Mantle cell lymphoma

Lymphoma: Pathology, Diagnosis and Treatment

Volumn , Issue , 2007, Pages 154-167

  Dreyling, Martin ^a   Williams, Michael E ^b  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^b UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 50449087670     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9780511663369.012     Document Type: Chapter

References (21)

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2. Fang, N. Y., Greiner, T. C., Weisenburger, D. D. et al. Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma. Proc. Natl. Acad. Sci. USA 100 (2003), 5372–5377.
3. Fernandez, V., Hartmann, E., Ott, G., Campo, E. and Rosenwald, A. Pathogenesis of mantle cell lymphoma: all oncogenic roads lead to dysregulation of cell cycle and DNA damage response pathways. J. Clin. Oncol. 23 (2005), 6364–6369.
4. Forstpointner, R., Dreyling, M., Repp, R. et al. The addition of rituximab to a combination of fludarabine, cyclophosphamide, mitoxantrone (FCM) significantly increases the response rate and prolongs survival as compared to FCM alone in patients with relapsed and refractory follicular and mantle cell lymphomas:results of a prospective randomized study of the German Low-Grade Lymphoma Study Group (GLSG). Blood 104 (2004), 3064–3071.
5. Forstpointner, R., Unterhalt M., Dreyling M. et al. Maintenance therapy with rituximab leads to a significant prolongation of response duration after salvage therapy with a combination of rituximab, fludarabine, cyclophosphamide and mitoxantrone (R-FCM) in patients with relapsed and refractory follicular and mantle cell lymphomas: results of a prospective randomized study of the German Low Grade Lymphoma Study Group (GLSG). Blood 108 (2006), 4003–4008.
6. Ghielmini, M., Schmitz Hsu, S. -F., Cogliatti, S. et al. Effect of single-agent rituximab given at the standard schedule or as prolonged treatment in patients with mantle cell lymphoma:a study of the Swiss Group for Clinical Cancer Research (SAKK). J. Clin. Oncol. 23 (2005), 705–711.
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17. Rosenberg, C. L., Wong, E., Petty, E. M. et al. PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma. Proc. Natl. Acad. Sci. USA 88 (1991),9638–9642.
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