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Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma

OBJECTIVES: Even though frequent, it is not known how HIV infection and treatment impact in the consolidation by radiotherapy of non-Hodgkin diffuse large B-cell lymphomas (DBCL). This article aim to assess that difference that HIV makes on radiation treatment. PATIENTS AND METHODS: A retrospective...

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Autores principales: Medici, Carolina Trindade Mello, Mauro, Geovanne Pedro, Casimiro, Lucas Coelho, Weltman, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296722/
https://www.ncbi.nlm.nih.gov/pubmed/32539797
http://dx.doi.org/10.1186/s13014-020-01589-1
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author Medici, Carolina Trindade Mello
Mauro, Geovanne Pedro
Casimiro, Lucas Coelho
Weltman, Eduardo
author_facet Medici, Carolina Trindade Mello
Mauro, Geovanne Pedro
Casimiro, Lucas Coelho
Weltman, Eduardo
author_sort Medici, Carolina Trindade Mello
collection PubMed
description OBJECTIVES: Even though frequent, it is not known how HIV infection and treatment impact in the consolidation by radiotherapy of non-Hodgkin diffuse large B-cell lymphomas (DBCL). This article aim to assess that difference that HIV makes on radiation treatment. PATIENTS AND METHODS: A retrospective cohort of all DBCL patients treated with chemotherapy and consolidative radiotherapy at a single institution between 2010 and 2018 was assessed. All patients had biopsy-proven lymphoma and were included if radiation was part of the treatment and had at least 6 months of follow-up or were followed until death. RESULTS: Three-hundred fifty-nine (359) patients were selected, with a median age at diagnosis of 57.7 years (13–90 years). Twenty-eight patients (7.8%) were HIV positive. Median follow-up was 48.0 months. Female patients were 51.3% and most had a good performance in the ECOG scale (78.8% are ECOG 0–1). Median overall survival was not reached, but mean OS was 50.1 months with 86 deaths. Median progression-free survival was 48.7 months. HIV infection had no impact on OS (p = 0.580) or PFS (p = 0.347) among patients treated with RT. HIV positive patients were more frequently staged only with CT (p > 0.05) with no impact on PFS (p = 0.191). No HIV positive patient received rituximab due to local policy restrictions and HIV positive patients were more prone to receive CHOP-like chemotherapy (p < 0.05), specially ones with etoposide (CHOEP). CHOP was associated with better survival (p = 0.015) in the overall population and in the HIV negative population (p = 0.002), but not in the HIV positive population (p = 0.982). RT toxicities were not overall more frequent in the HIV positive population (p = 0.567), except for fatigue (p < 0.05) and hematological toxicities (p = 0.022). CONCLUSION: HIV status did not influence on survival when patients were treated with consolidative radiotherapy. HIV infection was a bias on our sample for staging methods and chemotherapy regimens choices. For HIV positive patients there was an increase in fatigue and hematological toxicities of any grade with radiation.
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spelling pubmed-72967222020-06-16 Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma Medici, Carolina Trindade Mello Mauro, Geovanne Pedro Casimiro, Lucas Coelho Weltman, Eduardo Radiat Oncol Research OBJECTIVES: Even though frequent, it is not known how HIV infection and treatment impact in the consolidation by radiotherapy of non-Hodgkin diffuse large B-cell lymphomas (DBCL). This article aim to assess that difference that HIV makes on radiation treatment. PATIENTS AND METHODS: A retrospective cohort of all DBCL patients treated with chemotherapy and consolidative radiotherapy at a single institution between 2010 and 2018 was assessed. All patients had biopsy-proven lymphoma and were included if radiation was part of the treatment and had at least 6 months of follow-up or were followed until death. RESULTS: Three-hundred fifty-nine (359) patients were selected, with a median age at diagnosis of 57.7 years (13–90 years). Twenty-eight patients (7.8%) were HIV positive. Median follow-up was 48.0 months. Female patients were 51.3% and most had a good performance in the ECOG scale (78.8% are ECOG 0–1). Median overall survival was not reached, but mean OS was 50.1 months with 86 deaths. Median progression-free survival was 48.7 months. HIV infection had no impact on OS (p = 0.580) or PFS (p = 0.347) among patients treated with RT. HIV positive patients were more frequently staged only with CT (p > 0.05) with no impact on PFS (p = 0.191). No HIV positive patient received rituximab due to local policy restrictions and HIV positive patients were more prone to receive CHOP-like chemotherapy (p < 0.05), specially ones with etoposide (CHOEP). CHOP was associated with better survival (p = 0.015) in the overall population and in the HIV negative population (p = 0.002), but not in the HIV positive population (p = 0.982). RT toxicities were not overall more frequent in the HIV positive population (p = 0.567), except for fatigue (p < 0.05) and hematological toxicities (p = 0.022). CONCLUSION: HIV status did not influence on survival when patients were treated with consolidative radiotherapy. HIV infection was a bias on our sample for staging methods and chemotherapy regimens choices. For HIV positive patients there was an increase in fatigue and hematological toxicities of any grade with radiation. BioMed Central 2020-06-15 /pmc/articles/PMC7296722/ /pubmed/32539797 http://dx.doi.org/10.1186/s13014-020-01589-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Medici, Carolina Trindade Mello
Mauro, Geovanne Pedro
Casimiro, Lucas Coelho
Weltman, Eduardo
Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title_full Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title_fullStr Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title_full_unstemmed Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title_short Impact of HIV infection on consolidative radiotherapy for non-Hodgkin diffuse large B-cell lymphoma
title_sort impact of hiv infection on consolidative radiotherapy for non-hodgkin diffuse large b-cell lymphoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296722/
https://www.ncbi.nlm.nih.gov/pubmed/32539797
http://dx.doi.org/10.1186/s13014-020-01589-1
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