Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
Oxford Cancer and Haematology Centre, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, United Kingdom.
J Clin Oncol. 2021 Nov 10;39(32):3591-3601. doi: 10.1200/JCO.21.00408. Epub 2021 Aug 13.
The contemporary management of early-stage Hodgkin lymphoma (ES-HL) involves balancing the risk of late adverse effects of radiotherapy against the increased risk of relapse if radiotherapy is omitted. This study provides information on the risk of radiation-related cardiovascular disease to help personalize the delivery of radiotherapy in ES-HL.
We predicted 30-year absolute cardiovascular risk from chemotherapy and involved field radiotherapy in patients who were positron emission tomography (PET)-negative following three cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine chemotherapy within a UK randomized trial of PET-directed therapy for ES-HL. Cardiac and carotid radiation doses and chemotherapy exposure were combined with established dose-response relationships and population-based mortality and incidence rates.
Average mean heart dose was 4.0 Gy (range 0.1-24.0 Gy) and average bilateral common carotid artery dose was 21.5 Gy (range 0.6-38.1 Gy), based on individualized cardiovascular dosimetry for 144 PET-negative patients receiving involved field radiotherapy. The average predicted 30-year radiation-related absolute excess overall cardiovascular mortality was 0.56% (range 0.01%-6.79%; < 0.5% in 67% of patients and > 1% in 15%), whereas average predicted 30-year excess incidence was 6.24% (range 0.31%-31.09%; < 5% in 58% of patients and > 10% in 24%). For cardiac disease, the average predicted 30-year radiation-related absolute excess mortality was 0.42% (0.79% with mediastinal involvement and 0.05% without) and for stroke, it was 0.14%.
Predicted excess cardiovascular risk is small for most patients, so radiotherapy may provide net benefit. However, for a minority of patients receiving high doses of radiation to cardiovascular structures, it may be preferable to consider advanced radiotherapy techniques to reduce doses or to omit radiotherapy and accept the increased relapse risk. Individual assessment of cardiovascular and other risks before treatment would allow personalized decision making about radiotherapy in ES-HL.
早期霍奇金淋巴瘤(ES-HL)的现代治疗需要权衡放疗引起迟发性不良反应的风险与省略放疗导致复发风险增加之间的平衡。本研究旨在提供与放疗相关的心血管疾病风险信息,以帮助个体化决策 ES-HL 患者的放疗。
我们对英国一项 PET 引导治疗早期霍奇金淋巴瘤的随机试验中,三周期阿霉素、博来霉素、长春花碱和达卡巴嗪化疗后 PET 阴性的患者,预测化疗联合累及野放疗 30 年的绝对心血管风险。心脏和颈动脉剂量以及化疗暴露与已建立的剂量反应关系和人群死亡率及发病率相结合。
根据 144 例接受累及野放疗的 PET 阴性患者的个体化心血管剂量测定,平均平均心脏剂量为 4.0 Gy(范围 0.1-24.0 Gy),平均双侧颈总动脉剂量为 21.5 Gy(范围 0.6-38.1 Gy)。平均预测 30 年与放疗相关的绝对心血管死亡风险增加为 0.56%(范围 0.01%-6.79%;67%的患者<0.5%,15%的患者>1%),平均预测 30 年心血管疾病发病率增加为 6.24%(范围 0.31%-31.09%;58%的患者<5%,24%的患者>10%)。对于心脏病,平均预测 30 年与放疗相关的绝对死亡风险增加为 0.42%(纵隔受累者为 0.79%,无纵隔受累者为 0.05%),对于中风,为 0.14%。
大多数患者的预测心血管风险较小,因此放疗可能带来净获益。然而,对于少数接受大剂量心血管结构放疗的患者,可能更倾向于考虑先进的放疗技术以降低剂量,或省略放疗并接受复发风险增加的风险。治疗前对心血管风险和其他风险的个体化评估,可使 ES-HL 患者的放疗决策实现个体化。