Suppr超能文献

基于他汀类药物的肝细胞癌姑息治疗

Statin-Based Palliative Therapy for Hepatocellular Carcinoma.

作者信息

Shao Joni Yu-Hsuan, Lee Fei-Peng, Chang Chia-Lun, Wu Szu-Yuan

机构信息

From the Graduate Institute of Biomedical Informatics, Taipei Medical University, Taipei, Taiwan, R.O.C. (JY-HS); Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan, R.O.C. (S-YW); Department of Otorhinolaryngology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, R.O.C. (F-PL); Department of Hemato-Oncology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, R.O.C. (C-LC); Department of Radiation Oncology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, R.O.C. (S-YW); Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan, R.O.C. (S-YW); Department of Biotechnology, Hungkuang University, Taichung, Taiwan, R.O.C. (S-YW); and Division of Gastroenterology, Department of Internal Medicine, Wan Fang Medical Center, Taipei Medical University, Taipei, Taiwan; (G-SL, F-MS, M-SW, T-SC, C-NC).

出版信息

Medicine (Baltimore). 2015 Oct;94(42):e1801. doi: 10.1097/MD.0000000000001801.

Abstract

Most hepatocellular carcinoma (HCC) patients worldwide do not receive curative treatments. Alternative treatments for most HCC patients include palliative treatments, such as transarterial chemoembolization (TACE), chemotherapy, and radiotherapy. Although statins may be a chemopreventive treatment option for reducing hepatitis B virus (HBV)- and hepatitis C virus (HCV)-related HCC risks, their therapeutic effects are unknown. This study evaluated the effects of statin on HCC patients receiving palliative treatment.Data from the National Health Insurance claims database and cancer registry databases of The Collaboration Center of Health Information Application, Taiwan, were analyzed. We included HCC patients who were treated between January 1, 2001, and December 31, 2010, and followed them from the index date to December 31, 2012. The inclusion criteria were presence of HBV carrier-related HCC, age >20 years, and having received TACE, radiotherapy, or chemotherapy as palliative treatment. The exclusion criteria were cancer diagnosis before HCC was confirmed, surgery, liver transplantation, radiofrequency ablation, or percutaneous ethanol injection as curative treatment, missing sex-related information, HCC diagnosis before HBV, and age <20 years. We enrolled 20,200 HCC patients.The median follow-up duration was 1.66 years (interquartile range, 0.81). In total, 1988 and 18,212 patients received palliative treatment with and without statin use, respectively. HCC patients who received palliative treatment with statin use had lower HCC-specific deaths in all stages than those who received palliative treatment without statin use (P = 0.0001, 0.0002, 0.0012, and 0.0002, and relative risk (RR) = 0.763, 0.775, 0.839, and 0.718, for stages I-IV, respectively). In all-cause and HCC-specific deaths, decreasing trends (P for trend <0.0001) of adjusted hazard ratios (aHRs) were observed in all stages with no treatment, statin use only, palliative treatment only, and palliative treatment plus statin use. The aHRs of all-cause and HCC-specific deaths increased with the progress in cancer stage and reduced with the use of advanced therapeutic modalities (P for trend <0.0001). Differences in HBV- and non-HBV-related HCC were solely due to statin use. Statin use alone reduced HCC-specific deaths by 36% in non-HBV-related HCC in stage I and 50% in HBV-related HCC in stages II and III. With a relatively substantial reduction in mortality, the therapeutic effects of statin use were stronger in HBV-related HCC than in non-HBV-related HCC.Palliative treatments are critical for HCC patients. Multiple therapeutic methods with statin use reduced the mortality risk. Statins prolong the survival of patients with advanced HCC receiving palliative treatment, thus demonstrating its therapeutic value as an adjuvant treatment. Furthermore, statin-based palliative treatment in early stage HCC remarkably reduced the number of deaths. For patients who cannot tolerate palliative treatments, statin use only might possibly reduce mortality, particularly in HBV-related early stage HCC patients (>50% reduction in HCC deaths).

摘要

全球大多数肝细胞癌(HCC)患者未接受根治性治疗。大多数HCC患者的替代治疗包括姑息治疗,如经动脉化疗栓塞术(TACE)、化疗和放疗。尽管他汀类药物可能是一种化学预防治疗选择,用于降低乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)相关的HCC风险,但其治疗效果尚不清楚。本研究评估了他汀类药物对接受姑息治疗的HCC患者的影响。

分析了来自台湾健康信息应用合作中心的国民健康保险理赔数据库和癌症登记数据库的数据。我们纳入了2001年1月1日至2010年12月31日期间接受治疗的HCC患者,并从索引日期至2012年12月31日对他们进行随访。纳入标准为存在HBV携带者相关的HCC、年龄>20岁,且已接受TACE、放疗或化疗作为姑息治疗。排除标准为在HCC确诊前的癌症诊断、手术、肝移植、射频消融或经皮乙醇注射作为根治性治疗、缺少性别相关信息、HBV之前的HCC诊断以及年龄<20岁。我们纳入了20200例HCC患者。

中位随访时间为1.66年(四分位间距,0.81)。总共有1988例和18212例患者分别接受了使用和未使用他汀类药物的姑息治疗。与未使用他汀类药物接受姑息治疗的患者相比,使用他汀类药物接受姑息治疗的HCC患者在所有阶段的HCC特异性死亡人数均较低(I-IV期的P值分别为0.0001、0.0002、0.0012和0.0002,相对风险(RR)分别为0.763、0.775、0.839和0.718)。在全因死亡和HCC特异性死亡方面,在未治疗、仅使用他汀类药物、仅进行姑息治疗以及姑息治疗加使用他汀类药物的所有阶段均观察到调整后风险比(aHRs)的下降趋势(趋势P<0.0001)。全因死亡和HCC特异性死亡的aHRs随着癌症分期的进展而增加,并随着使用先进治疗方式而降低(趋势P<0.0001)。HBV相关和非HBV相关HCC的差异仅归因于他汀类药物的使用。单独使用他汀类药物可使I期非HBV相关HCC的HCC特异性死亡降低36%,使II期和III期HBV相关HCC的HCC特异性死亡降低50%。由于死亡率相对大幅降低,他汀类药物在HBV相关HCC中的治疗效果比在非HBV相关HCC中更强。

姑息治疗对HCC患者至关重要。使用他汀类药物的多种治疗方法降低了死亡风险。他汀类药物延长了接受姑息治疗的晚期HCC患者的生存期,从而证明了其作为辅助治疗的治疗价值。此外,早期HCC中基于他汀类药物的姑息治疗显著降低了死亡人数。对于无法耐受姑息治疗的患者,仅使用他汀类药物可能会降低死亡率,特别是在HBV相关的早期HCC患者中(HCC死亡降低>50%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bea/4620768/1f3ab405340e/medi-94-e1801-g005.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验