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NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas
BACKGROUND: Plexiform neurofibromas (PN) are found in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PN but limited data has been reported on its efficacy within a clinical trial. METHODS: This ongoing multicenter phase II trial includes patients...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164745/ http://dx.doi.org/10.1093/neuonc/noac079.472 |
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author | Kiaei, Dorsa Sadat Larouche, Valérie Décarie, Jean-Claude Tabori, Uri Hawkin, Cynthia Lippé, Sarah Ellezam, Benjamin Ospina, Luis H Théoret, Yves Desjardins, Léandra Métras, Marie-Élaine Sultan, Serge Cantin, Édith Routhier, Marie-Ève Mailloux, Chantal Bertrand, Marie-Claude Caru, Maxime Vairy, Stéphanie Legault, Geneviève Bouffet, Éric Ramaswamy, Vijay Coltin, Hallie Lafay-Cousin, Lucie Hukin, Juliette Erker, Craig Jabado, Nada Dehaes, Mathieu Perreault, Sébastien |
author_facet | Kiaei, Dorsa Sadat Larouche, Valérie Décarie, Jean-Claude Tabori, Uri Hawkin, Cynthia Lippé, Sarah Ellezam, Benjamin Ospina, Luis H Théoret, Yves Desjardins, Léandra Métras, Marie-Élaine Sultan, Serge Cantin, Édith Routhier, Marie-Ève Mailloux, Chantal Bertrand, Marie-Claude Caru, Maxime Vairy, Stéphanie Legault, Geneviève Bouffet, Éric Ramaswamy, Vijay Coltin, Hallie Lafay-Cousin, Lucie Hukin, Juliette Erker, Craig Jabado, Nada Dehaes, Mathieu Perreault, Sébastien |
author_sort | Kiaei, Dorsa Sadat |
collection | PubMed |
description | BACKGROUND: Plexiform neurofibromas (PN) are found in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PN but limited data has been reported on its efficacy within a clinical trial. METHODS: This ongoing multicenter phase II trial includes patients with pediatric low-grade glioma and PN. The primary objective for PN was to evaluate the overall response rate based on RECIST 1.1 criteria after daily oral trametinib administration for eighteen 28-day cycles. The volumes of PN were centrally quantified using a new semi-automatic 3D segmentation method. RESULTS: As of January 1, 2022, 45 patients with PN were enrolled in the study. Twenty-eight completed treatment and were available for analysis. For these patients, the median age was 11.4 years (range 0.7-19.8) including 16 males (57.1%). The majority did not receive prior systemic therapies (71.4%). The median volume of PN at baseline was 49.5 cm3 (range 2.6 to 469). Among the 28 patients, 25 (89.3%) completed 18 cycles as planned. One patient discontinued due to adverse reaction, one patient refused to continue treatment and one patient discontinued treatment based on physician decision. Median duration of treatment was 15.9 months (range 4.6 to 16.8). Median duration of follow-up was 29.7 months (range 17.7 to 38.1). A total of 32 PN were available for volumetric analysis. Using RECIST evaluation, the overall response rate was 24.1%. Volumetric assessment demonstrated an overall response rate of 60.7% and 62.5% of PN showed a decrease of more than 20% in volume. Median decrease in volume was -30% (range -93.5 to 14.3). Twenty-seven patients (93.1%) had durable response without progression (lasting ≥1 year). CONCLUSION: We report outcome and volumetric quantification of PN treated with trametinib within a large clinical trial. Based on the current results, trametinib appears effective and offers durable response. |
format | Online Article Text |
id | pubmed-9164745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91647452022-06-05 NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas Kiaei, Dorsa Sadat Larouche, Valérie Décarie, Jean-Claude Tabori, Uri Hawkin, Cynthia Lippé, Sarah Ellezam, Benjamin Ospina, Luis H Théoret, Yves Desjardins, Léandra Métras, Marie-Élaine Sultan, Serge Cantin, Édith Routhier, Marie-Ève Mailloux, Chantal Bertrand, Marie-Claude Caru, Maxime Vairy, Stéphanie Legault, Geneviève Bouffet, Éric Ramaswamy, Vijay Coltin, Hallie Lafay-Cousin, Lucie Hukin, Juliette Erker, Craig Jabado, Nada Dehaes, Mathieu Perreault, Sébastien Neuro Oncol Neurofibromatosis and other Predisposition Syndromes BACKGROUND: Plexiform neurofibromas (PN) are found in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PN but limited data has been reported on its efficacy within a clinical trial. METHODS: This ongoing multicenter phase II trial includes patients with pediatric low-grade glioma and PN. The primary objective for PN was to evaluate the overall response rate based on RECIST 1.1 criteria after daily oral trametinib administration for eighteen 28-day cycles. The volumes of PN were centrally quantified using a new semi-automatic 3D segmentation method. RESULTS: As of January 1, 2022, 45 patients with PN were enrolled in the study. Twenty-eight completed treatment and were available for analysis. For these patients, the median age was 11.4 years (range 0.7-19.8) including 16 males (57.1%). The majority did not receive prior systemic therapies (71.4%). The median volume of PN at baseline was 49.5 cm3 (range 2.6 to 469). Among the 28 patients, 25 (89.3%) completed 18 cycles as planned. One patient discontinued due to adverse reaction, one patient refused to continue treatment and one patient discontinued treatment based on physician decision. Median duration of treatment was 15.9 months (range 4.6 to 16.8). Median duration of follow-up was 29.7 months (range 17.7 to 38.1). A total of 32 PN were available for volumetric analysis. Using RECIST evaluation, the overall response rate was 24.1%. Volumetric assessment demonstrated an overall response rate of 60.7% and 62.5% of PN showed a decrease of more than 20% in volume. Median decrease in volume was -30% (range -93.5 to 14.3). Twenty-seven patients (93.1%) had durable response without progression (lasting ≥1 year). CONCLUSION: We report outcome and volumetric quantification of PN treated with trametinib within a large clinical trial. Based on the current results, trametinib appears effective and offers durable response. Oxford University Press 2022-06-03 /pmc/articles/PMC9164745/ http://dx.doi.org/10.1093/neuonc/noac079.472 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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 and other Predisposition Syndromes Kiaei, Dorsa Sadat Larouche, Valérie Décarie, Jean-Claude Tabori, Uri Hawkin, Cynthia Lippé, Sarah Ellezam, Benjamin Ospina, Luis H Théoret, Yves Desjardins, Léandra Métras, Marie-Élaine Sultan, Serge Cantin, Édith Routhier, Marie-Ève Mailloux, Chantal Bertrand, Marie-Claude Caru, Maxime Vairy, Stéphanie Legault, Geneviève Bouffet, Éric Ramaswamy, Vijay Coltin, Hallie Lafay-Cousin, Lucie Hukin, Juliette Erker, Craig Jabado, Nada Dehaes, Mathieu Perreault, Sébastien NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title | NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title_full | NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title_fullStr | NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title_full_unstemmed | NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title_short | NFB-08. TRAM-01: A Phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
title_sort | nfb-08. tram-01: a phase 2 study of trametinib for pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas |
topic | Neurofibromatosis and other Predisposition Syndromes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164745/ http://dx.doi.org/10.1093/neuonc/noac079.472 |
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