Yamazaki Haruhiko, Sugino Kiminori, Matsuzu Kenichi, Masaki Chie, Akaishi Junko, Hames Kiyomi, Tomoda Chisato, Suzuki Akifumi, Uruno Takashi, Ohkuwa Keiko, Kitagawa Wataru, Nagahama Mitsuji, Masuda Munetaka, Ito Koichi
Department of Surgery, Ito Hospital, 4-3-6, Jingumae, Shibuya-ku, Tokyo.
Department of Surgery, Yokohama City University School of Medicine, 3-9 Fukuura, Kanazawaku, Yokohama City, Kanagawa, Japan.
Medicine (Baltimore). 2020 Mar;99(11):e19408. doi: 10.1097/MD.0000000000019408.
Some thyroid cancer patients experience a rapid disease progression after the discontinuation of tyrosine kinase inhibitors (TKIs), which is called flare phenomenon. The incidence of the flare phenomenon of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) ranged from 4% to 11.1% and the median time to occurrence of the flare phenomenon ranged from 7 to 12 days in previous reports. In this study, we investigate the timing and incidence of the flare phenomenon in thyroid cancer patients treated with lenvatinib.The records of patients treated with lenvatinib were retrospectively reviewed. The primary outcomes were the incidence rate and timing of the flare phenomenon after the discontinuation of lenvatinib. The flare phenomenon was defined as death, hospitalization attributable to tumor progression, or unexpected event (e.g., pleural drainage) within 1 month of lenvatinib cessation. We excluded patients with progression of underlying diseases other than thyroid cancer or infection, those in whom the disease progressed, or those who died without achieving a clinical response (stable disease, partial response, or complete response).In total, 8 (14.3%) of the 56 patients experienced the flare phenomenon. The median time from lenvatinib cessation to the flare phenomenon was 9 (range, 4-30) days. Three patients in the flare group died within 1 month of lenvatinib cessation without an imaging evaluation. The remaining 5 patients had dyspnea and pleural effusion, and pleural drainage was performed in 3 of the 5 patients. Lenvatinib was resumed in 4 of the 8 patients in the flare group. Median overall survival (OS) was 15.1 months in the flare group and 41.9 months in the non-flare group. The OS tended to be poor in the flare group than in the non-flare group; however, this difference was not statistically significant (P = .051).In lenvatinib treatment for thyroid cancer, the incidence and timing of the flare phenomenon were similar to those observed with other TKIs. OS tended to be poor in the flare group than in the non-flare group. Further studies are needed to determine the mechanism of the flare phenomenon and establish measures and treatment policies.
一些甲状腺癌患者在停用酪氨酸激酶抑制剂(TKIs)后会经历疾病快速进展,这被称为“flare现象”。表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKI)的flare现象发生率在4%至11.1%之间,既往报道中flare现象出现的中位时间为7至12天。在本研究中,我们调查了接受乐伐替尼治疗的甲状腺癌患者中flare现象的发生时间和发生率。对接受乐伐替尼治疗的患者记录进行了回顾性分析。主要结局是乐伐替尼停药后flare现象的发生率和发生时间。flare现象定义为乐伐替尼停药后1个月内死亡、因肿瘤进展住院或意外事件(如胸腔引流)。我们排除了患有除甲状腺癌或感染以外的基础疾病进展的患者、疾病进展的患者或未达到临床缓解(疾病稳定、部分缓解或完全缓解)而死亡的患者。总共56例患者中有8例(14.3%)经历了flare现象。从乐伐替尼停药到flare现象的中位时间为9天(范围4至30天)。flare组中有3例患者在乐伐替尼停药后1个月内未进行影像学评估即死亡。其余5例患者出现呼吸困难和胸腔积液,5例中有3例进行了胸腔引流。flare组8例患者中有4例恢复使用乐伐替尼。flare组的中位总生存期(OS)为15.1个月,非flare组为41.9个月。flare组的OS倾向于比非flare组差;然而,这种差异无统计学意义(P = 0.051)。在乐伐替尼治疗甲状腺癌中,flare现象的发生率和发生时间与其他TKIs观察到的相似。flare组的OS倾向于比非flare组差。需要进一步研究以确定flare现象的机制并制定应对措施和治疗策略。