Dabrafenib Versus Dabrafenib + Trametinib in BRAF -Mutated Radioactive Iodine Refractory Differentiated Thyroid Cancer: Results of a Randomized, Phase 2, Open-Label Multicenter Trial

达布拉芬尼 曲美替尼 医学 内科学 实体瘤疗效评价标准 肿瘤科 临床终点 不利影响 甲状腺间变性癌 临床研究阶段 临床试验 甲状腺癌 癌症 生物 MAPK/ERK通路 威罗菲尼 激酶 细胞生物学 转移性黑色素瘤
作者
Naifa L. Busaidy,Bhavana Konda,Lai Wei,Lori J. Wirth,Catherine Devine,Gregory A. Daniels,Jonas DeSouza,Ming Poi,Nathan D. Seligson,Maria E. Cabanillas,Jennifer A. Sipos,Matthew D. Ringel,Ann‐Kathrin Eisfeld,Cynthia Timmers,Manisha H. Shah
出处
期刊:Thyroid [Mary Ann Liebert, Inc.]
卷期号:32 (10): 1184-1192 被引量:98
标识
DOI:10.1089/thy.2022.0115
摘要

Background: Oncogenic BRAF mutations are commonly found in advanced differentiated thyroid cancer (DTC), and reports have shown efficacy of BRAF inhibitors in these tumors. We investigated the difference in response between dabrafenib monotherapy and dabrafenib + trametinib therapy in patients with BRAF-mutated radioactive iodine refractory DTC. Methods: In this open-label randomized phase 2 multicenter trial, patients aged ≥18 years with BRAF-mutated radioactive iodine refractory DTC with progressive disease by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 within 13 months before enrollment were eligible. Patients were randomly assigned to receive dabrafenib alone or dabrafenib + trametinib. The primary endpoint was objective response rate by modified RECIST (minor response of -20% to -29%, partial and complete response) within the first 24 weeks of therapy. Trial Registration Number: NCT01723202. Results: A total of 53 patients were enrolled. The objective response rate (modified RECIST) was 42% (11/26 [95% confidence interval {CI} 23-63%]) with dabrafenib versus 48% (13/27 [CI 29-68%]) with dabrafenib + trametinib (p = 0.67). Objective response rate (RECIST 1.1) was 35% (9/26 [CI 17-56%]) with dabrafenib and 30% (8/27 [CI 14-51%]) with dabrafenib + trametinib. Most common treatment-related adverse events included skin and subcutaneous tissue disorders (17/26, 65%), fever (13/26, 50%), hyperglycemia (12/26, 46%) with dabrafenib alone and fever (16/27, 59%), nausea, chills, fatigue (14/27, 52% each) with dabrafenib + trametinib. There were no treatment-related deaths. Conclusions: Combination dabrafenib + trametinib was not superior in efficacy compared to dabrafenib monotherapy in patients with BRAF-mutated radioiodine refractory progressive DTC.
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