Genetic polymorphisms effect on cyclophosphamide's tolerability and clinical efficacy in Egyptian patients with lupus nephritis

被引:0
作者
Abuelsoud, Nermeen N. [1 ,3 ]
EL Khateeb, Engy M. [2 ]
机构
[1] Egyptian Russian Univ, Coll Pharm, Dept Pharm Practice & Clin Pharm, Cairo, Egypt
[2] Cairo Univ, Kasr Al Aini Sch Med, Dept Clin & Chem Pathol, Cairo, Egypt
[3] Egyptian Russian Univ, Suez Rd, Cairo 11829, Egypt
关键词
cyclophosphamide; CYP2B6 c.516G>T; Egyptians; lupus nephritis; systemic lupus erythematosus; VERSUS-HOST-DISEASE; MYCOPHENOLATE-MOFETIL; HUMAN CYP2B6; PHARMACOGENETICS; METABOLISM; PHARMACOKINETICS; TRANSPLANTATION; CLASSIFICATION; ASSOCIATION; DERIVATION;
D O I
10.1097/FPC.0000000000000506
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objectives Many studies were conducted to determine the association between genetic polymorphisms in CYP2B6 c.516G>T and cyclophosphamide (CYC) efficacy or toxicity, no studies were focused on both clinical efficacy and toxicity of CYC. This study aimed to investigate the relationship between the CYP2B6 c.516G>T polymorphism (rs 3745274) and 17 different parameters related to CYC efficacy and tolerability in Egyptian patients with lupus nephritis (LN).Methods A prospective cohort study on 142 LN patients with a mean age of 36.26 was conducted at Kasr Al Ainy School of Medicine, Cairo University, Egypt after the exclusion of 14 patients due to receiving an interacting medication with CYC. All clinical parameters related to CYC efficacy or toxicity were recorded and compared between the different genotypes.Results There was a statistically significant difference between different genotypes in 11 out of 13 of the studied efficacy-related parameters. Many of the studied clinical parameters revealed that CYC's efficacy was associated with the presence of the T allele. There was a statistically significant difference between different genotypes in hepatotoxicity, diarrhea, and blood-related toxicities.Conclusion To our knowledge, this study is the first study that focused on studying 17 different parameters related to CYC efficacy and tolerability. Our findings paint a picture of the function that CYP2B6 polymorphisms play in Egyptian LN patients. Pre-treatment evaluation of CYP2B6 rs 3745274 may account for some individual differences in treatment response.
引用
收藏
页码:172 / 180
页数:9
相关论文
共 38 条
  • [1] Q172H Replacement Overcomes Effects on the Metabolism of Cyclophosphamide and Efavirenz Caused by CYP2B6 Variant with Arg262
    Ariyoshi, Noritaka
    Ohara, Miyuki
    Kaneko, Mayumi
    Afuso, Sakino
    Kumamoto, Takuya
    Nakamura, Hiroyoshi
    Ishii, Itsuko
    Ishikawa, Tsutomu
    Kitada, Mitsukazu
    [J]. DRUG METABOLISM AND DISPOSITION, 2011, 39 (11) : 2045 - 2048
  • [2] Influence of glutathione S transferase A1 gene polymorphism (-69C > T, rs3957356) on intravenous cyclophosphamide efficacy and side effects: a case-control study in Egyptian patients with lupus nephritis
    Attia, Doaa H. S.
    Eissa, Mervat
    Samy, Lamees A.
    Khattab, Rasha A.
    [J]. CLINICAL RHEUMATOLOGY, 2021, 40 (02) : 753 - 762
  • [3] Cytochrome P450 2B6*5 Increases Relapse after Cyclophosphamide-Containing Conditioning and Autologous Transplantation for Lymphoma
    Bachanova, Veronika
    Shanley, Ryan
    Malik, Farhana
    Chauhan, Lata
    Lamba, Vishal
    Weisdorf, Daniel J.
    Burns, Linda J.
    Lamba, Jatinder Kaur
    [J]. BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2015, 21 (05) : 944 - 948
  • [4] DERIVATION OF THE SLEDAI - A DISEASE-ACTIVITY INDEX FOR LUPUS PATIENTS
    BOMBARDIER, C
    GLADMAN, DD
    UROWITZ, MB
    CARON, D
    CHANG, CH
    [J]. ARTHRITIS AND RHEUMATISM, 1992, 35 (06): : 630 - 640
  • [5] Influence of pharmacogenetics on response and toxicity in breast cancer patients treated with doxorubicin and cyclophosphamide
    Bray, J.
    Sludden, J.
    Griffin, M. J.
    Cole, M.
    Verrill, M.
    Jamieson, D.
    Boddy, A. V.
    [J]. BRITISH JOURNAL OF CANCER, 2010, 102 (06) : 1003 - 1009
  • [6] Using cyclophosphamide in inflammatory rheumatic diseases
    Brummaier, Tobias
    Pohanka, Erich
    Studnicka-Benke, Andrea
    Pieringer, Herwig
    [J]. EUROPEAN JOURNAL OF INTERNAL MEDICINE, 2013, 24 (07) : 590 - 596
  • [7] CHANG TKH, 1993, CANCER RES, V53, P5629
  • [8] Sequential therapies for proliferative lupus nephritis
    Contreras, G
    Pardo, V
    Leclercq, B
    Lenz, O
    Tozman, E
    O'Nan, P
    Roth, D
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (10) : 971 - 980
  • [9] Crow MK., 2017, Kelley and Firestein's textbook of rheumatology, V10th ed, P1329
  • [10] Influence of polymorphisms of drug metabolizing enzymes (CYP2136, CYP2C9, CYPX19, CYP3A4, CYP3A5, GSTA1, GSTP1, ALDH1A1 and ALDH3A1) on the pharmacokinetics of cyclophosphamide and 4-hydroxycyclophosphamide
    Ekhart, Corine
    Doodeman, Valerie D.
    Rodenhuis, Sjoerd
    Smits, Paul H. M.
    Beijnen, Jos H.
    Huitema, Alwin D. R.
    [J]. PHARMACOGENETICS AND GENOMICS, 2008, 18 (06) : 515 - 523