Congestive heart failure after anthracycline-containing treatment for Hodgkin lymphoma: A Swedish matched cohort study

EJHaem Pub Date : 2024-11-13 DOI:10.1002/jha2.1048
Joachim Baech, Tarec Christoffer El-Galaly, Joshua P. Entrop, Ingrid Glimelius, Daniel Molin, Sissel Johanne Godtfredsen, Michael J. Crowther, Karin E. Smedby, Sandra Eloranta, Caroline E. Dietrich
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Abstract

Introduction

Congestive heart failure (CHF) is a known complication after anthracyclines and radiotherapy for classical Hodgkin lymphoma (cHL). Contemporary cHL treatment may be associated with less risk because radiotherapy use and techniques have changed substantially over time.

Methods

In this study, Swedish cHL patients diagnosed in 2000–2018, and treated with adriamycin [doxorubicin], bleomycin, vinblastine, and dacarbazine (ABVD) or bleomycin, etoposide, Adriamycin [doxorubicin], cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP), were matched 1:10 to the general population on birth year and sex to investigate relative rates and cumulative risks of CHF.

Results

A total of 1994 cHL patients were included, with a median age of 34 years. The median follow-up was 8.1 years. The CHF rate was higher for patients versus comparators (adjusted hazard ratio [HR] = 3.02, 95% confidence interval [CI]: 2.26–4.02). Patients treated with ≤200 mg/m2 of anthracyclines had HR of 2.89 (95% CI: 1.51–3.47) versus 3.91 (95% CI: 2.72–5.60) for >200 mg/m2. Treatment with ABVD was associated with a significantly higher CHF rate (adjusted HR = 3.25, 95% CI: 2.31–4.23), while BEACOPP was not (adjusted HR = 1.95, 95% CI: 0.91–4.16). The increase in relative rates translated to the absolute scale, with an increased risk persisting up to 18 years for low cumulative doses.

Conclusion

These findings highlight that cHL survivors still face a substantial excess risk of CHF in the modern treatment era and that focus on cardiovascular health remains relevant.

Abstract Image

含蒽环类药物治疗霍奇金淋巴瘤后充血性心力衰竭:瑞典匹配队列研究。
简介:充血性心力衰竭(CHF)是蒽环类药物和放射治疗经典霍奇金淋巴瘤(cHL)后的已知并发症。由于放疗的使用和技术随着时间的推移发生了很大的变化,当代cHL治疗的风险可能较低。方法:在本研究中,2000-2018年诊断为cHL并接受阿霉素[阿霉素]、博来霉素、长春碱和达卡巴嗪(ABVD)或博来霉素、乙泊苷、阿霉素[阿霉素]、环磷酰胺、长春新碱、丙卡嗪和泼尼松(BEACOPP)治疗的瑞典cHL患者,按出生年和性别与普通人群进行1:10匹配,调查CHF的相对发病率和累积风险。结果:共纳入cHL患者1994例,中位年龄34岁。中位随访时间为8.1年。患者的CHF发生率高于对照组(校正风险比[HR] = 3.02, 95%可信区间[CI]: 2.26-4.02)。≤200mg /m2蒽环类药物组患者的风险比为2.89 (95% CI: 1.51-3.47),而≤200mg /m2组患者的风险比为3.91 (95% CI: 2.72-5.60)。ABVD治疗与较高的CHF发生率相关(调整后的HR = 3.25, 95% CI: 2.31-4.23),而BEACOPP治疗与此无关(调整后的HR = 1.95, 95% CI: 0.91-4.16)。相对比率的增加转化为绝对规模,低累积剂量的风险增加可持续18年。结论:这些发现强调,在现代治疗时代,cHL幸存者仍然面临大量的CHF超额风险,关注心血管健康仍然是相关的。
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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