de Vries Simone, Haaksma Miriam L, Jóźwiak Katarzyna, Schaapveld Michael, Hodgson David C, Lugtenburg Pieternella J, Krol Augustinus D G, Petersen Eefke J, van Spronsen Dick Johan, Ahmed Sameera, Hauptmann Michael, Aleman Berthe M P, van Leeuwen Flora E
Department of Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, the Netherlands.
J Clin Oncol. 2023 Jan 1;41(1):86-95. doi: 10.1200/JCO.21.02613. Epub 2022 Aug 10.
Previous efforts to predict absolute risk of treatment-related cardiovascular diseases (CVDs) have mostly focused on childhood cancer survivors. We aimed to develop prediction models for risk of coronary heart disease (CHD) and heart failure (HF) for survivors of adolescent/adult Hodgkin lymphoma (HL).
For model development, we used a multicenter cohort including 1,433 5-year HL survivors treated between 1965 and 2000 and age 18-50 years at HL diagnosis, with complete data on administered chemotherapy regimens, radiotherapy volumes and doses, and cardiovascular follow-up. Using cause-specific hazard models, covariate-adjusted cumulative incidences for CHD and HF were estimated in the presence of competing risks of death because of other causes than CHD and HF. Age at HL diagnosis, sex, smoking status, radiotherapy, and anthracycline treatment were included as predictors. External validation for the CHD model was performed using a Canadian cohort of 708 HL survivors treated between 1988 and 2004 and age 18-50 years at HL diagnosis.
After a median follow-up of 24 years, 341 survivors had developed CHD and 102 had HF. We were able to predict CHD and HF risk at 20 and 30 years after treatment with moderate to good overall calibration and moderate discrimination (areas under the curve: 0.68-0.74), which was confirmed by external validation for the CHD model (areas under the curve: 0.73-0.74). On the basis of our model including prescribed mediastinal radiation dose, 30-year risks ranged from 4% to 78% for CHD and 3% to 46% for HF, depending on risk factors.
We developed and validated prediction models for CHD and HF with good overall calibration and moderate discrimination. These models can be used to identify HL survivors who might benefit from targeted screening for CVD and early treatment for CVD risk factors.
以往预测与治疗相关的心血管疾病(CVD)绝对风险的研究大多集中在儿童癌症幸存者身上。我们旨在为青少年/成人霍奇金淋巴瘤(HL)幸存者开发冠心病(CHD)和心力衰竭(HF)风险的预测模型。
为了进行模型开发,我们使用了一个多中心队列,其中包括1433名在1965年至2000年间接受治疗的5年HL幸存者,他们在HL诊断时年龄为18至50岁,拥有关于所给予的化疗方案、放射治疗体积和剂量以及心血管随访的完整数据。使用特定病因风险模型,在存在除CHD和HF以外其他原因导致的死亡竞争风险的情况下,估计CHD和HF的协变量调整累积发病率。HL诊断时的年龄、性别、吸烟状况、放射治疗和蒽环类药物治疗被纳入作为预测因素。使用一个由708名在1988年至2004年间接受治疗且在HL诊断时年龄为18至50岁的HL幸存者组成的加拿大队列对CHD模型进行外部验证。
中位随访24年后,341名幸存者患CHD,102名患HF。我们能够在治疗后20年和30年预测CHD和HF风险,总体校准程度中等至良好,辨别能力中等(曲线下面积:0.68 - 0.74),CHD模型经外部验证得到证实(曲线下面积:0.73 - 0.74)。基于我们包含规定纵隔放射剂量的模型,CHD的30年风险范围为4%至78%,HF为3%至46%,具体取决于风险因素。
我们开发并验证了CHD和HF的预测模型,总体校准良好,辨别能力中等。这些模型可用于识别可能从针对CVD的靶向筛查和CVD风险因素的早期治疗中获益的HL幸存者。