Diffuse large B-cell lymphoma of Waldeyer's ring has distinct clinicopathologic features: a GELA study

被引:36
作者
de Leval, L. [1 ]
Bonnet, C. [2 ]
Copie-Bergman, C. [3 ,4 ,5 ]
Seidel, L. [6 ]
Baia, M. [3 ,4 ]
Briere, J. [7 ,8 ]
Molina, T. J. [9 ]
Fabiani, B. [10 ]
Petrella, T. [11 ]
Bosq, J. [12 ]
Gisselbrecht, C. [7 ]
Siebert, R. [13 ,14 ]
Tilly, H. [15 ]
Haioun, C. [3 ,4 ,5 ]
Fillet, G. [2 ]
Gaulard, P. [3 ,4 ,5 ]
机构
[1] CHU Vaudois, Inst Pathol, Dept Labs, CH-1011 Lausanne, Switzerland
[2] CHU Liege, Dept Clin Hematol, Liege, Belgium
[3] Hop Henri Mondor, Lymphoid Malignancies Unit, F-94010 Creteil, France
[4] Hop Henri Mondor, INSERM, U955, F-94010 Creteil, France
[5] Paris Est Univ, Dept Med, Creteil, France
[6] Univ Liege, Dept Biostat, Liege, Belgium
[7] Hop St Louis, INSERM, U728, Paris, France
[8] Hop St Louis, AP HP, Dept Pathol, Paris, France
[9] Paris Descartes Univ, AP HP, Hotel Dieu Hosp, Dept Pathol, Paris, France
[10] Hop St Antoine, Dept Pathol, F-75571 Paris, France
[11] CHU, Dept Pathol, Dijon, France
[12] Inst Gustave Roussy, Dept Biopathol, Morpol Unit, Villejuif, France
[13] Univ Kiel, Inst Human Genet, Kiel, Germany
[14] Univ Hosp Schleswig Holstein, Kiel, Germany
[15] Univ Rouen, Ctr Henri Becquerel, Dept Hematol, UMR918, Rouen, France
关键词
clinicopathologic features; diffuse large B-cell lymphomas; outcome; Waldeyer's ring; NON-HODGKINS-LYMPHOMA; BCL-2 PROTEIN EXPRESSION; CHOP PLUS RADIOTHERAPY; CENTRAL-NERVOUS-SYSTEM; FOLLICULAR LYMPHOMA; GERMINAL CENTER; ELDERLY-PATIENTS; GRADE; 3B; PROGNOSTIC-SIGNIFICANCE; CHEMOTHERAPY;
D O I
10.1093/annonc/mds150
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diffuse large B-cell lymphomas (DLBCLs) arising in specific extranodal sites have peculiar clinicopathologic features. We analyzed a cohort of 187 primary Waldeyer's ring (WR) DLBCLs retrieved from GELA protocols using anthracyclin-based polychemotherapy. Most patients (92%) had stage I-II disease. A germinal center B-cell-like (GCB) immunophenotype was observed in 61%, and BCL2 expression in 55%, of WR DLBCLs. BCL2, BCL6, IRF4 and MYC breakpoints were observed in, respectively, 3 of 42 (7%), 9 of 36 (25%), 2 of 26 (8%) and 4 of 40 (10%) contributive cases. A variable follicular pattern was evidenced in 30 of 68 (44%) large biopsy specimens. The 5-year progression-free survival (PFS) and the overall survival (OS) of 153 WR DLBCL patients with survival information were 69.5% and 77.8%, respectively. The GCB immunophenotype correlated with a better OS (P = 0.0015), while BCL2 expression predicted a worse OS (P = 0.037), an effect overcome by the GCB/non-GCB classification. Compared with matched nodal DLBCLs, WR DLBCLs with no age-adjusted international prognostic index factor disclosed a better 5-year PFS rate (77.5% versus 70.7%; P = 0.03). WR DLBCLs display distinct clinicopathologic features compared with conventional DLBCLs, with usual localized-stage disease, common follicular features and a high frequency of GCB immunophenotype contrasting with a low rate of BCL2 rearrangements. In addition, they seem to be associated with a better outcome than their nodal counterpart.
引用
收藏
页码:3143 / 3151
页数:9
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