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Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin
We present the case of a 78-year-old male patient who was diagnosed with anaplastic lymphoma kinase (ALK)-negative, CC chemokine receptor 4 (CCR4)-negative, and CD30-positive anaplastic large cell lymphoma (ALCL). The patient had a past medical history of adult T-cell leukemia/lymphoma and colon can...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772834/ https://www.ncbi.nlm.nih.gov/pubmed/33442363 http://dx.doi.org/10.1159/000511111 |
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author | Jo, Tatsuro Sakai, Takahiro Matsuzaka, Kaori Shioya, Haruna Tominaga, Hiroo Kaneko, Yohei Hayashi, Shizuka Matsuo, Masatoshi Taguchi, Jun Abe, Kuniko Shigematsu, Kazuto |
author_facet | Jo, Tatsuro Sakai, Takahiro Matsuzaka, Kaori Shioya, Haruna Tominaga, Hiroo Kaneko, Yohei Hayashi, Shizuka Matsuo, Masatoshi Taguchi, Jun Abe, Kuniko Shigematsu, Kazuto |
author_sort | Jo, Tatsuro |
collection | PubMed |
description | We present the case of a 78-year-old male patient who was diagnosed with anaplastic lymphoma kinase (ALK)-negative, CC chemokine receptor 4 (CCR4)-negative, and CD30-positive anaplastic large cell lymphoma (ALCL). The patient had a past medical history of adult T-cell leukemia/lymphoma and colon cancers that had developed simultaneously approximately 2 years prior to the development of ALCL that were treated with immunochemotherapy and resection, respectively. Initial treatment for ALCL included brentuximab vedotin, an anti-CD30 monoclonal antibody-monomethyl auristatin E conjugate; however, we were unable to achieve a sufficient treatment effect. Romidepsin, an oral histone deacetylase inhibitor, was introduced as salvage chemotherapy; complete remission was attained. Interestingly, a reversal of the CD4/CD8 ratio and a reduction in human T-lymphotropic virus type 1 (HTLV-1) virus load was observed after 2 cycles of immunochemotherapy; the patient experienced upregulation of HTLV-1 Tax-specific cytotoxic T lymphocytes after a herpes zoster infection and the completion of immunotherapy. The immunologic status was maintained from the time of diagnosis through the completion of romidepsin therapy. Our findings indicate that romidepsin can be used safely and effectively to treat ALCL without impairing cellular immunity to HTLV-1. |
format | Online Article Text |
id | pubmed-7772834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-77728342021-01-12 Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin Jo, Tatsuro Sakai, Takahiro Matsuzaka, Kaori Shioya, Haruna Tominaga, Hiroo Kaneko, Yohei Hayashi, Shizuka Matsuo, Masatoshi Taguchi, Jun Abe, Kuniko Shigematsu, Kazuto Case Rep Oncol Case Report We present the case of a 78-year-old male patient who was diagnosed with anaplastic lymphoma kinase (ALK)-negative, CC chemokine receptor 4 (CCR4)-negative, and CD30-positive anaplastic large cell lymphoma (ALCL). The patient had a past medical history of adult T-cell leukemia/lymphoma and colon cancers that had developed simultaneously approximately 2 years prior to the development of ALCL that were treated with immunochemotherapy and resection, respectively. Initial treatment for ALCL included brentuximab vedotin, an anti-CD30 monoclonal antibody-monomethyl auristatin E conjugate; however, we were unable to achieve a sufficient treatment effect. Romidepsin, an oral histone deacetylase inhibitor, was introduced as salvage chemotherapy; complete remission was attained. Interestingly, a reversal of the CD4/CD8 ratio and a reduction in human T-lymphotropic virus type 1 (HTLV-1) virus load was observed after 2 cycles of immunochemotherapy; the patient experienced upregulation of HTLV-1 Tax-specific cytotoxic T lymphocytes after a herpes zoster infection and the completion of immunotherapy. The immunologic status was maintained from the time of diagnosis through the completion of romidepsin therapy. Our findings indicate that romidepsin can be used safely and effectively to treat ALCL without impairing cellular immunity to HTLV-1. S. Karger AG 2020-11-30 /pmc/articles/PMC7772834/ /pubmed/33442363 http://dx.doi.org/10.1159/000511111 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Jo, Tatsuro Sakai, Takahiro Matsuzaka, Kaori Shioya, Haruna Tominaga, Hiroo Kaneko, Yohei Hayashi, Shizuka Matsuo, Masatoshi Taguchi, Jun Abe, Kuniko Shigematsu, Kazuto Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title | Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title_full | Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title_fullStr | Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title_full_unstemmed | Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title_short | Successful Treatment of a Patient with Brentuximab Vedotin-Refractory ALK-Negative Anaplastic Large Cell Lymphoma with Romidepsin |
title_sort | successful treatment of a patient with brentuximab vedotin-refractory alk-negative anaplastic large cell lymphoma with romidepsin |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772834/ https://www.ncbi.nlm.nih.gov/pubmed/33442363 http://dx.doi.org/10.1159/000511111 |
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