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Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma
AIM: To establish the safety and feasibility of rapidly infusing rituximab over 90 min in patients with primary CNS lymphoma (PCNSL). PATIENTS & METHODS: We retrospectively reviewed all patients with PCNSL who received rapid rituximab infusions (RRI) from January 2016 to January 2017. Primary en...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Medicine Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200062/ https://www.ncbi.nlm.nih.gov/pubmed/30221993 http://dx.doi.org/10.2217/cns-2018-0001 |
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author | Modelevsky, Lisa Tizon, Richard Reiss, Samantha N Smith, Marcel Garonce, Rachel Kaley, Thomas |
author_facet | Modelevsky, Lisa Tizon, Richard Reiss, Samantha N Smith, Marcel Garonce, Rachel Kaley, Thomas |
author_sort | Modelevsky, Lisa |
collection | PubMed |
description | AIM: To establish the safety and feasibility of rapidly infusing rituximab over 90 min in patients with primary CNS lymphoma (PCNSL). PATIENTS & METHODS: We retrospectively reviewed all patients with PCNSL who received rapid rituximab infusions (RRI) from January 2016 to January 2017. Primary end point was incidence of infusion reactions. RESULTS & CONCLUSION: 11 patients received a total of 44 RRIs. Rituximab was dosed at 500 or 750 mg/m(2). Premedication included acetaminophen and diphenhydramine. No infusion reactions occurred during any RRI. Two infusions were administered with steroids for neurologic symptoms at baseline (4.5%). Rapid administration of rituximab was safe and feasible for patients with PCNSL and at the higher doses received. |
format | Online Article Text |
id | pubmed-6200062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Future Medicine Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62000622018-10-26 Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma Modelevsky, Lisa Tizon, Richard Reiss, Samantha N Smith, Marcel Garonce, Rachel Kaley, Thomas CNS Oncol Research Article AIM: To establish the safety and feasibility of rapidly infusing rituximab over 90 min in patients with primary CNS lymphoma (PCNSL). PATIENTS & METHODS: We retrospectively reviewed all patients with PCNSL who received rapid rituximab infusions (RRI) from January 2016 to January 2017. Primary end point was incidence of infusion reactions. RESULTS & CONCLUSION: 11 patients received a total of 44 RRIs. Rituximab was dosed at 500 or 750 mg/m(2). Premedication included acetaminophen and diphenhydramine. No infusion reactions occurred during any RRI. Two infusions were administered with steroids for neurologic symptoms at baseline (4.5%). Rapid administration of rituximab was safe and feasible for patients with PCNSL and at the higher doses received. Future Medicine Ltd 2018-09-17 /pmc/articles/PMC6200062/ /pubmed/30221993 http://dx.doi.org/10.2217/cns-2018-0001 Text en © 2018 Lisa Modelevsky This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Article Modelevsky, Lisa Tizon, Richard Reiss, Samantha N Smith, Marcel Garonce, Rachel Kaley, Thomas Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title | Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title_full | Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title_fullStr | Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title_full_unstemmed | Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title_short | Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma |
title_sort | rapid infusion rituximab is well tolerated in patients with primary cns lymphoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200062/ https://www.ncbi.nlm.nih.gov/pubmed/30221993 http://dx.doi.org/10.2217/cns-2018-0001 |
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