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The lymphocyte to monocyte ratio improves the IPI-risk definition of diffuse large B-cell lymphoma when rituximab is added to chemotherapy

  • Alessandro Rambaldi
  • , Cristina Boschini
  • , Giuseppe Gritti
  • , Federica Delaini
  • , Elena Oldani
  • , Andrea Rossi
  • , Anna Maria Barbui
  • , Daniele Caracciolo
  • , Marco Ladetto
  • , Angela Gueli
  • , Alberto De Crescenzo
  • , Roberto Passera
  • , Liliana Devizzi
  • , Caterina Patti
  • , Alessandro Massimo Gianni
  • , Corrado Tarella

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

The peripheral blood lymphocyte to monocyte ratio (LMR) at diagnosis can be clinically relevant in patients with diffuse large B-cell lymphoma (DLBCL). We reviewed the outcome of 1,057 DLBCL patients followed from 1984 to 2012 at four centers. LMR was analyzed as a clinical biomarker by receiver-operating characteristic (ROC) analysis and Harrell's C-statistics. Patients were characterized by a median age of 61 years, International Prognostic Index (IPI) score of >2 in 39%, and were treated with a rituximab-containing chemotherapy in 66%. LMR proved strongly predictive for survival in patients treated with rituximab-based programs, but not in those receiving chemotherapy alone. Additionally, an LMR value of ≤2.6 (as determined by ROC analysis) was associated with a worst performance status, a higher lactate dehydrogenase (LDH) level, an advanced clinical stage, and a higher IPI score (P=0.000). In patients treated with rituximab-supplemented chemotherapy programs, an LMR value of <2.6 was found in most of the primary refractory patients (75%) which proved as the best cutoff to predict both response and survival (P=0.018). Finally, multivariate analysis and Harrell's C-statistics confirmed the IPI-independent role of LMR on survival (P=0.0000). In conclusion, LMR is a potent predictor of clinical response and survival in DLBCL treated with rituximab-containing chemotherapy.

Lingua originaleInglese
pagine (da-a)1062-1067
Numero di pagine6
RivistaAmerican Journal of Hematology
Volume88
Numero di pubblicazione12
DOI
Stato di pubblicazionePubblicato - dic 2013
Pubblicato esternamente

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