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[177Lu-DOTA 0-Tyr 3]-奥曲肽治疗胃肠胰神经内分泌肿瘤广泛转移患者:测量肾脏吸收剂量的价值。

[177Lu-DOTA 0-Tyr 3]-octreotate treatment in patients with disseminated gastroenteropancreatic neuroendocrine tumors: the value of measuring absorbed dose to the kidney.

机构信息

Department of Surgery, University of Gothenburg, Sahlgrenska University Hospital, 413 45, Göteborg, Sweden.

出版信息

World J Surg. 2010 Jun;34(6):1368-72. doi: 10.1007/s00268-009-0387-6.

Abstract

BACKGROUND

Peptide receptor radiation therapy (PRRT) using [(177)Lu-DOTA(0)-Tyr(3)]-octreotate is a new, promising option for treatment of disseminated gastroenteropancreatic neuroendocrine tumors (GEPNETs).

METHODS

During 2006-2008, 26 patients with disseminated GEPNETs were treated with (177)Lu-octreotate. Radiologic response (RECIST), biochemical response [plasma chromogranin-A (P-CgA)], hematologic toxicity [Common Toxicity Criteria (CTC)], absorbed dose to the kidneys (conjugate view method), and glomerular filtration rate (GFR) were analyzed.

RESULTS

(177)Lu-octreotate (8 GBq) was given one to five times (median = 3) with a 6-week interval between each. Sixteen of the 26 patients were evaluated radiologically; 6 (38%) had partial response (PR), 8 (50%) had stable disease (SD), and 2 (13%) had progressive disease (PD). Seventeen of the 26 patients were evaluated biochemically; 6 (35%) showed a >or=30% decrease, 8 (47%) showed a >or=20% increase, and 3 (18%) showed neither a >or=30% decrease nor a >or=20% increase. The mean absorbed dose to the kidneys was 24 Gy. With a dose limit of 27 Gy to the kidneys, 10 patients did not receive the planned four treatments, while four patients had the potential to receive additional treatment. A significant reduction (p = 0.0013) of GFR was observed at follow-up. Three patients experienced CTC grade 3 hematologic toxicity.

CONCLUSIONS

By using the absorbed dose to the kidneys as a limiting factor, treatment with (177)Lu-octreotate can be individualized, e.g., overtreatment can be avoided and patients with the potential to receive additional treatment can be identified. Further studies are needed to define tolerance doses to the kidneys so that treatment can be optimized.

摘要

背景

使用 [(177)Lu-DOTA(0)-Tyr(3)]-奥曲肽进行肽受体放射性治疗 (PRRT) 是治疗胃肠胰神经内分泌肿瘤 (GEPNETs) 扩散的一种新的、有前途的选择。

方法

在 2006 年至 2008 年期间,26 例患有扩散性 GEPNETs 的患者接受了 (177)Lu-奥曲肽治疗。分析了影像学反应 (RECIST)、生化反应 [血浆嗜铬粒蛋白 A (P-CgA)]、血液学毒性 [常见毒性标准 (CTC)]、肾脏吸收剂量(结合视图法)和肾小球滤过率 (GFR)。

结果

每 6 周间隔一次,26 例患者中的 26 例接受了 (177)Lu-奥曲肽 (8GBq) 治疗,1 至 5 次(中位数=3)。对 26 例患者中的 16 例进行了影像学评估;6 例(38%)有部分缓解(PR),8 例(50%)有稳定疾病(SD),2 例(13%)有进展性疾病(PD)。对 26 例患者中的 17 例进行了生化评估;6 例(35%)下降>或=30%,8 例(47%)增加>或=20%,3 例(18%)既没有下降>或=30%,也没有增加>或=20%。肾脏的平均吸收剂量为 24Gy。对于肾脏 27Gy 的剂量限制,10 名患者未接受计划的 4 次治疗,而 4 名患者有接受额外治疗的潜力。随访时观察到 GFR 显著下降(p=0.0013)。3 名患者发生 CTC 3 级血液学毒性。

结论

通过将肾脏吸收剂量用作限制因素,可以对 (177)Lu-奥曲肽治疗进行个体化,例如可以避免过度治疗,并确定有接受额外治疗潜力的患者。需要进一步研究以确定肾脏耐受剂量,从而优化治疗。

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