Takeda Haruhiko, Nishijima Norihiro, Nasu Akihiro, Komekado Hideyuki, Kita Ryuichi, Kimura Toru, Kudo Masatoshi, Osaki Yukio
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University, Kyoto.
Department of Gastroenterology and Hepatology, Osaka Red Cross Hospital, Osaka.
Hepatol Res. 2019 May;49(5):594-599. doi: 10.1111/hepr.13294. Epub 2019 Jan 31.
Lenvatinib is a novel multikinase inhibitor that has recently shown antitumor activity against hepatocellular carcinoma (HCC) in a phase III trial. We report the case of a woman in whom lenvatinib showed long-term antitumor activity, and in whom computed tomography (CT) scans revealed a series of suggestive radiological changes on the intratumor vascularity. A 68-year-old woman with hepatitis C virus-related liver disease presented with multiple HCCs. Following previous therapy, including six sessions of transcatheter arterial chemoembolization, we introduced lenvatinib monotherapy. Lenvatinib could rapidly cause hypovascularity in the main hypervascular target lesion, and portal vein tumor thrombosis also became undetectable 11 months after the initiation of lenvatinib. These radiological changes suggested that lenvatinib could exert not only anti-angiogenic activity but also direct antitumoral effect. Of note, CT scans during lenvatinib treatment revealed the target lesion as a low-density area in the early arterial phase, whereas scans during drug interruption due to proteinuria showed that the lesion was enhanced in the arterial phase. Finally, near-complete response could be achieved as the best response. We successfully managed various adverse events including proteinuria and hypertension, and the patient was able to continue this lenvatinib therapy for more than 4 years with well-controlled general condition. We report the first case of a patient with HCC in whom lenvatinib monotherapy demonstrated long-term antitumor activity. Suggestive radiological changes reflecting intratumor vascularity as presented here should be considered in patients receiving lenvatinib for HCC.
仑伐替尼是一种新型多激酶抑制剂,在一项III期试验中最近显示出对肝细胞癌(HCC)的抗肿瘤活性。我们报告了一例女性病例,仑伐替尼在该患者中显示出长期抗肿瘤活性,计算机断层扫描(CT)显示肿瘤内血管出现一系列提示性影像学变化。一名68岁患有丙型肝炎病毒相关肝病的女性出现多发性HCC。在接受包括六次经动脉化疗栓塞术在内的先前治疗后,我们采用了仑伐替尼单药治疗。仑伐替尼可迅速导致主要高血供靶病灶出现血管减少,在开始使用仑伐替尼11个月后门静脉肿瘤血栓也消失了。这些影像学变化表明仑伐替尼不仅可发挥抗血管生成活性,还可产生直接抗肿瘤作用。值得注意的是,在仑伐替尼治疗期间的CT扫描显示靶病灶在动脉早期为低密度区,而在因蛋白尿中断用药期间的扫描显示该病灶在动脉期强化。最终,最佳反应为接近完全缓解。我们成功处理了包括蛋白尿和高血压在内的各种不良事件,患者能够继续接受仑伐替尼治疗超过4年,总体状况得到良好控制。我们报告了首例接受仑伐替尼单药治疗显示长期抗肿瘤活性的HCC患者。对于接受仑伐替尼治疗HCC的患者,应考虑本文所呈现的反映肿瘤内血管情况的提示性影像学变化。