Literature DB >> 10764159

Ex vivo assessment of drug response by differential staining cytotoxicity (DiSC) assay suggests a biological basis for equality of chemotherapy irrespective of age for patients with chronic lymphocytic leukaemia.

A G Bosanquet1, M I Bosanquet.   

Abstract

With a mean age at diagnosis for chronic lymphocytic leukaemia (CLL) of 65 years, development of optimal therapeutic regimens has been hampered by the advanced age of patients. In general, because of comorbidity older patients are not treated with the intent of achieving a complete response and so do not attain the quality of response of younger patients and do not survive as long. We have investigated whether or not ex vivo cellular sensitivity to cytotoxic drugs could be an underlying biological basis for this age differential in response and survival by comparing ex vivo drug response with age in untreated CLL patients. Cells from 365 untreated CLL patients aged 31.1-87.1 years (average 65.3 years) were tested for drug response by differential staining cytotoxicity (DiSC) assay with a panel of 10 drugs. An average of 280 results (range 196-361) obtained for each drug was compared with patient age. For chlorambucil, cyclophosphamide, prednisolone, vincristine, doxorubicin, epirubicin, fludarabine, cladribine and methylprednisolone, no relationship was found between ex vivo drug response and age (r<0.12). For pentostatin, a possible but very weak relationship (r = 0.18; n = 210; P = 0.06) was found. We conclude that cellular sensitivity to cytotoxic drugs does not support the differential treatment of older and younger CLL patients.

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Year:  2000        PMID: 10764159     DOI: 10.1038/sj.leu.2401727

Source DB:  PubMed          Journal:  Leukemia        ISSN: 0887-6924            Impact factor:   11.528


  2 in total

1.  Determination of caspase-3 activation fails to predict chemosensitivity in primary acute myeloid leukemia blasts.

Authors:  Peter Staib; Jan Tiehen; Timo Strunk; Timo Schinköthe
Journal:  BMC Cancer       Date:  2005-06-11       Impact factor: 4.430

2.  In B-CLL, the codon 72 polymorphic variants of p53 are not related to drug resistance and disease prognosis.

Authors:  Isrid Sturm; Andrew G Bosanquet; Michael Hummel; Bernd Dörken; Peter T Daniel
Journal:  BMC Cancer       Date:  2005-08-18       Impact factor: 4.430

  2 in total

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