Treatment with Beta-Blockers and ACE-Inhibitors in Breast Cancer Patients Receiving Adjuvant Trastuzumab-Based Therapy and Developing Mild Cardiac Toxicity: A Prospective Study

被引:5
作者
Geuna, Elena [1 ]
Lombardi, Pasquale [2 ]
Martinello, Rossella [3 ]
Garino, Davide [2 ]
Bonzano, Alessandro [4 ]
Galizia, Danilo [1 ]
Nuzzo, Annamaria [5 ]
Berchialla, Paola [6 ]
Becco, Paolo [2 ]
Mangioni, Monica [7 ]
De Zarlo, Lorena [7 ]
Montemurro, Filippo [1 ]
机构
[1] FPO IRCCS, Candiolo Canc Inst, Multidisciplinary Oncol Outpatient Clin, I-10060 Candiolo, Italy
[2] Univ Turin, Med Sch, I-10124 Turin, Italy
[3] Osped Cardinal Massaia, Oncol Med, I-14100 Asti, Italy
[4] FPO IRCCS, Cardiol Unit, Candiolo Canc Inst, I-10060 Candiolo, Italy
[5] FPO IRCCS, Candiolo Canc Inst, Clin Res Off, I-10060 Candiolo, Italy
[6] Univ Turin, Dipartimento Sci Clin & Biol, I-10124 Turin, Italy
[7] FPO IRCCS, Clin Lab, Candiolo Canc Inst, I-10060 Candiolo, Italy
关键词
breast cancer; trastuzumab; cardiac toxicity; enalapril; carvedilol; ACE inhibitors; beta blockers; HERCEPTIN ADJUVANT; RANDOMIZED-TRIAL; PREVENTION; CARDIOTOXICITY; CANDESARTAN; CARVEDILOL;
D O I
10.3390/cancers12020327
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Angiotensin Converting Enzyme inhibitors (ACEis) and beta-blockers (BB) are suggested to prevent and treat trastuzumab-related cardiac toxicity. We performed a prospective clinical trial in women experiencing mild cardiac toxicity (MCT) while on adjuvant treatment with trastuzumab. Methods: MCT was defined as an asymptomatic absolute decrease in LVEF of >= 10 percentage units to >50%. Treatment consisted of enalapril 2.5 mg bid and carvedilol 3.75 mg bid, which were up-titrated to 10 mg bid for the enalapril and 6.25 mg bid of carvedilol. In patients receiving study drug, the primary study end-point was LVEF recovery, which was defined as a post-trastuzumab LVEF returning to no less than -5 percentage points of the baseline value. Results: 103 patients were enrolled, 100 started trastuzumab, and 98 completed the planned treatment. Sixteen patients (16%) had MCT and received study drugs until trastuzumab completion. None of these patients achieved a post-trastuzumab LVEF recovery. Nevertheless, treated patients had significantly higher median LVEF recovery from nadir to post-trastuzumab LVEF in (8% points vs. 4% points, respectively, p = 0.004), resulting in no difference in post-treatment LVEF values compared to patients without MCT. Conclusion: Treatment of MCT with ACEis and BB allows faster LVEF recovery from nadir values and should be further studied in this setting.
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页数:12
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