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NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB

BACKGROUND: Trametinib (Tr) has been applied in the treatment of children with various tumor types, often for prolonged periods. Little is known regarding immune function (IF) following prolonged Tr in this age group. OBJECTIVE: Describe laboratory measures of IF in children on Tr. METHOD: Patients...

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Autores principales: Moukhaiber, Perla, Samolej, Anna, Somsri, Palita, McCowage, Geoffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715110/
http://dx.doi.org/10.1093/neuonc/noaa222.620
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author Moukhaiber, Perla
Samolej, Anna
Somsri, Palita
McCowage, Geoffrey
author_facet Moukhaiber, Perla
Samolej, Anna
Somsri, Palita
McCowage, Geoffrey
author_sort Moukhaiber, Perla
collection PubMed
description BACKGROUND: Trametinib (Tr) has been applied in the treatment of children with various tumor types, often for prolonged periods. Little is known regarding immune function (IF) following prolonged Tr in this age group. OBJECTIVE: Describe laboratory measures of IF in children on Tr. METHOD: Patients receiving Tr had low grade glioma with BRAF anomalies (6), or neurofibromatosis-1 (16) with glioma or plexiform neurofibroma. IF was evaluated using leukocyte/lymphocyte counts, immunoglobulin levels, and antibody titres. RESULTS: 22 patients received Tr. 2 also received Dabrafenib. Median age at Tr initiation of Tr was 7.75 years. As of June 2020, 7 patients have had IFT; results are pending on 15. Median duration of Tr therapy at time of IF was 3.5 years (0.8 – 4). In these 7 patients, median white cell count was 6.9 x 10^9/L (4.1 – 12.6), neutrophils 4.2 x 10^9/L (1.8 – 6.8) and lymphocytes 3.2 x 10^9/L (1.4 – 7). IgG levels, B cells and CD8 cytotoxic T cells were normal across 7/7 patients:medians 9.47 g/L (8.62 – 17), 0.51 x 10^9/L (0.2 – 1.26) and 0.58 x 10^9/L (0.25 – 2.03) respectively. CD3 and CD4 T cells: median 2.08 x 10^9/L (0.67 – 4.62) and 1.34 x 10^9/L (0.35 – 2.31), borderline low in 1 heavily pre-treated patient. An adequate immune response was present in all 4 vaccine antigens tested in 5/5 patients. CONCLUSION: IF appears relatively intact, relevant for immunisation and infection precautions in children on Tr. Data on the complete cohort will be presented.
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spelling pubmed-77151102020-12-09 NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB Moukhaiber, Perla Samolej, Anna Somsri, Palita McCowage, Geoffrey Neuro Oncol Neurofibromatosis BACKGROUND: Trametinib (Tr) has been applied in the treatment of children with various tumor types, often for prolonged periods. Little is known regarding immune function (IF) following prolonged Tr in this age group. OBJECTIVE: Describe laboratory measures of IF in children on Tr. METHOD: Patients receiving Tr had low grade glioma with BRAF anomalies (6), or neurofibromatosis-1 (16) with glioma or plexiform neurofibroma. IF was evaluated using leukocyte/lymphocyte counts, immunoglobulin levels, and antibody titres. RESULTS: 22 patients received Tr. 2 also received Dabrafenib. Median age at Tr initiation of Tr was 7.75 years. As of June 2020, 7 patients have had IFT; results are pending on 15. Median duration of Tr therapy at time of IF was 3.5 years (0.8 – 4). In these 7 patients, median white cell count was 6.9 x 10^9/L (4.1 – 12.6), neutrophils 4.2 x 10^9/L (1.8 – 6.8) and lymphocytes 3.2 x 10^9/L (1.4 – 7). IgG levels, B cells and CD8 cytotoxic T cells were normal across 7/7 patients:medians 9.47 g/L (8.62 – 17), 0.51 x 10^9/L (0.2 – 1.26) and 0.58 x 10^9/L (0.25 – 2.03) respectively. CD3 and CD4 T cells: median 2.08 x 10^9/L (0.67 – 4.62) and 1.34 x 10^9/L (0.35 – 2.31), borderline low in 1 heavily pre-treated patient. An adequate immune response was present in all 4 vaccine antigens tested in 5/5 patients. CONCLUSION: IF appears relatively intact, relevant for immunisation and infection precautions in children on Tr. Data on the complete cohort will be presented. Oxford University Press 2020-12-04 /pmc/articles/PMC7715110/ http://dx.doi.org/10.1093/neuonc/noaa222.620 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neurofibromatosis
Moukhaiber, Perla
Samolej, Anna
Somsri, Palita
McCowage, Geoffrey
NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title_full NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title_fullStr NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title_full_unstemmed NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title_short NFB-18. IMMUNE FUNCTION IN CHILDREN TREATED WITH TRAMETINIB
title_sort nfb-18. immune function in children treated with trametinib
topic Neurofibromatosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715110/
http://dx.doi.org/10.1093/neuonc/noaa222.620
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