Literature DB >> 7779709

In vitro anthracycline cross-resistance pattern in childhood acute lymphoblastic leukaemia.

E Klumper1, R Pieters, M L den Boer, D R Huismans, A H Loonen, A J Veerman.   

Abstract

Daunorubicin (DNR) is a major front-line drug in the treatment of childhood acute lymphoblastic leukaemia (ALL). Previously, we showed that in vitro resistance to DNR at diagnosis is related to a poor long-term clinical outcome in childhood ALL and that relapsed ALL samples are more resistant to DNR than untreated ALL samples. In cell line studies, idarubicin (IDR), aclarubicin (ACR) and mitoxantrone (MIT) showed a (partial) lack of cross-resistance to the conventional anthracyclines DNR and doxorubicin (DOX), but clinical studies in childhood ALL have been inconclusive about the suggested lack of cross-resistance. In the present study we determined the in vitro cross-resistance pattern between DNR, DOX, IDR, ACR and MIT in 48 untreated and 39 relapsed samples from children with ALL using the MTT assay. The relapsed ALL group was about twice as resistant to DNR, DOX, IDR, ACR and MTT as the untreated ALL group. Thus, resistance developed to all five drugs. We found a significant cross-resistance between DNR, DOX, IDR, ACR and MIT, although in some individual cases in vitro anthracycline cross-resistance was less pronounced. We conclude that IDR, ACR and MIT cannot circumvent in vitro resistance to DNR in childhood ALL. Clinical studies may still prove whether IDR, ACR or MIT has a more favourable toxicity profile than DNR.

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Year:  1995        PMID: 7779709      PMCID: PMC2033825          DOI: 10.1038/bjc.1995.231

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  36 in total

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2.  Identification of anthracycline analogues with enhanced cytotoxicity and lack of cross-resistance to adriamycin using a series of mammalian cell lines in vitro.

Authors:  B T Hill; L Y Dennis; X T Li; R D Whelan
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

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

Authors:  R Pieters; D R Huismans; A H Loonen; K Hählen; A van der Does-van den Berg; E R van Wering; A J Veerman
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4.  Phase I trial of aclacinomycin A.

Authors:  D A Van Echo; M Y Whitacre; J Aisner; M M Applefeld; P H Wiernik
Journal:  Cancer Treat Rep       Date:  1982-05

5.  Mitoxantrone in refractory acute leukemia in children: a phase I study.

Authors:  K A Starling; A F Mulne; T S Vats; I Schoch; G Dukart
Journal:  Invest New Drugs       Date:  1985       Impact factor: 3.850

6.  Phase I and clinical pharmacological study of 4-demethoxydaunorubicin (idarubicin) in children with advanced cancer.

Authors:  C T Tan; C Hancock; P Steinherz; D M Bacha; L Steinherz; E Luks; N Winick; P Meyers; A Mondora; E Dantis
Journal:  Cancer Res       Date:  1987-06-01       Impact factor: 12.701

7.  Aggressive combination chemotherapy of bone marrow relapse in childhood acute lymphoblastic leukemia containing aclacinomycin-A: a multicentric trial.

Authors:  R Fengler; S Buchmann; H Riehm; F Berthold; R Dopfer; N Graf; J Holldack; A Jobke; H Jürgens; T Klingebiel
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Review 8.  Idarubicin (4-demethoxydaunorubicin). A preliminary overview of preclinical and clinical studies.

Authors:  F Ganzina; M A Pacciarini; N Di Pietro
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9.  Pharmacokinetics of mitoxantrone in humans following single-agent infusion or intra-arterial injection therapy or combined-agent infusion therapy.

Authors:  S J Van Belle; M M de Planque; I E Smith; A T van Oosterom; T J Schoemaker; W Deneve; J G McVie
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

10.  9-alkyl anthracyclines. Absence of cross-resistance to adriamycin in human and murine cell cultures.

Authors:  C A Scott; D Westmacott; M J Broadhurst; G J Thomas; M J Hall
Journal:  Br J Cancer       Date:  1986-05       Impact factor: 7.640

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2.  Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy.

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