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蒽环类药物心脏毒性风险增加的接受 R-CHOP 方案治疗的淋巴瘤患者中,一级心脏保护可降低死亡率。

Primary Cardioprotection Reduces Mortality in Lymphoma Patients with Increased Risk of Anthracycline Cardiotoxicity, Treated by R-CHOP Regimen.

机构信息

Department of Haematology, Jagiellonian University, Krakow,

Department of Experimental Oncology, European Institute of Oncology, Milan, Italy.

出版信息

Chemotherapy. 2018;63(4):238-245. doi: 10.1159/000492942. Epub 2018 Oct 29.

Abstract

BACKGROUND

Advances in anti-lymphoma therapy prolong overall survival, making late adverse effects, like doxorubicin-related cardiotoxicity, an even more important clinical issue. The effectiveness of cardioprotective strategies with close monitoring, angiotensin-converting enzyme inhibitors and/or β-blockers as well as liposomal doxorubicin are still unconfirmed in clinical practice.

METHODS

This study evaluated the role of a primary cardioprotection strategy in preventing cardiovascular mortality and heart failure occurrence in non-Hodgkin lymphoma (NHL) patients with a high risk of anthracycline cardiotoxicity. Thirty-five NHL patients were subjected prospectively to ramipril and/or bisoprolol at NHL diagnosis, before implementing doxorubicin-containing regimens. Additionally, patients with a diagnosis of asymptomatic/mild heart failure received the liposomal form of doxorubicin. The clinical outcome and frequency of all serious cardiac events were compared with the results in a historical cohort of 62 high-risk cases treated without primary cardioprotection.

RESULTS

NHL patients with a primary cardioprotection strategy did not experience cardiovascular deaths in contrast to the retrospective control group where cardiovascular mortality was 14.5% at 3 years (p < 0.05). Primary cardioprotection also decreased the frequency of new cardiotoxicity-related clinical symptoms (2.8 vs. 24.1%; p < 0.05) and prevented the occurrence of cardiac systolic dysfunction (0 vs. 8.5%, respectively; p < 0.05). Although the study was not planned to detect any survival benefit, it demonstrated a trend towards increased response rates (complete response 82 vs. 67%; p not significant) and prolonged survival (projected 5-year overall survival 74 vs. 60%; p < 0.05) for patients treated with primary cardioprotection.

CONCLUSIONS

A primary personalized cardioprotection strategy decreases the number of cardiac deaths and may potentially prolong overall survival in NHL patients with increased risk of anthracycline cardiotoxicity.

摘要

背景

抗淋巴瘤治疗的进步延长了总生存期,使得迟发性不良反应(如多柔比星相关的心脏毒性)成为一个更重要的临床问题。在临床实践中,通过密切监测、使用血管紧张素转换酶抑制剂和/或β受体阻滞剂以及使用脂质体多柔比星等心脏保护策略的有效性仍未得到证实。

方法

本研究评估了一种主要的心脏保护策略在预防高蒽环类药物心脏毒性风险的非霍奇金淋巴瘤(NHL)患者中心血管死亡和心力衰竭发生中的作用。35 例 NHL 患者在开始多柔比星方案前,前瞻性地接受雷米普利和/或比索洛尔治疗。此外,诊断为无症状/轻度心力衰竭的患者接受脂质体多柔比星治疗。将临床结果和所有严重心脏事件的频率与未进行主要心脏保护的 62 例高危病例的历史队列结果进行比较。

结果

与回顾性对照组(3 年时心血管死亡率为 14.5%,p < 0.05)相比,接受主要心脏保护策略的 NHL 患者未发生心血管死亡。主要心脏保护还降低了新发与心脏毒性相关的临床症状的频率(2.8% vs. 24.1%;p < 0.05),并预防了心脏收缩功能障碍的发生(0% vs. 8.5%;p < 0.05)。尽管该研究未计划检测任何生存获益,但显示出接受主要心脏保护治疗的患者具有更高的缓解率(完全缓解 82% vs. 67%;p 无显著差异)和更长的生存时间(预计 5 年总生存率 74% vs. 60%;p < 0.05)的趋势。

结论

对于蒽环类药物心脏毒性风险增加的 NHL 患者,个性化的主要心脏保护策略可降低心脏死亡人数,并可能潜在地延长总生存期。

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