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P2Y12 inhibitors: do they increase cancer risk?

机译:P2Y12抑制剂:它们会增加癌症风险吗?

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摘要

Treatment with dual antiplatelet therapy (DAPT), typically combining a P2Y12 inhibitor with aspirin, is the standard of care for the prevention of coronary stent thrombosis, especially post revascularization and in the setting of acute coronary syndromes (ACS). Determining the appropriate duration has been debated as prolonged courses have been associated with reduced thrombotic complications. Despite proven benefit, there have been reports of a potential cancer risk associated with DAPT following the FDA’s review of the TRITON-TIMI 38 trial and the DAPT trial. The latter revealed an increased risk of non-cardiovascular death, which was driven by more bleeding and cancer-related deaths. This further clouds the decision if longer courses of DAPT should be recommended. Several trials and meta-analyses have been conducted to further review this cancer risk with P2Y12 inhibitors. This manuscript intends to evaluate current literature to determine if there is a risk of cancer for patients on DAPT and its consequences in the management of cardiovascular disease.
机译:双重抗血小板治疗(DAPT)的治疗通常是将P2Y12抑制剂与阿司匹林联合使用,是预防冠状动脉支架血栓形成的护理标准,尤其是在血运重建后和急性冠脉综合征(ACS)发生时。由于延长疗程与减少血栓形成并发症相关,因此确定合适的持续时间一直存在争议。尽管已证明有益处,但在FDA对TRITON-TIMI 38试验和DAPT试验进行审查之后,有报道称DAPT有潜在的癌症风险。后者显示非心血管死亡的风险增加,这是由更多的出血和与癌症相关的死亡驱动的。如果需要建议更长的DAPT疗程,这将使决定更加模糊。已经进行了一些试验和荟萃分析,以进一步评估P2Y12抑制剂的这种癌症风险。该手稿旨在评估当前的文献,以确定DAPT患者是否有患癌症的风险及其在心血管疾病管理中的后果。

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