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Outcome on Mesenteric Mass Response of Small-Intestinal Neuroendocrine Tumors Treated by177Lu-DOTATATE Peptide Receptor Radionuclide Therapy: The MesenLuth Study, a National Study from the French Group of Endocrine Tumors and Endocan-RENATEN Network

放射性核素治疗 肽受体 神经内分泌肿瘤 医学 临床终点 实体瘤疗效评价标准 内科学 无进展生存期 核医学 耐火材料(行星科学) 胃肠病学 化疗 受体 临床试验 临床研究阶段 生物 天体生物学
作者
Laure Al Mansour,Louis de Mestier,Magalie Haissaguerre,Pauline Afchain,Julien Hadoux,Thierry Lecomte,David Morland,Anne‐Ségolène Cottereau,Ophélie De Rycke,Ghoufrane Tlili,Jérémie Tordo,M. Janier,A. Deville,Thomas Walter
出处
期刊:The Journal of Nuclear Medicine [Society of Nuclear Medicine]
卷期号:65 (2): 258-263 被引量:3
标识
DOI:10.2967/jnumed.123.266063
摘要

A mesenteric mass (MM), characterized by fibrotic reaction, is present in most small-intestinal neuroendocrine tumors (SI-NETs). 177Lu-DOTATATE peptide receptor radionuclide therapy (PRRT) has shown its efficacy in patients with progressive SI-NETs. However, because of specific tissue characteristics of desmoplastic MMs, we hypothesize that these lesions may be refractory to 177Lu-DOTATATE PRRT. Methods: From the national French Groupe d'étude des Tumeurs Endocrines database, we identified patients with an advanced SI-NET and a MM (≥2 cm with a retractile aspect) of a SI-NET treated by at least 1 course of 177Lu-DOTATATE PRRT. The primary endpoint was a MM objective response rate (ORR) of less than 5%. Secondary endpoints were metabolic response, MM-related safety, and clinical response, as well as MM progression-free survival (PFS) and non-MM PFS. Results: In total, 52 patients were included. The MM ORR was 4% (n = 2), and the non-MM ORR was 8% (n = 4). No patient had a MM metabolic response, and the non-MM metabolic response rate was 12% (n = 6). Among the 26 patients with baseline MM-related symptoms, 46% had a clinical response. Four patients presented with gastrointestinal complications during PRRT. The median MM-related PFS was not reached, and the non-MM PFS was 50.3 mo (95% CI, 38.2–61.7 mo). Conclusion: This study confirms that 177Lu-DOTATATE PRRT does not lead to morphologic response on MMs (ORR < 5%). However, it allows MM stability, with few MM-related side effects, and has a relevant impact on MM-related symptoms.

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