Literature DB >> 8905031

L-Asparagine depletion in plasma and cerebro-spinal fluid of children with acute lymphoblastic leukemia during subsequent exposures to Erwinia L-asparaginase.

D Gentili1, V Conter, C Rizzari, B Tschuemperlin, M Zucchetti, D Orlandoni, M D'Incalci, G Masera.   

Abstract

BACKGROUND: Monitoring L-asparagine (L-ASN) plasma levels could provide information useful for determining whether the dosage or schedule of L-asparaginase (L-ASE) administration is adequate. Very few data are available on depletion caused by the Erwinia chrysanthemi (E. chrysanthemi) product. Since it has been suggested that L-ASN depletion may have been overestimated in the past due to residual L-ASE activity, samples in this study have been analyzed after deproteinization with sulphosalicylic acid. Patients undergoing subsequent exposures to L-ASE derived from E. chrysanthemi have been investigated. PATIENTS AND METHODS: Fifty-four children with newly diagnosed acute lymphoblastic leukemia (ALL) at our institution entered this study. L-ASE was given at conventional doses (10,000 IU/sqm) every three days during the induction phase (8 doses, first exposure) or twice a week (4 doses, second exposure) during the reinduction phase. High-dose L-ASE (i.e., HD-L-ASE 25,000 IU/sqm) was given weekly, for a total of 20 doses, as a second or third exposure during the reinduction and/or maintenance phases. To determine the plasma levels of L-ASN, samples were deproteinized with sulphosalicylic acid, stored at -80 degrees C and then analyzed by HPLC after precolumn derivatization with o-phthaldialdehyde. The CSF samples were analyzed by the same procedure. An experiment was carried out to detect in vitro L-ASE deactivation in patients' plasma.
RESULTS: L-ASN plasma depletion was observed in 80% of the cases during the first exposure to conventional doses of L-ASE and only in 25% of the cases during the second or third exposures to either conventional or high doses of L-ASE. A correlation was found between plasma and CSF L-ASN levels. Activity inhibitory to L-ASE was found in the plasma of patients not depleted during L-ASE treatment and was not found in the plasma of those in whom L-ASN plasma depletion was obtained.
CONCLUSIONS: L-ASN plasma depletion is regularly obtained in the majority of patients during the first exposure to conventional doses of E. chrysanthemi L-ASE. Conversely, in most cases depletion does not occur during subsequent exposures. Studies should be performed to evaluate whether L-ASE derived from different species or conjugated with polyethylene-glycole are effective in obtaining L-ASN plasma depletion in patients previously treated with Erwinia C. L-ASE. The clinical impact of L-ASN depletion should also be investigated in large cohorts of patients.

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Year:  1996        PMID: 8905031     DOI: 10.1093/oxfordjournals.annonc.a010722

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  8 in total

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Authors:  Xavier Thomas; Caroline Le Jeune
Journal:  Int J Hematol Oncol       Date:  2016-05-05

2.  A prospective study on drug monitoring of PEGasparaginase and Erwinia asparaginase and asparaginase antibodies in pediatric acute lymphoblastic leukemia.

Authors:  Wing H Tong; Rob Pieters; Gertjan J L Kaspers; D Maroeska W M te Loo; Marc B Bierings; Cor van den Bos; Wouter J W Kollen; Wim C J Hop; Claudia Lanvers-Kaminsky; Mary V Relling; Wim J E Tissing; Inge M van der Sluis
Journal:  Blood       Date:  2014-01-21       Impact factor: 22.113

3.  Erwinia asparaginase achieves therapeutic activity after pegaspargase allergy: a report from the Children's Oncology Group.

Authors:  Wanda L Salzer; Barbara Asselin; Jeffrey G Supko; Meenakshi Devidas; Nicole A Kaiser; Paul Plourde; Naomi J Winick; Gregory H Reaman; Elizabeth Raetz; William L Carroll; Stephen P Hunger
Journal:  Blood       Date:  2013-06-05       Impact factor: 22.113

4.  Clinical utility of ammonia concentration as a diagnostic test in monitoring of the treatment with L-asparaginase in children with acute lymphoblastic leukemia.

Authors:  Małgorzata Czogała; Walentyna Balwierz; Krystyna Sztefko; Iwona Rogatko
Journal:  Biomed Res Int       Date:  2014-07-23       Impact factor: 3.411

5.  Purification, Characterization and Comparison between Two New L-asparaginases from Bacillus PG03 and Bacillus PG04.

Authors:  Mahsa Rahimzadeh; Manijeh Poodat; Sedigheh Javadpour; Fatemeh Izadpanah Qeshmi; Fereshteh Shamsipour
Journal:  Open Biochem J       Date:  2016-11-04

6.  Assessment of l-Asparaginase Pharmacodynamics in Mouse Models of Cancer.

Authors:  Thomas D Horvath; Wai Kin Chan; Michael A Pontikos; Leona A Martin; Di Du; Lin Tan; Marina Konopleva; John N Weinstein; Philip L Lorenzi
Journal:  Metabolites       Date:  2019-01-09

7.  Pharmacodynamics of cerebrospinal fluid asparagine after asparaginase.

Authors:  John C Panetta; Yiwei Liu; Teodoro Bottiglieri; Erland Arning; Cheng Cheng; Seth E Karol; Jun J Yang; Yinmei Zhou; Hiroto Inaba; Ching-Hon Pui; Sima Jeha; Mary V Relling
Journal:  Cancer Chemother Pharmacol       Date:  2021-06-25       Impact factor: 3.288

8.  Asparagine levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia treated with pegylated-asparaginase in the induction phase of the AIEOP-BFM ALL 2009 study.

Authors:  Carmelo Rizzari; Claudia Lanvers-Kaminsky; Maria Grazia Valsecchi; Andrea Ballerini; Cristina Matteo; Joachim Gerss; Gudrun Wuerthwein; Daniela Silvestri; Antonella Colombini; Valentino Conter; Andrea Biondi; Martin Schrappe; Anja Moericke; Martin Zimmermann; Arend von Stackelberg; Christin Linderkamp; Michael C Frühwald; Sabine Legien; Andishe Attarbaschi; Bettina Reismüller; David Kasper; Petr Smisek; Jan Stary; Luciana Vinti; Elena Barisone; Rosanna Parasole; Concetta Micalizzi; Massimo Zucchetti; Joachim Boos
Journal:  Haematologica       Date:  2019-01-31       Impact factor: 9.941

  8 in total

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