Fei Fei Gong, Eli Grunblatt, Woo Bin Voss, Vibhav Rangarajan, Sasan Raissi, Kimberly Chow, Lua Jafari, Nikita P Patel, Inga Vaitenas, Milica Marion, Haydee Ramirez, Manyun Zhao, Adin-Christian Andrei, Abigail S Baldridge, Gillian Murtagh, Kameswari Maganti, Vera H Rigolin, Nausheen Akhter
{"title":"对接受抗 HER2 治疗的早期乳腺癌患者进行应变指导的心脏保护试验(PROTECT HER2)。","authors":"Fei Fei Gong, Eli Grunblatt, Woo Bin Voss, Vibhav Rangarajan, Sasan Raissi, Kimberly Chow, Lua Jafari, Nikita P Patel, Inga Vaitenas, Milica Marion, Haydee Ramirez, Manyun Zhao, Adin-Christian Andrei, Abigail S Baldridge, Gillian Murtagh, Kameswari Maganti, Vera H Rigolin, Nausheen Akhter","doi":"10.1186/s40959-024-00291-5","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Global longitudinal strain (GLS) has been used to identify patients at risk for cancer-therapy related cardiac dysfunction (CTRCD). However, there is limited data on the effectiveness of initiating cardioprotective therapy based on a strain-guided strategy in early stage HER2+ breast cancer patients. This randomized clinical trial assessed if treatment with carvedilol based on a strain-guided strategy can prevent development of CTRCD in HER2+ breast cancer patients on non-anthracycline based regimens.</p><p><strong>Methods: </strong>Study participants were prospectively assigned to one of four arms. Patients with normal LVEF and GLS remained in Arm A. Patients whose GLS decreased by > 15% from baseline or to < -15% during follow up were randomized 1:1 to prophylactic carvedilol (Arm B) or no therapy (Arm C). Patients who developed CTRCD were assigned to Arm D. The primary endpoint was GLS stability. The secondary endpoints were development of CTRCD and rate of anti-HER2 treatment interruption.</p><p><strong>Results: </strong>Among 110 patients who completed follow up, 84 were assigned to Arm A, 10 each were randomized to Arms B or C, and 6 were assigned to Arm D. At the end of the study period, there were no significant differences in GLS stability, development of CTRCD, or number of cancer therapy cycles completed between patients who did and did not receive cardioprotective therapy.</p><p><strong>Conclusions: </strong>In this prospective randomized GLS-guided study of prophylactic carvedilol in early stage HER2+ breast cancer patients on non-anthracycline regimens, there were no significant difference between groups in GLS stability, CTRCD or trastuzumab cycles held. These findings may identify a low-risk group of patients who may be considered for less intensive cardiac surveillance.</p><p><strong>Trial registration: </strong>https://clinicaltrials.gov/study/NCT02993198 . Start date: 4/2015. 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However, there is limited data on the effectiveness of initiating cardioprotective therapy based on a strain-guided strategy in early stage HER2+ breast cancer patients. This randomized clinical trial assessed if treatment with carvedilol based on a strain-guided strategy can prevent development of CTRCD in HER2+ breast cancer patients on non-anthracycline based regimens.</p><p><strong>Methods: </strong>Study participants were prospectively assigned to one of four arms. Patients with normal LVEF and GLS remained in Arm A. Patients whose GLS decreased by > 15% from baseline or to < -15% during follow up were randomized 1:1 to prophylactic carvedilol (Arm B) or no therapy (Arm C). Patients who developed CTRCD were assigned to Arm D. The primary endpoint was GLS stability. The secondary endpoints were development of CTRCD and rate of anti-HER2 treatment interruption.