Literature DB >> 3480081

Cellular and plasma adriamycin concentrations in long-term infusion therapy of leukemia patients.

P A Speth1, P C Linssen, J B Boezeman, H M Wessels, C Haanen.   

Abstract

To determine whether long-term adriamycin (ADM) infusions resulted in cellular ADM concentrations at least comparable to those observed after bolus injections, ADM cellular and plasma concentrations were measured in 18 patients with leukemia. ADM was administered at 30 mg/m2 per day for 3 days, either as bolus injections or as 4-, 8-, or 72-h infusions. Negligible accumulation of plasma ADM was observed. Peak plasma ADM concentrations after bolus injections were 1640 +/- 470 ng/ml (n = 7). Maximum levels were 176 +/- 34 ng/ml during 4-h infusion (n = 5); 85 +/- 50 ng/ml during 8-h infusion (n = 4); and 47 +/- 5 ng/ml (n = 2) after 72-h infusion. ADM concentrations in nucleated blood and bone marrow cells correlated well (r = 0.82, n = 47). ADM accumulated in leukemic cells up to 30-100 times the plasma concentrations. The shorter the administration time-span, the higher the peak leukemic cell concentration and the greater the loss of drug immediately after the end of the administration. The final cellular ADM half-life was approximately 85-110 h. After long-term infusion and bolus injection of the same dose, similar areas under the curve for plasma or leukemic blast cell ADM concentrations were attained. Since comparable therapeutic efficacy was observed in all regimens, the antileukemic effect appeared not to be related to the peak plasma concentrations, while acute toxicity phenomena decreased with increasing duration of the infusion. Long-term ADM infusion deserves more attention in the treatment of patients with anthracyclines.

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Year:  1987        PMID: 3480081     DOI: 10.1007/BF00262581

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  19 in total

1.  Rapid quantitative determination of four anthracyclines and their main metabolites in human nucleated haematopoietic cells.

Authors:  P A Speth; P C Linssen; J B Boezeman; J M Wessels; C Haanen
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2.  Clinical evaluation of long-term, continuous-infusion doxorubicin.

Authors:  M B Garnick; G R Weiss; G D Steele; M Israel; D Schade; M J Sack; E Frei
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3.  Significance of cellular pharmacokinetics for the cytotoxic effects of daunorubicin.

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4.  Cytofluorescence localization of anthracycline antibiotics.

Authors:  M J Egorin; R E Clawson; J L Cohen; L A Ross; N R Bachur
Journal:  Cancer Res       Date:  1980-12       Impact factor: 12.701

5.  Cellular pharmacokinetics of doxorubicin in cultured mouse sarcoma cells originating from autochthonous tumors.

Authors:  T Nguyen-Ngoc; P Vrignaud; J Robert
Journal:  Oncology       Date:  1984       Impact factor: 2.935

6.  Daunomycin administered by continuous intravenous infusion is effective in the treatment of acute nonlymphocytic leukaemia.

Authors:  J P Lewis; F J Meyers; L Tanaka
Journal:  Br J Haematol       Date:  1985-10       Impact factor: 6.998

7.  Experimental evaluation of anthracycline analogs.

Authors:  A M Casazza
Journal:  Cancer Treat Rep       Date:  1979-05

8.  Plasma pharmacokinetics of adriamycin and adriamycinol: implications for the design of in vitro experiments and treatment protocols.

Authors:  R F Greene; J M Collins; J F Jenkins; J L Speyer; C E Myers
Journal:  Cancer Res       Date:  1983-07       Impact factor: 12.701

9.  Kinetics and sensitivity of daunorubicin in patients with acute leukemia.

Authors:  M W DeGregorio; W M Holleran; B A Macher; C A Linker; J R Wilbur
Journal:  Cancer Chemother Pharmacol       Date:  1984       Impact factor: 3.333

10.  Leukemic cell and plasma daunomycin concentrations after bolus injection and 72 h infusion.

Authors:  P A Speth; P C Linssen; J B Boezeman; H M Wessels; C Haanen
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

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  20 in total

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Journal:  Pharm Weekbl Sci       Date:  1992-12-11

2.  Doxorubicin and doxorubicinol: intra- and inter-individual variations of pharmacokinetic parameters.

Authors:  J M Jacquet; F Bressolle; M Galtier; M Bourrier; D Donadio; J Jourdan; J F Rossi
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3.  New data on the pharmacokinetics of adriamycin and its major metabolite, adriamycinol.

Authors:  F Leca; D Marchiset-Leca; A Noble; M Antonetti
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1991 Apr-Jun       Impact factor: 2.441

4.  Multiple actions of doxorubicin on the sphingolipid network revealed by flux analysis.

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5.  Chemotherapy exposure increases leukemia cell stiffness.

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6.  Co-variation of glutathione transferase expression and cytostatic drug resistance in HeLa cells: establishment of class Mu glutathione transferase M3-3 as the dominating isoenzyme.

Authors:  X Y Hao; M Widersten; M Ridderström; U Hellman; B Mannervik
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7.  Reversing multidrug-resistant by RNA interference through silencing MDR1 gene in human hepatocellular carcinoma cells subline Bel-7402/ADM.

Authors:  Long Sheng; Maoming Xiong; Cong Li; Xiangling Meng
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Review 8.  Clinical pharmacokinetics of idarubicin.

Authors:  J Robert
Journal:  Clin Pharmacokinet       Date:  1993-04       Impact factor: 6.447

9.  siRNA-based targeting of antiapoptotic genes can reverse chemoresistance in P-glycoprotein expressing chondrosarcoma cells.

Authors:  Dae Won Kim; Kyung-Ok Kim; Mike J Shin; Jung Hee Ha; Sung Wook Seo; Jay Yang; Francis Y Lee
Journal:  Mol Cancer       Date:  2009-05-15       Impact factor: 27.401

10.  Cellular pharmacokinetics of doxorubicin in patients with chronic lymphocytic leukemia: comparison of bolus administration and continuous infusion.

Authors:  C Muller; E Chatelut; V Gualano; M De Forni; F Huguet; M Attal; P Canal; G Laurent
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

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