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177Lu 肽受体放射性核素治疗神经内分泌肿瘤的疗效:一项荟萃分析。

Efficacy of 177Lu Peptide Receptor Radionuclide Therapy for the Treatment of Neuroendocrine Tumors: A Meta-analysis.

机构信息

From the Departments of Surgery.

Family Medicine.

出版信息

Clin Nucl Med. 2019 Sep;44(9):719-727. doi: 10.1097/RLU.0000000000002646.

DOI:10.1097/RLU.0000000000002646
PMID:31205149
Abstract

OBJECTIVE

The purpose of this study was to assess the efficacy of Lu-labeled peptide receptor radionuclide therapy (PRRT) induction treatments for patients with unresectable metastatic neuroendocrine tumors.

METHODS

MEDLINE, EMBASE, and Ovid were systematically searched with keywords "lutetium," "Lu-177," "PRRT," "neuroendocrine," and "prognosis." Studies evaluating treatment with Lu-labeled PRRT were assessed for disease response and/or disease control rate by Response Evaluation Criteria in Solid Tumors (RECIST) 1.0 or 1.1, modified RECIST, Southwest Oncology Group (SWOG), or modified SWOG criteria. Pooled proportions of disease response and control rates were calculated for both fixed- and random-effects models.

RESULTS

Eighteen studies with 1920 patients were included (11 with 1268 patients using RECIST and 6 with 804 patients using SWOG). By RECIST criteria, the pooled disease response rate by random-effects model was 29.1% (95% confidence interval [CI], 20.2%-38.9%), and disease control rate was 74.1% (95% CI, 67.8%-80.0%). By SWOG criteria, the pooled disease response rate by random-effects model was 30.6% (95% CI, 20.7%-41.5%), and disease control rate was 81.1% (95% CI, 76.4%-85.4%).

CONCLUSIONS

Induction therapy, typically 4 treatments, with Lu PRRT is an effective method of treating unresectable metastatic neuroendocrine tumors with significant disease response and control rates.

摘要

目的

本研究旨在评估 Lu 标记的肽受体放射性核素治疗 (PRRT) 诱导治疗对不可切除转移性神经内分泌肿瘤患者的疗效。

方法

通过关键词“镥”、“Lu-177”、“PRRT”、“神经内分泌”和“预后”,系统地在 MEDLINE、EMBASE 和 Ovid 上进行了搜索。评估了使用 Lu 标记的 PRRT 治疗的研究,根据实体瘤反应评估标准 (RECIST) 1.0 或 1.1、改良 RECIST、西南肿瘤协作组 (SWOG) 或改良 SWOG 标准,评估疾病缓解率和/或疾病控制率。采用固定效应模型和随机效应模型计算疾病缓解率和控制率的合并比例。

结果

纳入了 18 项研究,共 1920 例患者(11 项研究使用 RECIST,共 1268 例患者;6 项研究使用 SWOG,共 804 例患者)。根据 RECIST 标准,随机效应模型的疾病缓解率的合并比例为 29.1%(95%置信区间 [CI],20.2%-38.9%),疾病控制率为 74.1%(95% CI,67.8%-80.0%)。根据 SWOG 标准,随机效应模型的疾病缓解率的合并比例为 30.6%(95% CI,20.7%-41.5%),疾病控制率为 81.1%(95% CI,76.4%-85.4%)。

结论

Lu PRRT 的诱导治疗,通常为 4 个疗程,是治疗不可切除转移性神经内分泌肿瘤的有效方法,具有显著的疾病缓解率和控制率。

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