• Media type: E-Article
  • Title: First third-generation CAR T cell application targeting CD19 for the treatment of systemic IgM AL amyloidosis with underlying marginal zone lymphoma
  • Contributor: Korell, Felix; Schönland, Stefan; Schmitt, Anita; Jansen, Madelaine; Farid, Kiavasch; Müller-Tidow, Carsten; Dreger, Peter; Schmitt, Michael; Hegenbart, Ute
  • imprint: Springer Science and Business Media LLC, 2023
  • Published in: Biomarker Research
  • Language: English
  • DOI: 10.1186/s40364-023-00532-2
  • ISSN: 2050-7771
  • Keywords: Biochemistry (medical) ; Clinical Biochemistry ; Molecular Medicine
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>Light chain amyloidosis (AL) is a rare disease caused by the generalized deposition of misfolded free light chains. Patients with immunoglobulin M gammopathy (IgM) and indolent B-cell lymphoma such as marginal zone lymphoma (MZL) may in some instances develop AL amyloidosis. So far, CAR T cells for AL amyloidosis have only been reported utilizing the B cell maturation antigen as target, while CD19 has so far not been used in AL amyloidosis.</jats:p><jats:p>We report the case of a 71-year-old male, diagnosed with systemic AL kappa amyloidosis and MZL, receiving third-generation CAR T cell therapy targeting CD19. Prior treatment included bendamustine/rituximab and cyclophosphamide/ dexamethasone with subsequent autologous stem cell transplantation. CAR T application was well tolerated despite heart and kidney amyloid manifestations, and only early low-grade procedure-specific toxicities were observed. A continuous decrease in IgM, kappa light chains and kappa-to-lambda light chain difference was observed in the patient from day + 30 on, resulting in a deep hematological response six months after treatment.</jats:p><jats:p>In summary, we present a novel case of CAR T cell treatment with third generation CD19 directed infusion for AL amyloidosis with an underlying secretory active B cell lymphoma, showing that this is an effective treatment modality and can be applied to patients with subsequent AL amyloidosis.</jats:p>
  • Access State: Open Access