Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group
Mature T-cell and natural killer (NK)–cell lymphomas are rare and heterogeneous diseases following an aggressive clinical course which necessitates immediate therapy. Outcome is generally believed poor although only 1 recent study1 comprises all major T-cell lymphoma subtypes according to the World...
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| Main Authors: | , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
July 21, 2010
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| In: |
Blood
Year: 2010, Volume: 116, Issue: 18, Pages: 3418-3425 |
| ISSN: | 1528-0020 |
| DOI: | 10.1182/blood-2010-02-270785 |
| Online Access: | Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1182/blood-2010-02-270785 Verlag, lizenzpflichtig, Volltext: https://ashpublications.org/blood/article/116/18/3418/27966/Treatment-and-prognosis-of-mature-T-cell-and-NK 
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| Author Notes: | Norbert Schmitz, Lorenz Trümper, Marita Ziepert, Maike Nickelsen, Anthony D. Ho, Bernd Metzner, Norma Peter, Markus Loeffler, Andreas Rosenwald, and Michael Pfreundschuh |
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| 520 | |a Mature T-cell and natural killer (NK)–cell lymphomas are rare and heterogeneous diseases following an aggressive clinical course which necessitates immediate therapy. Outcome is generally believed poor although only 1 recent study1 comprises all major T-cell lymphoma subtypes according to the World Health Organization classification2,3 with spin-off studies reporting on clinical outcome and prognostic factors of various subtypes. In contrast to the progress made in the treatment of aggressive B-cell lymphoma, evidence for similar therapeutic improvements in T- and NK-cell lymphoma is largely absent. Therefore, we analyzed a large cohort of patients with T-cell lymphoma who have been treated on protocols of the German High-Grade Non-Hodgkin Lymphoma Study Group (Deutsche Studiengruppe Hochmaligne Non-Hodgkin Lymphome [DSHNHL]). We were particularly interested in the long-term results achieved with “standard” CHOP (cyclophosphamide, hydroxydaunorubicin (doxorubicin), Oncovin (vincristine), and prednisone/prednisolone) and CHOP-like therapy and wanted to define prognostic factors which should influence the decision which patients should be treated on standard or experimental protocols in the future. | ||
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