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Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases
OBJECTIVE: The risk of developing diffuse large B-cell lymphoma (DLBCL) is increased in many rheumatic diseases (RDs). It is possible that RD-associated DLBCL is a distinct subset within the category of ‘DLBCL’, exhibiting characteristic biological features and clinical behaviour. However, informati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596057/ https://www.ncbi.nlm.nih.gov/pubmed/34785569 http://dx.doi.org/10.1136/lupus-2021-000561 |
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author | Gorodetskiy, Vadim Probatova, Natalya Obukhova, Tatiana Vasilyev, Vladimir |
author_facet | Gorodetskiy, Vadim Probatova, Natalya Obukhova, Tatiana Vasilyev, Vladimir |
author_sort | Gorodetskiy, Vadim |
collection | PubMed |
description | OBJECTIVE: The risk of developing diffuse large B-cell lymphoma (DLBCL) is increased in many rheumatic diseases (RDs). It is possible that RD-associated DLBCL is a distinct subset within the category of ‘DLBCL’, exhibiting characteristic biological features and clinical behaviour. However, information on RD-associated DLBCL is limited. METHODS: We searched the V.A. Nasonova Research Institute of Rheumatology (Russia) database from 1996 to 2021 for patients with RDs and coexisting DLBCL. Prognostic factors including the International Prognostic Index (IPI), bulk disease and c-MYC/8q24 gene rearrangements were analysed. Furthermore, we stratified DLBCLs as germinal centre B-cell (GCB) subtype and non-GCB subtype based on Hans’ immunohistochemical algorithm and also examined Epstein-Barr virus (EBV) status. RESULTS: Twenty-seven patients with RD-associated DLBCL were identified. Twenty patients had primary Sjogren’s syndrome, three had systemic lupus erythematosus, two had rheumatoid arthritis and two had systemic sclerosis. Secondary Sjogren’s syndrome was found in four patients. The median age at the time of diagnosis of DLBCL was 59 years with a female predominance (26:1). Based on IPI, 16 patients were assigned to the intermediate-high and high-risk groups. Bulk disease was detected in 29% of patients. Of the 20 examined cases, 4 (20%) were classified as the GCB subtype and 16 (80%) were classified as the non-GCB subtype. EBV was detected in 2 of the 21 tested cases (10%), and the c-MYC/8q24 gene rearrangement was not found in any of the 19 examined cases. After the lymphoma diagnosis, the median overall survival (OS) was 10 months (range: 0–238 months). CONCLUSIONS: Except for the more common non-GCB subtype, we did not identify any other prognostic factor that could influence the prognosis of patients with RD-associated DLBCL. We believe that short OS in our patients was predominantly associated with decreased tolerance to lymphoma treatment. |
format | Online Article Text |
id | pubmed-8596057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-85960572021-11-24 Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases Gorodetskiy, Vadim Probatova, Natalya Obukhova, Tatiana Vasilyev, Vladimir Lupus Sci Med Co-Morbidities OBJECTIVE: The risk of developing diffuse large B-cell lymphoma (DLBCL) is increased in many rheumatic diseases (RDs). It is possible that RD-associated DLBCL is a distinct subset within the category of ‘DLBCL’, exhibiting characteristic biological features and clinical behaviour. However, information on RD-associated DLBCL is limited. METHODS: We searched the V.A. Nasonova Research Institute of Rheumatology (Russia) database from 1996 to 2021 for patients with RDs and coexisting DLBCL. Prognostic factors including the International Prognostic Index (IPI), bulk disease and c-MYC/8q24 gene rearrangements were analysed. Furthermore, we stratified DLBCLs as germinal centre B-cell (GCB) subtype and non-GCB subtype based on Hans’ immunohistochemical algorithm and also examined Epstein-Barr virus (EBV) status. RESULTS: Twenty-seven patients with RD-associated DLBCL were identified. Twenty patients had primary Sjogren’s syndrome, three had systemic lupus erythematosus, two had rheumatoid arthritis and two had systemic sclerosis. Secondary Sjogren’s syndrome was found in four patients. The median age at the time of diagnosis of DLBCL was 59 years with a female predominance (26:1). Based on IPI, 16 patients were assigned to the intermediate-high and high-risk groups. Bulk disease was detected in 29% of patients. Of the 20 examined cases, 4 (20%) were classified as the GCB subtype and 16 (80%) were classified as the non-GCB subtype. EBV was detected in 2 of the 21 tested cases (10%), and the c-MYC/8q24 gene rearrangement was not found in any of the 19 examined cases. After the lymphoma diagnosis, the median overall survival (OS) was 10 months (range: 0–238 months). CONCLUSIONS: Except for the more common non-GCB subtype, we did not identify any other prognostic factor that could influence the prognosis of patients with RD-associated DLBCL. We believe that short OS in our patients was predominantly associated with decreased tolerance to lymphoma treatment. BMJ Publishing Group 2021-11-16 /pmc/articles/PMC8596057/ /pubmed/34785569 http://dx.doi.org/10.1136/lupus-2021-000561 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Co-Morbidities Gorodetskiy, Vadim Probatova, Natalya Obukhova, Tatiana Vasilyev, Vladimir Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title | Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title_full | Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title_fullStr | Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title_full_unstemmed | Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title_short | Analysis of prognostic factors in diffuse large B-cell lymphoma associated with rheumatic diseases |
title_sort | analysis of prognostic factors in diffuse large b-cell lymphoma associated with rheumatic diseases |
topic | Co-Morbidities |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596057/ https://www.ncbi.nlm.nih.gov/pubmed/34785569 http://dx.doi.org/10.1136/lupus-2021-000561 |
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