Annals of Oncology 15:369-374, 2004
© 2004 European Society for Medical Oncology
Diagnosis and actual therapy strategies in peripheral T-cell lymphomas: summary of an international meeting
1 Department of Medicine III, JW-Goethe University, Frankfurt/Main; 2 Department of Medicine III, University of Erlangen Nürnberg, Erlangen; 3 Medizinische Poliklinik, University of Würzburg, Würzburg, Germany
Received 13 May 2003; revised 31 July 2003; accepted 13 August 2003
Key words: histopathology, immunology, molecular biology and genetics, peripheral T-cell lymphoma, treatment
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Introduction
Peripheral T-cell lymphomas (PTCL) according to the REAL classification (mature T-cell lymphomas of the WHO classification) comprise no more than 10% of all non-Hodgkins lymphomas in the Western hemisphere [1]. Until now, uncertainties regarding many features of these rather heterogeneous diseases have prevented progress in developing effective therapies. PTCL has often been assessed as part of clinical studies focusing on the more common B-cell lymphomas and, consequently, our understanding of how to treat this group of lymphomas remains less clear than for B-cell lymphomas.
With the exception of a few subgroups, the prognosis of PTCL is poor, partly due to a limited understanding of their pathophysiological features. There is considerable variability in clinical presentation, which may greatly prolong the time taken to reach an accurate diagnosis in an individual patient. Additionally, treatment standards in PTCL have not yet been established [2].
Challenged by this variety of
Immunology and histological classification
Cytogenetics and molecular genetics
Treatment of primary cutaneous and disseminated T-cell lymphomas
Antibody treatment of T-cell malignancies
Introduction of current treatment studies in peripheral T-cell lymphomas
Conclusions
Acknowledgements
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