Neoplasma. 2018;65(2):216-221. doi: 10.4149/neo_2018_170111N23.
This meta-analysis aimed to clarify the actual association between the phosphodiesterase type 5 inhibitors (PDE5-Is) use and the risk of melanoma in erectile dysfunction (ED) patients. A systematic literature search was conducted in online databases in October, 2016 to identify studies focusing on the association between PDE5-Is use and the risk of melanoma. Summarized multivariate adjusted risk ratios (RRs) and 95% confidence intervals (CIs) were calculated to assess the strength of associations. A total of six clinical trials containing more than one million participants were included. ED patients using PDE5-Is shared a significant high risk of melanoma (RR=1.12, 95% CI=1.03-1.21, p=0.006). Positive associations were observed in all kinds of prescriptions: single prescription (RR=1.20, 95% CI=1.06-1.35, p=0.003), medium number of prescription (RR=1.15, 95% CI=1.01-1.30, p=0.03), and high number of prescription (RR=1.18, 95% CI=1.05-1.34, P=0.006). Additionally, PDE5-Is were also found to be significantly associated with increased risk of basal cell carcinoma (RR=1.14, 95% CI=1.09-1.19, p<0.00001). Our study indicates that PDE5-Is use could significantly increase the risk of melanoma and basal cell carcinoma. However, the risk of melanoma did not rise significantly with the increased number of prescriptions. Consequently, owing to the lack of information about other potential synergistic factors, it is difficult for us to make a solid conclusion that application of PDE5-Is is the direct cause of increased risk of melanoma. Their relationship needs to be validated by further evidences.
本荟萃分析旨在阐明磷酸二酯酶 5 抑制剂(PDE5-Is)的使用与勃起功能障碍(ED)患者黑色素瘤风险之间的实际关联。2016 年 10 月,我们在在线数据库中进行了系统文献检索,以确定专注于 PDE5-Is 使用与黑色素瘤风险之间关联的研究。计算了汇总的多变量调整风险比(RR)和 95%置信区间(CI),以评估关联的强度。共有六项包含超过一百万参与者的临床试验被纳入。使用 PDE5-Is 的 ED 患者黑色素瘤风险显著升高(RR=1.12,95%CI=1.03-1.21,p=0.006)。各种处方均观察到阳性关联:单处方(RR=1.20,95%CI=1.06-1.35,p=0.003)、中等数量的处方(RR=1.15,95%CI=1.01-1.30,p=0.03)和大量处方(RR=1.18,95%CI=1.05-1.34,P=0.006)。此外,还发现 PDE5-Is 与基底细胞癌风险增加显著相关(RR=1.14,95%CI=1.09-1.19,p<0.00001)。我们的研究表明,PDE5-Is 的使用可显著增加黑色素瘤和基底细胞癌的风险。然而,随着处方数量的增加,黑色素瘤的风险并未显著增加。因此,由于缺乏有关其他潜在协同因素的信息,我们很难得出 PDE5-Is 的应用是黑色素瘤风险增加的直接原因的明确结论。需要进一步的证据来验证它们之间的关系。