Pharmacokinetics of mitoxantrone, etoposide and cytosine arabinoside in leukemic cells during treatment of acute myelogenous leukemia—Relationship to treatment outcome and bone marrow toxicity-Reference-Cited by-同舟云学术

Pharmacokinetics of mitoxantrone, etoposide and cytosine arabinoside in leukemic cells during treatment of acute myelogenous leukemia—Relationship to treatment outcome and bone marrow toxicity

Published:1995-10 Issue:10 Volume:19 Page:757-761
ISSN:0145-2126
Container-title:Leukemia Research
language:en
Short-container-title:Leukemia Research

Author:

Gruber Astrid,Liliemark Eva,Tidefelt Ulf,Paul Christer,Björkholm Magnus,Peterson Curt,Liliemark Jan

Publisher

Elsevier BV

Subject

Cancer Research,Oncology,Hematology

Reference18 articles.

1. The biochemistry of the P-glycoprotein-mediated multidrug resistance;Endicott;Annu. Rev. Biochem.,1989

2. Chemosensitisation and drug accumulation effects of cyclosporin A, PSC-833 and verapamil in human MDR large cell lung cancer cells expressing a 190k membrane protein distinct from P-glycoprotein;Barrand;Eur. J. Cancer,1993

3. Effects of verapamil on the cellular accumulation of daunorubicin in blast cells and on the chemosensitivity of leukaemic blast progenitors in acute myelogenous leukaemia;Maruyama;Br. J. Haematol.,1989

4. Relationship of 1-β-d-arabinofuranosylcytosine in plasma to 1-β-d-arabinofuranosyl-cytosine 5′-triphosphate levels in leukemic cells during treatment with high-dose 1-β-d-arabinofuranosylcytosine;Liliemark;Cancer Res.,1985

5. Pharmacokinetics of mitoxantrone in plasma and leukemic cells during treatment of patients with acute non-lymphocytic leukemia;Gruber;Leukemia Lymphoma,1992

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