</p><p><strong>Results: </strong>Among 110 patients who completed follow up, 84 were assigned to Arm A, 10 each were randomized to Arms B or C, and 6 were assigned to Arm D. At the end of the study period, there were no significant differences in GLS stability, development of CTRCD, or number of cancer therapy cycles completed between patients who did and did not receive cardioprotective therapy.</p><p><strong>Conclusions: </strong>In this prospective randomized GLS-guided study of prophylactic carvedilol in early stage HER2+ breast cancer patients on non-anthracycline regimens, there were no significant difference between groups in GLS stability, CTRCD or trastuzumab cycles held. These findings may identify a low-risk group of patients who may be considered for less intensive cardiac surveillance.</p><p><strong>Trial registration: </strong>https://clinicaltrials.gov/study/NCT02993198 . Start date: 4/2015. 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引用次数: 0
摘要
背景:全球纵向应变(GLS)已被用于识别癌症治疗相关心功能障碍(CTRCD)的高危患者。然而,基于应变指导策略对早期 HER2+ 乳腺癌患者启动心脏保护治疗的有效性数据有限。这项随机临床试验评估了基于应变指导策略的卡维地洛治疗是否能预防接受非蒽环类药物治疗的HER2+乳腺癌患者发生CTRCD:研究参与者被前瞻性地分配到四组中的一组。随访期间GLS从基线下降>15%或降至<-15%的患者按1:1随机分配至预防性卡维地洛(B组)或不治疗(C组)。出现 CTRCD 的患者被分配到 D 组。次要终点是出现 CTRCD 和抗 HER2 治疗中断率:在完成随访的 110 名患者中,84 人被分配到 A 组,10 人被随机分配到 B 组或 C 组,6 人被分配到 D 组。在研究期结束时,接受和未接受心脏保护疗法的患者在 GLS 稳定性、CTRCD 发生率或完成癌症治疗周期数方面没有显著差异:在这项前瞻性随机GLS指导研究中,对使用非蒽环类疗法的早期HER2+乳腺癌患者进行预防性卡维地洛治疗后,各组间在GLS稳定性、CTRCD或曲妥珠单抗治疗周期方面没有明显差异。这些发现可能会确定一组低风险患者,可考虑对其进行强度较低的心脏监测。试验注册:https://clinicaltrials.gov/study/NCT02993198 。开始日期:2015 年 4 月。该试验包括回顾性登记的患者。
A strain-guided trial of cardioprotection in early-stage breast cancer patients on anti-HER2 therapy (PROTECT HER2).
Background: Global longitudinal strain (GLS) has been used to identify patients at risk for cancer-therapy related cardiac dysfunction (CTRCD). However, there is limited data on the effectiveness of initiating cardioprotective therapy based on a strain-guided strategy in early stage HER2+ breast cancer patients. This randomized clinical trial assessed if treatment with carvedilol based on a strain-guided strategy can prevent development of CTRCD in HER2+ breast cancer patients on non-anthracycline based regimens.
Methods: Study participants were prospectively assigned to one of four arms. Patients with normal LVEF and GLS remained in Arm A. Patients whose GLS decreased by > 15% from baseline or to < -15% during follow up were randomized 1:1 to prophylactic carvedilol (Arm B) or no therapy (Arm C). Patients who developed CTRCD were assigned to Arm D. The primary endpoint was GLS stability. The secondary endpoints were development of CTRCD and rate of anti-HER2 treatment interruption.
Results: Among 110 patients who completed follow up, 84 were assigned to Arm A, 10 each were randomized to Arms B or C, and 6 were assigned to Arm D. At the end of the study period, there were no significant differences in GLS stability, development of CTRCD, or number of cancer therapy cycles completed between patients who did and did not receive cardioprotective therapy.
Conclusions: In this prospective randomized GLS-guided study of prophylactic carvedilol in early stage HER2+ breast cancer patients on non-anthracycline regimens, there were no significant difference between groups in GLS stability, CTRCD or trastuzumab cycles held. These findings may identify a low-risk group of patients who may be considered for less intensive cardiac surveillance.
Trial registration: https://clinicaltrials.gov/study/NCT02993198 . Start date: 4/2015. This trial included patients who were retrospectively registered.