Faulkes Rosemary E, Rehman Zaira, Palanichamy Swetha, Zakeri Nekisa, Coldham Chris, Dasari Bobby V M, Perera M Thamara P R, Rajoriya Neil, Shetty Shishir, Shah Tahir
Liver Unit, Queen Elizabeth Hospital, Birmingham B15 2GW, UK.
Institute Immunology and Immunotherapy, University of Birmingham, Birmingham B15 2TT, UK.
Cancers (Basel). 2023 Feb 3;15(3):978. doi: 10.3390/cancers15030978.
Hepatocellular carcinoma (HCC) is the third leading cause of cancer death, and its incidence is rising. Mortality from HCC is predicted to increase by 140% by 2035. Surveillance of high-risk patients with cirrhosis or chronic liver disease may be one means of reducing HCC mortality, but the level of supporting evidence for international guidelines is low/moderate. This study explores the real-world experience of HCC surveillance at a tertiary referral centre. Electronic patient records for all new HCCs diagnosed between August 2012 and December 2021 were retrospectively reviewed. Patient and tumour characteristics were evaluated, including the co-existence of chronic liver disease, cancer treatment and survival, and categorised according to HCC diagnosis within or outside a surveillance programme. Patients with HCC who presented through surveillance had smaller tumours diagnosed at an earlier stage, but this did not translate into improved overall survival. All patients in surveillance had chronic liver disease, including 91% ( = 101) with cirrhosis, compared to 45% ( = 29) in the non-surveillance cohort. We propose that the immune dysfunction associated with cirrhosis predisposes patients to a more aggressive tumour biology than the largely non-cirrhotic population in the non-surveillance group.
肝细胞癌(HCC)是癌症死亡的第三大主要原因,且其发病率正在上升。预计到2035年,HCC导致的死亡率将增加140%。对肝硬化或慢性肝病高危患者进行监测可能是降低HCC死亡率的一种手段,但国际指南的支持证据水平为低/中等。本研究探讨了一家三级转诊中心HCC监测的实际情况。对2012年8月至2021年12月期间诊断的所有新发HCC患者的电子病历进行了回顾性审查。评估了患者和肿瘤特征,包括慢性肝病的共存情况、癌症治疗和生存情况,并根据监测计划内或外的HCC诊断进行分类。通过监测发现的HCC患者肿瘤较小且诊断较早,但这并未转化为总体生存率的提高。所有接受监测的患者都患有慢性肝病,其中91%(n = 101)患有肝硬化,而非监测队列中的这一比例为45%(n = 29)。我们认为,与肝硬化相关的免疫功能障碍使患者比非监测组中大多无肝硬化的人群更容易出现侵袭性更强的肿瘤生物学行为。