Role of neoadjuvant peptide receptor radionuclide therapy in unresectable and metastatic gastro-entero-pancreatic neuroendocrine neoplasms: A scoping review.

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM Journal of Neuroendocrinology Pub Date : 2024-06-27 DOI:10.1111/jne.13425
Raghava Kashyap, Senthil Raja, Ajay Adusumilli, Murali Mohan Reddy Gopireddy, Benjamin P T Loveday, Ramin Alipour, Grace Kong
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Abstract

Peptide receptor radionuclide therapy (PRRT) is an established therapy for metastatic neuroendocrine neoplasms (NEN). The role of PRRT as a neoadjuvant treatment prior to surgery or other local therapies is uncertain. This scoping review aimed to define the landscape of evidence available detailing the utility of PRRT in the neo-adjuvant setting, including the clinical contexts, efficacy, and levels of evidence. A comprehensive literature search of PUBMED, SCOPUS, and EMBASE through to December 2022 was performed to identify reports of PRRT use as neoadjuvant therapy prior to local therapies. Observational studies and clinical trials were included. A total of 369 records were identified by the initial search, and 17 were included in the final analysis, comprising 179 patients treated with neoadjuvant PRRT. Publications included case reports, retrospective cohort series and a phase 2 trial. Definitions of unresectable disease were variable. Radioisotopes used included 177Lu (n = 142) and 90Y (n = 36), used separately (n = 178) or in combination (n = 1). A combination of PRRT with chemotherapy was also explored (n = 2). Toxicity data was reported in 11/17 studies. Survival analysis was reported in 3/17 studies. Surgical resection following PRRT was reported for both the primary tumor (n = 71) and metastases (n = 12). Resection rates could not be calculated as not all publications reported whether resection was completed. Published literature exploring the use of PRRT in the neoadjuvant setting is mostly limited to case reports and retrospective cohort studies. From these limited data there is reported to be a role of PRRT in neoadjuvant setting in the literature. However, the low quality of evidence precludes any definite conclusion on the grade of disease, site of primary, isotope used or use of concomitant chemotherapy that can benefit from this application. Further prospective studies will require collaboration between multiple centers to gain sufficient high-quality evidence.

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新辅助肽受体放射性核素疗法在不可切除和转移性胃肠胰神经内分泌肿瘤中的作用:范围综述。
肽受体放射性核素疗法(PRRT)是一种治疗转移性神经内分泌肿瘤(NEN)的成熟疗法。在手术或其他局部疗法之前,PRRT 作为新辅助疗法的作用尚不确定。本次范围界定综述旨在明确现有证据的范围,详细说明 PRRT 在新辅助治疗中的作用,包括临床背景、疗效和证据级别。我们对截至 2022 年 12 月的 PUBMED、SCOPUS 和 EMBASE 进行了全面的文献检索,以确定在局部治疗前将 PRRT 用作新辅助治疗的报告。研究纳入了观察性研究和临床试验。初步搜索共发现 369 条记录,其中 17 条被纳入最终分析,包括 179 名接受新辅助 PRRT 治疗的患者。文献包括病例报告、回顾性队列系列研究和一项二期试验。不可切除性疾病的定义各不相同。使用的放射性同位素包括177Lu(n = 142)和90Y(n = 36),分别使用(n = 178)或联合使用(n = 1)。还探讨了 PRRT 与化疗的联合应用(n = 2)。11/17 项研究报告了毒性数据。3/17 项研究报告了生存期分析。有报告称,PRRT 治疗后对原发肿瘤(71 例)和转移瘤(12 例)进行了手术切除。由于并非所有文献都报告了切除是否完成,因此无法计算切除率。探讨在新辅助治疗中使用 PRRT 的已发表文献大多局限于病例报告和回顾性队列研究。从这些有限的数据来看,有文献报道 PRRT 在新辅助治疗中的作用。然而,由于证据质量不高,因此无法就可从该应用中获益的疾病分级、原发部位、使用的同位素或同时使用的化疗得出明确结论。进一步的前瞻性研究需要多个中心合作才能获得足够的高质量证据。
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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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