocrine tumors from 2018 to 2019 at our institution. Patients were assessed with computed tomography/magnetic resonance imaging and Ga-DOTATATE-positron emission tomography before and after 2 or 4 cycles of peptide receptor radionuclide therapy. Tumor response was evaluated by RECIST 1.1. Statistics included multinomial logistic regression models and Fisher exact test.
Twenty-seven patients underwent 92 cycles of peptide receptor radionuclide therapy: pancreas (n = 11), small bowel (n = 7), and other (n = 9) neuroendocrine tumors. Overall, 30% (8 of 27) had partial response, 59% (16 of 27) stable disease, and 11% (3 of 27) progressed. Pancreatic neuroendocrine tumors responded differently from small bowel neuroendocrine tumors regardless of cycle number (P = .01). The majority of pancreatic neuroendocrine tumors (6 of 11) had partial response to peptide receptor radionuclide therapy, while all small bowel neuroendocrine tumors had stable disease. Pancreatic neuroendocrine tumors stable after 2 cycles were more likely to respond to additional cycles versus other neuroendocrine tumors (probability: 60% vs 11%).
Patients with unresectable advanced or metastatic pancreatic neuroendocrine tumors may benefit from a full course of peptide receptor radionuclide therapy, whereas other neuroendocrine tumors appear less likely to respond. Large prospective studies are needed to confirm these findings.
肽受体放射性核素治疗是一种用于治疗不可切除的生长抑素受体阳性神经内分泌肿瘤的靶向治疗方法。本研究的目的是评估不同原发灶神经内分泌肿瘤的缓解率,并确定与未来治疗策略相关的因素。
我们回顾性分析了 2018 年至 2019 年在我院接受肽受体放射性核素治疗的神经内分泌肿瘤患者。患者在接受 2 或 4 个周期肽受体放射性核素治疗前后接受了计算机断层扫描/磁共振成像和 Ga-DOTATATE 正电子发射断层扫描。根据 RECIST 1.1 评估肿瘤反应。统计学分析包括多项逻辑回归模型和 Fisher 精确检验。
27 例患者共进行了 92 个周期的肽受体放射性核素治疗:胰腺(n=11)、小肠(n=7)和其他(n=9)神经内分泌肿瘤。总体而言,30%(8/27)有部分缓解,59%(16/27)为稳定疾病,11%(3/27)为进展。无论周期数如何,胰腺神经内分泌肿瘤的反应均不同于小肠神经内分泌肿瘤(P=0.01)。大多数胰腺神经内分泌肿瘤(11 例中的 6 例)对肽受体放射性核素治疗有部分缓解,而所有小肠神经内分泌肿瘤均为稳定疾病。2 个周期后稳定的胰腺神经内分泌肿瘤比其他神经内分泌肿瘤更有可能对额外周期有反应(概率:60%比 11%)。
不可切除的晚期或转移性胰腺神经内分泌肿瘤患者可能受益于完整的肽受体放射性核素治疗,而其他神经内分泌肿瘤似乎反应较差。需要进行大型前瞻性研究来证实这些发现。