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Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report
INTRODUCTION: In diffuse large B-cell lymphoma, first-line treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; salvage with cisplatin-based regimens for relapsing patients; and autologous stem cell therapy are standards of care. Treatment approaches are less clear fo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191682/ https://www.ncbi.nlm.nih.gov/pubmed/25277681 http://dx.doi.org/10.1186/1752-1947-8-325 |
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author | Krawczyk, Katarzyna Jurczak, Wojciech Gałązka, Krystyna Gruchała, Andrzej Skotnicki, Aleksander B |
author_facet | Krawczyk, Katarzyna Jurczak, Wojciech Gałązka, Krystyna Gruchała, Andrzej Skotnicki, Aleksander B |
author_sort | Krawczyk, Katarzyna |
collection | PubMed |
description | INTRODUCTION: In diffuse large B-cell lymphoma, first-line treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; salvage with cisplatin-based regimens for relapsing patients; and autologous stem cell therapy are standards of care. Treatment approaches are less clear for patients who are refractory or who are not candidates for autologous stem cell therapy. Options may include palliative regimens or clinical trial enrollment. One therapy under investigation in diffuse large B-cell lymphoma is lenalidomide, an immunomodulatory agent with antiangiogenic activity. CASE PRESENTATION: We present the case of a 55-year-old Caucasian male patient diagnosed with diffuse large B-cell lymphoma who had an early relapse after treatment with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone. He then had a subsequent early relapse after cisplatin-based salvage consolidated with autologous stem cell therapy. The efficacy of gemcitabine-cisplatin-rituximab was limited to five months, followed by systemic and central nervous system progression. Fourth-line treatment with lenalidomide plus rituximab and involved-field radiotherapy followed by lenalidomide monotherapy greatly improved this patient’s quality of life and performance status, allowing over two years of progression-free survival to date (excluding a brief relapse due to treatment interruption). CONCLUSION: A lenalidomide-based regimen was highly effective in this patient with diffuse large B-cell lymphoma. |
format | Online Article Text |
id | pubmed-4191682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41916822014-10-10 Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report Krawczyk, Katarzyna Jurczak, Wojciech Gałązka, Krystyna Gruchała, Andrzej Skotnicki, Aleksander B J Med Case Rep Case Report INTRODUCTION: In diffuse large B-cell lymphoma, first-line treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; salvage with cisplatin-based regimens for relapsing patients; and autologous stem cell therapy are standards of care. Treatment approaches are less clear for patients who are refractory or who are not candidates for autologous stem cell therapy. Options may include palliative regimens or clinical trial enrollment. One therapy under investigation in diffuse large B-cell lymphoma is lenalidomide, an immunomodulatory agent with antiangiogenic activity. CASE PRESENTATION: We present the case of a 55-year-old Caucasian male patient diagnosed with diffuse large B-cell lymphoma who had an early relapse after treatment with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone. He then had a subsequent early relapse after cisplatin-based salvage consolidated with autologous stem cell therapy. The efficacy of gemcitabine-cisplatin-rituximab was limited to five months, followed by systemic and central nervous system progression. Fourth-line treatment with lenalidomide plus rituximab and involved-field radiotherapy followed by lenalidomide monotherapy greatly improved this patient’s quality of life and performance status, allowing over two years of progression-free survival to date (excluding a brief relapse due to treatment interruption). CONCLUSION: A lenalidomide-based regimen was highly effective in this patient with diffuse large B-cell lymphoma. BioMed Central 2014-10-02 /pmc/articles/PMC4191682/ /pubmed/25277681 http://dx.doi.org/10.1186/1752-1947-8-325 Text en Copyright © 2014 Krawczyk et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Krawczyk, Katarzyna Jurczak, Wojciech Gałązka, Krystyna Gruchała, Andrzej Skotnicki, Aleksander B Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title | Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title_full | Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title_fullStr | Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title_full_unstemmed | Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title_short | Lenalidomide in heavily pretreated refractory diffuse large B-cell lymphoma: a case report |
title_sort | lenalidomide in heavily pretreated refractory diffuse large b-cell lymphoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191682/ https://www.ncbi.nlm.nih.gov/pubmed/25277681 http://dx.doi.org/10.1186/1752-1947-8-325 |
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