Wolter P, Stefan C, Decallonne B, Dumez H, Bex M, Carmeliet P, Schöffski P
Department of General Medical Oncology, University Hospital Gasthuisberg, Catholic University Leuven, Leuven Cancer Institute, Herestraat 49, Leuven B-3000, Belgium.
Br J Cancer. 2008 Aug 5;99(3):448-54. doi: 10.1038/sj.bjc.6604497.
Sunitinib is approved for the treatment of metastatic renal cell carcinoma (RCC) and imatinib-resistant or -intolerant gastrointestinal stromal tumours (GIST). Several studies have identified unexpected rates of thyroid dysfunction with sunitinib treatment. We performed a prospective observational study with the aim of more accurately defining the incidence and severity of hypothyroidism in RCC or GIST patients receiving sunitinib. Thyroid function was assessed at baseline and on days 1 and 28 of each treatment cycle. Thyroid antibodies were assessed at baseline and during follow-up if abnormal thyroid function tests were recorded. Sixteen patients (27%) developed sub- or clinical hypothyroidism and required hormone replacement and 20 patients (34%) showed at least one elevated thyroid-stimulating hormone not requiring therapeutic intervention. Twenty patients (34%) did not develop any biochemical thyroid abnormality. Thus, sunitinib can induce (sub-) clinical hypothyroidism, warranting close monitoring of thyroid function. We propose a new algorithm for managing this side effect in clinical practise.
舒尼替尼被批准用于治疗转移性肾细胞癌(RCC)以及对伊马替尼耐药或不耐受的胃肠道间质瘤(GIST)。多项研究已发现舒尼替尼治疗时出现甲状腺功能障碍的意外发生率。我们进行了一项前瞻性观察性研究,旨在更准确地确定接受舒尼替尼治疗的RCC或GIST患者甲状腺功能减退的发生率和严重程度。在基线以及每个治疗周期的第1天和第28天评估甲状腺功能。如果记录到甲状腺功能检查异常,则在基线和随访期间评估甲状腺抗体。16例患者(27%)出现亚临床或临床甲状腺功能减退并需要激素替代治疗,20例患者(34%)至少有一次促甲状腺激素升高但无需治疗干预。20例患者(34%)未出现任何甲状腺生化异常。因此,舒尼替尼可诱发(亚)临床甲状腺功能减退,需要密切监测甲状腺功能。我们提出了一种在临床实践中管理这种副作用的新算法。