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Title: | Bone marrow biopsy superiority over PET/CT in predicting progression-free survival in a homogeneously-treated cohort of diffuse large B-cell lymphoma. |
Authors: | Chen-Liang, Tzu-Hua Martín-Santos, Taida Jerez, Andrés Rodríguez-García, Guillermo Senent, Leonor Martínez-Millán, Cristina Muiña, Begoña Orero, Mayte Teruel, Anabel Martín, Alejandro Gómez-Espuch, Joaquín Kennedy, Kyra Benet, Carmen Raya, José María Fernández-González, Marta de la Cruz, Fátima Guinot, Marta Villegas, Carolina Ballester, Isabel Baile, Mónica Moya, María López-Jiménez, Javier Frutos, Laura Navarro, José Luis Uña, Jon Fernández-López, Rosa Igua, Carolina Contreras, José Sánchez-Vañó, Raquel Cozar, María Del Puig Tamayo, Pilar Mucientes, Jorge Sánchez-Blanco, José Javier Pérez-Ceballos, Elena Ortuño, Francisco José |
Keywords: | Bone marrow biopsy;PET/CT;diffuse large B-cell lymphoma;outcomes research |
metadata.dc.subject.mesh: | Adolescent Adult Age Factors Aged Aged, 80 and over Antibodies, Monoclonal, Murine-Derived Antineoplastic Combined Chemotherapy Protocols Biopsy Bone Marrow Cyclophosphamide Disease-Free Survival Doxorubicin Female Follow-Up Studies Health Status Humans Lymphoma, Large B-Cell, Diffuse Male Middle Aged Multivariate Analysis Positron Emission Tomography Computed Tomography Predictive Value of Tests Prednisone Retrospective Studies Rituximab Survival Rate Vincristine Young Adult beta 2-Microglobulin |
Issue Date: | 27-Sep-2017 |
Abstract: | Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B-cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R-CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow-up of 25 months the estimated 3-year progression-free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB-BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS > 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age >60 years old (HR: 2.4), ECOG PS >1 (HR: 2.4), and abnormally elevated B2-microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first-line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS. |
URI: | http://hdl.handle.net/10668/11625 |
metadata.dc.identifier.doi: | 10.1002/cam4.1205 |
Appears in Collections: | Producción 2020 |
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