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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
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Updated: Sep 27, 2025

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Immune targeted therapy for diffuse large B cell lymphoma.

Yaxin Zheng1, Junqi Si1, Tian Yuan1

  • 1Department of Hematology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China.

Blood Science (Baltimore, Md.)
|April 11, 2022
PubMed
Summary
This summary is machine-generated.

Diffuse large B-cell lymphoma (DLBCL) is a common cancer with a poor prognosis for some. This review covers advancements in immune-targeted therapies, including bispecific T-cell engagers and CAR T-cell therapy, for refractory and relapsed DLBCL patients.

Keywords:
Antibody-drug conjugatesCheckpoint inhibitorsDLBCLMonoclonal antibodiesSignaling pathway inhibitors

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Area of Science:

  • Oncology
  • Immunology

Background:

  • Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma, characterized by heterogeneity and invasiveness.
  • While many patients respond to standard chemoimmunotherapy (R-CHOP), approximately one-third face a poor prognosis.
  • Refractory and relapsed DLBCL present significant clinical challenges.

Purpose of the Study:

  • To review the current progress and advancements in immune-targeted therapies for DLBCL.
  • To highlight the efficacy of novel immunotherapies in managing refractory and relapsed DLBCL cases.

Main Methods:

  • Literature review of recent clinical studies and research on immune-targeted therapies for DLBCL.
  • Analysis of data concerning bispecific T-cell engagers and CAR T-cell therapy efficacy.

Main Results:

  • Immune-targeted therapies, including bispecific T-cell engagers and CAR T-cell therapy, demonstrate significant efficacy in patients with refractory and relapsed DLBCL.
  • These novel approaches offer promising alternatives for a subset of DLBCL patients who do not respond to conventional treatments.

Conclusions:

  • Immune-targeted therapy represents a rapidly evolving and effective strategy for treating difficult-to-manage DLBCL.
  • Continued research and development in this area hold potential for improving outcomes for a broader range of DLBCL patients.