Division of Medical Oncology, Department of Medicine, School of Medicine, University of Colorado Denver, Aurora, USA.
Clin Genitourin Cancer. 2012 Dec;10(4):225-31. doi: 10.1016/j.clgc.2012.08.002. Epub 2012 Sep 25.
Sunitinib and sorafenib are tyrosine kinase inhibitors used in metastatic renal cell carcinoma and are known to cause hypothyroidism in a subset of patients. The goal of this study was to better characterize the development of hypothyroidism in patients and to examine its relationship to progression-free survival.
A retrospective chart review was performed on patients treated with sunitinib or sorafenib from January 1, 2005, to January 1, 2011. Data pertaining to the treatment course and development of hypothyroidism were extracted. Patients with hypothyroidism at the beginning of treatment were analyzed separately.
A total of 73 treatment periods had sufficient data to analyze. Among patients with normal baseline thyroid function, 15 (44%) of 34 patients treated with sunitinib and 6 (27%) of 22 patients treated with sorafenib developed hypothyroidism. The hazard ratio for the development of hypothyroidism with sorafenib vs. sunitinib treatment was significant, at 0.38 (95% CI, 0.14-0.97). There was a statistically significant difference in the progression-free survival between patients who developed hypothyroidism while receiving treatment compared with those who did not, 18.2 vs. 10.1 months (P = .01).
This study demonstrated a significant difference in the incidence of hypothyroidism during treatment with sunitinib and sorafenib, with a higher incidence of hypothyroidism in patients treated with sunitinib. The development of hypothyroidism was associated with a longer progression-free survival.
舒尼替尼和索拉非尼是用于转移性肾细胞癌的酪氨酸激酶抑制剂,已知会在一部分患者中引起甲状腺功能减退。本研究的目的是更好地描述患者甲状腺功能减退的发生情况,并研究其与无进展生存期的关系。
对 2005 年 1 月 1 日至 2011 年 1 月 1 日期间接受舒尼替尼或索拉非尼治疗的患者进行了回顾性病历审查。提取了与治疗过程和甲状腺功能减退发展相关的数据。对治疗开始时患有甲状腺功能减退的患者进行了单独分析。
共有 73 个治疗期的数据足以进行分析。在基线甲状腺功能正常的患者中,34 名接受舒尼替尼治疗的患者中有 15 名(44%)和 22 名接受索拉非尼治疗的患者中有 6 名(27%)发生了甲状腺功能减退。与索拉非尼治疗相比,索拉非尼治疗发生甲状腺功能减退的风险比为 0.38(95%CI,0.14-0.97),有统计学意义。与未发生甲状腺功能减退的患者相比,治疗期间发生甲状腺功能减退的患者无进展生存期显著延长,分别为 18.2 个月和 10.1 个月(P=0.01)。
本研究表明,在接受舒尼替尼和索拉非尼治疗期间,甲状腺功能减退的发生率存在显著差异,接受舒尼替尼治疗的患者甲状腺功能减退的发生率更高。甲状腺功能减退的发生与无进展生存期延长相关。