PRRT 治疗高级别消化道神经内分泌肿瘤(NET G3 和 NEC)。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Halfdan Sorbye, Grace Kong, Simona Grozinsky-Glasberg, Jonathan Strosberg
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引用次数: 0

摘要

肽受体放射性核素疗法(PRRT)主要针对中低度消化道神经内分泌肿瘤(NET G1-G2)进行研究。对高级别消化道神经内分泌肿瘤(NEN)也有类似疗效的文献还很有限。本综述评估了 PRRT 在高级别消化道神经内分泌肿瘤(分化良好的 G3 级 NET 和分化不良的神经内分泌癌 [NEC])中的应用。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超过 10 例消化道高级别 NEN 患者的 PRRT 治疗结果。回顾性单臂研究表明,PRRT 对 G3 级 NET 有益。随机III期NETTER-2试验表明,在NET G3亚组的一线治疗中,PRRT的PFS优于体生长激素类似物疗法。PRRT 现在可被视为体生长激素受体阳性 NET G3 患者的潜在一线治疗方法,但是否应作为所有 NET G3 患者的一线标准治疗方法仍未明确。对于 NEC,目前可获得的数据很少,而且当 Ki-67 低于 55% 时,病理学上很难区分 NEC 和 NET G3。在体生长抑素受体成像摄取率高、Ki-67低于55%且肿瘤没有快速进展的极个别病例中,可考虑将PRRT作为难治性NEC的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PRRT in high-grade digestive neuroendocrine neoplasms (NET G3 and NEC).

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.

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CiteScore
7.20
自引率
4.30%
发文量
567
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