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**Brentuximab vedotin + lenalidomide + rituximab** is a combination therapy approved for the treatment of adult patients with relapsed or refractory large B-cell lymphoma (LBCL), including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, DLBCL arising from indolent lymphoma, or high-grade B-cell lymphoma (HGBL), after two or more lines of systemic therapy who are ineligible for autologous hematopoietic stem cell transplantation or CAR T-cell therapy. - **Brentuximab vedotin** is an antibody-drug conjugate (ADC) targeting CD30, in which a monoclonal antibody is linked to the cytotoxic agent monomethyl auristatin E. It delivers the cytotoxic agent to CD30-expressing cells, leading to cell death. - **Lenalidomide** is an immunomodulatory small molecule that exerts antineoplastic activity through multiple mechanisms, including inhibition of angiogenesis, modulation of the immune response, and direct cytotoxicity to tumor cells. - **Rituximab** is a monoclonal antibody targeting CD20 on B lymphocytes, resulting in B-cell depletion through cytotoxic and apoptotic mechanisms[1][2][4][5][7][8]. This combination demonstrated a statistically significant survival benefit in patients with relapsed/refractory DLBCL in phase 3 clinical trials.
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