Department of Oncology, Shanghai Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, People's Republic of China.
Department of Oncology, the 903rd Hospital of PLA, 14 Lingyin Road, Hangzhou, 310013, China.
BMC Cancer. 2019 Nov 8;19(1):1062. doi: 10.1186/s12885-019-6287-8.
The majority of patients diagnosed with hepatocellular carcinoma (HCC) have advanced diseases and many are not eligible for curative therapies.
We report a rare case of HCC from a patient who had a complete response (CR) with the use of combination of Lenvatinib and Pembrolizumab. A 63-year-old man presented at the hospital with serious abdominal pain and was found to have a mass with heterogeneous enhancement and with hemorrhage in segment III of the liver after the examination of abdominal computerized tomography (CT) scan. The patient's history of viral hepatitis B infection, liver cirrhosis and the ɑ-fetoprotein (AFP) level of 14,429.3 ng/ml supported the clinical diagnosis of HCC and laboratory results demonstrated liver function damage status (Child-Pugh class B, Score 8). The patient first received hepatic arterial embolization treatment on 28th November 2017. At this stage supportive care was recommended for poor liver function. In February 2018, combined immunotherapy of Pembrolizumab (2 mg/kg, q3w) and Lenvatinib (8 mg-4 mg, qd) were performed. Nine months following the treatment he had a CR and now, 22 months since the initial treatment, there is no clinical evidence of disease progression. The current overall survival is 22 months.
HCC is a potentially lethal malignant tumor and the combination of immunotherapy plus anti-angiogenic inhibitors shows promising outcome for advanced diseases.
大多数诊断为肝细胞癌(HCC)的患者患有晚期疾病,许多患者不符合治愈性治疗的条件。
我们报告了一例 HCC 患者的罕见病例,该患者使用仑伐替尼和帕博利珠单抗联合治疗后获得完全缓解(CR)。一名 63 岁男性因严重腹痛就诊,腹部计算机断层扫描(CT)检查发现肝 III 段有肿块,呈异质性增强,伴出血。患者的乙型肝炎病毒感染史、肝硬化和α-胎蛋白(AFP)水平为 14,429.3ng/ml 支持 HCC 的临床诊断,实验室结果显示肝功能损害状态(Child-Pugh 分级 B,评分 8)。该患者于 2017 年 11 月 28 日首次接受肝动脉栓塞治疗。在此阶段,建议对肝功能不良进行支持性治疗。2018 年 2 月,接受 Pembrolizumab(2mg/kg,q3w)和仑伐替尼(8mg-4mg,qd)联合免疫治疗。治疗后 9 个月达到 CR,目前初始治疗后 22 个月,无疾病进展的临床证据。目前总生存时间为 22 个月。
HCC 是一种潜在致命的恶性肿瘤,免疫治疗联合抗血管生成抑制剂对晚期疾病显示出有希望的结果。