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Chimeric antigen receptor T-cell therapy in hematologic malignancies: Successes, challenges, and opportunities.
Ho, Matthew; Zanwar, Saurabh; Paludo, Jonas.
Afiliação
  • Ho M; Division of General Internal Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Zanwar S; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Paludo J; Division of General Internal Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Eur J Haematol ; 112(2): 197-210, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37545132
ABSTRACT
The success of chimeric antigen receptor T-cell (CAR-T) therapy in hematologic malignancies has realized a longstanding effort toward harnessing the immune system to fight cancer in a truly personalized fashion. Second generation chimeric antigen receptors (CAR) incorporating co-stimulatory molecules like 4-1BB or CD28 were able to overcome some of the hindrances with initial CAR constructs resulting in efficacious products. Many second-generation CAR-T products have been approved in the treatment of relapsed/refractory hematologic malignancies including multiple myeloma (MM), non-Hodgkin lymphoma (NHL), and acute lymphoblastic leukemia. However, challenges remain in optimizing the manufacturing, timely access, limiting the toxicity from CAR-T infusions and improving sustainability of responses derived with CAR-T therapy. Here, we summarize the clinical trial data leading to approval CAR-T therapies in MM and NHL, discuss the limitations with current CAR-T therapy strategies and review emerging strategies for overcoming these limitations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Neoplasias Hematológicas / Receptores de Antígenos Quiméricos / Mieloma Múltiplo Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Neoplasias Hematológicas / Receptores de Antígenos Quiméricos / Mieloma Múltiplo Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article