Late Cardiac Toxicity After Anthracyclines and Radiotherapy for Lymphoma—A Regression Analysis of Dose-Response

IF 3.9 4区 医学 Q2 HEMATOLOGY
Lotte Nygård, Ivan Richter Vogelius, Klaus F. Kofoed, Søren Bentzen, Lena Specht
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Abstract

Late cardiac toxicity after radiation therapy and/or systemic therapy with anthracyclines for lymphomas is a serious concern. To estimate the risks with different treatment combinations, reliable estimates of the dose-response relationships are needed. We performed a literature-based regression analysis of long-term cardiac events after lymphoma treatment. The objective was to identify dose-response relationships for anthracycline and radiotherapy regarding congestive heart failure (CHF), ischemic heart disease (IHD), and valvular heart disease (VHD). We included papers published January 2000-December 2022 with data on long term cardiac outcomes in lymphoma patients, radiation doses to the heart, and anthracycline doses. Papers without dose/response information were excluded. We identified six eligible papers including 22,916 patients. The excess relative risk (ERR) of CHF for anthracyclines per 100 mg/m2 (corresponding to 2 cycles of ABVD or CHOP chemotherapy) was 92% (CI: 74%–101%), and for radiotherapy per Gray (Gy) of mean heart dose it was 6.1% (CI: 4.4%–7.6%). Corresponding numbers for the other endpoints were: IHD: No effect of anthracyclines, ERR = 4.4%/Gy (CI: 2.7%–6.1%) and VHD: ERR = 25%/100 mg/m2 (CI: 13%–37%) and ERR = 10%/Gy (CI: 6%–13%). Data agree with a linear no threshold dose-response relationship for related endpoints, that is, there are no “safe” lower doses of either anthracyclines or radiotherapy. Late cardiac toxicity risks for all three endpoints can be assessed in each patient by a combined estimate from the cumulative doses of anthracyclines and radiation to the heart. This estimate can guide future treatment allocation in lymphoma patients.

Abstract Image

蒽环类药物和放疗治疗淋巴瘤后的晚期心脏毒性——剂量-反应的回归分析
放疗和/或蒽环类药物治疗淋巴瘤后的晚期心脏毒性是一个严重的问题。为了估计不同治疗组合的风险,需要对剂量-反应关系进行可靠的估计。我们对淋巴瘤治疗后的长期心脏事件进行了基于文献的回归分析。目的是确定蒽环类药物和放疗治疗充血性心力衰竭(CHF)、缺血性心脏病(IHD)和瓣膜性心脏病(VHD)的剂量-反应关系。我们纳入了2000年1月至2022年12月发表的论文,其中包含淋巴瘤患者长期心脏结局、心脏辐射剂量和蒽环类药物剂量的数据。没有剂量/反应信息的论文被排除在外。我们确定了6篇符合条件的论文,包括22,916例患者。每100 mg/m2蒽环类药物(对应2个ABVD或CHOP化疗周期)的CHF的超额相对危险度(ERR)为92% (CI: 74%-101%),每格雷(Gy)平均心脏剂量放疗的超额相对危险度(ERR)为6.1% (CI: 4.4%-7.6%)。其他终点对应的数字为:IHD:蒽环类药物无影响,ERR = 4.4%/Gy (CI: 2.7%-6.1%), VHD: ERR = 25%/100 mg/m2 (CI: 13%-37%), ERR = 10%/Gy (CI: 6%-13%)。相关终点的数据与线性无阈值剂量-反应关系一致,即蒽环类药物或放疗均不存在“安全”的较低剂量。所有三个终点的晚期心脏毒性风险都可以通过对蒽环类药物累积剂量和对心脏辐射的综合估计来评估。这一估计可以指导未来淋巴瘤患者的治疗分配。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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