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Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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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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Related Experiment Video

Updated: Jul 15, 2025

Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
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CD19-Targeted Chimeric Antigen Receptor T-cell Therapy for Concomitant Diffuse Large B-cell Lymphoma and Multiple

Tyler D'Ovidio1, Kathryn Ciccolini1, Matko Kalac1

  • 1Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, USA.

Cureus
|October 4, 2023
PubMed
Summary

This case report details a rare instance of simultaneous multiple myeloma (MM) and diffuse large B-cell lymphoma (DLBCL). CD19-targeted CAR T-cell therapy successfully treated both hematologic malignancies.

Keywords:
car t-cell therapyconcomitant malignanciesdiffuse large b-cell lymphomamultiple myelomanon-hodgkin’s lymphoma

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A Syngeneic Mouse B-Cell Lymphoma Model for Pre-Clinical Evaluation of CD19 CAR T Cells
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Area of Science:

  • Hematology
  • Oncology
  • Immunotherapy

Background:

  • Multiple myeloma (MM) and diffuse large B-cell lymphoma (DLBCL) are distinct hematologic malignancies.
  • The co-occurrence of MM and DLBCL in a single patient is exceptionally rare.
  • Chimeric antigen receptor (CAR) T-cell therapies targeting CD19 or B-cell maturation antigen (BCMA) show efficacy in hematologic cancers.

Observation:

  • A patient presented with findings consistent with MM on bone marrow biopsy.
  • A subsequent lymph node biopsy confirmed DLBCL.
  • The patient had concurrent, distinct diagnoses of MM and DLBCL.

Findings:

  • The patient received CD19-targeted CAR T-cell therapy.
  • Post-treatment evaluation showed no detectable evidence of either MM or DLBCL.
  • This represents the first reported case of concomitant MM and DLBCL treated with CD19-targeted CAR T-cell therapy.

Implications:

  • CD19-targeted CAR T-cell therapy may be effective in treating patients with both MM and DLBCL.
  • This case expands the understanding of CAR T-cell therapy applications in rare hematologic malignancy combinations.
  • Further investigation is warranted to explore the efficacy of CAR T-cell therapy in similar rare co-occurring hematologic cancers.