Iten Fabienne, Muller Beat, Schindler Christian, Rasch Helmut, Rochlitz Christoph, Oertli Daniel, Maecke Helmut R, Muller-Brand Jan, Walter Martin A
Institute of Nuclear Medicine, University Hospital Basel, Switzerland.
Cancer. 2009 May 15;115(10):2052-62. doi: 10.1002/cncr.24272.
The authors aimed to explore the efficacy of (90)Yttrium-1,4,7,10-tetra-azacyclododecane N,N',N'',N'''-tetraacetic acid [(90)Y-DOTA]-Tyr(3)-octreotide (TOC) in advanced iodine-refractory thyroid cancer.
In a phase 2 trial, the authors investigated biochemical response (assessed by serum thyroglobulin levels), survival, and the long-term safety profile of systemic [(90)Y-DOTA]-TOC treatment in metastasized iodine-refractory thyroid cancer. Adverse events were assessed according to the National Cancer Institute criteria. Survival analyses were performed by using multiple regression models.
A total of 24 patients were enrolled. A median cumulative activity of 13.0 GBq (range, 1.7-30.3 GBq) was administered. Response was found in 7 (29.2%) patients. Eight (33.3%) patients developed hematologic toxicity grade 1-3, and 4 (16.7%) patients developed renal toxicity grade 1-4. The median survival was 33.4 months (range, 3.6-126.8 months) from time of diagnosis and 16.8 months (range, 1.8-99.1 months) from time of first [(90)Y-DOTA]-TOC treatment. Response to treatment was associated with longer survival from time of diagnosis (hazard ratio [HR], 0.17; 95% confidence interval [CI], 0.03-0.92; P = .04) and from time of first [(90)Y-DOTA]-TOC therapy (HR, 0.20; 95% CI, 0.04-0.94; P = .04). The visual grade of scintigraphic tumor uptake was not associated with treatment response (odds ratio [OR], 0.98; 95% CI, 0.26-3.14; P = 1.00).
Response to [(90)Y-DOTA]-TOC in metastasized iodine-refractory thyroid cancer was associated with longer survival. Upcoming trials should aim to increase the number of treatment cycles.
作者旨在探讨钇-1,4,7,10-四氮杂环十二烷-N,N',N'',N'''-四乙酸[(90)Y-DOTA]-酪氨酰-3-奥曲肽(TOC)在晚期碘难治性甲状腺癌中的疗效。
在一项2期试验中,作者研究了转移性碘难治性甲状腺癌全身应用[(90)Y-DOTA]-TOC治疗的生化反应(通过血清甲状腺球蛋白水平评估)、生存率和长期安全性。根据美国国立癌症研究所的标准评估不良事件。使用多元回归模型进行生存分析。
共纳入24例患者。给予的中位累积活度为13.0GBq(范围1.7-30.3GBq)。7例(29.2%)患者有反应。8例(33.3%)患者出现1-3级血液学毒性,4例(16.7%)患者出现1-4级肾毒性。从诊断时起中位生存期为33.4个月(范围3.6-126.8个月),从首次[(90)Y-DOTA]-TOC治疗时起为16.8个月(范围1.8-99.1个月)。治疗反应与从诊断时起(风险比[HR],0.17;95%置信区间[CI],0.03-0.92;P=0.04)和从首次[(90)Y-DOTA]-TOC治疗时起(HR,0.20;95%CI,0.04-0.94;P=0.04)的较长生存期相关。闪烁显像肿瘤摄取的视觉分级与治疗反应无关(优势比[OR],0.98;95%CI,0.26-3.14;P=1.00)。
转移性碘难治性甲状腺癌对[(90)Y-DOTA]-TOC的反应与较长生存期相关。即将开展的试验应旨在增加治疗周期数。