Therapeutic drug monitoring of asparaginase in the ALL-BFM 2000 protocol between 2000 and 2007.

Schrey D, Borghorst S, Lanvers-Kaminsky C, Hempel G, Gerss J, Möricke A, Schrappe M, Boos J

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

BACKGROUND: On a voluntary basis therapeutic drug monitoring (TDM) was implemented in the ALL-BFM 2000 protocol for the three currently used asparaginase (ASNase) preparations (first line: native Escherichia coli ASNase; second line: pegylated ASNase and third line: Erwinia chrysanthemi ASNase). PROCEDURE: Between 2000 and 2007, 2,074 ASNase samples from 763 patients out of 114 hospitals were evaluated (5,000 U/m2 E. coli ASNase (n = 318), 1,000 U/m2 pegylated ASNase (n = 416) and 10,000 U/m2 Erwinia chrysanthemi ASNase (n = 29)). RESULTS: First-line therapy with 5,000 U/m2 E. coli ASNase resulted in an ASNase activity of <100 U/L in 10% of all samples from day +3 after administration. Second-line treatment with 1,000 U/m2 PEG ASNase led to activity values below 100 U/L in approximately 30% of all samples taken +7 days. Relating ASNase activity to route of administration, 10,000 U/m2 Erwinia ASNase IM compared to IV as third-line treatment, led to a higher median activity (IM: median 151.5 U/L, range (0-750 U/L); IV: median 115 U/L, range (0-884 U/L), P = 0.3) and fewer samples below 100 U/L (IM: 15% vs. IV: 45%) at day +2. CONCLUSION: The reduced dose of 5,000 U/m2 E. coli ASNase for induction treatment succeeded to achieve an activity level above 100 U/L in more than 90% of all samples. They confirm that dose reduction is reasonable and provide the basis for future treatment strategies employing ASNase.

Details zur Publikation

FachzeitschriftPediatric Blood and Cancer
Jahrgang / Bandnr. / Volume54
Ausgabe / Heftnr. / Issue7
Seitenbereich952-958
StatusVeröffentlicht
Veröffentlichungsjahr2010
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1002/pbc.22417
StichwörterFemale; Clinical Trials as Topic; Antineoplastic Agents; Adolescent; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Infant; Child Preschool; Antineoplastic Combined Chemotherapy Protocols; Drug Monitoring; Humans; Male; Pectobacterium chrysanthemi; Drug Hypersensitivity; Asparaginase; Escherichia coli; Child; Female; Clinical Trials as Topic; Antineoplastic Agents; Adolescent; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Infant; Child Preschool; Antineoplastic Combined Chemotherapy Protocols; Drug Monitoring; Humans; Male; Pectobacterium chrysanthemi; Drug Hypersensitivity; Asparaginase; Escherichia coli; Child

Autor*innen der Universität Münster

Boos, Joachim
Klinik für Kinder- und Jugendmedizin - Pädiatrische Hämatologie und Onkologie - (UKM PHO)
Borghorst, Stephan
Institut für Pharmazeutische und Medizinische Chemie
Gerß, Joachim
Institut für Biometrie und Klinische Forschung (IBKF)
Hempel, Georg
Professur für Klinische Pharmazie (Prof. Hempel) (apl.)
Lanvers-Kaminsky, Claudia
Klinik für Kinder- und Jugendmedizin - Pädiatrische Hämatologie und Onkologie - (UKM PHO)
Schrey, Dominik Friedhelm
Klinik für Kinder- und Jugendmedizin - Pädiatrische Hämatologie und Onkologie - (UKM PHO)