Department of Medicine, University of Alabama at Birmingham, 321 Lyons Harrison Research Building, 1720 2nd Ave South, Birmingham, AL, 35294, USA.
Division of Cardiology, Department of Medicine, University of Colorado, 12631 E. 17th Ave, Mail Stop B130, Aurora, CO, 80045, USA.
Curr Treat Options Oncol. 2020 Apr 8;21(4):32. doi: 10.1007/s11864-020-0722-6.
Cardiovascular disease is a leading cause of death among cancer survivors. While the field of cardiology as a whole is driven by evidence generated through robust clinical trials, data in cardio-oncology is limited to a relatively small number of prospective clinical trials with heterogeneous groups of cancer patients. In addition, many pharmaceutical trials in oncology are flawed from a cardiovascular perspective because they exclude patients with significant cardiovascular (CV) history and have wide variation in the definitions of CV events and cardiotoxicity. Ultimately, oncology trials often underrepresent the possibility of cardiovascular events in a "real world" population. Thus, the signal for CV toxicity from a cancer treatment is often not manifested until phase IV studies; where we are often caught trying to mitigate the CV effects rather than preventing them. Most of the data about cardiotoxicity from cancer therapy and cardioprotective strategies has been developed from our experience in using anthracyclines for over 50 years with dramatic improvement in cancer survivorship. However, as we are in an era where cancer drug discovery is moving at lightning pace with increasing survival rates, it is imperative to move beyond anthracyclines and commit to research on the cardiovascular side effects of all aspects of cancer therapy with a focus on prevention. We emphasize the role of pre-cancer treatment CV assessment to anticipate cardiac issues and ultimately optimizing CV risk prior to cancer therapy as an opportunity to mitigate cardiovascular risk from cancer therapy.
心血管疾病是癌症幸存者死亡的主要原因。虽然整个心脏病学领域都是由通过强大的临床试验产生的证据推动的,但心血管肿瘤学的数据仅限于少数相对较少的前瞻性临床试验,且这些临床试验的癌症患者群体存在异质性。此外,许多肿瘤学的药物试验从心血管角度来看存在缺陷,因为它们排除了有严重心血管病史的患者,并且心血管事件和心脏毒性的定义差异很大。最终,肿瘤学试验往往不能代表“真实世界”人群中发生心血管事件的可能性。因此,癌症治疗的心血管毒性信号往往直到 IV 期研究才显现出来;那时我们常常试图减轻心血管影响,而不是预防它们。关于癌症治疗和心脏保护策略的心脏毒性的大部分数据都是从我们使用蒽环类药物超过 50 年的经验中发展而来的,这使得癌症患者的存活率显著提高。然而,随着癌症药物发现的步伐在以闪电般的速度前进,癌症治疗的各个方面的心血管副作用的研究都取得了进步,我们必须超越蒽环类药物,并致力于研究,重点是预防。我们强调在癌症治疗前进行心血管评估,以预测心脏问题,并最终在癌症治疗前优化心血管风险,以减轻癌症治疗的心血管风险。