MDR1 gene expression and treatment outcome in acute myeloid leukemia. 1991

R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
First Medical Clinic, University of Vienna, Austria.

To prospectively assess the role of MDR1 gene expression in patients with de novo acute myeloid leukemia (AML), levels of MDR1 RNA in blast cells were determined at diagnosis and correlated with treatment outcome in 63 patients. MDR1 RNA levels were negative in 29% and positive in 71% of the patients. The complete remission rate in response to induction chemotherapy was 89% for MDR1 RNA-negative patients and 53% for MDR1 RNA-positive patients (P = .008). Expression of the MDR1 gene was observed in most patients who died early or had resistant disease. Kaplan-Meier curves revealed a decrease in both disease-free survival and overall survival of patients with detectable MDR1 gene expression compared with the disease-free survival and overall survival of MDR1 RNA-negative patients (P = .029 and P = .009, respectively). These data indicate that MDR1 gene expression is an unfavorable prognostic factor and suggest that multidrug resistance is important in AML.

UI MeSH Term Description Entries
D007948 Leukemia, Monocytic, Acute An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. Leukemia, Monoblastic, Acute,Leukemia, Myeloid, Acute, M5,Leukemia, Myeloid, Schilling-Type,Monoblastic Leukemia, Acute,Monocytic Leukemia, Acute,Myeloid Leukemia, Acute, M5,Myeloid Leukemia, Schilling-Type,Leukemia, Acute Monocytic,Leukemia, Myeloid, Schilling Type,Acute Monoblastic Leukemia,Acute Monoblastic Leukemias,Acute Monocytic Leukemia,Acute Monocytic Leukemias,Leukemia, Schilling-Type Myeloid,Leukemias, Acute Monoblastic,Leukemias, Acute Monocytic,Monoblastic Leukemias, Acute,Monocytic Leukemias, Acute,Myeloid Leukemia, Schilling Type,Schilling-Type Myeloid Leukemia
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011379 Prognosis A prediction of the probable outcome of a disease based on a individual's condition and the usual course of the disease as seen in similar situations. Prognostic Factor,Prognostic Factors,Factor, Prognostic,Factors, Prognostic,Prognoses
D004351 Drug Resistance Diminished or failed response of an organism, disease or tissue to the intended effectiveness of a chemical or drug. It should be differentiated from DRUG TOLERANCE which is the progressive diminution of the susceptibility of a human or animal to the effects of a drug, as a result of continued administration. Resistance, Drug
D004915 Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. Di Guglielmo's Disease,Erythremic Myelosis,Erythroblastic Leukemia, Acute,Erythroleukemia,Leukemia, Myeloid, Acute, M6,Myeloid Leukemia, Acute, M6,Di Guglielmo Disease,Acute Erythroblastic Leukemia,Acute Erythroblastic Leukemias,Di Guglielmos Disease,Disease, Di Guglielmo,Disease, Di Guglielmo's,Erythremic Myeloses,Erythroblastic Leukemias, Acute,Erythroleukemias,Leukemia, Acute Erythroblastic,Leukemias, Acute Erythroblastic,Myeloses, Erythremic,Myelosis, Erythremic
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
March 1995, Journal of the Formosan Medical Association = Taiwan yi zhi,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
September 2002, Cancer research,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
July 2002, Leukemia & lymphoma,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
February 2005, British journal of haematology,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
March 2008, Zhonghua nei ke za zhi,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
May 2002, Haematologica,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
January 1997, Anticancer research,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
September 1992, Leukemia,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
January 2007, Neoplasma,
R Pirker, and J Wallner, and K Geissler, and W Linkesch, and O A Haas, and P Bettelheim, and M Hopfner, and R Scherrer, and P Valent, and L Havelec
June 2001, Blood,
Copied contents to your clipboard!