Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency

被引:113
|
作者
Grace, Rachael F. [1 ,2 ]
Rose, Christian [4 ]
Layton, D. Mark [6 ]
Galacteros, Frederic [5 ]
Barcellini, Wilma [7 ]
Morton, D. Holmes [8 ]
van Beers, Eduard J. [11 ]
Yaish, Hassan [12 ]
Ravindranath, Yaddanapudi [13 ]
Kuo, Kevin H. M. [14 ]
Sheth, Sujit [15 ]
Kwiatkowski, Janet L. [9 ,10 ]
Barbier, Ann J. [3 ]
Bodie, Susan [3 ]
Silver, Bruce [16 ]
Hua, Lei [3 ]
Kung, Charles [3 ]
Hawkins, Peter [3 ]
Jouvin, Marie-Helene [3 ]
Bowden, Chris [3 ]
Glader, Bertil [17 ]
机构
[1] Dana Farber Boston Childrens Canc & Blood Disorde, Boston, MA USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Agios Pharmaceut, Cambridge, MA USA
[4] Hop St Vincent de Paul, Lille, France
[5] Ctr Hosp Univ Henri Mondor, Unite Malad Genet Globule Rouge, Creteil, France
[6] Imperial Coll Healthcare NHS Trust, Hammersmith Hosp, London, England
[7] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy
[8] Cent Penn Clin, Belleville, PA USA
[9] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[10] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[11] Univ Med Ctr Utrecht, Van Creveldklin, Utrecht, Netherlands
[12] Univ Utah, Salt Lake City, UT USA
[13] Wayne State Univ, Childrens Hosp Michigan, Sch Med, Detroit, MI USA
[14] Univ Toronto, Toronto, ON, Canada
[15] Weill Cornell Med Coll, New York, NY USA
[16] Bruce A Silver Clin Sci & Dev, Dunkirk, MD USA
[17] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2019年 / 381卷 / 10期
关键词
RED-CELL DISTORTION; EXTREME HEMOLYSIS; PK DEFICIENCY; BLOOD-CELL;
D O I
10.1056/NEJMoa1902678
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Pyruvate kinase deficiency is caused by mutations in PKLR and leads to congenital hemolytic anemia. Mitapivat is an oral, small-molecule allosteric activator of pyruvate kinase in red cells. Methods In this uncontrolled, phase 2 study, we evaluated the safety and efficacy of mitapivat in 52 adults with pyruvate kinase deficiency who were not receiving red-cell transfusions. The patients were randomly assigned to receive either 50 mg or 300 mg of mitapivat twice daily for a 24-week core period; eligible patients could continue treatment in an ongoing extension phase. Results Common adverse events, including headache and insomnia, occurred at the time of drug initiation and were transient; 92% of the episodes of headache and 47% of the episodes of insomnia resolved within 7 days. The most common serious adverse events, hemolytic anemia and pharyngitis, each occurred in 2 patients (4%). A total of 26 patients (50%) had an increase of more than 1.0 g per deciliter in the hemoglobin level. Among these patients, the mean maximum increase was 3.4 g per deciliter (range, 1.1 to 5.8), and the median time until the first increase of more than 1.0 g per deciliter was 10 days (range, 7 to 187); 20 patients (77%) had an increase of more than 1.0 g per deciliter in the hemoglobin level at more than 50% of visits during the core study period, with improvement in markers of hemolysis. The response was sustained in all 19 patients remaining in the extension phase, with a median follow-up of 29 months (range, 22 to 35). Hemoglobin responses were observed only in patients who had at least one missense PKLR mutation and were associated with the red-cell pyruvate kinase protein level at baseline. Conclusions The administration of mitapivat was associated with a rapid increase in the hemoglobin level in 50% of adults with pyruvate kinase deficiency, with a sustained response during a median follow-up of 29 months during the extension phase. Adverse effects were mainly low-grade and transient.
引用
收藏
页码:933 / 944
页数:12
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