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Patient preferences for treatment in relapsed/refractory diffuse large B-cell lymphoma: a discrete choice experiment.
Birch, Kelly; Snider, Julia T; Chiu, Kevin; Baumgardner, James; Wade, Sally W; Shah, Gunjan.
Afiliación
  • Birch K; PRECISIONheor, 6550 Rock Spring Dr #155, Bethesda, MD 20817, USA.
  • Snider JT; Kite Pharmaceuticals, 2400 Broadway, Santa Monica, CA 90404, USA.
  • Chiu K; OnPoint Analytics, 200 Powell St #860, Emeryville, CA 94608, USA.
  • Baumgardner J; PRECISIONheor, 6550 Rock Spring Dr #155, Bethesda, MD 20817, USA.
  • Wade SW; Kite Pharmaceuticals, 2400 Broadway, Santa Monica, CA 90404, USA.
  • Shah G; Wade Outcomes Research & Consulting, 136 U Street, Salt Lake City, UT 84103, USA.
Future Oncol ; 18(25): 2791-2804, 2022 08.
Article en En | MEDLINE | ID: mdl-35837970
Chimeric antigen receptor (CAR) T-cell therapy is a new treatment for patients with diffuse large B-cell lymphoma. CAR T-cell therapies are made from a patient's own cells, modified in a laboratory and used to attack cancer cells. While CAR T-cell therapies may increase long-term survival, they can also cause temporary but serious side effects, including neurological issues (e.g., headache, confusion, brain swelling) and cytokine-release syndrome (CRS), an inflammatory condition that can cause fever, breathing difficulties and organ dysfunction. To understand how patients' perspectives of CAR T-cell therapy compared with their perspectives on other treatments for diffuse large B-cell lymphoma, we surveyed 224 patients in the USA and Europe. They were asked to choose between two treatments in a series of choice sets, each displaying varying levels of aspects of cancer therapies, including survival and risks of serious side effects. Their choices allowed us to measure which factors were most important to patients when making decisions about treatment. We found that increasing the probability of survival was most important, followed by avoiding risks of neurological complications and CRS. Patients were willing to accept increased risks of neurological toxicities and CRS if they could obtain a 13­14 percentage point increase in the probability of surviving for at least 1 year after treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma no Hodgkin / Linfoma de Células B Grandes Difuso Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Future Oncol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma no Hodgkin / Linfoma de Células B Grandes Difuso Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Future Oncol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos