Mei Zubing, Liang Mining, Li Lezhi, Zhang Yi, Wang Qingming, Yang Wei
Department of Anorectal Surgery, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of Psychiatry, the Second Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Int J Cancer. 2017 Mar 1;140(5):1068-1081. doi: 10.1002/ijc.30526.
Statins have been implicated in the regulation of cell proliferation, apoptosis and tumor progression in cancer patients and statin use at the time of cancer diagnosis has been reported to be associated with reduced cancer risk and improved survival, irrespective of concomitant anti-cancer therapy. A systematic literature search of relevant databases through May 2015 was conducted to identify studies assessing the prognostic impact of statin use on prognostic outcomes in cancer patients. Literature search identified 95 cohort studies that met the inclusion criteria. A meta-analysis of 55 articles showed that statin use was significantly associated with decreased risk of all-cause mortality (HR 0.70, 95% Cl 0.66 to 0.74) compared with nonusers. The observed pooled estimates were retained for cancer-specific mortality (HR 0.60, 95% Cl 0.47 to 0.77), progression-free survival (HR 0.67, 95% Cl 0.56 to 0.81), recurrence-free survial (HR 0.74, 95% Cl 0.65 to 0.83) and disease-free survival (HR 0.53, 95% Cl 0.40 to 0.72). These associations almost remained consistent across those outcomes when stratified by publication type, tumour location, study design, sample size, initiation of statins, disease stage, research country, follow-up duration or research hospital involved. Subgroup analyses according to initiation of statins showed postdiagnosis statin users (HR 0.65, 95% Cl 0.54 to 0.79) gained significantly more recurrence-free survival benefit than prediagnosis statin users (HR 0.86, 95% Cl 0.77 to 0.96) (p for interaction = 0.018). Statin therapy has potential survival benefit for patients with malignancy. Further large-scale prospective studies emphasising survival outcomes of individual cancer type are strongly encouraged.
他汀类药物已被证明与癌症患者的细胞增殖、凋亡及肿瘤进展的调控有关,并且据报道,在癌症诊断时使用他汀类药物与降低癌症风险及改善生存率相关,无论是否同时进行抗癌治疗。通过检索截至2015年5月的相关数据库进行了一项系统的文献研究,以确定评估他汀类药物使用对癌症患者预后结果的预后影响的研究。文献检索确定了95项符合纳入标准的队列研究。对55篇文章的荟萃分析表明,与未使用者相比,使用他汀类药物与全因死亡率风险降低显著相关(风险比0.70,95%置信区间0.66至0.74)。观察到的汇总估计值在癌症特异性死亡率(风险比0.60,95%置信区间0.47至0.77)、无进展生存期(风险比0.67,95%置信区间0.56至0.81)、无复发生存期(风险比0.74,95%置信区间0.65至0.83)和无病生存期(风险比0.53,95%置信区间0.40至0.72)方面保持不变。当按发表类型、肿瘤位置、研究设计、样本量、他汀类药物起始使用时间、疾病分期、研究国家、随访时间或所涉及的研究医院进行分层时,这些关联在这些结果中几乎保持一致。根据他汀类药物起始使用时间进行的亚组分析表明,诊断后使用他汀类药物的患者(风险比0.65,95%置信区间0.54至0.79)比诊断前使用他汀类药物的患者(风险比0.86,95%置信区间0.77至0.96)获得的无复发生存期益处显著更多(交互作用p值 = 0.018)。他汀类药物治疗对恶性肿瘤患者有潜在的生存益处。强烈鼓励开展进一步的大规模前瞻性研究,重点关注个体癌症类型的生存结果。