Philippi Zachary, Reddy Keerthi D, Malik Sheza, Al-Khalil Zeina, Dbouk Nader
Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Rochester General Hospital, Rochester, NY 14621, USA.
Int J Mol Sci. 2025 Jun 22;26(13):5994. doi: 10.3390/ijms26135994.
Hepatocellular carcinoma (HCC), the most common primary liver cancer, remains a leading cause of cancer-related mortality worldwide. Its often-silent progression results in late-stage diagnosis, limiting curative options and necessitating systemic therapy for many patients. The presence of underlying cirrhosis in most cases further complicates treatment decisions. While the approval of sorafenib in 2007 marked a major milestone in systemic therapy for HCC, the treatment landscape has since evolved significantly, particularly with the advent of immune checkpoint inhibitors and anti-angiogenic agents. Combination regimens, such as atezolizumab plus bevacizumab, have demonstrated superior outcomes and are now considered standard first-line options. Despite these advances, efforts to translate insights from HCC's molecular pathogenesis into personalized treatments have been limited. This narrative review explores the current systemic therapy options for HCC, from first-line to subsequent-line treatments, and highlights emerging strategies, including novel immunotherapies and targeted agents. We emphasize the need for individualized treatment approaches that consider tumor biology, liver function, and performance status, and we outline future directions for research aimed at improving outcomes in this complex and evolving field.
肝细胞癌(HCC)是最常见的原发性肝癌,仍然是全球癌症相关死亡的主要原因。其进展往往隐匿,导致晚期诊断,限制了治愈选择,许多患者需要进行全身治疗。大多数情况下存在的潜在肝硬化使治疗决策更加复杂。虽然2007年索拉非尼的获批标志着HCC全身治疗的一个重要里程碑,但此后治疗格局发生了显著变化,尤其是随着免疫检查点抑制剂和抗血管生成药物的出现。联合方案,如阿替利珠单抗加贝伐单抗,已显示出更好的疗效,现在被认为是标准的一线选择。尽管取得了这些进展,但将HCC分子发病机制的见解转化为个性化治疗的努力仍然有限。这篇叙述性综述探讨了HCC目前的全身治疗选择,从一线治疗到后续治疗,并强调了新兴策略,包括新型免疫疗法和靶向药物。我们强调需要考虑肿瘤生物学、肝功能和体能状态的个体化治疗方法,并概述了旨在改善这一复杂且不断发展领域治疗结果的未来研究方向。