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Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient
Primary central nervous system lymphoma (PCNSL) remains a therapeutic challenge due to impaired drugs diffusion as a result of the blood‐brain barrier and high risk of relapse. Patients with good performance status, chemo‐sensitive disease, and eligible for autologous stem cell transplant (ASCT) may...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099056/ https://www.ncbi.nlm.nih.gov/pubmed/30147874 http://dx.doi.org/10.1002/ccr3.1630 |
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author | Camus, Vincent Dubois, Sydney Lepretre, Stéphane Jardin, Fabrice Tilly, Hervé |
author_facet | Camus, Vincent Dubois, Sydney Lepretre, Stéphane Jardin, Fabrice Tilly, Hervé |
author_sort | Camus, Vincent |
collection | PubMed |
description | Primary central nervous system lymphoma (PCNSL) remains a therapeutic challenge due to impaired drugs diffusion as a result of the blood‐brain barrier and high risk of relapse. Patients with good performance status, chemo‐sensitive disease, and eligible for autologous stem cell transplant (ASCT) may benefit from salvage therapy and therapeutic intensification that may allow long‐term remission. |
format | Online Article Text |
id | pubmed-6099056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60990562018-08-24 Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient Camus, Vincent Dubois, Sydney Lepretre, Stéphane Jardin, Fabrice Tilly, Hervé Clin Case Rep Case Reports Primary central nervous system lymphoma (PCNSL) remains a therapeutic challenge due to impaired drugs diffusion as a result of the blood‐brain barrier and high risk of relapse. Patients with good performance status, chemo‐sensitive disease, and eligible for autologous stem cell transplant (ASCT) may benefit from salvage therapy and therapeutic intensification that may allow long‐term remission. John Wiley and Sons Inc. 2018-06-04 /pmc/articles/PMC6099056/ /pubmed/30147874 http://dx.doi.org/10.1002/ccr3.1630 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Camus, Vincent Dubois, Sydney Lepretre, Stéphane Jardin, Fabrice Tilly, Hervé Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title | Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title_full | Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title_fullStr | Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title_full_unstemmed | Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title_short | Prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
title_sort | prolonged third complete remission after busulfan, thiotepa, and autologous stem cell transplant in a primary central nervous system lymphoma patient |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099056/ https://www.ncbi.nlm.nih.gov/pubmed/30147874 http://dx.doi.org/10.1002/ccr3.1630 |
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