Update on the molecular pathogenesis and clinical treatment of mantle cell lymphoma: report of the 10th annual conference of the European Mantle Cell Lymphoma Network

被引:24
作者
Dreyling, Martin [1 ]
Kluin-Nelemans, Hanneke C. [2 ]
Bea, Silvia [3 ]
Hartmann, Elena [4 ]
Salaverria, Itziar [5 ]
Hutter, Grit [7 ]
Perez-Galan, Patricia [3 ]
Roue, Gael [3 ]
Pott, Christiane [6 ]
Le Gouill, Steven [8 ]
Cortelazzo, Sergio [9 ,10 ]
Rule, Simon [11 ]
Hess, Georg [12 ]
Zaja, Francesco [13 ]
Vitolo, Umberto [14 ]
Szymczyk, Michal [15 ,16 ]
Walewski, Jan [15 ,16 ]
Ribrag, Vincent [17 ]
Unterhalt, Michael [18 ]
Hermine, Olivier [18 ]
Hoster, Eva [1 ]
机构
[1] Univ Hosp Grosshadern LMU Munich, Dept Med 3, Munich, Germany
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Hematol, NL-9713 AV Groningen, Netherlands
[3] Hosp Clin Barcelona, Hematopathol Unit, Dept Pathol, IDIBAPS, Barcelona, Spain
[4] Univ Wurzburg, Inst Pathol, D-8700 Wurzburg, Germany
[5] Univ Kiel, Univ Hosp Schleswig Holstein Campus Kiel, Inst Human Genet, D-24098 Kiel, Germany
[6] Univ Kiel, Univ Hosp Schleswig Holstein Campus Kiel, Dept Med 2, D-24098 Kiel, Germany
[7] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Munich, Germany
[8] Hosp Hotel Dieu, Dept Hematol, Nantes, France
[9] Gen Hosp Bolzano, Div Hematol, Bolzano, Italy
[10] Gen Hosp Bolzano, BMT, Bolzano, Italy
[11] Derriford Hosp, Dept Haematol, Plymouth PL6 8DH, Devon, England
[12] Univ Hosp Mainz, Dept Med 3, Munich, Germany
[13] Azienda Osped Univ, Clin Ematol, DIRM, Udine, Italy
[14] Ematol II Osp San Giovanni Battista, Turin, Italy
[15] Maria Sklodowska Curie Inst, Warsaw, Poland
[16] Ctr Oncol, Warsaw, Poland
[17] Inst Gustave Roussy, Dept Hematol, Villejuif, France
[18] Univ Paris 05, Necker Hosp, AP HP, Dept Hematol,Fac Med, Paris, France
关键词
Mantle cell lymphoma; clinical treatment; BENDAMUSTINE PLUS RITUXIMAB; PROGRESSION-FREE SURVIVAL; GENE-EXPRESSION; B-CELL; IMMUNOCHEMOTHERAPY; TRANSLOCATION; AMPLIFICATION; MULTICENTER; MONOTHERAPY; REMISSION;
D O I
10.3109/10428194.2011.600488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mantle cell lymphoma (MCL) is a distinct subtype of malignant lymphoma characterized by the chromosomal translocation t(11;14)(q13;q32), resulting in constitutional overexpression of cyclin D1 and cell cycle dysregulation in virtually all cases. Clinically, MCL shows an aggressive clinical course with a continuous relapse pattern and a median survival of only 3-5 years. However, recently a subset of up to 15% long-term survivors has been identified with a rather indolent clinical course. Advanced stage disease is usually apparent already at first clinical manifestation; in general, conventional chemotherapy is only palliative and median duration of remissions is only 1-2 years. In 2000, the European MCL Network (http://www.europeanmcl.net) was founded, which consists of 15 national lymphoma study groups supplemented by experts in hematopathology, cytogenetics and molecular genetics. During the last decade, the European consortium has successfully initiated the largest phase III trials in MCL worldwide. In the current study generation, the addition of high-dose Ara-C to a rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP)-like regimen followed by myeloablative consolidation achieved a significant improvement of progression-free survival. Similarly, in elderly patients, rituximab maintenance until progression led to a marked prolongation of remission duration. Emerging strategies include proteasome inhibitors, immune modulatory drugs (IMiDs), mammalian target of rapamycin (mTOR) inhibitors and others, all based on the dysregulated control of cell cycle machinery and impairment of several apoptotic pathways. Combination strategies are currently being investigated in numerous trials, but their introduction into clinical practice and current treatment algorithms remains a challenge. Future strategies will apply individualized approaches according to the molecular risk profile of the patient. At the annual conference in Warsaw, recent results of molecular pathogenesis, analyses of current clinical trials and new study concepts were discussed.
引用
收藏
页码:2226 / 2236
页数:11
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