Morsica Giulia, Bertoni Costanza, Hasson Hamid, Messina Emanuela, Uberti Foppa Caterina
Department of Infectious Diseases, IRCCS, San Raffaele, Scientific Institute, Milan, Italy.
Faculty of Medicine and Surgery, Vita-Salute University, Milan, Italy.
Front Oncol. 2023 Dec 5;13:1242741. doi: 10.3389/fonc.2023.1242741. eCollection 2023.
The use and choice of the best systemic treatment is gaining increasing interest in people living with HIV (PLWH) because hepatocellular carcinoma (HCC) represents an increasing cause of morbidity and mortality in this setting and most HCCs are diagnosed in the advanced stage. Ten years ago, the multi-kinase inhibitor lenvatinib was approved in the first-line setting. However, to date, no data on the efficacy and tolerability of lenvatinib in PLWH from clinical trials and real-life studies are available. Case 1 was a gentleman with hepatitis B virus-related cirrhosis who underwent orthotopic liver transplantation for HCC and developed peritoneal metastasis several years later. Lenvatinib treatment was selected at HCC recurrence. This participant maintained undetectable HIV viremia and a relatively preserved immune status during 6 months of systemic treatment with lenvatinib. After 6 months, he discontinued lenvatinib for progression of the disease (growing of peritoneal metastasis) and uncontrolled hypertension. Case 2 was a gentleman with hepatitis C-genotype 1a-related cirrhosis who experienced unresectable recurrences after radiofrequency thermal ablation of the tumor. At the first recurrence, HCC was treated with six cycles of trans-catheter arterial chemoembolization; at the second recurrence, the participant underwent trans-catheter arterial radioembolization; and at the third recurrence, he received lenvatinib. A week after the start of lenvatinib, the participant had liver decompensation and discontinued therapy. The presently reported cases showed low tolerability of systemic therapy with lenvatinib in PLWH. Cumulative data are necessary to define the position of lenvatinib in this setting.
由于肝细胞癌(HCC)在人类免疫缺陷病毒感染者(PLWH)中导致发病和死亡的情况日益增多,且大多数HCC在晚期才被诊断出来,因此最佳全身治疗的使用和选择在PLWH中越来越受到关注。十年前,多激酶抑制剂仑伐替尼被批准用于一线治疗。然而,迄今为止,尚无来自临床试验和真实研究的关于仑伐替尼在PLWH中的疗效和耐受性的数据。病例1是一位患有乙型肝炎病毒相关肝硬化的男性,因HCC接受了原位肝移植,几年后出现腹膜转移。在HCC复发时选择了仑伐替尼治疗。该参与者在接受仑伐替尼全身治疗的6个月期间,HIV病毒血症检测不到,免疫状态相对保持良好。6个月后,他因疾病进展(腹膜转移增大)和无法控制的高血压而停用了仑伐替尼。病例2是一位患有丙型肝炎基因1a型相关肝硬化的男性,在肿瘤进行射频热消融后出现不可切除的复发。第一次复发时,HCC接受了六个周期的经动脉化疗栓塞治疗;第二次复发时,该参与者接受了经动脉放射性栓塞治疗;第三次复发时,他接受了仑伐替尼治疗。开始使用仑伐替尼一周后,该参与者出现肝失代偿并停止治疗。目前报告的病例显示,仑伐替尼全身治疗在PLWH中的耐受性较低。需要累积数据来确定仑伐替尼在这种情况下的地位。