Thrombosis and meningococcal infection rates in pegcetacoplan-treated patients with paroxysmal nocturnal hemoglobinuria in the clinical trial and postmarketing settings

被引:8
作者
Kelly, Richard J. [1 ,7 ]
Nishimori, Hisakazu [2 ,3 ]
Horneff, Regina [4 ]
Hillmen, Peter [5 ]
Al-Adhami, Mohammed [5 ]
Lallier, Stacie [5 ]
Gerber, Gloria F. [6 ]
机构
[1] St James Univ Hosp, Leeds, England
[2] Okayama Univ Hosp, Dept Hematol, Okayama, Japan
[3] Hiroshima City Hiroshima Citizens Hosp, Hiroshima, Japan
[4] Swedish Orphan Biovitrum AB, Stockholm, Sweden
[5] Apellis Pharmaceut Inc, Waltham, MA USA
[6] Johns Hopkins Univ, Sch Med, Dept Med, Div Hematol, Baltimore, MD USA
[7] St James Univ Hosp, Dept Haematol, Leeds LS7 9TF, England
关键词
LONG-TERM SAFETY; ECULIZUMAB; EFFICACY; DISEASE;
D O I
10.1016/j.rpth.2024.102416
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hematologic disease characterized by complement-mediated hemolysis and thrombosis. Complement component 5 (C5) inhibitors have decreased PNH-related thrombosis rates and reduced mortality compared with those of age-matched controls. A small but significantly increased risk of life-threatening Neisseria infections, especially N meningitidis, represents a long-term safety risk of complement inhibition. Objectives: To evaluate the rates of thrombosis and meningococcal infections in patients with PNH treated with the complement component 3-targeted therapy pegcetacoplan. Methods: Cumulative patient-year exposure to pegcetacoplan was calculated, and thrombotic events and meningococcal infections were reviewed in 7 clinical trials and in the postmarketing setting. The clinical trial protocols and pegcetacoplan labeling required vaccination against Streptococcus pneumoniae, N meningitidis, and Haemophilus influenzae before pegcetacoplan use; the label allowed for prophylactic antibiotic use if pegcetacoplan must be administered before vaccination. Results: As of November 13, 2022, 464 patients with PNH had 619.4 patient-years of pegcetacoplan exposure in completed/ongoing clinical trials and the postmarketing setting. Seven thrombotic events were reported: 5 in clinical trials (2 in the same patient) and 2 in the postmarketing setting. The overall thrombosis rate was 1.13 events per 100 patient-years (clinical trials: 1.22 events/100 patient-years in 409.4 years; postmarketing: 0.95 events/100 patient-years in 210.0 years). No infections with meningococcal bacteria were reported. Conclusion: Event rates for thrombosis were comparable between pegcetacoplan and previously reported rates of C5 inhibitors in patients with PNH, and no cases of meningococcal infection were reported with pegcetacoplan. Continued follow-up is required.
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页数:8
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