Department of Internal Medicine, Santa Croce Hospital, 12100 Cuneo, Piedmont, Italy.
World J Gastroenterol. 2013 Jun 7;19(21):3207-16. doi: 10.3748/wjg.v19.i21.3207.
To analyze the epidemiology, clinical characteristics, treatment patterns and outcome in hepatocellular carcinoma (HCC) patients.
We analyzed clinical, pathological and therapeutic data from 256 consecutive patients, examined at S. Croce Hospital in Cuneo-Piedmont, with a diagnosis of HCC between 30(th) June 2000 and 1(st) July 2010. We analyzed the hospital imaging database and examined all medical records, including the diagnosis code for HCC (155.0 according to the ICD-9M classification system), both for inpatients and outpatients, and discovered 576 relevant clinical records. After the exclusion of reports relating to multiple admissions for the same patient, we identified 282 HCC patients. Moreover, from this HCC series, we excluded 26 patients: 1 patient because of an alternative final diagnosis, 8 patients because of a lack of complete clinical data in the medical record and 17 patients because they were admitted to different health care facilities, leaving 256 HCC patients. To highlight possible changes in HCC patterns over the ten-year period, we split the population into two five-year groups, according to the diagnosis period: 30(th) June 2000-30(th) June 2005 and 1(st) July 2005-1(st) July 2010. Patients underwent a 6-mo follow up.
Two hundred and fifty-six HCC patients were included (male/female 182/74; mean age 70 years), 133 in the first period and 123 in the second. Hepatitis C virus (HCV) infection was the most common HCC risk factor (54.1% in the first period, 50.4% in the second; P = 0.63); in the first period, 21.8% of patients were alcoholics and 15.5% were alcoholics in the second period (P > 0.05); the non-viral/non-alcoholic etiology rate was 3.7% in the first period and 20.3% in the second period (P < 0.001). Child class A patients increased significantly in the second period (P < 0.001). Adjusting for age, gender and etiology, there was a significant increase in HCC surveillance during the second period (P = 0.01). Differences between the two periods were seen in tumor parameters: there was an increase in the number of unifocal HCC patients, from 53 to 69 (P = 0.01), as well as an increase in the number of cases where the HCC was < 3 cm [from 22 to 37 (P = 0.01)]. The combined incidence of stage Barcelona Clinic Liver Cancer 0 (very-early) and A (early) HCC was 46 (34.6%) between 2000-2005, increasing to 62 (50.4%) between 2005-2010 (P = 0.01). Of the patients, 62.4% underwent specific treatment in the first group, which increased to 90.2% in the second group (P < 0.001). Diagnosis period (P < 0.01), Barcelona-Clinic Liver Cancer stage (P < 0.01) and treatment per se (P < 0.05) were predictors of better prognosis; surveillance was not related to survival (P = 0.20).
This study showed that, between 2000-2005 and 2005-2010, the number of HCV-related HCC decreased, non-viral/non alcoholic etiologies increased and of surveillance programs were more frequently applied.
分析肝细胞癌(HCC)患者的流行病学、临床特征、治疗模式和结局。
我们分析了 2000 年 6 月 30 日至 2010 年 7 月 1 日期间在库内奥-皮埃蒙特的圣十字医院就诊并诊断为 HCC 的 256 例连续患者的临床、病理和治疗数据。我们分析了医院的影像数据库,并检查了包括 HCC 诊断代码(ICD-9M 分类系统中的 155.0)在内的所有病历,包括住院和门诊患者,并发现了 576 份相关病历记录。在排除了同一患者多次住院的报告后,我们确定了 282 例 HCC 患者。此外,我们从这个 HCC 系列中排除了 26 例患者:1 例患者因为最终诊断不同,8 例患者因为病历中缺乏完整的临床数据,17 例患者因为他们在不同的医疗机构就诊,剩下 256 例 HCC 患者。为了突出这十年中 HCC 模式的可能变化,我们根据诊断期将人群分为两个五年组:2000 年 6 月 30 日至 2005 年 6 月 30 日和 2005 年 7 月 1 日至 2010 年 7 月 1 日。患者接受了 6 个月的随访。
共纳入 256 例 HCC 患者(男/女 182/74;平均年龄 70 岁),其中第一组 133 例,第二组 123 例。丙型肝炎病毒(HCV)感染是最常见的 HCC 危险因素(第一组 54.1%,第二组 50.4%;P = 0.63);第一组中 21.8%的患者为酗酒者,第二组中 15.5%为酗酒者(P > 0.05);非病毒性/非酒精性病因率第一组为 3.7%,第二组为 20.3%(P < 0.001)。第二期儿童 A 级患者显著增加(P < 0.001)。调整年龄、性别和病因后,第二期 HCC 监测显著增加(P = 0.01)。两个时期之间在肿瘤参数上存在差异:单发 HCC 患者数量增加,从 53 例增加到 69 例(P = 0.01),并且 HCC < 3 cm 的病例数量也增加[从 22 例增加到 37 例(P = 0.01)]。巴塞罗那临床肝癌 0 期(极早期)和 A 期(早期)HCC 的合并发生率在 2000-2005 年为 46%(34.6%),在 2005-2010 年增加到 62%(50.4%)(P = 0.01)。第一组中 62.4%的患者接受了特定治疗,第二组中这一比例增加到 90.2%(P < 0.001)。诊断期(P < 0.01)、巴塞罗那临床肝癌分期(P < 0.01)和治疗本身(P < 0.05)是更好预后的预测因素;监测与生存无关(P = 0.20)。
本研究表明,在 2000-2005 年和 2005-2010 年期间,HCV 相关 HCC 的数量减少,非病毒性/非酒精性病因增加,监测计划更频繁地应用。