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基于生长抑素的放射性肽治疗与 [177Lu-DOTA]-TOC 与 [90Y-DOTA]-TOC 在神经内分泌肿瘤中的比较。

Somatostatin-based radiopeptide therapy with [177Lu-DOTA]-TOC versus [90Y-DOTA]-TOC in neuroendocrine tumours.

机构信息

Institute of Nuclear Medicine, University Hospital Basel, Basel, Switzerland.

出版信息

Eur J Nucl Med Mol Imaging. 2014 Feb;41(2):214-22. doi: 10.1007/s00259-013-2559-8. Epub 2013 Oct 2.

DOI:10.1007/s00259-013-2559-8
PMID:24085501
Abstract

PURPOSE

Somatostatin-based radiopeptide treatment is generally performed using the β-emitting radionuclides (90)Y or (177)Lu. The present study aimed at comparing benefits and harms of both therapeutic approaches.

METHODS

In a comparative cohort study, patients with advanced neuroendocrine tumours underwent repeated cycles of [(90)Y-DOTA]-TOC or [(177)Lu-DOTA]-TOC until progression of disease or permanent adverse events. Multivariable Cox regression and competing risks regression were employed to examine predictors of survival and adverse events for both treatment groups.

RESULTS

Overall, 910 patients underwent 1,804 cycles of [(90)Y-DOTA]-TOC and 141 patients underwent 259 cycles of [(177)Lu-DOTA]-TOC. The median survival after [(177)Lu-DOTA]-TOC and after [(90)Y-DOTA]-TOC was comparable (45.5 months versus 35.9 months, hazard ratio 0.91, 95% confidence interval 0.63-1.30, p = 0.49). Subgroup analyses revealed a significantly longer survival for [(177)Lu-DOTA]-TOC over [(90)Y-DOTA]-TOC in patients with low tumour uptake, solitary lesions and extra-hepatic lesions. The rate of severe transient haematotoxicities was lower after [(177)Lu-DOTA]-TOC treatment (1.4 vs 10.1%, p = 0.001), while the rate of severe permanent renal toxicities was similar in both treatment groups (9.2 vs 7.8%, p = 0.32).

CONCLUSION

The present results revealed no difference in median overall survival after [(177)Lu-DOTA]-TOC and [(90)Y-DOTA]-TOC. Furthermore, [(177)Lu-DOTA]-TOC was less haematotoxic than [(90)Y-DOTA]-TOC.

摘要

目的

生长抑素受体放射性肽治疗通常采用β发射放射性核素(90)Y 或(177)Lu 进行。本研究旨在比较这两种治疗方法的益处和危害。

方法

在一项比较队列研究中,患有晚期神经内分泌肿瘤的患者接受了多次(90)Y-DOTA-TOC 或(177)Lu-DOTA-TOC 治疗,直到疾病进展或出现永久性不良反应。采用多变量 Cox 回归和竞争风险回归分析来检查两组治疗的生存和不良反应的预测因素。

结果

总体而言,910 例患者接受了 1804 个周期的(90)Y-DOTA-TOC 治疗,141 例患者接受了 259 个周期的(177)Lu-DOTA-TOC 治疗。(177)Lu-DOTA-TOC 和(90)Y-DOTA-TOC 治疗后的中位生存时间相似(45.5 个月与 35.9 个月,风险比 0.91,95%置信区间 0.63-1.30,p=0.49)。亚组分析显示,在肿瘤摄取低、单发病变和肝外病变患者中,(177)Lu-DOTA-TOC 的生存时间明显长于(90)Y-DOTA-TOC。(177)Lu-DOTA-TOC 治疗后严重短暂血液毒性的发生率较低(1.4%与 10.1%,p=0.001),而两组严重永久性肾毒性的发生率相似(9.2%与 7.8%,p=0.32)。

结论

本研究结果显示,(177)Lu-DOTA-TOC 和(90)Y-DOTA-TOC 治疗后的中位总生存时间无差异。此外,(177)Lu-DOTA-TOC 的血液毒性小于(90)Y-DOTA-TOC。

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