UPFR des Sports, Université de Bourgogne Franche-Comté, Besançon, France; EA 3920: Marqueurs pronostiques et facteurs de régulation des pathologies cardiaques et vasculaires, CHU Jean-Minjoz, Besançon, France.
INSERM UMR 1098: Unité de méthodologie et de qualité de vie en cancérologie, CHU Jean-Minjoz, Besançon, France.
Breast. 2018 Oct;41:1-7. doi: 10.1016/j.breast.2018.06.001. Epub 2018 Jun 15.
Cardiac toxicity with a decrease of the left ventricular ejection fraction (LVEF) is the main side effect induced by trastuzumab. This study reports the fluctuation of LVEF over the 12 months of adjuvant trastuzumab in PHARE trial (NCT00381901).
LVEF assessment was performed every 3 months while patients received trastuzumab and after completion of treatment over the first 2 years and then every 6 months afterwards. The fluctuations of LVEF over time were described and a logistic regression model was performed investigating associated factors to LVEF perfect recovery at baseline value.
A total of 1631 patients who received 12 months of trastuzumab from PHARE trial, were considered in the analysis. A total of 13 881 LVEF measurements were assessed. Baseline mean LVEF was 66.08% (standard error (SE): 0.15) and the mean relative LVEF decrease observed at 12-month was 3.61% (SE: 0.31). No clinical characteristic was significantly associated to LVEF fluctuation. After completion of trastuzumab, the relative difference progressively disappeared with beyond 30 months a relative difference value of 0.08% (SE: 0.42). Nevertheless, at 30 months, 48.53% of patients with available measures (379/781) did not fully recover their baseline LVEF value.
The LVEF decreased during treatment with trastuzumab and rose up after the completion of treatment without coming back to the initial values for a substantial subset. These results would suggest investigating some strategies aimed to improve the ability to achieve a full recovery.
曲妥珠单抗会导致心脏毒性,使左心室射血分数(LVEF)降低,这是其主要的副作用。本研究报告了 PHARE 试验(NCT00381901)中曲妥珠单抗辅助治疗 12 个月期间 LVEF 的波动情况。
在接受曲妥珠单抗治疗期间以及治疗结束后的前 2 年内每 3 个月评估一次 LVEF,此后每 6 个月评估一次。描述了 LVEF 的随时间波动情况,并进行了逻辑回归模型分析,以探讨与 LVEF 恢复至基线值相关的因素。
在 PHARE 试验中,共有 1631 例患者接受了 12 个月的曲妥珠单抗治疗,纳入了本分析。共评估了 13881 次 LVEF 测量。基线时 LVEF 的平均值为 66.08%(标准误差(SE):0.15),在 12 个月时观察到的平均相对 LVEF 下降为 3.61%(SE:0.31)。没有临床特征与 LVEF 波动显著相关。曲妥珠单抗治疗结束后,相对差异逐渐消失,超过 30 个月时相对差异值为 0.08%(SE:0.42)。然而,在 30 个月时,有 781 例患者中有 48.53%(379/781)可获得的测量值未完全恢复至基线 LVEF 值。
曲妥珠单抗治疗期间 LVEF 下降,治疗结束后 LVEF 升高,但对于相当一部分患者,无法恢复到初始值。这些结果表明,需要研究一些策略来提高完全恢复的能力。