Limouris G S, Karfis I, Chatzioannou A, Paphiti M I, Lyra M, Gennatas K, Nikou G, Voros D, Pragulidis G P, Polydorou A A, Gouliamos A
Nuclear Medicine Division, Radiology Department I, "Aretaieion" Hospital, Athens University Medical Faculty, Greece.
Q J Nucl Med Mol Imaging. 2012 Dec;56(6):551-8.
Aim of this study was to evaluate the effectiveness of non-carrier added (n. c. a.) [177Lu]DOTA-TATE in inoperable liver metastases, positive for sst2 receptor overexpression (verified by Octreoscan and confirmed by biopsy) due to neuroendocrine gastroenteropancreatic (GEP) tumors. [177Lu]DOTA-TATE has been infused after selective catheterization of the hepatic artery, minimising in parallel the toxicity of non-target tissues.
The dose per session administered to each patient (12 cases in total) was 7400 MBq (200 mCi). Repetitions did not exceed 6-fold with treatment intervals of 5-8 weeks. Response assessment was classified according to the therapeutic benefit. Absorbed doses delivered to metastases, kidneys and red marrow were calculated according to OLINDA 1.1 program and the derived values were correlated to the Response Evaluating Criteria in Solid Tumors (RECIST). CT/MRI scans were performed as baseline before, during and after the end of treatment and monthly ultrasound images for follow-up estimation and measurements. Toxicity (World Health Organization criteria) was measured using blood and urine tests of renal, hepatic and bone marrow function.
None of the patients resulted complete response (0.0%); partial response was assessed in 8 (66.7%), disease stabilization in 3 (25%) and progressive disease in 1(8.3%). A 14-month median survival time was estimated for all patients, so far. Eight of 12 (66.7%) showed a mean target diameter shrinkage ranging from 33% to 45%. The organ average radiation dose estimation was found as follows: a) liver tumor 20.8 mGy/MBq; b) liver 0.14 mGy/MBq; c) kidneys 0.41 mGy/MBq; d) spleen 1.4 mGy/MBq; and f) bone marrow 0.022 mGy/MBq. The average absorbed dose per session to a tumor for a spherical mass of 20 g was estimated to be 20.8 mGy/MBq, depending on the histotype of the tumor. WHO toxicity grade 2 to 3 erythro-, leuko- and thrombo-cytopenia occurred in 9 (75%) cases observed about after the third session.
In unresectable metastatic liver lesions positive for somatostatin receptors repeated, trans-hepatic high doses of [177Lu]DOTA-TATE resulted in a more than promising therapeutic outcome with a partial response in 75% of the treated patients. Given the loco-regional modality character of the administration technique, no nephro-toxicity has been so far observed whereas a remarkable myelotoxicity was noticed.
本研究旨在评估非载体添加(n.c.a.)[177Lu]DOTA - TATE对不可切除的肝转移瘤的疗效,这些肝转移瘤因神经内分泌胃肠胰腺(GEP)肿瘤而对生长抑素受体2(sst2)过表达呈阳性(经奥曲肽扫描验证并经活检确认)。[177Lu]DOTA - TATE在肝动脉选择性插管后注入,同时将非靶组织的毒性降至最低。
每位患者(共12例)每次给药剂量为7400 MBq(200 mCi)。重复给药不超过6次,治疗间隔为5 - 8周。根据治疗获益对反应进行评估。根据OLINDA 1.1程序计算转移灶、肾脏和红骨髓的吸收剂量,并将得出的值与实体瘤疗效评价标准(RECIST)相关联。在治疗开始前、治疗期间和治疗结束后进行CT/MRI扫描作为基线检查,并每月进行超声图像检查以进行随访评估和测量。使用肾脏、肝脏和骨髓功能的血液和尿液检测来测量毒性(世界卫生组织标准)。
无患者达到完全缓解(0.0%);8例(66.7%)评估为部分缓解,3例(25%)疾病稳定,1例(8.3%)疾病进展。目前估计所有患者的中位生存时间为14个月。12例中的8例(66.7%)显示平均靶直径缩小33%至45%。器官平均辐射剂量估计如下:a)肝肿瘤20.8 mGy/MBq;b)肝脏0.14 mGy/MBq;c)肾脏0.41 mGy/MBq;d)脾脏1.4 mGy/MBq;f)骨髓0.022 mGy/MBq。对于一个20 g的球形肿块,每次治疗对肿瘤的平均吸收剂量估计为20.8 mGy/MBq,具体取决于肿瘤的组织类型。在大约第三次治疗后观察到9例(75%)患者出现世界卫生组织2至3级的红细胞、白细胞和血小板减少毒性反应。
在生长抑素受体阳性的不可切除转移性肝病变中,重复经肝高剂量给予[177Lu]DOTA - TATE产生了非常有前景的治疗效果,75%的治疗患者出现部分缓解。鉴于给药技术的局部区域方式特点,目前尚未观察到肾毒性,而观察到明显的骨髓毒性。