Feng Shijian, Zhou Liang, Liu Qinyu, He Qing, Liao Banghua, Wei Xin, Li Hong, Wang Kunjie, Zhu Yuchun
Department of Urology, Institute of Urology (Laboratory of Reconstructive Urology), West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.
Medicine (Baltimore). 2018 Jan;97(3):e9601. doi: 10.1097/MD.0000000000009601.
Phosphodiesterase type 5 (PDE5) inhibitors are recommended for patients with erectile dysfunction by American Urological Association and European Association Urology guidelines. However, recent researches have shown that PDE5 inhibitors may lead to increased melanoma risk. Thus, we aimed to explore whether PDE5 inhibitors are associated with increased melanoma risk based on published literatures.We conducted a systematic online search on PubMed, EMBASE, Cochrane Library, Chinese Biochemical Literature, China National Knowledge Infrastructure, and Chinese Science and Technology Periodical databases to identify the related studies. Odds ratios (ORs), risk ratios, and hazard ratios with 95% confidence intervals (CIs) were extracted and calculated to assess the strength of associations between PDE5 inhibitors and melanoma risk. We also extracted the basal cell carcinoma (BCC) to validate the association in this study.We included 5 studies containing 100,932 participants in our systematic review and meta-analysis. The calculated results suggested positive results of PDE5 inhibitors on melanoma risk (OR: 1.13; 95%CI: 1.04-1.23). For localized and nonlocalized melanoma, the results were different (OR: 1.22; 95%CI: 1.04-1.43 for localized melanoma) (OR: 0.62; 95%CI: 0.39-0.98 for nonlocalized melanoma). It also showed that PDE5 inhibitors were associated with increased BCC risk (OR: 1.18; 95%CI: 1.11-1.27).The association between PDE5 inhibitors and melanoma might not be causal due to potential bias (patient selection, and so on) and limitations.
5型磷酸二酯酶(PDE5)抑制剂被美国泌尿外科学会和欧洲泌尿外科学会指南推荐用于治疗勃起功能障碍患者。然而,最近的研究表明,PDE5抑制剂可能会增加患黑色素瘤的风险。因此,我们旨在根据已发表的文献探讨PDE5抑制剂是否与黑色素瘤风险增加有关。我们在PubMed、EMBASE、Cochrane图书馆、中国生物医学文献数据库、中国知网和中国科技期刊数据库进行了系统的在线搜索,以识别相关研究。提取并计算了比值比(OR)、风险比和风险比以及95%置信区间(CI),以评估PDE5抑制剂与黑色素瘤风险之间关联的强度。我们还提取了基底细胞癌(BCC)的数据,以验证本研究中的关联。我们的系统评价和荟萃分析纳入了5项研究,共100932名参与者。计算结果表明,PDE5抑制剂与黑色素瘤风险呈阳性关联(OR:1.13;95%CI:1.04-1.23)。对于局限性和非局限性黑色素瘤,结果有所不同(局限性黑色素瘤的OR:1.22;95%CI:1.04-1.43)(非局限性黑色素瘤的OR:0.62;95%CI:0.39-0.98)。研究还表明,PDE5抑制剂与基底细胞癌风险增加有关(OR:1.18;95%CI:1.11-1.27)。由于潜在的偏倚(患者选择等)和局限性,PDE5抑制剂与黑色素瘤之间的关联可能不是因果关系。