Efficacy and safety of lomitapide in homozygous familial hypercholesterolaemia: the pan-European retrospective observational study

被引:33
作者
D'Erasmo, Laura [1 ]
Steward, Kim [2 ]
Cefalu, Angelo Baldassare [3 ]
Di Costanzo, Alessia [1 ]
Boersma, Eric [4 ]
Bini, Simone [1 ]
Arca, Marcello [1 ]
van Lennep, Jeanine Roeters [2 ]
机构
[1] Sapienza Univ Rome, Dept Translat & Precis Med, Viale Univ 35, I-00161 Rome, Italy
[2] Univ Med Ctr Rotterdam, Dept Internal Med, Erasmus MC, Doctor Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
[3] Univ Palermo, Dipartimento Promoz Salute Materno Infantile Med, Via Vespro 129, I-90127 Palermo, Italy
[4] Univ Med Ctr Rotterdam, Dept Cardiol, Erasmus MC, Doctor Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
关键词
Homozygous familial hypercholesterolaemia; Lomitapide; Medium-term efficacy; Medium-term safety; Atherosclerosis; LONG-TERM EFFICACY; TRANSFER PROTEIN INHIBITOR; LIPOPROTEIN APHERESIS; MANAGEMENT; REDUCTION; PCSK9; HOFH;
D O I
10.1093/eurjpc/zwab229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Lomitapide is a lipid-lowering agent indicated as an adjunct therapy for adult homozygous familial hypercholesterolaemia (HoFH). This study evaluated the medium-term effectiveness and safety of lomitapide in a large cohort of HoFH patients in Europe. Methods and results In a multicentre retrospective, observational study including 75 HoFH patients treated with lomitapide in a real-world clinical setting from 9 European countries, low-density lipoprotein cholesterol (LDL-C) changes, adverse events (AEs), and major adverse cardiovascular events (MACE) were assessed. After a median 19 months (interquartile range 11-41 months) of treatment with a mean dosage of 20 mg of lomitapide. Low-density lipoprotein cholesterol decreased by 60%, from baseline 280.5 mg/dL (191.8-405.0 mg/dL) to 121.6 mg/dL (61.0-190.5 mg/dL). At the last visit, 32.0% of patients achieved LDL-C <100 mg/dL and 18.7% <70 mg/dL. At baseline, 38 HoFH patients were receiving LDL apheresis (LA), but after initiation of lomitapide 36.8% of patients discontinued LA. During follow-up, lomitapide was permanently interrupted in 13% of patients. Gastrointestinal AEs occurred in 40% and liver transaminases increased (3-5 x upper limits of normal) in 13% of patients. Among patients with liver ultrasound evaluation (n = 45), a modest increase in hepatic steatosis was noted during treatment; however, liver stiffness measured by elastography in 30 of them remained within the normal range. Among HoFH patients exposed to lomitapide for at least 2 years, MACE incident rate was 7.4 per 1000 person-years in the 2 years after as compared to 21.2 per 1000 person-years before treatment with lomitapide. Conclusion In this medium-term real-world experience, lomitapide proved to be very effective in reducing LDL-C in HoFH. Gastrointestinal AEs were common, but liver safety was reassuring with no sign of increased risk of liver fibrosis. A signal of cardiovascular protection was also observed.
引用
收藏
页码:832 / 841
页数:10
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