Determinants of Interpatient Variability in Treosulfan Pharmacokinetics in AML Patients Undergoing Autologous Stem Cell Transplantation

被引:2
作者
Aycicek, Selin G. [1 ]
Akhoundova, Dilara [1 ]
Bacher, Ulrike [2 ]
Hayoz, Michael [3 ,4 ]
Aebi, Yolanda [3 ,4 ]
Largiader, Carlo R. [3 ,4 ]
Pabst, Thomas [1 ]
机构
[1] Univ Bern, Dept Med Oncol, Inselspital, CH-3010 Bern, Switzerland
[2] Univ Bern, Dept Hematol, Inselspital, CH-3010 Bern, Switzerland
[3] Univ Bern, Ctr Lab Med ZLM, Inselspital, CH-3010 Bern, Switzerland
[4] Univ Bern, Dept Clin Chem, Inselspital, CH-3010 Bern, Switzerland
关键词
acute myeloid leukemia (AML); treosulfan; pharmacokinetics; interpatient variability; exposure; high-dose chemotherapy (HDCT); autologous stem cell transplantation (ASCT); adverse events; clinical outcome; ACUTE MYELOID-LEUKEMIA; INTRAVENOUS TREOSULFAN; PREPARATIVE REGIMEN; ACTIVE MONOEPOXIDE; CHILDREN PRIOR; BLOOD; 1,23,4-DIEPOXYBUTANE; HYDROLYSIS; ACTIVATION; TOXICITY;
D O I
10.3390/ijms25158215
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Limited data on treosulfan pharmacokinetics in adults, particularly regarding autologous stem cell transplantation (ASCT) in acute myeloid leukemia (AML), is available to date. Furthermore, correlations between treosulfan exposure, toxicity, and clinical outcome remain understudied. In this single-center retrospective study, we analyzed data from 55 AML patients who underwent HDCT with treosulfan (14 g/m2) and melphalan (140 mg/m2 or 200 mg/m2) (TreoMel) between August 2019 and November 2023 at the University Hospital of Bern. We assessed treosulfan pharmacokinetics and correlations with several physiological parameters with potential impact on its interpatient variability. We further analyzed how treosulfan exposure correlates with toxicity and clinical outcomes. Women above 55 years showed higher area under the curve (AUC) levels (median: 946 mg*h/L, range: 776-1370 mg*h/L), as compared to women under 55 (median: 758 mg*h/L, range: 459-1214 mg*h/L, p = 0.0487). Additionally, women above 55 showed higher peak levels (median: 387 mg/L, range: 308-468 mg/L), as compared to men of the same age range (median: 326 mg/L, range: 264-395 mg/L, p = 0.0159). Treosulfan levels varied significantly with body temperature, liver enzymes, hemoglobin/hematocrit., and treosulfan exposure correlated with diarrhea severity in women over 55 (p = 0.0076). Our study revealed age- and gender-related variability in treosulfan pharmacokinetics, with higher plasma levels observed in female patients above 55. Moreover, our data suggest that treosulfan plasma levels may vary with several physiological parameters and that higher treosulfan exposure may impact toxicity. Our study underlines the need for further research on treosulfan pharmacokinetics, especially in older patients undergoing HDCT in the ASCT setting.
引用
收藏
页数:18
相关论文
共 55 条
  • [1] [Anonymous], 2010, COMMON TERMINOLOGY C
  • [2] Treosulfan compared with reduced-intensity busulfan improves allogeneic hematopoietic cell transplantation outcomes of older acute myeloid leukemia and myelodysplastic syndrome patients: Final analysis of a prospective randomized trial
    Beelen, Dietrich W.
    Stelljes, Matthias
    Remenyi, Peter
    Wagner-Drouet, Eva-Maria
    Dreger, Peter
    Bethge, Wolfgang
    Ciceri, Fabio
    Stoelzel, Friedrich
    Junghanss, Christian
    Labussiere-Wallet, Helene
    Schaefer-Eckart, Kerstin
    Grigoleit, Goetz U.
    Scheid, Christof
    Patriarca, Francesca
    Rambaldi, Alessandro
    Niederwieser, Dietger
    Hilgendorf, Inken
    Russo, Domenico
    Socie, Gerard
    Holler, Ernst
    Glass, Bertram
    Casper, Jochen
    Wulf, Gerald
    Basara, Nadezda
    Bieniaszewska, Maria
    Stuhler, Gernot
    Verbeek, Mareike
    La Rocca, Ursula
    Finke, Juergen
    Benedetti, Fabio
    Pichlmeier, Uwe
    Klein, Anja
    Baumgart, Joachim
    Markiewicz, Miroslaw
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2022, 97 (08) : 1023 - 1034
  • [3] Dose-escalated treosulphan in combination with cyclophosphamide as a new preparative regimen for allogeneic haematopoietic stem cell transplantation in patients with an increased risk for regimen-related complications
    Beelen, DW
    Trenschel, R
    Casper, J
    Freund, M
    Hilger, RA
    Scheulen, ME
    Basara, N
    Fauser, AA
    Hertenstein, B
    Mylius, HA
    Baumgart, J
    Pichlmeier, U
    Hahn, JR
    Holler, E
    [J]. BONE MARROW TRANSPLANTATION, 2005, 35 (03) : 233 - 241
  • [4] Prophylactic corticosteroid use prevents engraftment syndrome in patients after autologous stem cell transplantation
    Betticher, Christophe
    Bacher, Ulrike
    Legros, Myriam
    Zimmerli, Stefan
    Banz, Yara
    Mansouri Taleghani, Behrouz
    Pabst, Thomas
    [J]. HEMATOLOGICAL ONCOLOGY, 2021, 39 (01) : 97 - 104
  • [5] The role of hydrolysis in the detoxification of 1,2:3,4-diepoxybutane by human, rat, and mouse liver and lung in vitro
    Boogaard, PJ
    Bond, JA
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 141 (02) : 617 - 627
  • [6] Autologous stem cell transplantation in favorable-risk acute myeloid leukemia: single-center experience and current challenges
    Capria, Saveria
    Trisolini, Silvia Maria
    Diverio, Daniela
    Minotti, Clara
    Breccia, Massimo
    Cartoni, Claudio
    Carmini, Daniela
    Gozzer, Maria
    La Rocca, Ursula
    Bafti, Mahnaz Shafii
    Martelli, Maurizio
    [J]. INTERNATIONAL JOURNAL OF HEMATOLOGY, 2022, 116 (04) : 586 - 593
  • [7] Chiesa R, 2014, BONE MARROW TRANSPL, V49, pS380
  • [8] Danielak D, 2020, PHARMACOL REP, V72, P1297, DOI 10.1007/s43440-020-00115-0
  • [9] Population pharmacokinetics of treosulfan and development of a limited sampling strategy in children prior to hematopoietic stem cell transplantation
    Danielak, Dorota
    Twardosz, Jadwiga
    Kasprzyk, Anna
    Wachowiak, Jacek
    Kalwak, Krzysztof
    Glowka, Franciszek
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 74 (01) : 79 - 89
  • [10] Treosulfan-based conditioning before hematopoietic SCT: more than a BU look-alike
    Danylesko, I.
    Shimoni, A.
    Nagler, A.
    [J]. BONE MARROW TRANSPLANTATION, 2012, 47 (01) : 5 - 14