Evaluation of pentamidine tolerability and efficacy between CYP2C19 phenotypes

被引:0
|
作者
Koon, Alexis [1 ]
He, Jiaxian [2 ]
Patel, Jai [3 ]
Morse, Allison [4 ]
Boseman, Victoria [5 ]
Hamilton, Alicia [6 ]
Knight, Thomas [7 ]
Shah, Nilay [7 ]
Ragon, Brittany [7 ]
Chojecki, Aleksander [7 ]
Ai, Jing [7 ]
Steuerwald, Nury [6 ]
Gerber, Jonathan [8 ]
Copelan, Edward [7 ]
Grunwald, Michael [7 ]
Arnall, Justin [9 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Coll Pharm, N Chicago, IL 60064 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Clin Trials & Evidence Synth, Baltimore, MD 21205 USA
[3] Atrium Hlth, Levine Canc Inst, Dept Canc Pharmacol, Charlotte, NC 28204 USA
[4] Atrium Hlth, Levine Canc Inst, Dept Pharm, Charlotte, NC 28204 USA
[5] Atrium Hlth, Levine Canc Inst, Dept Biostat & Data Sci, Charlotte, NC 28204 USA
[6] Atrium Hlth, Mol Biol Core Lab, Levine Canc Inst, Charlotte, NC 28204 USA
[7] Atrium Hlth, Levine Canc Inst, Dept Hematol Oncol & Blood Disorders, Charlotte, NC 28204 USA
[8] UMass Mem Med Ctr, Div Hematol Oncol, Worcester, MA 01655 USA
[9] Atrium Hlth, Specialty Pharm Serv, Charlotte 28204, NC USA
关键词
allogeneic hematopoietic stem cell transplant; hematopoietic stem cell transplant; pentamidine; Pneumocystis jirovecii pneumonia; PNEUMOCYSTIS-JIROVECI PNEUMONIA; CELL TRANSPLANTATION; PJP PROPHYLAXIS;
D O I
10.2217/pgs-2023-0093
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intravenous pentamidine is used for prophylaxis against Pneumocystis jirovecii pneumonia, an infection seen in hematopoietic stem cell transplant recipients. Pentamidine is partially metabolized by CYP2C19, which is vulnerable to pharmacogenetic variation. This retrospective study evaluated allogeneic hematopoietic stem cell transplant patients who received intravenous pentamidine as P. jirovecii pneumonia prophylaxis. The primary objective was the association between CYP2C19 phenotype and discontinuation of pentamidine due to drug-related side effects based on univariate logistic regression (N = 81). Ten patients (12.3%) discontinued pentamidine because of side effects. There was no difference in discontinuation between phenotype groups (p = 0.18) or discontinuation due to side effects (p = 0.76). Overall, no association was seen between phenotypes and pentamidine-related side effects (p = 0.475). Drug discontinuation rates and P. jirovecii pneumonia infection rates were low.
引用
收藏
页码:821 / 830
页数:10
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