Literature DB >> 1678081

Relation of cellular drug resistance to long-term clinical outcome in childhood acute lymphoblastic leukaemia.

R Pieters1, D R Huismans, A H Loonen, K Hählen, A van der Does-van den Berg, E R van Wering, A J Veerman.   

Abstract

The clinical relevance of cellular drug resistance in children with acute lymphoblastic leukaemia (ALL) is unknown. The relation between in-vitro sensitivity to chemotherapeutic drugs at initial diagnosis and long-term clinical outcome was investigated in 44 children with ALL. The short-term MTT assay was used to assess sensitivity to prednisolone, vincristine, colaspase (asparaginase), daunorubicin, and thioguanine (instead of mercaptopurine which is unstable in vitro). For vincristine and colaspase there was no difference in outcome (probability of continuous complete remission) between sensitive and resistant patients. However, the probability of continuous complete remission was significantly lower in patients with resistant cells than in those with sensitive cells for thioguanine (p less than 0.01), daunorubicin (p less than 0.02), and prednisolone (p less than 0.05). For prednisolone there was a significant worsening of the prognosis (p less than 0.05) from the extremely sensitive patients through an intermediate group to the most resistant group. The prognostic significance of cellular drug resistance was independent of white-blood-cell count, age, sex, and hepatosplenomegaly. Leukaemic cells from boys were more resistant to thioguanine than those from girls. Thus, the short-term highly efficient MTT assay can help to predict long-term response to chemotherapy in childhood ALL.

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Year:  1991        PMID: 1678081     DOI: 10.1016/0140-6736(91)91029-t

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  40 in total

Review 1.  Therapeutic trials in childhood ALL: what's their future?

Authors:  O B Eden
Journal:  J Clin Pathol       Date:  2000-01       Impact factor: 3.411

Review 2.  Molecular pharmacodynamics in childhood leukemia.

Authors:  R Pieters; M L den Boer
Journal:  Int J Hematol       Date:  2003-12       Impact factor: 2.490

3.  A genome-wide approach identifies that the aspartate metabolism pathway contributes to asparaginase sensitivity.

Authors:  S-H Chen; W Yang; Y Fan; G Stocco; K R Crews; J J Yang; S W Paugh; C-H Pui; W E Evans; M V Relling
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4.  Selection of chemotherapy by ex vivo assessment of tumor sensitivity to cytotoxic drugs: results of a clinical trial.

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Journal:  Med Oncol       Date:  2002       Impact factor: 3.064

5.  Hydrocortisone does not influence glucocorticoid sensitivity of acute lymphoblastic leukemia cells.

Authors:  Lidewij T Warris; Marry M van den Heuvel-Eibrink; Ingrid M Ariës; Rob Pieters; Erica L T van den Akker; Monique L den Boer
Journal:  Haematologica       Date:  2014-11-25       Impact factor: 9.941

6.  Two groups of Philadelphia chromosome-positive childhood acute lymphoblastic leukemia classified by pretreatment multidrug sensitivity or resistance in in vitro testing.

Authors:  Teruaki Hongo; Shuichi Okada; Noriko Inoue; Sayuri Yamada; Shuhei Yajima; Chieko Watanabe; Yuji Fujii; Yasuo Horikoshi
Journal:  Int J Hematol       Date:  2002-10       Impact factor: 2.490

7.  The expression of 70 apoptosis genes in relation to lineage, genetic subtype, cellular drug resistance, and outcome in childhood acute lymphoblastic leukemia.

Authors:  Amy Holleman; Monique L den Boer; Renée X de Menezes; Meyling H Cheok; Cheng Cheng; Karin M Kazemier; Gritta E Janka-Schaub; Ulrich Göbel; Ulrike B Graubner; William E Evans; Rob Pieters
Journal:  Blood       Date:  2005-09-27       Impact factor: 22.113

Review 8.  Cellular drug resistance in childhood leukemia.

Authors:  A J Veerman; G J Kaspers; R Pieters
Journal:  Ann Hematol       Date:  1994       Impact factor: 3.673

9.  Indirect two-sided relative ranking: a robust similarity measure for gene expression data.

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10.  Methotrexate cytotoxicity determination using the MTT assay following enzymatic depletion of thymidine and hypoxanthine.

Authors:  M Haber; J Madafiglio; M D Norris
Journal:  J Cancer Res Clin Oncol       Date:  1993       Impact factor: 4.553

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