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Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience
CONTEXT: Primary central nervous system lymphoma (PCNSL) is a variant of extranodal lymphoma, accounting for 4% of primary central nervous system tumors. PCNSL was more common in immunocompetent individuals. International Extranodal Lymphoma Study Group (IELSG) scoring was used for prognostication....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759068/ https://www.ncbi.nlm.nih.gov/pubmed/29333016 http://dx.doi.org/10.4103/ijmpo.ijmpo_202_16 |
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author | Puligundla, Chaitanya Krishna Bala, Stalin Karnam, Ashok Kumar Gundeti, Sadashivudu Paul, Tara Roshni Uppin, Megha S Maddali, Lakshmi Srinivas |
author_facet | Puligundla, Chaitanya Krishna Bala, Stalin Karnam, Ashok Kumar Gundeti, Sadashivudu Paul, Tara Roshni Uppin, Megha S Maddali, Lakshmi Srinivas |
author_sort | Puligundla, Chaitanya Krishna |
collection | PubMed |
description | CONTEXT: Primary central nervous system lymphoma (PCNSL) is a variant of extranodal lymphoma, accounting for 4% of primary central nervous system tumors. PCNSL was more common in immunocompetent individuals. International Extranodal Lymphoma Study Group (IELSG) scoring was used for prognostication. High-dose methotrexate regimens along with radiotherapy improved outcomes in PCNSL. AIMS: The aim of this study is to analyze the clinical and pathological features, progression-free survival (PFS), and overall survival (OS) in patients with PCNSL. MATERIALS AND METHODS: Data of patients with PCNSL between 2005 and 2016 were retrospectively analyzed. Outcome was analyzed in patients who received chemotherapy. GraphPad Prism software for Windows Version 6 was used to plot the Kaplan–Meier curves for PFS and OS. Log-rank test was used to calculate P values. P < 0.05 was considered as statistically significant. RESULTS: A total of 42 patients were available for analysis. Of these, 34 patients who received chemotherapy were evaluable for outcome parameters. The median age at presentation was 46 years (range, 10–75) with male-to-female ratio of 2.2:1. Only 2 (4.7%) patients were HIV positive. Diffuse large B-cell lymphoma (DLBCL) was the most common histology seen in 41 (97.6%) patients. Using IELSG risk scoring, scores of 8 (19%), 19 (45.2%), and 15 (35.8%) were stratified into low, intermediate, and high risk. The median PFS and OS were 11 months (range, 2–72) and 15.9 months (2.4–80.4), respectively. The median OS was 36.2 months (range, 8.8–72), 15.6 months (2–36), and 6.1 months (2.6–12.7) in low-, intermediate-, and high-risk groups, respectively, which was statistically significant (P = 0.0002). CONCLUSIONS: Immunocompetent patients with PCNSL outnumber immunocompromised patients. DLBCL was the most common histology, and IELSG risk stratification significantly predicts the outcome in PCNSL. |
format | Online Article Text |
id | pubmed-5759068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57590682018-01-12 Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience Puligundla, Chaitanya Krishna Bala, Stalin Karnam, Ashok Kumar Gundeti, Sadashivudu Paul, Tara Roshni Uppin, Megha S Maddali, Lakshmi Srinivas Indian J Med Paediatr Oncol Original Article CONTEXT: Primary central nervous system lymphoma (PCNSL) is a variant of extranodal lymphoma, accounting for 4% of primary central nervous system tumors. PCNSL was more common in immunocompetent individuals. International Extranodal Lymphoma Study Group (IELSG) scoring was used for prognostication. High-dose methotrexate regimens along with radiotherapy improved outcomes in PCNSL. AIMS: The aim of this study is to analyze the clinical and pathological features, progression-free survival (PFS), and overall survival (OS) in patients with PCNSL. MATERIALS AND METHODS: Data of patients with PCNSL between 2005 and 2016 were retrospectively analyzed. Outcome was analyzed in patients who received chemotherapy. GraphPad Prism software for Windows Version 6 was used to plot the Kaplan–Meier curves for PFS and OS. Log-rank test was used to calculate P values. P < 0.05 was considered as statistically significant. RESULTS: A total of 42 patients were available for analysis. Of these, 34 patients who received chemotherapy were evaluable for outcome parameters. The median age at presentation was 46 years (range, 10–75) with male-to-female ratio of 2.2:1. Only 2 (4.7%) patients were HIV positive. Diffuse large B-cell lymphoma (DLBCL) was the most common histology seen in 41 (97.6%) patients. Using IELSG risk scoring, scores of 8 (19%), 19 (45.2%), and 15 (35.8%) were stratified into low, intermediate, and high risk. The median PFS and OS were 11 months (range, 2–72) and 15.9 months (2.4–80.4), respectively. The median OS was 36.2 months (range, 8.8–72), 15.6 months (2–36), and 6.1 months (2.6–12.7) in low-, intermediate-, and high-risk groups, respectively, which was statistically significant (P = 0.0002). CONCLUSIONS: Immunocompetent patients with PCNSL outnumber immunocompromised patients. DLBCL was the most common histology, and IELSG risk stratification significantly predicts the outcome in PCNSL. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5759068/ /pubmed/29333016 http://dx.doi.org/10.4103/ijmpo.ijmpo_202_16 Text en Copyright: © 2017 Indian Journal of Medical and Paediatric Oncology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Puligundla, Chaitanya Krishna Bala, Stalin Karnam, Ashok Kumar Gundeti, Sadashivudu Paul, Tara Roshni Uppin, Megha S Maddali, Lakshmi Srinivas Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title | Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title_full | Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title_fullStr | Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title_full_unstemmed | Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title_short | Clinicopathological Features and Outcomes in Primary Central Nervous System Lymphoma: A 10-year Experience |
title_sort | clinicopathological features and outcomes in primary central nervous system lymphoma: a 10-year experience |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759068/ https://www.ncbi.nlm.nih.gov/pubmed/29333016 http://dx.doi.org/10.4103/ijmpo.ijmpo_202_16 |
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