Vulsteke Christof, Pfeil Alena M, Maggen Charlotte, Schwenkglenks Matthias, Pettengell Ruth, Szucs Thomas D, Lambrechts Diether, Dieudonné Anne-Sophie, Hatse Sigrid, Neven Patrick, Paridaens Robert, Wildiers Hans
Integrated Cancer Center Ghent, AZ Maria Middelares, Ghent, Belgium.
Institute of Pharmaceutical Medicine (ECPM), University of Basel, Basel, Switzerland.
Breast Cancer Res Treat. 2015 Jul;152(1):67-76. doi: 10.1007/s10549-015-3437-9. Epub 2015 May 28.
Anthracycline-induced cardiotoxicity (ACT) is a well-known serious adverse drug reaction leading to substantial morbidity. The purpose of this study was to assess ACT occurrence and clinical and genetic risk factors in early breast cancer patients. In 6 genes of interest (ABCC1, ABCC2, CYBA, NCF4, RAC2, SLC28A3), 10 single nucleotide polymorphisms (SNPs) involved in ACT were selected based on a literature search. Eight hundred and seventy-seven patients treated between 2000 and 2010 with 3-6 cycles of (neo) adjuvant 5-fluorouracil, epirubicin and cyclophosphamide (FEC) were genotyped for these SNPs using Sequenom MassARRAY. Main outcome measures were asymptomatic decrease of left ventricular ejection fraction (LVEF) > 10 % and cardiac failure grade 3-5 (CTCAE 4.0). To evaluate the impact of these 10 SNPs as well as clinical factors (age, relative dose intensity of epirubicin, left-sided radiotherapy, occurrence of febrile neutropenia, and planned and received cycles of epirubicin) on decrease of LVEF and cardiac failure, we performed uni- and multivariable logistic regression analysis. Additionally, exploratory analyses including 11 additional SNPs related to the metabolism of anthracyclines were performed. After a median follow-up of 3.62 years (range 0.40-9.60), a LVEF decline of > 10 % occurred in 153 patients (17.5 %) and cardiac failure in 16 patients (1.8 %). In multivariable analysis, six cycles of FEC compared to three cycles received and heterozygous carriers of the rs246221 T-allele in ABCC1 relative to homozygous carriers of the T-allele were significantly associated with LVEF decline of > 10 % (OR 1.3, 95 % CI 1.1-1.4, p < 0.001 and OR 1.6, 95 % CI 1.1-2.3, p = 0.02). Radiotherapy for left-sided breast cancer was associated with cardiac failure (OR 3.7, 95 % CI 1.2-11.5, p 0.026). The other 9 SNPs and clinical factors tested were not significantly associated. In our exploratory analysis, no other SNPs related to anthracycline metabolism were retained in the multivariate model for prediction of LVEF decline. ACT in breast cancer patients is related to number of received cycles of epirubicin and left-sided radiotherapy. Additional studies should be performed to independently confirm the potential association between rs246221 in ABCC1 and LVEF.
蒽环类药物所致心脏毒性(ACT)是一种众所周知的严重药物不良反应,可导致严重发病。本研究的目的是评估早期乳腺癌患者中ACT的发生情况以及临床和遗传风险因素。基于文献检索,在6个感兴趣的基因(ABCC1、ABCC2、CYBA、NCF4、RAC2、SLC28A3)中,选择了10个与ACT相关的单核苷酸多态性(SNP)。对2000年至2010年间接受3 - 6周期(新)辅助5-氟尿嘧啶、表柔比星和环磷酰胺(FEC)治疗的877例患者,使用Sequenom MassARRAY对这些SNP进行基因分型。主要观察指标为左心室射血分数(LVEF)无症状下降>10%和3 - 5级心力衰竭(CTCAE 4.0)。为评估这10个SNP以及临床因素(年龄、表柔比星的相对剂量强度、左侧放疗、发热性中性粒细胞减少症的发生情况以及表柔比星的计划和实际周期数)对LVEF下降和心力衰竭的影响,我们进行了单变量和多变量逻辑回归分析。此外,还进行了探索性分析,包括另外11个与蒽环类药物代谢相关的SNP。中位随访3.62年(范围0.40 - 9.60年)后,153例患者(17.5%)出现LVEF下降>10%,16例患者(1.8%)发生心力衰竭。在多变量分析中,与接受3个周期FEC相比,接受6个周期FEC以及相对于T等位基因纯合子,ABCC1中rs246221 T等位基因的杂合携带者与LVEF下降>10%显著相关(OR 1.3,95%CI 1.1 - 1.4,p < 0.001和OR 1.6,95%CI 1.1 - 2.3,p = 0.02)。左侧乳腺癌放疗与心力衰竭相关(OR 3.7,95%CI 1.2 - 11.5,p = 0.026)。测试的其他9个SNP和临床因素无显著相关性。在我们的探索性分析中,多变量模型中没有其他与蒽环类药物代谢相关的SNP被保留用于预测LVEF下降。乳腺癌患者的ACT与表柔比星的实际周期数和左侧放疗有关。应进行更多研究以独立证实ABCC1中rs246221与LVEF之间的潜在关联。