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肽受体放射性核素治疗在高级别消化系统神经内分泌肿瘤(神经内分泌瘤G3级和神经内分泌癌)中的应用

PRRT in high-grade digestive neuroendocrine neoplasms (NET G3 and NEC).

作者信息

Sorbye Halfdan, Kong Grace, Grozinsky-Glasberg Simona, Strosberg Jonathan

机构信息

Department of Oncology, Haukeland University Hospital, Bergen, Norway.

Department of Clinical Sciences, University of Bergen, Bergen, Norway.

出版信息

J Neuroendocrinol. 2025 Mar;37(3):e13443. doi: 10.1111/jne.13443. Epub 2024 Sep 7.

Abstract

Peptide receptor radionuclide therapy (PRRT) has been primarily studied in low and intermediate-grade digestive neuroendocrine tumors (NET G1-G2). The documentation of a similar benefit for high-grade digestive neuroendocrine neoplasms (NEN) has been limited. This review evaluates the use of PRRT for high-grade digestive NEN (well-differentiated NET G3 and poorly differentiated neuroendocrine carcinomas [NEC]). We identified one phase III trial and seven retrospective studies reporting specifically on PRRT outcome of >10 digestive high-grade NEN patients. The retrospective single-arm studies indicate a benefit for PRRT in NET G3. The randomized phase III NETTER-2 trial demonstrates major PFS superiority of PRRT versus somatostatin analog therapy as the first-line treatment for the NET G3 subgroup. PRRT can now be considered a potential first-line treatment for somatostatin receptor-positive NET G3 patients, but whether it should be the first-line standard of care for all NET G3 patients is still not clarified. For NEC, scarce data are available, and pathologic distinction between NEC and NET G3 can be difficult when Ki-67 is below 55%. PRRT could be considered as a treatment for refractory NEC in very selected cases when there is a high uptake on somatostatin receptor imaging, Ki-67 is below 55%, and there is no rapid tumor progression.

摘要

肽受体放射性核素治疗(PRRT)主要用于低级别和中级别的消化神经内分泌肿瘤(NET G1-G2)。关于高级别消化神经内分泌肿瘤(NEN)有类似疗效的文献报道有限。本综述评估PRRT用于高级别消化NEN(高分化NET G3和低分化神经内分泌癌[NEC])的情况。我们确定了一项III期试验和七项回顾性研究,这些研究专门报告了10例以上消化高级别NEN患者的PRRT治疗结果。回顾性单臂研究表明PRRT对NET G3有益。随机III期NETTER-2试验表明,作为NET G3亚组的一线治疗,PRRT在主要无进展生存期方面明显优于生长抑素类似物治疗。现在可以认为PRRT是生长抑素受体阳性NET G3患者的潜在一线治疗方法,但它是否应成为所有NET G3患者的一线标准治疗仍不明确。对于NEC,可用数据稀少,当Ki-67低于55%时,NEC与NET G3之间的病理区分可能很困难。在非常特殊的情况下,当生长抑素受体显像摄取高、Ki-67低于55%且肿瘤无快速进展时,PRRT可被视为难治性NEC的一种治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/214d/11919471/1ed77123b5dd/JNE-37-e13443-g001.jpg

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