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Immunohistochemical subtypes of diffuse large B-cell lymphoma in the head and neck region
1Department of Pathology, Sichuan Cancer Hospital, Chengdu, China lijiman_ljm@126.com.
Insights
This study found that head and neck diffuse large B-cell lymphoma (DLBCL) is predominantly the activated B-cell (ABC) subtype, not the germinal center B-cell (GCB) subtype. The Hans, Choi, and Tally algorithms showed no significant differences in classifying DLBCL subtypes.
Area of Science:
- Oncology
- Immunohistochemistry
- Molecular Pathology
Background:
- Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous lymphoid malignancy.
- Accurate subtyping of DLBCL is crucial for predicting patient outcomes and guiding treatment strategies.
- Head and neck DLBCL presents unique characteristics that warrant specific investigation.
Purpose of the Study:
- To determine the immunohistochemical subtypes of head and neck DLBCL using established algorithms.
- To compare the performance of the Hans, Choi, and Tally algorithms in classifying DLBCL subtypes.
- To investigate the correlation between protein expression (CD10, Bcl-6, MUM1, GCET1, FOXP1, LMO2) and DLBCL subtypes.
Main Methods:
- Immunohistochemistry was performed on 103 head and neck DLBCL patient samples.
- Proteins analyzed included CD10, B-cell lymphoma 6 protein (Bcl-6), mutated melanoma-associated antigen 1 (MUM1), germinal center B-cell-expressed transcript 1 (GCET1), forkhead box protein P1 (FOXP1), and LIM domain only 2 (LMO2).
- DLBCL subtypes were classified using the Hans, Choi, and Tally algorithms.
Main Results:
- The majority of head and neck DLBCL cases were classified as the activated B-cell (ABC) subtype (74.8% by Hans, 75.7% by Choi, 80.6% by Tally), rather than the germinal center B-cell (GCB) subtype.
- Expression of CD10, MUM1, GCET1, FOXP1, and LMO2 showed significant correlation with the determined subtypes across algorithms (P < 0.05).
- Bcl-6 expression did not correlate with the Hans and Choi algorithms.
Conclusions:
- Head and neck DLBCL predominantly exhibits the ABC subtype.
- The Hans, Choi, and Tally algorithms demonstrated comparable performance in classifying head and neck DLBCL subtypes.
- Protein expression analysis provides valuable insights into the molecular characteristics of different DLBCL subtypes.
Abstract:
The objectives of this study were to detect immunohistochemical subtypes of diffuse large B-cell lymphoma (DLBCL) of the head and neck, to compare the Hans, Choi, and Tally algorithms and to examine the significance of protein expression in these algorithms. This study included 103 DLBCL patients at Sichuan Cancer Hospital between May 2010 and October 2012. Immunohistochemistry was per-formed for CD10, B-cell lymphoma 6 protein (Bcl-6), mutated melanoma-associated antigen 1 (MUM1), germinal center B-cell-expressed transcript 1 (GCET1), forkhead box protein P1 (FOXP1), and LIM do-main only 2 (LMO2). Subtypes were determined according to the Hans, Choi, and Tally algorithms. Positive staining for CD10 was detected in 16 patients (15.53%), for Bcl-6 in 68 patients (66.02%), for MUM1 in 69 patients (66.99%), for GCET1 in 21 patients (20.39%), for FOXP1 in 75 patients (72.82%), and for LMO2 in 50 patients (48.54%). The Hans algorithm identified 26 patients (25.2%) with the germinal center B-cell (GCB) subtype and 77 (74.8%) with the activated B-cell (ABC) subtype. In the Choi algorithm, 25 patients (24.3%) were identified with the GCB subtype and 78 (75.7%) with the ABC subtype. In the Tally algorithm, 20 patients (19.4%) had the GCB subtype and 83 (80.6%) had the ABC subtype. Expression of CD10, MUM1, GCET1, FOXP1, and LMO2 correlated with algorithm (P < 0.05); however, Bcl-6 did not correlate with the Hans and Choi algorithms. DLBCL of the head and neck is most commonly the ABC subtype, not GCB. The Hans, Choi, and Tally algorithms were not significantly different.
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