Frakes Jessica M, Abuodeh Yazan A, Naghavi Arash O, Echevarria Michelle I, Shridhar Ravi, Friedman Mark, Kim Richard, El-Haddad Ghassan, Kis Bela, Biebel Benjamin, Sweeney Jennifer, Choi Junsung, Anaya Daniel, Giuliano Anna R, Hoffe Sarah E
Department of Radiation Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
Department of Radiation Oncology, Florida Hospital Cancer Institute, Orlando, FL, USA.
J Gastrointest Oncol. 2018 Jun;9(3):546-552. doi: 10.21037/jgo.2018.03.04.
Viral associated (VA) malignancies have recently been correlated with improved outcomes. We sought to evaluate outcomes of patients with hepatocellular carcinoma (HCC) with and without viral hepatitis (hepatitis B and C) treated with lobar yttrium-90 radioembolization (Y-90 RE).
After IRB approval, an institutional database of patients with HCC who received RE between 2009-2014 was queried and 99 patients were identified that received a total of 122 lobar RE. Charts were reviewed to capture previous treatments, viral hepatitis status, α-fetoprotein values (AFP), Child-Pugh class (CP), albumin-bilirubin score (ALBI), portal vein thrombosis (PVT), volumes treated and doses delivered. Comparison was made with Chi-square and Mann-Whitney U test. Intrahepatic control (IHC), extrahepatic control (EHC), progression free survival (PFS), and overall survival (OS) were calculated according to the Kaplan-Meier method stratified by cause of underlying liver disease (viral non-viral) and survival differences were assessed via the log-rank test. Hazard ratios were calculated using Cox regression.
Median follow up for VA HCC and non-VA (NVA) HCC patients was 10.9 months (range, 0.8-46.7 months) and 11.8 months (range, 1.1-62.8 months), respectively. Patients with VA HCC (n=44) were younger (P<0.001) and had smaller pretreatment liver volumes (P<0.001); however, there was no difference with respect to gender, pre-treatment AFP, CP, ALBI, PVT, extrahepatic disease, previous treatment, or dose delivered. Median doses for VA and NVA HCC patients were 129.5 Gy (range, 90-215.8 Gy) and 131 Gy (range, 100.9-265 Gy), respectively (P=0.75). One year IHC showed a strong trend to better control for VA HCC at 67% versus 34% for NVA HCC (P=0.067) but 1 year EHC was significantly worse at 63% for VA HCC versus 86% for NVA HCC (P=0.027). There were no significant differences in survival, with a 1-year PFS of 45% for VA HCC versus 31% for NVA HCC (P=0.56) and 1 year OS of 46% versus 55% (P=0.55). Patients that received salvage treatments, CP A, no PVT, and those without extrahepatic disease had improved OS.
Patients with VA HCC had a trend to improved IHC and significantly worse EHC. Prospective investigation of novel systemic therapies following Y-90 RE in patients with VA HCC is warranted to potentially further extend survival in VA HCC patients by addressing extra-hepatic disease.
病毒相关性(VA)恶性肿瘤最近被认为与预后改善相关。我们试图评估接受叶钇-90放射性栓塞(Y-90 RE)治疗的伴有和不伴有病毒性肝炎(乙型和丙型肝炎)的肝细胞癌(HCC)患者的预后。
经机构审查委员会批准,查询了2009年至2014年间接受RE治疗的HCC患者的机构数据库,确定了99例接受了总共122次叶RE治疗的患者。查阅病历以获取既往治疗、病毒性肝炎状态、甲胎蛋白值(AFP)、Child-Pugh分级(CP)、白蛋白-胆红素评分(ALBI)、门静脉血栓形成(PVT)、治疗体积和给予的剂量。采用卡方检验和曼-惠特尼U检验进行比较。根据Kaplan-Meier方法,按潜在肝病病因(病毒性与非病毒性)分层计算肝内控制(IHC)、肝外控制(EHC)、无进展生存期(PFS)和总生存期(OS),并通过对数秩检验评估生存差异。使用Cox回归计算风险比。
VA HCC和非VA(NVA)HCC患者的中位随访时间分别为10.9个月(范围0.8 - 46.7个月)和11.8个月(范围1.1 - 62.8个月)。VA HCC患者(n = 44)更年轻(P < 0.001)且治疗前肝脏体积更小(P < 0.001);然而,在性别、治疗前AFP、CP、ALBI、PVT、肝外疾病、既往治疗或给予的剂量方面没有差异。VA和NVA HCC患者的中位剂量分别为129.5 Gy(范围90 - 215.8 Gy)和131 Gy(范围100.9 - 265 Gy)(P = 0.75)。1年IHC显示VA HCC有更好控制的强烈趋势,为67%,而NVA HCC为34%(P = 0.067),但1年EHC明显更差,VA HCC为63%,而NVA HCC为86%(P = 0.027)。生存率无显著差异,VA HCC的1年PFS为45%,NVA HCC为31%(P = 0.56),1年OS为46%对5�%(P = 0.55)。接受挽救性治疗、CP A级、无PVT以及无肝外疾病的患者OS有所改善。
VA HCC患者有IHC改善的趋势,但EHC明显更差。对VA HCC患者在Y-90 RE后进行新型全身治疗进行前瞻性研究是必要的,以通过解决肝外疾病潜在地进一步延长VA HCC患者的生存期。