Lineaue determination of CD20-B-cell neoplasms: An inummohistochemical study

被引:45
作者
Chu, Peiguo G. [1 ]
Loera, Sofia [1 ]
Huang, Qin [1 ]
Weiss, Lawrence M. [1 ]
机构
[1] City Hope Natl Med Ctr, Div Pathol, Duarte, CA 91010 USA
关键词
CD20; Pax-5; BOB.1; OCT.2; B lineage; rituximab; rituxan;
D O I
10.1309/3WG32YRAMQ7RB9D4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We studied 61 CD20- B-cell lymphomas, including 29 cases of precursor B-cell lymphoblastic leukemia,lymphoblastic lymphoma (B-ALL/B-LBL), 25 cases of CD20-recurrent mature B-cell lymphoma after rituximab therapy, and 7 cases of CD20-diffuse large B cell lymphoma (DLBCL). We used markers specific for B lineage: CD79a, Pax-5, OCT.2, and BOB.1. All B-ALL/B-LBLs expressed Pax-5 (29/29 [100%]), 25 (93%) of 27 expressed BOB.1, 23 (79%) of 29 expressed CD79a, and 6 (22%) of 27 expressed OCT.2. The percentages of cases expressing Pax-5, CD79a, OCT.2, and BOB.1 in CD20- recurrent mature B-cell lymphomas after rituximab treatment were 88% (21/24), 84% (21/25), 81% (17/21), and 73% (16/22), respectively. CD20- DLBCLs rarely express routine B-lineage markers, such as CD79a and Pax-5, but they expressed OCT.2 or BOB.1. Pax-5, BOB.1, and CD79a antigens are the most reliable B-lineage markers for paraffin immunophenotyping B-ALL/B-LBL. CD79a and Pax-5 should be used as the first-line B lineage-specific markers for rituximab-treated CD20-mature B-cell lymphomas. If negative, OCT.2 or BOB. I may be useful. The newly identified B-lineage markers, OCT 2 and BOB.1, may be the most useful for the B-lineage determination of CD20-plasmablastic or primary effusion subtypes of DLBCL.
引用
收藏
页码:534 / 544
页数:11
相关论文
共 42 条
[1]   CD20-negative DLBCL transformation after rituximab treatment in follicular lymphoma:: a new case report and review of the literature [J].
Alvaro-Naranjo, T ;
Jaén-Martínez, J ;
Gumá-Padró, J ;
Bosch-Príncep, R ;
Salvadó-Usach, MT .
ANNALS OF HEMATOLOGY, 2003, 82 (09) :585-588
[2]  
Arber DA, 1996, AM J PATHOL, V149, P1105
[3]   PROPOSED REVISED CRITERIA FOR THE CLASSIFICATION OF ACUTE MYELOID-LEUKEMIA - A REPORT OF THE FRENCH-AMERICAN-BRITISH COOPERATIVE GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :620-625
[4]   Rituximab using a thrice weekly dosing schedule in B-Cell chronic lymphocytic leukemia and small lymphocytic lymphoma demonstrates clinical activity and acceptable toxicity [J].
Byrd, JC ;
Murphy, T ;
Howard, RS ;
Lucas, MS ;
Goodrich, A ;
Park, K ;
Pearson, M ;
Waselenko, JK ;
Ling, G ;
Grever, MR ;
Grillo-Lopez, AJ ;
Rosenberg, J ;
Kunkel, L ;
Flinn, IW .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (08) :2153-2164
[5]  
Chang KL, 1996, APPL IMMUNOHISTOCHEM, V4, P1
[6]  
Chu PG, 2002, LEUKEMIA LYMPHOMA, V43, P2335, DOI 10.1080/1042819021000040044
[7]   CD79: A review [J].
Chu, PG ;
Arber, DA .
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2001, 9 (02) :97-106
[8]   CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. [J].
Coiffier, B ;
Lepage, E ;
Brière, J ;
Herbrecht, R ;
Tilly, H ;
Bouabdallah, R ;
Morel, P ;
Van den Neste, E ;
Salles, G ;
Gaulard, P ;
Reyes, F ;
Gisselbrecht, C .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :235-242
[9]   Rituximab (anti-CD20 monoclonal antibody) as single first-line therapy for patients with follicular lymphoma with a low tumor burden:: clinical and molecular evaluation [J].
Colombat, P ;
Salles, G ;
Brousse, N ;
Eftekhari, P ;
Soubeyran, P ;
Delwail, V ;
Deconinck, E ;
Haïoun, C ;
Foussard, C ;
Sebban, C ;
Stamatoullas, A ;
Milpied, N ;
Boué, F ;
Taillan, B ;
Lederlin, P ;
Najman, A ;
Thièblemont, C ;
Montestruc, F ;
Mathieu-Boué, A ;
Benzohra, A ;
Solal-Céligny, P .
BLOOD, 2001, 97 (01) :101-106
[10]  
Davis TA, 2000, CLIN CANCER RES, V6, P2644