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Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy
Despite the prominent effects of BCR-ABL tyrosine kinase inhibitors (TKI) therapy in patients with chronic phase-chronic myeloid leukemia (CP-CML) and thus low incidence of blastic transformation, blast phase (BP)-CML remains a major therapeutic challenge in the TKI era. The “gatekeeper” mutation T3...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917542/ https://www.ncbi.nlm.nih.gov/pubmed/31997880 http://dx.doi.org/10.2147/OTT.S232102 |
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author | Zhou, Lu Shi, Huiping Shi, Wenyu Yang, Li Zhang, Yaping Xu, Mengqi Chen, Xiufang Zhu, Yanv Mu, Hui Wan, Xiaochun Yang, Zhonghua Zeng, Ying Liu, Hong |
author_facet | Zhou, Lu Shi, Huiping Shi, Wenyu Yang, Li Zhang, Yaping Xu, Mengqi Chen, Xiufang Zhu, Yanv Mu, Hui Wan, Xiaochun Yang, Zhonghua Zeng, Ying Liu, Hong |
author_sort | Zhou, Lu |
collection | PubMed |
description | Despite the prominent effects of BCR-ABL tyrosine kinase inhibitors (TKI) therapy in patients with chronic phase-chronic myeloid leukemia (CP-CML) and thus low incidence of blastic transformation, blast phase (BP)-CML remains a major therapeutic challenge in the TKI era. The “gatekeeper” mutation T315I in BCR-ABL1 kinase, which often coupled with a poor prognosis, is quite common and resistant to all TKIs except for ponatinib. The occurrence of T315I mutation in BP-CML makes the situation more complex. Anti-CD19 chimeric antigen receptor T cell (CAR-T) technology is a new immunotherapy which has significantly improved the efficacy of B cell hematologic malignances. Here we report a lymphoid BP-CML patient harboring T315I mutation who achieved complete molecular remission and returned to chronic phase by anti-CD19 CAR-T therapy. Our study provides a new therapeutic strategy for patients in BP-CML. |
format | Online Article Text |
id | pubmed-6917542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-69175422020-01-29 Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy Zhou, Lu Shi, Huiping Shi, Wenyu Yang, Li Zhang, Yaping Xu, Mengqi Chen, Xiufang Zhu, Yanv Mu, Hui Wan, Xiaochun Yang, Zhonghua Zeng, Ying Liu, Hong Onco Targets Ther Case Report Despite the prominent effects of BCR-ABL tyrosine kinase inhibitors (TKI) therapy in patients with chronic phase-chronic myeloid leukemia (CP-CML) and thus low incidence of blastic transformation, blast phase (BP)-CML remains a major therapeutic challenge in the TKI era. The “gatekeeper” mutation T315I in BCR-ABL1 kinase, which often coupled with a poor prognosis, is quite common and resistant to all TKIs except for ponatinib. The occurrence of T315I mutation in BP-CML makes the situation more complex. Anti-CD19 chimeric antigen receptor T cell (CAR-T) technology is a new immunotherapy which has significantly improved the efficacy of B cell hematologic malignances. Here we report a lymphoid BP-CML patient harboring T315I mutation who achieved complete molecular remission and returned to chronic phase by anti-CD19 CAR-T therapy. Our study provides a new therapeutic strategy for patients in BP-CML. Dove 2019-12-13 /pmc/articles/PMC6917542/ /pubmed/31997880 http://dx.doi.org/10.2147/OTT.S232102 Text en © 2019 Zhou et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Zhou, Lu Shi, Huiping Shi, Wenyu Yang, Li Zhang, Yaping Xu, Mengqi Chen, Xiufang Zhu, Yanv Mu, Hui Wan, Xiaochun Yang, Zhonghua Zeng, Ying Liu, Hong Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title | Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title_full | Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title_fullStr | Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title_full_unstemmed | Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title_short | Durable Molecular Remission in a Lymphoid BP-CML Patient Harboring T315I Mutation Treated with Anti-CD19 CAR-T Therapy |
title_sort | durable molecular remission in a lymphoid bp-cml patient harboring t315i mutation treated with anti-cd19 car-t therapy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917542/ https://www.ncbi.nlm.nih.gov/pubmed/31997880 http://dx.doi.org/10.2147/OTT.S232102 |
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