Literature DB >> 35045358

Image-guided interventional radiological delivery of chimeric antigen receptor (CAR) T cells for pleural malignancies in a phase I/II clinical trial.

Mario Ghosn1, Waseem Cheema2, Amy Zhu2, Jennifer Livschitz2, Majid Maybody1, Franz E Boas1, Ernesto Santos1, DaeHee Kim1, Jason A Beattie3, Michael Offin4, Valerie W Rusch2, Marjorie G Zauderer5, Prasad S Adusumilli6, Stephen B Solomon1.   

Abstract

OBJECTIVES: We describe techniques and results of image-guided delivery of mesothelin-targeted chimeric antigen receptor (CAR) T cells in patients with pleural malignancies in a phase I/II trial (ClinicalTrials.gov: NCT02414269).
MATERIALS AND METHODS: Patients without a pleural catheter or who lack effusion for insertion of a catheter (31 of 41) were administered intrapleural CAR T cells by interventional radiologists under image guidance by computed tomography or ultrasound. CAR T cells were administered through a needle in an accessible pleural loculation (intracavitary) or following an induced loculated artificial pneumothorax. In patients where intracavitary infusion was not feasible, CAR T cells were injected via percutaneous approach either surrounding and/or in the pleural nodule/thickening (intratumoral). Pre- and post-procedural clinical, laboratory, and imaging findings were assessed.
RESULTS: CAR T cells were administered intrapleurally in 31 patients (33 procedures, 2 patients were administered a second dose) with successful delivery of planned dose (10-186 mL); 14/33 (42%) intracavitary and 19/33 (58%) intratumoral. All procedures were completed within 2 h of T-cell thawing. There were no procedure-related adverse events greater than grade 1 (1 in 3 patients had prior ipsilateral pleural fusion procedures). The most common imaging finding was ground glass opacities with interlobular septal thickening and/or consolidation, observed in 12/33 (36%) procedures. There was no difference in the incidence of fever, CRP, IL-6, and peak vector copy number in the peripheral blood between infusion methods.
CONCLUSION: Image-guided intrapleural delivery of CAR T cells using intracavitary or intratumoral routes is feasible, repeatable and safe across anatomically variable pleural cancers.
Copyright © 2022 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Adoptive cell therapy; Malignant pleural effusion; Malignant pleural mesothelioma; Pleural metastases; Regional delivery

Year:  2022        PMID: 35045358      PMCID: PMC9256852          DOI: 10.1016/j.lungcan.2022.01.003

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   6.081


  46 in total

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Journal:  J Thorac Oncol       Date:  2013-04       Impact factor: 15.609

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Journal:  Sci Transl Med       Date:  2014-03-05       Impact factor: 17.956

Review 7.  Lipiodol transarterial chemoembolization for hepatocellular carcinoma: A systematic review of efficacy and safety data.

Authors:  Riccardo Lencioni; Thierry de Baere; Michael C Soulen; William S Rilling; Jean-Francois H Geschwind
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Journal:  Sci Immunol       Date:  2017-05-19

Review 9.  CAR T-cell therapy for pleural mesothelioma: Rationale, preclinical development, and clinical trials.

Authors:  Navin K Chintala; David Restle; Hue Quach; Jasmeen Saini; Rebecca Bellis; Michael Offin; Jason Beattie; Prasad S Adusumilli
Journal:  Lung Cancer       Date:  2021-05-05       Impact factor: 6.081

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Authors:  Mythili Koneru; Roisin O'Cearbhaill; Swati Pendharkar; David R Spriggs; Renier J Brentjens
Journal:  J Transl Med       Date:  2015-03-28       Impact factor: 5.531

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  1 in total

1.  Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities.

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  1 in total

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