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Unanticipated Cardiotoxicity Associated with Targeted Anticancer Therapy in Patients with Hematologic Malignancies Patients: Natural History and Risk Factors

机译:血液恶性肿瘤患者靶向抗癌治疗的意外心脏毒性:自然病史和危险因素

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摘要

Our aim is to study unanticipated cardiotoxicity associated with the use of anticancer targeted agents, a problem that remains poorly understood. Using diagnosis codes, we retrospectively identified patients with both hematologic malignancies (HM) and cardiovascular diseases (n = 820 patients). Cardiotoxicity was defined per published criteria. The targeted agents of interest included tyrosine kinase inhibitors, proteasome inhibitors, monoclonal antibodies, and immunomodulatory agents. Patients found with cardiotoxicity (n = 29) were compared with 70 case-matched reference subjects. Median time from targeted therapy exposure to cardiotoxicity was 132 days. A higher percentage of patients had prior exposure to anthracyclines in study versus reference group (65.5 vs. 42.8%, P = 0.04), however, did not stay significant in multivariate analysis. Two variables were significant predictors, prior of DVT/PE and Karnofsky score of ≥ 80% (P ≤ 0.011). Only 2 study group patients died of cardiac causes. Most cardiotoxicity patients (23/29) had remained stable or improved, while 21 patients received further chemotherapy. OS was lower in the study group (P = 0.018) versus the reference group. In conclusion, a small number patients with HM experience unanticipated cardiotoxicity with low related mortality. Risk of cardiotoxicity was significantly associated with history of DVT/PE. Most patients do well, but despite that, their OS is significantly poorer.
机译:我们的目标是研究与使用抗癌靶向药物相关的意外心脏毒性,这一问题仍知之甚少。使用诊断代码,我们回顾性地确定了同时患有血液系统恶性肿瘤(HM)和心血管疾病的患者(n = 820例)。根据公开的标准定义心脏毒性。感兴趣的靶向药物包括酪氨酸激酶抑制剂,蛋白酶体抑制剂,单克隆抗体和免疫调节剂。将发现具有心脏毒性的患者(n = 29)与70例匹配的参考对象进行比较。从靶向治疗暴露到心脏毒性的中位时间为132天。与参考组相比,研究中有更高比例的患者曾经接受蒽环类药物治疗(65.5 vs. 42.8%,P = 0.04),但是在多变量分析中没有显着意义。有两个变量是显着的预测指标,即DVT / PE之前和Karnofsky评分≥80%(P≤0.011)。只有2个研究组患者死于心脏原因。大多数心脏毒性患者(23/29)保持稳定或好转,而21例患者接受了进一步的化疗。研究组的OS低于参考组(P = 0.018)。总之,少数患有HM的患者会发生意料之外的心脏毒性,相关死亡率也较低。心脏毒性风险与DVT / PE病史显着相关。大多数患者表现良好,但尽管如此,他们的OS仍然很差。

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