TY - JOUR
T1 - CLIPI
T2 - A new prognostic index for indolent cutaneous B cell lymphoma proposed by the International Extranodal Lymphoma Study Group (IELSG 11)
AU - Mian, Michael
AU - Marcheselli, Luigi
AU - Luminari, Stefano
AU - Federico, Massimo
AU - Cantonetti, Maria
AU - Sarris, Andreas H.
AU - Rossi, Andrea
AU - Rambaldi, Alessandro
AU - Frontani, Marina
AU - Devizzi, Liliana
AU - Gianni, Alessandro Massimo
AU - Busetto, Mario
AU - Berti, Emilio
AU - Martinelli, Giovanni
AU - Tsang, Richard W.
AU - Ferreri, Andrés J M
AU - Pinotti, Graziella
AU - Pogliani, Enrico
AU - Zucca, Emanuele
AU - Cortelazzo, Sergio
PY - 2011/4
Y1 - 2011/4
N2 - Indolent primary cutaneous B cell lymphomas (PCBCL) generally have a good prognosis, but they often relapse leading in some cases to extracutaneous disease and therefore, to poor survival. We developed a prognostic model to improve the therapeutic approach to these lymphomas. Two hundred and seventeen patients with diagnosis of indolent PCBCL stage IE or IIE were assessed retrospectively. The prognostic model was built to fit a Cox proportional hazard model using all the covariates affecting progression-free survival (PFS) at p<0.1 in the univariate analysis, and the final model was selected based on the Bayes Information Criteria. Elevated serum lactate dehydrogenase, morphology of the lesion (nodule vs. other), and >2 lesions were independent predictors for PFS. To each prognostic factor was assigned a value of 1. Patients were then stratified to three risk groups: score 0 (28%), low risk; score 1 (55%), intermediate risk; score 2 and 3 (17%), high risk with a 5-year PFS of 91%, 64%, and 48%, respectively (p
AB - Indolent primary cutaneous B cell lymphomas (PCBCL) generally have a good prognosis, but they often relapse leading in some cases to extracutaneous disease and therefore, to poor survival. We developed a prognostic model to improve the therapeutic approach to these lymphomas. Two hundred and seventeen patients with diagnosis of indolent PCBCL stage IE or IIE were assessed retrospectively. The prognostic model was built to fit a Cox proportional hazard model using all the covariates affecting progression-free survival (PFS) at p<0.1 in the univariate analysis, and the final model was selected based on the Bayes Information Criteria. Elevated serum lactate dehydrogenase, morphology of the lesion (nodule vs. other), and >2 lesions were independent predictors for PFS. To each prognostic factor was assigned a value of 1. Patients were then stratified to three risk groups: score 0 (28%), low risk; score 1 (55%), intermediate risk; score 2 and 3 (17%), high risk with a 5-year PFS of 91%, 64%, and 48%, respectively (p
KW - B cell
KW - CLIPI
KW - Cutaneous
KW - Lymphoma
KW - Prognostic index
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U2 - 10.1007/s00277-010-1083-1
DO - 10.1007/s00277-010-1083-1
M3 - Article
C2 - 20872000
AN - SCOPUS:79955934467
VL - 90
SP - 401
EP - 408
JO - Revue d'hématologie
JF - Revue d'hématologie
SN - 0939-5555
IS - 4
ER -