High Ki67 Index and Bulky Disease Remain Significant Adverse Prognostic Factors in Patients with Diffuse Large B Cell Lymphoma before and after the Introduction of Rituximab
Authors:
- Francesco GaudioFGFrancesco Gaudio
- Annamaria GiordanoAGAnnamaria Giordano
- Tommasina PerroneTPTommasina Perrone
- Domenico PastoreDPDomenico Pastore
- Paola CurciPCPaola Curci
- Mario DeliaMDMario Delia
- Anna NapoliANAnna Napoli
- Clara De’ RisiCRClara De’ Risi
- Alessandro SpinaASAlessandro Spina
- Rosalia RiccoRRRosalia Ricco
- Vincenzo LisoVLVincenzo Liso
- Giorgina SpecchiaGSGiorgina Specchia
- 24 March 2011
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 126 (1) , 44-51
Abstract
The aim of this study was to evaluate the impact of clinical variables and biologic features on response rate (RR), overall survival (OS) and progression-free survival (PFS) in 111 patients with de novo diffuse large B cell lymphoma (DLBCL). Fifty-three patients were treated with CHOP (cyclophosphamide, doxorubicin, vincristine and prednisolone) and 58 patients were treated with R-CHOP (rituximab + CHOP). The variables predictive of RR in the CHOP group were B symptoms, age, clinical stage, bone marrow involvement, bulky disease, International Prognostic Index (IPI) and Bcl-2; in the R-CHOP group, these variables were bulky disease, bone marrow involvement, IPI and Ki67 expression >80%. Multivariate analysis showed that in patients treated with CHOP, the independent prognostic factors associated with PFS were age, bulky disease, IPI and Bcl-2 and those associated with OS were performance status, clinical stage, IPI and bone marrow involvement. In contrast, in patients treated with R-CHOP, the variable shown by multivariate analysis to be an independent prognostic factor associated with PFS was bulky disease, whereas Ki67 expression >80% was associated with OS and PFS. Our data show that a high Ki67 expression and bulky disease could represent possible predictive factors of poor prognosis, which would help to identify a high-risk subgroup of newly diagnosed DLBCL.Keywords
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