Department of Nuclear Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Department of General Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Endocrine. 2022 Oct;78(1):68-76. doi: 10.1007/s12020-022-03113-9. Epub 2022 Jun 29.
Management of progressive, metastatic radioactive iodine refractory differentiated thyroid cancer (RAIR-DTC) has been a great challenge due to its poor prognosis and limited treatment options. Recently, apatinib, an orally anti-angiogenic tyrosine kinase inhibitor (TKI) is reported to be useful for treatment of progressive RAIR-DIC. The aim of this study was to evaluate the antitumour effect of apatinib and the combination therapy with radioactive iodine (RAI) in patients with progressive metastatic DTC.
Five patients (all female, mean age 62 ± 8 years, ranged from 51 to 69 years) with distant metastatic DTC (dmDTC) after total thyroidectomy (TTE) and neck lymph node dissection were treated with apatinib at a dose 500 mg per day after F-Fluorodeoxyglucose (F-FDG) PET/CT. The effects of apatinib on DTC were evaluated at 4 ± 1 months after treatment with apatinib. RAI therapy was then initiated. The response to apatinib and the combination therapy with RAI treatment was evaluated by Response Evaluation Criteria in Solid Tumours (RECIST, version 1.1) and metabolic activity using serum thyroglobulin (Tg) and F-FDG PET/CT.
Positive F-FDG PET/CT results were found in all patients before apatinib therapy. The immunohistochemical analysis of primary tumour tissues showed high expression of vascular endothelial growth factor receptor-2 (VEGFR-2). Four patients with follicular thyroid carcinoma (FTC) showed partial response (PR) with significant decrease in tumour size and maximum standardized uptake value (SUVmax) after 4 ± 1 month's treatment with apatinib. Further significant reduction of tumour size and SUVmax were observed in three patients after combination therapy with apatinib and RAI. Only one patient with both FTC and papillary thyroid cancer (PTC) demonstrated progressive disease (PD) after treatment with apatinib alone, however, a decrease in tumour size and SUVmax as well as serum Tg levels was achieved after the combination with RAI therapy and apatinib.
Apatinib had significant antitumour effects on progressive distant metastatic DTC. Moreover, beneficial synergistic and complementary effects were shown when apatinib combined with RAI therapy.
NCT04180007, Registered November 26, 2019.
由于预后较差且治疗选择有限,进展性、转移性放射性碘难治性分化型甲状腺癌(RAIR-DTC)的管理一直是一个巨大的挑战。最近,阿帕替尼是一种口服抗血管生成酪氨酸激酶抑制剂(TKI),据报道对治疗进展性 RAIR-DIC 有效。本研究的目的是评估阿帕替尼对进展性转移性 DTC 患者的抗肿瘤作用以及与放射性碘(RAI)联合治疗的效果。
5 名患者(均为女性,平均年龄 62±8 岁,年龄 51~69 岁)在接受全甲状腺切除术(TTE)和颈部淋巴结清扫术后患有远处转移性 DTC(dmDTC),在 F-氟脱氧葡萄糖(F-FDG)PET/CT 后每天接受 500mg 阿帕替尼治疗。在治疗后 4±1 个月,评估阿帕替尼对 DTC 的影响。然后开始进行 RAI 治疗。通过实体瘤反应评估标准(RECIST,版本 1.1)和血清甲状腺球蛋白(Tg)和 F-FDG PET/CT 评估阿帕替尼和 RAI 联合治疗的反应。
所有患者在阿帕替尼治疗前的 F-FDG PET/CT 结果均为阳性。原发肿瘤组织的免疫组织化学分析显示血管内皮生长因子受体-2(VEGFR-2)高表达。4 名滤泡状甲状腺癌(FTC)患者在接受 4±1 个月的阿帕替尼治疗后,肿瘤大小和最大标准化摄取值(SUVmax)均有部分缓解(PR),且显著减小。在接受阿帕替尼和 RAI 联合治疗的 3 名患者中,进一步观察到肿瘤大小和 SUVmax 的显著减小。仅 1 名 FTC 和乳头状甲状腺癌(PTC)患者在单独使用阿帕替尼后出现疾病进展(PD),但在联合 RAI 治疗和阿帕替尼后,肿瘤大小和 SUVmax 以及血清 Tg 水平均降低。
阿帕替尼对进展性远处转移性 DTC 具有显著的抗肿瘤作用。此外,阿帕替尼与 RAI 联合治疗显示出有益的协同和互补作用。
NCT04180007,注册于 2019 年 11 月 26 日。