Cardiovascular Disease Mortality Risk among Long-term Survivors of Different Hodgkin Lymphoma Types.

IF 1.3 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Reviews in cardiovascular medicine Pub Date : 2025-06-30 eCollection Date: 2025-06-01 DOI:10.31083/RCM24981
Zhenxing Lu, Liyu Guo, Huijuan He, Linglong Liu, Manting Feng, Xueqi Xiao, Xin Lin, Yingyu Deng, Tianwang Guan, Xiaoping Peng
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Abstract

Background: The temporal trend and disparities in cardiovascular disease (CVD) mortality risk among long-term survivors of different Hodgkin lymphoma (HL) types are unclear. Therefore, we aimed to examine the temporal trend and disparities in CVD mortality risk among survivors of various HL subtypes.

Methods: This multicenter cohort included 20,423 patients with HL diagnosed between 1975 and 2018, with an average follow-up time of 18.5 years. Proportional mortality ratio, cumulative cause-specific mortality accounting for competing risks, standardized mortality ratio, and absolute excess risk were calculated.

Results: Patients with nodular lymphocyte-predominant HL (NLPHL) and classical HL exhibited higher CVD-related deaths than HL-related deaths after approximately 12 and 120 months of follow-up, respectively. From the initial diagnosis to >500 months of follow-up, the cumulative CVD mortality increased continuously without a plateau and exceeded that of HL at different times in most patients with various HL types. However, CVD mortality risk exceeded that of HL earlier in NLPHL than in other types. Black or male patients with nodular sclerosing classical HL exhibited a higher CVD mortality risk, while a contrary trend was noted among those with lymphocyte-rich classical HL or lymphocyte-depleted classical HL. Over the past decades, CVD mortality risk has decreased slowly or remained unchanged. Patients with HL exhibited higher risks of CVD mortality than the general population.

Conclusions: CVD mortality risk exceeded that of HL over time among many survivors. This temporal trend was significantly different among various HL subtypes. Thus, more effective strategies are required to reduce the risk of CVD mortality, depending on subtypes.

不同霍奇金淋巴瘤类型长期存活者的心血管疾病死亡率风险
背景:不同类型霍奇金淋巴瘤(HL)长期存活者心血管疾病(CVD)死亡风险的时间趋势和差异尚不清楚。因此,我们旨在研究各种HL亚型幸存者CVD死亡风险的时间趋势和差异。方法:该多中心队列纳入了1975年至2018年间诊断为HL的20,423例患者,平均随访时间为18.5年。计算了比例死亡率、考虑竞争风险的累积病因特异性死亡率、标准化死亡率和绝对超额风险。结果:在大约12个月和120个月的随访后,结节性淋巴细胞占主导地位的HL (NLPHL)和典型HL的cvd相关死亡率分别高于HL相关死亡率。从初诊到随访50 ~ 500个月,各种类型的大多数患者CVD累计死亡率持续上升,无平台期,不同时期均超过HL。然而,与其他类型相比,NLPHL的CVD死亡风险早于HL。黑人或男性结节硬化型经典HL患者CVD死亡风险较高,而淋巴细胞丰富型经典HL或淋巴细胞减少型经典HL患者CVD死亡风险则相反。在过去的几十年里,心血管疾病的死亡风险缓慢下降或保持不变。HL患者的心血管疾病死亡率高于一般人群。结论:随着时间的推移,许多幸存者的心血管疾病死亡率风险超过了HL。这一时间趋势在不同HL亚型之间存在显著差异。因此,根据不同的亚型,需要更有效的策略来降低心血管疾病死亡率的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reviews in cardiovascular medicine
Reviews in cardiovascular medicine 医学-心血管系统
CiteScore
2.70
自引率
3.70%
发文量
377
审稿时长
1 months
期刊介绍: RCM is an international, peer-reviewed, open access journal. RCM publishes research articles, review papers and short communications on cardiovascular medicine as well as research on cardiovascular disease. We aim to provide a forum for publishing papers which explore the pathogenesis and promote the progression of cardiac and vascular diseases. We also seek to establish an interdisciplinary platform, focusing on translational issues, to facilitate the advancement of research, clinical treatment and diagnostic procedures. Heart surgery, cardiovascular imaging, risk factors and various clinical cardiac & vascular research will be considered.
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