Cytogenetic abnormalities are among the most important factors affecting the outcome of patients with acute myeloid leukaemia (AML), but approximately 40-50% of AML cases display a normal karyotype at diagnosis. Multidrug resistance (MDR) proteins overexpression is associated with worse prognosis in acute leukaemias, but its role in normal karyotype AML is less defined. We analysed the expression of P-glycoprotein (PGP), MDR-related protein (MRP) and lung resistance protein (LRP) in 135 adult patients with normal karyotype AML and its correlation with other biological features of the disease, to evaluate the impact of MDR proteins on response to therapy and on survival. Increased PGP expression was associated with lower rate of complete remission (CR; p = 0.006), similarly to advanced age. Cases overexpressing PGP displayed also a shorter event-free survival (EFS; 4 vs. 10 months, p = 0.035) and the increased expression of at least one MDR protein was associated with a reduced overall survival (OS; p = 0.038). Also age was predictive of worse prognosis. Our data confirm the prognostic role of MDR proteins, in particular of PGP, also in AML patients with normal karyotype at diagnosis. This finding could be used to stratify patients with different prognosis and to design risk-adapted therapeutic strategies. Copyright © 2007 John Wiley & Sons, Ltd.

The role of MDR-related proteins in the prognosis of adult acute myeloid leukaemia (AML) with normal karyotype / Damiani, D.; Tiribelli, M.; Raspadori, D.; Michelutti, A.; Gozzetti, A.; Calistri, E.; Candoni, A.; Chiarvesio, A.; Lenoci, M.; Russo, D.; Fanin, R.. - In: HEMATOLOGICAL ONCOLOGY. - ISSN 0278-0232. - 25:1(2007), pp. 38-43. [10.1002/hon.806]

The role of MDR-related proteins in the prognosis of adult acute myeloid leukaemia (AML) with normal karyotype

Candoni A.;
2007-01-01

Abstract

Cytogenetic abnormalities are among the most important factors affecting the outcome of patients with acute myeloid leukaemia (AML), but approximately 40-50% of AML cases display a normal karyotype at diagnosis. Multidrug resistance (MDR) proteins overexpression is associated with worse prognosis in acute leukaemias, but its role in normal karyotype AML is less defined. We analysed the expression of P-glycoprotein (PGP), MDR-related protein (MRP) and lung resistance protein (LRP) in 135 adult patients with normal karyotype AML and its correlation with other biological features of the disease, to evaluate the impact of MDR proteins on response to therapy and on survival. Increased PGP expression was associated with lower rate of complete remission (CR; p = 0.006), similarly to advanced age. Cases overexpressing PGP displayed also a shorter event-free survival (EFS; 4 vs. 10 months, p = 0.035) and the increased expression of at least one MDR protein was associated with a reduced overall survival (OS; p = 0.038). Also age was predictive of worse prognosis. Our data confirm the prognostic role of MDR proteins, in particular of PGP, also in AML patients with normal karyotype at diagnosis. This finding could be used to stratify patients with different prognosis and to design risk-adapted therapeutic strategies. Copyright © 2007 John Wiley & Sons, Ltd.
25
1
38
43
The role of MDR-related proteins in the prognosis of adult acute myeloid leukaemia (AML) with normal karyotype / Damiani, D.; Tiribelli, M.; Raspadori, D.; Michelutti, A.; Gozzetti, A.; Calistri, E.; Candoni, A.; Chiarvesio, A.; Lenoci, M.; Russo, D.; Fanin, R.. - In: HEMATOLOGICAL ONCOLOGY. - ISSN 0278-0232. - 25:1(2007), pp. 38-43. [10.1002/hon.806]
Damiani, D.; Tiribelli, M.; Raspadori, D.; Michelutti, A.; Gozzetti, A.; Calistri, E.; Candoni, A.; Chiarvesio, A.; Lenoci, M.; Russo, D.; Fanin, R.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1294019
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 28
  • ???jsp.display-item.citation.isi??? 26
social impact