肽受体放射性核素疗法或依维莫司治疗转移性神经内分泌肿瘤:SeqEveRIV研究,法国内分泌肿瘤小组和Endocan-RENATEN网络的一项全国性研究。

Aurelien Fosse, Julien Hadoux, Paul Girot, Amandine Beron, Pauline Afchain, Anne-Segolene Cottereau, Eric Baudin, Lawrence O Dierickx, Thierry Lecomte, Marine Perrier, Come Lepage, Karine Bouhier-Leporrier, Bernard Goichot, Boumediene Lachachi, Thomas Walter, Alice Durand
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引用次数: 0

摘要

依维莫司和肽受体放射性核素疗法(PRRT,177Lu-DOTATATE)是指南推荐的胃肠胰转移性神经内分泌肿瘤的两种治疗方法。然而,最佳治疗顺序仍是未知数。方法:我们设计了一项回顾性多中心研究,纳入了2004年4月至2022年10月期间接受依维莫司和PRRT治疗的内分泌肿瘤研究小组国家前瞻性数据库中的患者。主要目的是比较两种疗法(依维莫司和PRRT)的疗效和安全性,次要目的是根据转移性神经内分泌肿瘤患者的总无进展生存期(PFS)(第一次治疗期间的无进展生存期+第二次治疗期间的无进展生存期)评估治疗顺序(先PRRT后依维莫司或先依维莫司后PRRT)。研究结果84名患者接受了两种治疗。依维莫司的客观反应率和中位生存期分别为 5 个月(6.0%)和 16.1 个月(95% CI,11.5-20.7 个月),而 PRRT 的客观反应率和中位生存期分别为 19 个月(22.6%)和 24.5 个月(95% CI,17.7-31.3 个月)。PRRT 的安全性也更好。依维莫司-PRRT序列的中位总生存期为43.2个月(95% CI,33.7-52.7个月),PRRT-依维莫司序列的中位总生存期为30.6个月(95% CI,17.8-43.4个月)(危险比为0.69;95% CI,0.39-1.24;P = 0.22)。结论PRRT比依维莫司更有效,毒性更低。两种序列的总生存期相似,建议患者在符合两种治疗条件的情况下根据具体情况进行讨论,但在需要客观反应或身体虚弱的人群中,应首先使用 PRRT。
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Peptide Receptor Radionuclide Therapy or Everolimus in Metastatic Neuroendocrine Tumors: The SeqEveRIV Study, a National Study from the French Group of Endocrine Tumors and Endocan-RENATEN Network.

Everolimus and peptide receptor radionuclide therapy (PRRT, 177Lu-DOTATATE) are 2 treatments recommended in guidelines for gastroenteropancreatic metastatic neuroendocrine tumors. However, the best treatment sequence remains unknown. Methods: We designed a retrospective multicenter study that included patients from the national prospective database of the Groupe d'Étude des Tumeurs Endocrines who had been treated using everolimus and PRRT between April 2004 and October 2022. The primary aim was to compare the 2 treatments (everolimus and PRRT) in terms of efficacy and safety, and the secondary aim was to evaluate the sequences (PRRT followed by everolimus or everolimus followed by PRRT) based on overall progression-free survival (PFS) (PFS during first treatment + PFS during second treatment) in patients with metastatic neuroendocrine tumors. Results: Both treatments were used for 84 patients. The objective response rate and median PFS were 5 (6.0%) and 16.1 mo (95% CI, 11.5-20.7 mo), respectively, under everolimus and 19 (22.6%) and 24.5 mo (95% CI, 17.7-31.3 mo), respectively, for PRRT. The safety profile was also better for PRRT. Median overall PFS was 43.2 mo (95% CI, 33.7-52.7 mo) for the everolimus-PRRT sequence and 30.6 mo (95% CI, 17.8-43.4 mo) for the PRRT-everolimus sequence (hazard ratio, 0.69; 95% CI, 0.39-1.24; P = 0.22). Conclusion: PRRT was more effective and less toxic than everolimus. Overall PFS was similar between the 2 sequences, suggesting case-by-case discussion if the patient is eligible for both treatments, but PRRT should be used first when an objective response is needed or in frail populations.

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