Endocrinology and Diabetes Unit, Department of Medicine I, University of Wuerzburg, Oberduerrbacher Strasse 6, D-97080 Wuerzburg, Germany.
J Clin Endocrinol Metab. 2012 Mar;97(3):914-22. doi: 10.1210/jc.2011-2765. Epub 2011 Dec 14.
In advanced adrenocortical carcinoma (ACC), many patients have progressive disease despite standard treatment, indicating a need for new treatment options. We have shown high and specific retention of [123I]metomidate ([123I]IMTO) in ACC lesions, suggesting that labeling of metomidate with 131I offers targeted radionuclide therapy for advanced ACC.
Safety and efficacy of radionuclide therapy with [131I]IMTO in advanced ACC.
DESIGN/SETTING: This monocentric case series comprised 19 treatments in 11 patients with nonresectable ACC.
Between 2007 and 2010, patients with advanced ACC not amenable to radical surgery and exhibiting high uptake of [123I]IMTO in their tumor lesions were offered treatment with [131I]IMTO (1.6-20 GBq in one to three cycles of [131I]IMTO).
Tumor response was assessed according to response evaluation criteria in solid tumors (RECIST version 1.1) criteria, and side effects were assessed by Common Toxicity Criteria (version 4.0).
Best response was classified as partial response in one case with a change in target lesions of -51% from baseline, as stable disease in five patients, and as progressive disease in four patients. One patient died 11 d after treatment with [131I]IMTO unrelated to radionuclide therapy. In patients responding to treatment, median progression-free survival was 14 months (range, 5-33) with ongoing disease stabilization in three patients at last follow-up. Treatment was well tolerated, but transient bone marrow depression was observed. Adrenal insufficiency developed in two patients.
Radionuclide therapy with [131I]IMTO is a promising treatment option for selected patients with ACC, deserving evaluation in prospective clinical trials.
在晚期肾上腺皮质癌(ACC)中,尽管采用了标准治疗,许多患者仍出现疾病进展,这表明需要新的治疗选择。我们已经证明,[123I]美替拉酮([123I]IMTO)在 ACC 病变中有很高且特异性的保留,这表明美替拉酮的 131I 标记为晚期 ACC 提供了靶向放射性核素治疗。
用[131I]IMTO 进行放射性核素治疗晚期 ACC 的安全性和疗效。
设计/设置:这项单中心病例系列研究包括 11 名无法切除的 ACC 患者的 19 次治疗。
在 2007 年至 2010 年期间,对不适合根治性手术且肿瘤病变摄取[123I]IMTO 较高的晚期 ACC 患者,给予[131I]IMTO 治疗(在一个至三个[131I]IMTO 周期中给予 1.6-20GBq)。
根据实体瘤反应评估标准(RECIST 版本 1.1)评估肿瘤反应,根据通用毒性标准(版本 4.0)评估不良反应。
最佳反应在 1 例患者中被归类为部分缓解,目标病灶从基线下降了-51%,5 例患者为稳定疾病,4 例患者为进展性疾病。1 例患者在接受[131I]IMTO 治疗后 11d 死亡,与放射性核素治疗无关。在对治疗有反应的患者中,中位无进展生存期为 14 个月(范围为 5-33),3 例患者在最后一次随访时疾病稳定仍在继续。治疗耐受性良好,但观察到短暂的骨髓抑制。两名患者出现肾上腺皮质功能不全。
用[131I]IMTO 进行放射性核素治疗是一种有前途的治疗选择,值得在前瞻性临床试验中评估。