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用于考虑接受 Lu-177-DOTATATE 治疗的神经内分泌肿瘤患者的临床评分。

A clinical score for neuroendocrine tumor patients under consideration for Lu-177-DOTATATE therapy.

机构信息

Vanderbilt University Medical Center, Division of Hematology and Oncology, Department of Medicine, Nashville, Tennessee, USA.

Vanderbilt University of Medical Center, Department of Biostatistics, Nashville, Tennessee, USA.

出版信息

Endocr Relat Cancer. 2021 Mar;28(3):203-212. doi: 10.1530/ERC-20-0482.

Abstract

We developed a clinical score (CS) at Vanderbilt Ingram Cancer Center (VICC) that we hoped would predict outcomes for patients with progressive well-differentiated neuroendocrine tumors (NETs) receiving therapy with Lutetium-177 (177Lu)-DOTATATE. Patients under consideration for 177Lu-DOTATATE between March 1, 2016 and March 17, 2020 at VICC were assigned a CS prospectively. The CS included 5 categories: available treatments for tumor type outside of 177Lu-DOTATATE, prior systemic treatments, patient symptoms, tumor burden in critical organs and presence of peritoneal carcinomatosis. The primary outcome of the analysis was progression-free survival (PFS). To evaluate the effect of the CS on PFS, a multivariable Cox regression analysis was performed adjusting for tumor grade, primary tumor location, and the interaction between 177Lu-DOTATATE doses received (zero, 1-2, 3-4) and CS. A total of 91 patients and 31 patients received 3-4 doses and zero doses of 177Lu-DOTATATE, respectively. On multivariable analysis, in patients treated with 3-4 doses of 177Lu-DOTATATE, for each 1-point increase in CS, the estimated hazard ratio (HR) for PFS was 2.0 (95% CI 1.61-2.48). On multivariable analysis, in patients who received zero doses of 177Lu-DOTATATE, for each 1-point increase in CS, the estimated HR for PFS was 1.22 (95% CI 0.91-1.65). Among patients treated with 3-4 doses of 177Lu-DOTATATE, those with lower CS experienced improved PFS with the treatment compared to patients with higher CS. This PFS difference, based upon CS, was not observed in patients who did not receive 177Lu-DOTATATE, suggesting the predictive utility of the score.

摘要

我们在范德比尔特英格拉姆癌症中心(VICC)开发了一种临床评分(CS),我们希望该评分能够预测接受镥-177(177Lu)-DOTATATE 治疗的进展性分化良好的神经内分泌肿瘤(NET)患者的结局。2016 年 3 月 1 日至 2020 年 3 月 17 日期间,在 VICC 考虑接受 177Lu-DOTATATE 治疗的患者前瞻性地分配了 CS。CS 包括 5 个类别:除 177Lu-DOTATATE 以外的肿瘤类型的可用治疗方法、既往全身治疗、患者症状、关键器官中的肿瘤负担以及腹膜癌病的存在。分析的主要结果是无进展生存期(PFS)。为了评估 CS 对 PFS 的影响,进行了多变量 Cox 回归分析,该分析调整了肿瘤分级、原发肿瘤位置以及接受的 177Lu-DOTATATE 剂量(零、1-2、3-4)与 CS 之间的相互作用。共有 91 名患者和 31 名患者分别接受了 3-4 剂量和零剂量的 177Lu-DOTATATE。多变量分析显示,在接受 3-4 剂量 177Lu-DOTATATE 治疗的患者中,CS 每增加 1 分,PFS 的估计风险比(HR)为 2.0(95%CI1.61-2.48)。多变量分析显示,在未接受 177Lu-DOTATATE 治疗的患者中,CS 每增加 1 分,PFS 的估计 HR 为 1.22(95%CI0.91-1.65)。在接受 3-4 剂量 177Lu-DOTATATE 治疗的患者中,CS 较低的患者与 CS 较高的患者相比,治疗后 PFS 得到改善。在未接受 177Lu-DOTATATE 治疗的患者中,未观察到基于 CS 的 PFS 差异,这表明评分具有预测效用。

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