Department of Oncology, Affiliated Hospital of Qinghai University, No. 29 Tongren Road, Xining, 810000, China.
Department of geriatric diseases, Zaozhuang Mental Health Center, Zaozhuang, China.
Arch Osteoporos. 2018 Dec 17;14(1):1. doi: 10.1007/s11657-018-0552-3.
Several previous studies have shown that oral bisphosphonates (BPs) are associated with the incidence of 13 specific cancers, including lung cancer, esophageal cancer, gastric cancer, and colorectal cancer (CRC). However, the findings are heterogeneous.
Relevant studies published in databases such as PubMed, Embase database, and Cochrane library were systematically retrieved from inception to August 25th, 2018, regardless of language, by two investigators independently. Afterwards, the maximum adjusted hazard ratios (HRs) and corresponding 95% confidence intervals (CIs) were extracted from the retrieved studies. Finally, 13 cohort studies involving 1,510,763 participants were enrolled into this meta-analysis. No significant relationship was found between oral BPs and the risk of all-cause cancer in osteoporosis (OP) patients among the entire population (HR 0.97, 95% CI 0.80-1.18; I 92.5%). Besides, oral BPs could remarkably reduce the incidence of breast cancer (HR 0.79, 95% CI 0.68-0.92; I 54%) and endometrial cancer (HR 0.79, 95% CI 0.64-0.96; I 0%) in postmenopausal OP females. In addition, oral BPs were also found to evidently reduce the incidence of upper gastrointestinal cancer in OP patients among the entire population (HR 0.73, 95% CI 0.54-0.98; I 36.1%). However, oral BPs may lead to increased risk of liver cancer in mixed genders (HR 1.69, 95% CI 1.03-2.77; I 30.7%).
Taken together, oral BPs do not increase the risk of incidence of all-cause cancer; instead, they can reduce the incidence of breast, endometrial, and upper gastrointestinal cancers among the postmenopausal OP females. Our analysis stratified by gender suggests that oral BPs may increase the incidence of liver cancer in mixed genders, while no significant association was observed in females. Careful analysis of post-marketing data should be conducted to address the clinical relevance of our results on the putative association of oral BP use and liver cancer suggested by our meta-analysis.
几项先前的研究表明,口服双膦酸盐(BPs)与 13 种特定癌症的发病率有关,包括肺癌、食管癌、胃癌和结直肠癌(CRC)。然而,这些发现存在异质性。
两位研究者独立地从数据库(如 PubMed、Embase 数据库和 Cochrane 图书馆)中系统地检索了截至 2018 年 8 月 25 日发表的相关研究,无论语言如何。之后,从检索到的研究中提取最大调整后的危险比(HRs)和相应的 95%置信区间(CIs)。最后,纳入了 13 项队列研究,共纳入 1510763 名参与者进行荟萃分析。在所有人群中,口服 BPs 与骨质疏松症(OP)患者的所有原因癌症风险之间没有显著关系(HR 0.97,95%CI 0.80-1.18;I 92.5%)。此外,口服 BPs 可显著降低绝经后 OP 女性乳腺癌(HR 0.79,95%CI 0.68-0.92;I 54%)和子宫内膜癌(HR 0.79,95%CI 0.64-0.96;I 0%)的发病率。此外,还发现口服 BPs 可显著降低所有人群中 OP 患者上消化道癌症的发病率(HR 0.73,95%CI 0.54-0.98;I 36.1%)。然而,口服 BPs 可能会增加混合性别的肝癌风险(HR 1.69,95%CI 1.03-2.77;I 30.7%)。
综上所述,口服 BPs 不会增加所有原因癌症的发病风险;相反,它们可以降低绝经后 OP 女性乳腺癌、子宫内膜癌和上消化道癌症的发病率。我们按性别进行的分析表明,口服 BPs 可能会增加混合性别的肝癌发病率,而女性中未观察到显著相关性。应该仔细分析上市后数据,以解决我们的荟萃分析提示的口服 BP 使用与肝癌之间可能存在关联的临床意义。