MYC-rearranged lymphomas other than Burkitt: Comparison between R-CHOP and Burkitt-type immunochemotherapy
Med Clin (Barc). 2017 Oct 23;149(8):339-342.
doi: 10.1016/j.medcli.2017.03.056.
Epub 2017 Jun 23.
[Article in
English,
Spanish]
Affiliations
- 1 Departamento de Hematología, Institut Català d'Oncologia (ICO)-Hospital Universitari Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Barcelona, España.
- 2 Departamento de Anatomía Patológica, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Barcelona, España.
- 3 Departamento de Hematología, Hospital Universitario Infanta Leonor, Universidad Complutense de Madrid, Madrid, España.
- 4 Departamento de Hematología, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, España.
- 5 Departamento de Hematología, Institut Català d'Oncologia (ICO)-Hospital Universitari Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Barcelona, España. Electronic address: [email protected].
Abstract
Background and objective:
MYC-rearranged (MYC-R) lymphomas other than Burkitt lymphoma (BL) are very aggressive, with poor prognosis when treated with standard regimens. We aimed to study the characteristics and outcome of a series of MYC-R lymphomas comparing the treatment results between R-CHOP based and a specific intensive regimen for BL (BURKIMAB).
Patients and methods:
Retrospective study of patients diagnosed with MYC-R. Translocations of MYC, BCL2 and BCL6 were evaluated by fluorescent in situ hybridization. Patients were treated with either, R-CHOP based immunochemotherapy or the Burkitt type regimen, BURKIMAB.
Results:
Thirty-four MYC-R lymphoma cases were studied: 21 treated with R-CHOP and 13 treated with BURKIMAB. There were no differences in CR rate; 45% (9/20) for R-CHOP and 42% (5/12) for BURKIMAB (P=.99). Although overall survival (OS) and progression free survival (PFS) of BURKIMAB-treated patients were better than those of R-CHOP-treated (3y-OS: 46 vs. 24%; 3y-PFS: 46 vs. 10%), the differences were not statistically significant.
Conclusion:
MYC-R lymphomas show poor outcomes even when treated with intensive immunochemotherapy for BL.
Keywords:
Immunochemotherapy; Inmunoquimioterapia; Linfoma; Lymphoma; MYC; Prognosis; Pronóstico.
Copyright © 2017 Elsevier España, S.L.U. All rights reserved.
MeSH terms
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Adult
-
Aged
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Aged, 80 and over
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Antibodies, Monoclonal, Murine-Derived / therapeutic use
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Biomarkers, Tumor / genetics*
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Cyclophosphamide / therapeutic use
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Doxorubicin / therapeutic use
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Female
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Follow-Up Studies
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Genes, myc / genetics*
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Humans
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Immunologic Factors / therapeutic use*
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In Situ Hybridization, Fluorescence
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Lymphoma / drug therapy*
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Lymphoma / genetics
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Lymphoma / mortality
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Male
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Middle Aged
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Prednisone / therapeutic use
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Retrospective Studies
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Rituximab
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Survival Analysis
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Translocation, Genetic*
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Treatment Outcome
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Vincristine / therapeutic use
Substances
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Antibodies, Monoclonal, Murine-Derived
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Biomarkers, Tumor
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Immunologic Factors
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R-CHOP protocol
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Rituximab
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Vincristine
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Doxorubicin
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Cyclophosphamide
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Prednisone