晚期肝细胞癌治疗模式的演变:整合所有的治疗方法。
The evolving treatment paradigm of advanced hepatocellular carcinoma: putting all the pieces back together.
机构信息
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
出版信息
Curr Opin Oncol. 2021 Jul 1;33(4):386-394. doi: 10.1097/CCO.0000000000000744.
PURPOSE OF REVIEW
The therapeutic landscape of advanced hepatocellular carcinoma (HCC) has become notably complex in recent years. With this review, we aimed to put the most recent findings in perspective and tried to delineate the rapidly changing treatment algorithm.
RECENT FINDINGS
The combination of atezolizumab and bevacizumab has become the new first-line standard of care treatment for unresectable HCC after the positive results of the phase 3 IMbrave150 study. Nivolumab monotherapy failed to demonstrate advantage versus sorafenib in the CheckMate 459 trial, while two different therapeutic strategies (sintilimab and bevacizumab biosimilar and donafenib) outperformed sorafenib in two phase 2/3 studies conducted in the Chinese population. Several immunotherapy combinations are currently under study in large phase 3 trials after promising results in earlier phase studies. About further lines of treatment, the combination of ipilimumab and nivolumab was approved for sorafenib-pretreated patients after the positive results of the phase 1/2 CheckMate 040 study and apatinib was proven effective in the Chinese population in a phase 2/3 study, while pembrolizumab as monotherapy did not show statistically significant superiority when compared with placebo in the KEYNOTE-240 study.
SUMMARY
Because of the growing complexity of advanced HCC treatment, the implementation of predictive biomarkers of response is eagerly needed.
目的综述
近年来,晚期肝细胞癌(HCC)的治疗领域变得异常复杂。本文旨在结合最近的研究结果,阐述迅速变化的治疗方案。
最近的发现
IMbrave150 期研究的阳性结果使阿替利珠单抗联合贝伐珠单抗成为不可切除 HCC 的新一线治疗标准。纳武利尤单抗单药治疗在 CheckMate 459 试验中未能优于索拉非尼,而两项在中国人群中进行的 2/3 期研究中,两种不同的治疗策略(替雷利珠单抗联合贝伐珠单抗生物类似药和多纳非尼)优于索拉非尼。在早期临床试验取得良好结果后,目前正在进行几项免疫联合治疗的大型 3 期试验。关于进一步的治疗线,在 CheckMate 040 期 1/2 研究阳性结果后,伊匹单抗联合纳武利尤单抗被批准用于索拉非尼预处理患者,阿帕替尼在一项 2/3 期研究中被证明对中国人群有效,而在 KEYNOTE-240 研究中,与安慰剂相比,帕博利珠单抗单药治疗并未显示出统计学上的优越性。
总结
由于晚期 HCC 治疗的复杂性不断增加,迫切需要预测疗效的生物标志物。