Centre for Big Data Research in Health, University of New South Wales, Level 2, AGSM Building (G27), Sydney, NSW, 2052, Australia.
NHMRC Clinical Trials Centre, University of Sydney, Levels 4-6 Medical Foundation Building, 92-94 Parramatta Rd, Camperdown, NSW, 2050, Australia.
Breast Cancer Res Treat. 2021 Jun;187(3):893-902. doi: 10.1007/s10549-021-06135-5. Epub 2021 Feb 22.
Cardiac function assessment is important for detecting and managing trastuzumab-associated cardiotoxicity. Our study estimates rates and predictors of cardiac assessment among patients receiving trastuzumab for HER2-positive early breast cancer (HER2+EBC) in Australia.
We conducted a retrospective cohort study of Australians initiating (neo)adjuvant trastuzumab for HER2+EBC between 1 January 2015 and 15 April 2019. We used administrative claims to determine the number of patients receiving guideline-recommended assessment, i.e. evidence of baseline cardiac assessment (between 120 days before and 30 days after trastuzumab initiation) and regular on-treatment cardiac assessments (at least every 120 days). We examined factors associated with baseline and regular on-treatment cardiac assessment.
Our study includes 5621 patients (median age 56 years), of whom 4984 (88.7%) had a baseline cardiac function test. Among 4280 patients with at least 12 months of follow-up, 2702 (63.1%) had guideline-recommended cardiac assessment. Rates of guideline-recommended assessment increased with later year of diagnosis (60.9% in 2015 vs 68.3% in 2018, OR 1.34, 95% CI 1.06-1.69). Patients with higher baseline comorbidities and greater socioeconomic disadvantage were less likely to have guideline-recommended cardiac assessment. Cardiac assessment practices varied by State/Territory. There was no association between baseline cardiac risk or anthracycline use and the likelihood of receiving guideline-recommended cardiac assessment.
The majority of patients receiving (neo)adjuvant trastuzumab had guideline-recommended baseline and on-treatment cardiac assessment. Variations in cardiac assessment predominantly related to system-level factors, such as year of diagnosis and geography, rather than individual patient factors.
心脏功能评估对于检测和管理曲妥珠单抗相关心脏毒性至关重要。本研究旨在评估澳大利亚接受曲妥珠单抗治疗的人表皮生长因子受体 2 阳性早期乳腺癌(HER2+EBC)患者进行心脏评估的比例和预测因素。
我们对 2015 年 1 月 1 日至 2019 年 4 月 15 日期间接受曲妥珠单抗(新)辅助治疗的澳大利亚人进行了回顾性队列研究。我们利用行政索赔数据确定接受指南推荐评估的患者数量,即基线心脏评估(曲妥珠单抗起始前 120 天至起始后 30 天之间)和常规治疗期间心脏评估(至少每 120 天一次)的证据。我们研究了与基线和常规治疗期间心脏评估相关的因素。
本研究共纳入 5621 例患者(中位年龄 56 岁),其中 4984 例(88.7%)进行了基线心脏功能检查。在 4280 例至少随访 12 个月的患者中,有 2702 例(63.1%)接受了指南推荐的心脏评估。指南推荐评估的比例随诊断年份的推移而增加(2015 年为 60.9%,2018 年为 68.3%,OR 1.34,95%CI 1.06-1.69)。基线合并症较多和社会经济劣势较大的患者更不可能接受指南推荐的心脏评估。各州/领地的心脏评估实践存在差异。基线心脏风险或蒽环类药物的使用与接受指南推荐的心脏评估的可能性之间没有关联。
大多数接受(新)辅助曲妥珠单抗治疗的患者接受了指南推荐的基线和治疗期间的心脏评估。心脏评估的差异主要与系统层面的因素相关,如诊断年份和地理位置,而不是个体患者的因素。