胸部放射治疗中的早期心脏肿瘤学干预:前瞻性单臂先导研究。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Samuel C Zhang, Jordan O Gasho, Celeste Eno, Katrina D Silos, Felicity Pendergast, Wenjuan Zhang, Eric Vail, Mitchell Kamrava, Behrooz Hakimian, Amin Mirhadi, Raymond H Mak, Andriana P Nikolova, Katelyn M Atkins
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引用次数: 0

摘要

背景:虽然人们越来越认识到癌症幸存者的心血管疾病发病率,包括胸部放疗后加速动脉粥样硬化,但患者的心血管风险往往没有得到充分的优化。方法:在这项前瞻性单臂队列先导研究中,患者接受高剂量胸部放疗并早期咨询心脏肿瘤学。20名患者入组。主要终点是心脏肿瘤学会诊的依从性。次要终点是心血管药物干预率和患者报告的干预观点。克隆造血潜能不确定,这是癌症患者中主要的心血管风险标志物,由辐射暴露诱导,作为一个探索性终点进行测量。结果:队列中位年龄为71岁。大多数患者为女性(13/20),原发肺癌或食管癌(16/20),7/20有既往心血管疾病。我们发现,心血管肿瘤会诊依从性很高(19/20),并导致大多数患者(12/19)心血管药物优化改变,最常见的是开始或加强他汀类药物治疗(8/12)。有8/12的患者在入组前接受了初级心脏病专家的治疗,建议他们改变用药。大多数(12/17)参与者很高兴了解他们在癌症治疗期间的心脏健康状况。8/20的患者在治疗前可检测到克隆造血,3例患者在治疗后出现新的变异(1/3为新生)。结论:我们观察到早期心脏肿瘤学咨询是可行的,导致大多数参与者(bbb60 %)心血管药物优化,最常见的是开始或加强他汀类药物治疗。放疗后可早期发现新的克隆造血变异,其对治疗后心血管风险的影响值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early cardio-oncology intervention in thoracic radiotherapy: prospective single-arm pilot study.

Background: While there is increasing recognition of the morbidity of cardiovascular disease in cancer survivors, including accelerated atherosclerosis following thoracic radiotherapy, patients are frequently under-optimized for cardiovascular risk.

Methods: In this prospective single-arm cohort pilot study, patients were treated with high-dose thoracic radiotherapy and had early consultation with cardio-oncology. Twenty patients were enrolled. The primary endpoint was adherence to cardio-oncology consultation. Secondary endpoints were cardiovascular medication intervention rate and patient-reported intervention perspectives. Clonal hematopoiesis of indeterminate potential, a major cardiovascular risk marker enriched in patients with cancer and induced by radiation exposure, was measured as an exploratory endpoint.

Results: The cohort median age is 71 years. Most patients are female (13/20), have primary lung or esophageal carcinoma (16/20), and 7/20 have pre-existing cardiovascular disease. We show that cardio-oncology consultation adherence is high (19/20) and results in cardiovascular medication optimization changes in most patients (12/19), most commonly to initiate or intensify statin therapy (8/12). 8/12 patients with a primary cardiologist prior to enrollment have medication changes recommended. Most (12/17) participants are glad to learn about their heart health during cancer treatment. Clonal hematopoiesis is detectable prior to treatment in 8/20 patients and three develop new variants after treatment (1/3 de novo).

Conclusions: We observe that early cardio-oncology consultation is feasible, leads to cardiovascular medication optimization in the majority (>60%) of participants, most commonly to initiate or intensify statin therapy. New clonal hematopoiesis variants are detectable early after radiotherapy and the impact on post-treatment cardiovascular risk is worthy of further study.

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