Division of Gastrointestinal Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi, Sunto-gun, Shizuoka, 411-8777, Japan.
Invest New Drugs. 2024 Aug;42(4):361-368. doi: 10.1007/s10637-024-01449-9. Epub 2024 May 29.
The oral multikinase inhibitors sorafenib and lenvatinib are currently available as first-line treatment for patients with unresectable or metastatic thyroid cancer. However, treatment options for patients who are refractory to these multikinase inhibitors are limited. This study aimed to evaluate the safety and efficacy of rechallenged lenvatinib after failure of both lenvatinib and sorafenib in patients with metastatic thyroid cancer in the real-world clinical practice. We retrospectively reviewed the data of consecutive 16 patients with metastatic thyroid cancer who received lenvatinib as a rechallenge after failure of initial lenvatinib and sorafenib treatment at Shizuoka Cancer Center between 2016 and 2023. Of these, the initial lenvatinib was discontinued in 12 patients owing to progressive disease, in 3 patients owing to adverse events, and in 1 patient owing to both. The overall response rate was 6.7%, and disease control was achieved by rechallenge with lenvatinib in all patients with the target lesions. The median progression free survival after rechallenging with lenvatinib was 15.0 months. No new signs of toxicity were observed after rechallenging with lenvatinib. Our findings suggest that rechallenge with lenvatinib after failure of both lenvatinib and sorafenib showed manageable safety and modest efficacy in patients with metastatic thyroid cancer in clinical practice. The strategy of lenvatinib rechallenge may provide an alternative option for patients with no targetable driver genes or when selective kinase inhibitors are not indicated.
口服多激酶抑制剂索拉非尼和仑伐替尼目前可作为不可切除或转移性甲状腺癌患者的一线治疗药物。然而,对于对这些多激酶抑制剂耐药的患者,治疗选择有限。本研究旨在评估在真实临床实践中,对接受多激酶抑制剂治疗失败的转移性甲状腺癌患者重新使用仑伐替尼的安全性和疗效。我们回顾性分析了 2016 年至 2023 年在静冈癌症中心连续接受转移性甲状腺癌治疗的 16 例患者的数据,这些患者在初始仑伐替尼和索拉非尼治疗失败后接受了仑伐替尼的重新挑战。其中,12 例患者因疾病进展而停止使用仑伐替尼,3 例患者因不良反应而停止使用仑伐替尼,1 例患者因两者均而停止使用仑伐替尼。总的客观缓解率为 6.7%,所有患者的目标病灶均通过重新使用仑伐替尼实现了疾病控制。重新使用仑伐替尼后无进展生存期的中位数为 15.0 个月。重新使用仑伐替尼后未观察到新的毒性迹象。我们的研究结果表明,在多激酶抑制剂治疗失败后重新使用仑伐替尼在转移性甲状腺癌患者的临床实践中显示出可管理的安全性和适度的疗效。仑伐替尼重新挑战的策略可能为无靶向驱动基因的患者或当选择激酶抑制剂不适用时提供替代选择。