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Cyclophosphamide, doxorubicin, vincristine, methotrexate, bleomicin and prednisone plus rituximab in untreated young patients with low-risk (age-adjusted international prognostic index 0-1) diffuse large B-cell lymphoma.

Authors :
Derenzini, Enrico
Stefoni, Vittorio
Pellegrini, Cinzia
Fina, Maria Paola
Broccoli, Alessandro
Venturini, Filippo
Gandolfi, Letizia
Pileri, Stefano A.
Martelli, Maurizio
Petti, Maria Concetta
Perrotti, Alessio
De Renzo, Amalia
Zaja, Francesco
Baccarani, Michele
Zinzani, Pier Luigi
Source :
Leukemia & Lymphoma; Nov2009, Vol. 50 Issue 11, p1824-1829, 6p, 3 Charts
Publication Year :
2009

Abstract

Young patients (aged 18-60 years) with good-prognosis diffuse large B-cell lymphoma (DLBCL) [0 and 1 risk factor according to age-adjusted international prognostic index (aa-IPI)] are distinguished from patients with poor-prognosis. Six cycles of cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) in combination with rituximab achieved best results in young patients with low-risk DLBCL. We retrospectively analyzed the data of 82 patients (18-60 years) with untreated aa-IPI 0-1 DLBCL, from six Italian institutions, who underwent, between January 2002 and January 2007, rituximab-cyclophosphamide, doxorubicin, vincristine, methotrexate, bleomicin and prednisone (R-MACOP-B) therapy followed, in patients with bulky presentation, by 30-36 Gy involved-field radiation therapy (34 patients). An overall response rate was noted in 77 out of 82 (94%) patients (75 patients had a complete response (91%), 2 patients had a partial response). With a median follow-up of 46 months, 7-year progression-free and overall survival were estimated to be 91% and 94%, respectively. R-MACOP-B regimen followed by involved-field radiation on bulky presentation is safe and very effective in the treatment of young patients with low-risk DLBCL. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10428194
Volume :
50
Issue :
11
Database :
Complementary Index
Journal :
Leukemia & Lymphoma
Publication Type :
Academic Journal
Accession number :
73501697
Full Text :
https://doi.org/10.3109/10428190903216796