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Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma

Low lymphocyte‐to‐monocyte‐ratio (LMR) has been associated with unfavorable survival in patients with diffuse large B‐cell lymphoma (DLBCL). To date, however, the impact of LMR on survival has not been examined in a uniformly treated cohort of patients with high‐risk aggressive large B‐cell lymphoma...

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Autores principales: Vajavaara, Heli, Leivonen, Suvi‐Katri, Jørgensen, Judit, Holte, Harald, Leppä, Sirpa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421995/
https://www.ncbi.nlm.nih.gov/pubmed/36051040
http://dx.doi.org/10.1002/jha2.409
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author Vajavaara, Heli
Leivonen, Suvi‐Katri
Jørgensen, Judit
Holte, Harald
Leppä, Sirpa
author_facet Vajavaara, Heli
Leivonen, Suvi‐Katri
Jørgensen, Judit
Holte, Harald
Leppä, Sirpa
author_sort Vajavaara, Heli
collection PubMed
description Low lymphocyte‐to‐monocyte‐ratio (LMR) has been associated with unfavorable survival in patients with diffuse large B‐cell lymphoma (DLBCL). To date, however, the impact of LMR on survival has not been examined in a uniformly treated cohort of patients with high‐risk aggressive large B‐cell lymphoma. We collected peripheral blood absolute lymphocyte counts (ALCs) and absolute monocyte counts (AMC) prior to treatment and calculated LMR from 112 adult patients, who were less than 65 years of age, had age‐adjusted International Prognostic Index 2–3, or site‐specific risk factors for central nervous system (CNS) recurrence, and were treated in a Nordic Lymphoma Group LBC‐05 trial with dose‐dense immunochemotherapy and early systemic CNS prophylaxis (www.ClinicalTrials.gov, number NCT01325194). Median pretreatment ALC was 1.40 × 10(9)/l (range, 0.20–4.95), AMC 0.68 × 10(9)/l (range, 0.10–2.62), and LMR 2.08 (range, 0.10–12.00). ALC did not correlate with tumor‐infiltrating lymphocytes, AMC did not correlate with tumor‐associated macrophages, and neither ALC nor AMC correlated with survival. However, low LMR (<1.72) translated to unfavourable progression‐free survival (PFS) (5‐year PFS 70% vs. 92%, p = 0.002) and overall survival (OS) (5‐year OS, 77% vs. 92%, p = 0.020). In the patients with low LMR, relative risk of progression was 4.4‐fold (95% confidence interval [CI] 1.60–12.14, p = 0.004), and relative risk of death was 3.3‐fold (95% CI 1.18–9.50, p = 0.024) in comparison to the patients with high LMR. We conclude that low LMR is an adverse prognostic factor in uniformly treated young patients with high‐risk aggressive large B‐cell lymphoma.
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spelling pubmed-94219952022-08-31 Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma Vajavaara, Heli Leivonen, Suvi‐Katri Jørgensen, Judit Holte, Harald Leppä, Sirpa EJHaem Haematologic Malignancy ‐ Lymphoid Low lymphocyte‐to‐monocyte‐ratio (LMR) has been associated with unfavorable survival in patients with diffuse large B‐cell lymphoma (DLBCL). To date, however, the impact of LMR on survival has not been examined in a uniformly treated cohort of patients with high‐risk aggressive large B‐cell lymphoma. We collected peripheral blood absolute lymphocyte counts (ALCs) and absolute monocyte counts (AMC) prior to treatment and calculated LMR from 112 adult patients, who were less than 65 years of age, had age‐adjusted International Prognostic Index 2–3, or site‐specific risk factors for central nervous system (CNS) recurrence, and were treated in a Nordic Lymphoma Group LBC‐05 trial with dose‐dense immunochemotherapy and early systemic CNS prophylaxis (www.ClinicalTrials.gov, number NCT01325194). Median pretreatment ALC was 1.40 × 10(9)/l (range, 0.20–4.95), AMC 0.68 × 10(9)/l (range, 0.10–2.62), and LMR 2.08 (range, 0.10–12.00). ALC did not correlate with tumor‐infiltrating lymphocytes, AMC did not correlate with tumor‐associated macrophages, and neither ALC nor AMC correlated with survival. However, low LMR (<1.72) translated to unfavourable progression‐free survival (PFS) (5‐year PFS 70% vs. 92%, p = 0.002) and overall survival (OS) (5‐year OS, 77% vs. 92%, p = 0.020). In the patients with low LMR, relative risk of progression was 4.4‐fold (95% confidence interval [CI] 1.60–12.14, p = 0.004), and relative risk of death was 3.3‐fold (95% CI 1.18–9.50, p = 0.024) in comparison to the patients with high LMR. We conclude that low LMR is an adverse prognostic factor in uniformly treated young patients with high‐risk aggressive large B‐cell lymphoma. John Wiley and Sons Inc. 2022-06-23 /pmc/articles/PMC9421995/ /pubmed/36051040 http://dx.doi.org/10.1002/jha2.409 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Haematologic Malignancy ‐ Lymphoid
Vajavaara, Heli
Leivonen, Suvi‐Katri
Jørgensen, Judit
Holte, Harald
Leppä, Sirpa
Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title_full Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title_fullStr Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title_full_unstemmed Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title_short Low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large B‐cell lymphoma
title_sort low lymphocyte‐to‐monocyte ratio predicts poor outcome in high‐risk aggressive large b‐cell lymphoma
topic Haematologic Malignancy ‐ Lymphoid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421995/
https://www.ncbi.nlm.nih.gov/pubmed/36051040
http://dx.doi.org/10.1002/jha2.409
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