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CAR T-cell therapy in relapsed/refractory diffuse large B-cell lymphoma: physician preferences trading off benefits, risks and time to infusion.
Boeri, Marco; Purdum, Anna G; Sutphin, Jessie; Hauber, Brett; Kaye, James A.
Afiliação
  • Boeri M; RTI Health Solutions, Belfast BT2 8LA, UK.
  • Purdum AG; Queen's University Belfast, Belfast BT7 1NN, UK.
  • Sutphin J; Kite Pharma, A Gilead Company, Santa Monica, CA 90404, USA.
  • Hauber B; RTI Health Solutions, Research Triangle Park, NC 27709, USA.
  • Kaye JA; RTI Health Solutions, Research Triangle Park, NC 27709, USA.
Future Oncol ; 17(34): 4697-4709, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34581197
Lay abstract CAR-T therapy is a treatment option for patients with diffuse large B-cell lymphoma that has not responded to at least two other kinds of treatments. CAR-T therapies are manufactured from a patient's white blood cells, modified to attack lymphoma cells. A CAR-T therapy takes time to manufacture after these cells are collected. CAR-T therapies can result in the reduction or disappearance of lymphoma tumors and can increase the chances of survival, but also cause serious side effects for a few patients. One of these is cytokine release syndrome (CRS), in which high levels of inflammation throughout the body may cause fever, heart problems or difficulty breathing. Another is the development of temporary but serious neurological problems such as confusion, seizures and memory problems. To understand how important physicians consider certain features of CAR-T therapies to be when deciding whether to recommend them, we asked physicians to choose between two treatment options resembling CAR-T therapies in a series of questions, with the CAR-T features varying in each question. Their answers indicated whether disappearance of tumors, a patient's chances of survival after 1 and 2 years of treatment, manufacturing time, or the risk of CRS or neurological problems was the most important factor. Physicians most wanted to reduce manufacturing time from 113 to 16 days, but also were willing to accept a >20% increase in risk of severe CRS and a 15% increase in risk of severe neurological events to increase a patient's chance of survival from 40 to 55% at 2 years.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Linfoma Difuso de Grandes Células B / Tomada de Decisão Clínica / Síndrome da Liberação de Citocina / Recidiva Local de Neoplasia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Linfoma Difuso de Grandes Células B / Tomada de Decisão Clínica / Síndrome da Liberação de Citocina / Recidiva Local de Neoplasia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article