Tomonari Tetsu, Sato Yasushi, Tanaka Hironori, Tanaka Takahiro, Taniguchi Tatsuya, Sogabe Masahiro, Okamoto Koichi, Miyamoto Hiroshi, Muguruma Naoki, Saito Yu, Imura Satoru, Bando Yoshimi, Shimada Mitsuo, Takayama Tetsuji
Department of Gastroenterology and Oncology, Institute of Biomedical Sciences, Tokushima University Graduate School.
Department of Digestive and Transplant Surgery, Tokushima University.
Medicine (Baltimore). 2020 Oct 16;99(42):e22782. doi: 10.1097/MD.0000000000022782.
Lenvatinib (LEN) is a novel potent multi-tyrosine kinase inhibitor, approved as first-line treatment for unresectable hepatocellular carcinoma (HCC). Considering its high objective response rate, LEN therapy could be expected to achieve downstaging of tumors and lead to conversion therapy with hepatectomy or ablation. However, the feasibility of conversion therapy after LEN treatment in unresectable HCC remains largely unknown.
Here, we reported 3 cases of unresectable HCC: case 1, a 69-year-old man diagnosed with ruptured HCC; case 2, a 72-year-old woman with nonalcoholic steatohepatitis-based HCC; and case 3, a 73-year-old man with a history of alcoholic cirrhosis-based HCC.
In all cases, cirrhosis was classified as Child-Pugh 5 and modified albumin-bilirubin grade 1 or 2a. HCC was diagnosed as Barcelona Clinic Liver Cancer (BCLC) stage B.
In all cases, LEN was initiated after conventional-transcatheter arterial embolization enforcement, while maintaining liver function.
In all cases, the main tumor size decreased after 6 months of LEN treatment and no satellite nodes were detected, indicating downstaging of HCC to BCLC stage A. Subsequently, conversion hepatectomy or ablation was performed. After successful conversion therapy, the general condition of the patients was good, without tumor recurrence during the observation period (median 10 months).
This study demonstrated that LEN enables downstaging of HCC and thus represents a bridge to successful surgery or ablation therapy. In particular, LEN treatment may facilitate the possibility for conversion therapy of initially unresectable HCC, while maintaining the hepatic functional reserve.
仑伐替尼(LEN)是一种新型强效多酪氨酸激酶抑制剂,被批准作为不可切除肝细胞癌(HCC)的一线治疗药物。鉴于其较高的客观缓解率,预计仑伐替尼治疗可实现肿瘤降期,并导致采用肝切除术或消融术的转化治疗。然而,在不可切除的HCC中,仑伐替尼治疗后转化治疗的可行性在很大程度上仍不清楚。
在此,我们报告了3例不可切除的HCC病例:病例1,一名69岁男性,诊断为破裂性HCC;病例2,一名72岁女性,患有非酒精性脂肪性肝炎相关性HCC;病例3,一名73岁男性,有酒精性肝硬化相关性HCC病史。
所有病例中,肝硬化均被分类为Child-Pugh 5级,改良白蛋白-胆红素分级为1级或2a级。HCC被诊断为巴塞罗那临床肝癌(BCLC)分期B期。
所有病例中,在常规经动脉导管栓塞强化治疗后开始使用仑伐替尼,同时维持肝功能。
所有病例中,仑伐替尼治疗6个月后主要肿瘤大小减小,未检测到卫星结节,表明HCC降期至BCLC分期A期。随后进行了转化性肝切除术或消融术。成功的转化治疗后,患者的一般状况良好,观察期内(中位时间10个月)无肿瘤复发。
本研究表明,仑伐替尼可实现HCC降期,因此是成功手术或消融治疗的桥梁。特别是,仑伐替尼治疗可能有助于初始不可切除HCC转化治疗的可能性,同时维持肝功能储备。