Lymphomas with pseudo-double-hit BCL6-MYC translocations due to t(3;8)(q27;q24) are associated with a germinal center immunophenotype, extranodal involvement, and frequent BCL2 translocations

被引:27
作者
Johnson, Steven M. [1 ]
Umakanthan, Jayadev Manikkam [2 ]
Yuan, Ji [3 ]
Fedoriw, Yuri [1 ,4 ]
Bociek, R. Gregory [2 ]
Kaiser-Rogers, Kathleen [1 ,5 ,6 ]
Sanmann, Jennifer N. [7 ]
Montgomery, Nathan D. [1 ,4 ]
机构
[1] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[2] Univ Nebraska Med Ctr, Dept Internal Med, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Dept Pathol, Omaha, NE 68198 USA
[4] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Sch Med, Dept Pediat, Chapel Hill, NC 27514 USA
[6] Univ N Carolina, Sch Med, Dept Genet, Genetics, NC 27514 USA
[7] Univ Nebraska Med Ctr, Munroe Meyer Inst, Human Genet Lab, Omaha, NE 68131 USA
关键词
Double-hit lymphoma; High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements; t(3; 8)(q27; q24); Triple-hit lymphoma; Lymphoma cytogenetics; B-CELL LYMPHOMA; MYC TRANSLOCATIONS; HODGKIN-LYMPHOMA; BURKITT-LYMPHOMA; REARRANGEMENTS; PROGNOSIS; FEATURES; LYMPHOMA/LEUKEMIA; CLASSIFICATION; JUXTAPOSITION;
D O I
10.1016/j.humpath.2018.06.006
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
High-grade B-cell lymphomas with MYC, BCL2, and/or BCL6 rearrangements, "double-hit" or "triple-hit" lymphomas (DTHL), are aggressive neoplasms associated with a poor prognosis. A t(3;8) (q27;q24) rarely occurs in B-cell lymphomas that results in a unique "pseudo double-hit" BCL6-MYC fusion, indistinguishable by interphase fluorescence in situ hybridization (FISH) from more conventional DTHL with independent MYC and BCL6 translocations. Reports of t(3;8)(q27;q24) lymphomas are sparse, and to better characterize their pathologic, cytogenetic, and clinical features, 6 new cases from 2 institutions and 19 previously published cases were reviewed. All new cases displayed aggressive morphologic features, and most previously published cases were classified as aggressive lymphomas. Collectively, all t(3;8)(q27; q24) cases had a germinal center (GC) phenotype, and most had complex karyotypes (22/24, 92%), including frequent concomitant BCL2 rearrangements (17/24, 71%). When compared to two large published DTHL cohorts, t(3;8)(q27;q24) lymphomas less often expressed BCL2 (P<.01), had a greater likelihood of extranodal involvement (P<.01), and more frequently appeared triple-hit by FISH analysis (P<.01). Despite presenting with aggressive clinicopathologic features, 100% (6/6) of t(3;8;)(q27;q24) patients achieved complete remission after intensive induction regimens, and 2- and 3-year overall survival rates were 63% (10/16) and 57% (8/14), respectively. These findings suggest that lymphomas with t (3;8)(q27;q24) may represent a subset of GC B-cell lymphomas distinct from conventional DTHL. Our results further highlight the value of routine karyotype assessment in aggressive B-cell lymphomas, and the importance of recognizing the t(3;8)(q27;q24) so that its clinical significance can be more fully explored. (C) 2018 Elsevier Inc. All rights reserved.
引用
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页码:192 / 200
页数:9
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