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Tafasitamab for the treatment of patients with diffuse large B-cell lymphoma.
Pirosa, Maria Cristina; Stathis, Anastasios; Zucca, Emanuele.
Afiliação
  • Pirosa MC; Clinic of Medical Oncology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Stathis A; Institute of Oncology Research, Bellinzona, Switzerland.
  • Zucca E; Faculty of Biomedical Science, Universita' della Svizzera italiana, Lugano, Switzerland.
Hum Vaccin Immunother ; 20(1): 2309701, 2024 Dec 31.
Article em En | MEDLINE | ID: mdl-38299612
ABSTRACT
Patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) require additional treatments, especially those not eligible or not responding to high dose cytotoxic chemotherapy and stem cell transplantation. Over the last few years, several new treatments have been developed and approved for these patients, among them of particular relevance are those targeting CD19. Tafasitamab is a humanized monoclonal antibody targeting CD19, composed of a modified fragment crystallizable (Fc) region engineered with higher affinity for Fc gamma receptors (FcγR) receptors, leading to increased cytotoxicity through natural killer cells and macrophages (antibody-dependent cellular cytotoxicity and antibody-dependent cell-mediated phagocytosis). In this product review, we will discuss its mechanism of action, safety profile and efficacy results from clinical trials that led to its approval in combination with lenalidomide for patients with R/R DLBCL ineligible for high-dose chemotherapy and autologous transplantation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Linfoma Difuso de Grandes Células B / Antineoplásicos Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: Hum Vaccin Immunother Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Linfoma Difuso de Grandes Células B / Antineoplásicos Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: Hum Vaccin Immunother Ano de publicação: 2024 Tipo de documento: Article