Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. Thyroid Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Clin Cancer Res. 2015 Mar 1;21(5):1028-35. doi: 10.1158/1078-0432.CCR-14-2915. Epub 2014 Dec 30.
To determine whether the selective BRAF inhibitor, dabrafenib, can stimulate radioiodine uptake in BRAF V600E-mutated unresectable or metastatic iodine-refractory papillary thyroid cancer (PTC).
Ten patients with BRAF V600E-mutant iodine-refractory PTC were enrolled. Absence of radioiodine uptake on iodine-131 whole body scan obtained within 14 months of study entry was required. Each patient received dabrafenib (150 mg twice daily) for 25 days before thyrotropin α-stimulated iodine-131 whole body scan (4 mCi/148 MBq). Patients whose scan showed new sites of radioiodine uptake remained on dabrafenib for 17 more days, and then were treated with 150 mCi (5.5 GBq) iodine-131. The primary endpoint of the study was the percentage of patients with new radioiodine uptake after treatment with dabrafenib.
Six of 10 patients (60%) demonstrated new radioiodine uptake on whole body scan after treatment with dabrafenib. All 6 were treated with 5.5 GBq iodine-131. Two patients had partial responses and 4 patients had stable disease on standard radiographic restaging at 3 months. Thyroglobulin decreased in 4 of 6 treated patients. One patient developed squamous cell carcinoma of the skin. There were no other significant adverse events attributed to dabrafenib.
Dabrafenib can stimulate radioiodine uptake in patients with metastatic BRAF V600E-mutant iodine-refractory PTC, representing a potential new therapeutic approach for these patients.
确定选择性 BRAF 抑制剂 dabrafenib 是否能刺激 BRAF V600E 突变型不可切除或转移性碘难治性甲状腺乳头状癌(PTC)摄取放射性碘。
纳入了 10 名 BRAF V600E 突变型碘难治性 PTC 患者。研究入组前 14 个月内碘-131 全身扫描未见放射性碘摄取。每位患者在促甲状腺素 α 刺激碘-131 全身扫描(4 mCi/148 MBq)前接受 dabrafenib(150 mg 每日两次)治疗 25 天。扫描显示新部位放射性碘摄取的患者继续接受 dabrafenib 治疗 17 天,然后接受 150 mCi(5.5 GBq)碘-131 治疗。该研究的主要终点是治疗后新出现放射性碘摄取的患者比例。
10 名患者中有 6 名(60%)在接受 dabrafenib 治疗后全身扫描显示新的放射性碘摄取。所有 6 名患者均接受 5.5 GBq 碘-131 治疗。2 名患者有部分缓解,4 名患者在 3 个月的标准影像学复查时疾病稳定。4 名接受治疗的患者中甲状腺球蛋白水平下降。1 名患者发生皮肤鳞状细胞癌。无其他与 dabrafenib 相关的严重不良事件。
dabrafenib 可刺激转移性 BRAF V600E 突变型碘难治性 PTC 患者摄取放射性碘,为这些患者提供了一种潜在的新治疗方法。