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CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer
Pancreatic cancer lacks effective therapy. Here, we reported two metastatic pancreatic cancer patients administrated with Claudin 18.2 (CLDN 18.2) CART therapy after the failure of standard therapy (NCT04581473 and NCT03874897). In case 1, with CLDN 18.2 expression of 2+, 70%, 250 × 10(6) cells were...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492318/ https://www.ncbi.nlm.nih.gov/pubmed/37689733 http://dx.doi.org/10.1186/s13045-023-01491-9 |
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author | Qi, Changsong Xie, Tong Zhou, Jun Wang, Xicheng Gong, Jifang Zhang, Xiaotian Li, Jian Yuan, Jiajia Liu, Chang Shen, Lin |
author_facet | Qi, Changsong Xie, Tong Zhou, Jun Wang, Xicheng Gong, Jifang Zhang, Xiaotian Li, Jian Yuan, Jiajia Liu, Chang Shen, Lin |
author_sort | Qi, Changsong |
collection | PubMed |
description | Pancreatic cancer lacks effective therapy. Here, we reported two metastatic pancreatic cancer patients administrated with Claudin 18.2 (CLDN 18.2) CART therapy after the failure of standard therapy (NCT04581473 and NCT03874897). In case 1, with CLDN 18.2 expression of 2+, 70%, 250 × 10(6) cells were infused after lymphodepletion. Grade 1 cytokine release syndrome (CRS) occurred on d1 which was later controlled by tocilizumab. Partial response (PR) was achieved according to RECIST v1.1, with great shrinkage of lung metastasis. An increasing CD8+ T cell and Treg cells and declining CD4+ T cell and B cell were observed. In case 2, IHC result of ClDN18.2 showed 3+, 60%. 250 × 10(6) CLDN18.2 CART cells were subsequently administered. Patient experienced grade 2 CRS, which was controlled with tocilizumab. Target lesions of lung metastasis further achieved complete response. Similar increasing CD8+ T cell and Treg cell was detected from peripheral blood. Elevating IL-8 and declining TGF-β1 were also observed. The tumor is still under well control until the last follow-up on July 18, 2023. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-023-01491-9. |
format | Online Article Text |
id | pubmed-10492318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104923182023-09-10 CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer Qi, Changsong Xie, Tong Zhou, Jun Wang, Xicheng Gong, Jifang Zhang, Xiaotian Li, Jian Yuan, Jiajia Liu, Chang Shen, Lin J Hematol Oncol Correspondence Pancreatic cancer lacks effective therapy. Here, we reported two metastatic pancreatic cancer patients administrated with Claudin 18.2 (CLDN 18.2) CART therapy after the failure of standard therapy (NCT04581473 and NCT03874897). In case 1, with CLDN 18.2 expression of 2+, 70%, 250 × 10(6) cells were infused after lymphodepletion. Grade 1 cytokine release syndrome (CRS) occurred on d1 which was later controlled by tocilizumab. Partial response (PR) was achieved according to RECIST v1.1, with great shrinkage of lung metastasis. An increasing CD8+ T cell and Treg cells and declining CD4+ T cell and B cell were observed. In case 2, IHC result of ClDN18.2 showed 3+, 60%. 250 × 10(6) CLDN18.2 CART cells were subsequently administered. Patient experienced grade 2 CRS, which was controlled with tocilizumab. Target lesions of lung metastasis further achieved complete response. Similar increasing CD8+ T cell and Treg cell was detected from peripheral blood. Elevating IL-8 and declining TGF-β1 were also observed. The tumor is still under well control until the last follow-up on July 18, 2023. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-023-01491-9. BioMed Central 2023-09-09 /pmc/articles/PMC10492318/ /pubmed/37689733 http://dx.doi.org/10.1186/s13045-023-01491-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence Qi, Changsong Xie, Tong Zhou, Jun Wang, Xicheng Gong, Jifang Zhang, Xiaotian Li, Jian Yuan, Jiajia Liu, Chang Shen, Lin CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title | CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title_full | CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title_fullStr | CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title_full_unstemmed | CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title_short | CT041 CAR T cell therapy for Claudin18.2-positive metastatic pancreatic cancer |
title_sort | ct041 car t cell therapy for claudin18.2-positive metastatic pancreatic cancer |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492318/ https://www.ncbi.nlm.nih.gov/pubmed/37689733 http://dx.doi.org/10.1186/s13045-023-01491-9 |
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