Left ventricular ejection fraction decrease related to BRAF and/or MEK inhibitors in metastatic melanoma patients: A retrospective analysis

被引:18
作者
Berger, Mathilde [1 ]
Amini-Adle, Mona [1 ]
Maucort-Boulch, Delphine [2 ,3 ]
Robinson, Philip [4 ]
Thomas, Luc [1 ,5 ]
Dalle, Stephane [1 ,5 ]
Courand, Pierre-Yves [6 ,7 ,8 ]
机构
[1] Hosp Civils Lyon, Ctr Hosp Lyon Sud, Serv Dermatol, Pierre Benite, France
[2] Univ Lyon 1, Hosp Civils Lyon, Serv Biostatist, Lyon, France
[3] Univ Lyon, CNRS, Equipe Biostat Sante, Lab Biometrie & Biol Evolut, Villeurbanne, France
[4] Hosp Civils Lyon, Direct Rech Clin & Innovat, Lyon, France
[5] Univ Claude Bernard, Ctr Rech Cancerol Lyon, Univ Lyon, Lyon, France
[6] Hop Croix Rousse, Serv Cardiol, Hosp Civils Lyon, Lyon, France
[7] Ctr Hosp Lyon Sud, Lyon, France
[8] Univ Lyon, Creatis Umr Inserm U1044, INSA, Lyon, France
关键词
adverse events; BRAF inhibitor; cardiac toxicity; heart failure; left ventricular ejection fraction; left ventricular systolic dysfunction; MEK inhibitor; metastatic melanoma; ACTIVATED PROTEIN-KINASE; HEART-FAILURE; TROPONIN-I; CHEMOTHERAPEUTIC-AGENTS; EUROPEAN ASSOCIATION; MAPK PATHWAY; DOUBLE-BLIND; CANCER; HYPERTROPHY; CARDIOTOXICITY;
D O I
10.1002/cam4.2922
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BRAF and MEKis have revolutionized the management of BRAF(V600)-mutated melanoma patients. Left ventricular ejection fraction decrease (LVEF-D) related to these treatments has not been thoroughly evaluated to date. The main objective of this study was to describe characteristics of LVEF-D in melanoma patients treated with BRAF and/or MEKis. Metastatic melanoma patients treated with BRAF and/or MEKis between March 1, 2012 and May 18, 2018 were included retrospectively (Lyon Sud University Hospital, Hospices Civils de Lyon). LVEF-D was defined as a reduction in LVEF >= 10% from baseline to a value <55%; normalization was defined as a value >= 55%. Among the 88 patients included, 12 (13.6%) experienced a LVEF-D, including 10 grade 2 and 2 grade 3. The median onset of which was 11 months (IQR [3-21]). No patient previously treated with beta-blockers (n = 12) experienced a LVEF-D. Analysis of laboratory parameters, electrocardiogram, and transthoracic echocardiography during the follow-up did not find any predictive marker of LVEF-D. All patients who benefited from a specific treatment of LVEF-D had a normalization of LVEF at the end of follow-up. LVEF recovery was significantly better for patients treated with angiotensin converting enzyme inhibitors and beta-blockers than those who did not (P = .019). Ophthalmological adverse events were significantly more frequent in patients who experienced a LVEF-D (P = .006) and the latter did not influence overall-survival (P = .117) or progression-free-survival (P = .297). LVEF-D is a common and easily manageable adverse event due to BRAF and MEKis. Its association with ocular toxicity suggests a close ophthalmological monitoring when LVEF-D occurs.
引用
收藏
页码:2611 / 2620
页数:10
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