CD19-targeted immunotherapies for treatment of patients with non-Hodgkin B-cell lymphomas

Expert Opin Investig Drugs. 2018 Jul;27(7):601-611. doi: 10.1080/13543784.2018.1492549. Epub 2018 Jul 5.

Abstract

Introduction: Ubiquitous expression of CD19 on B cell non-Hodgkin lymphoma identified it as a potential target for immune-based therapies.

Areas covered: This article reviews the current literature on anti-CD19 therapies currently in clinical trials including monoclonal antibodies (mAb), antibody targeted cytotoxic drug conjugates (ADC), bispecific antibodies, and chimeric antigen receptor (CAR) modified T cells.

Expert opinion: Naked anti-CD19 mAbs have shown little clinical benefit in B cell lymphomas. Despite unusual toxicity profiles with many anti-CD19 ADCs slowing development, durable remissions in a substantial minority of patients with refractory aggressive lymphomas should encourage continued efforts in this area. Blinatumomab, an anti-CD19 bispecific T cell engager, has shown impressive responses in relapse/refractory diffuse large B cell lymphoma (DLBCL), but is plagued by neurotoxicity issues and the need for continuous infusion. CD19 targeting CAR-T cell therapies are the most promising, with the potential for curing a third of refractory DLBCL patients. There is still much work to be done to address potentially life-threatening cytokine release syndrome and neurotoxicity, an extended production time precluding patients with rapidly progressive disease, and treatment expense. However, if the promise of CAR-T cell technology is confirmed, this will likely change the approach and prognosis for relapse/refractory aggressive lymphoma.

Keywords: B cell lymphoma; CAR-T cells; CD19; antibody drug conjugates; blinatumomab.

Publication types

  • Review

MeSH terms

  • Antibodies, Bispecific / administration & dosage
  • Antibodies, Bispecific / immunology
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / immunology
  • Antigens, CD19 / immunology*
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacology
  • Humans
  • Immunoconjugates / administration & dosage
  • Immunoconjugates / adverse effects
  • Immunoconjugates / immunology
  • Immunotherapy / adverse effects
  • Immunotherapy / methods*
  • Lymphoma, Large B-Cell, Diffuse / immunology
  • Lymphoma, Large B-Cell, Diffuse / pathology
  • Lymphoma, Large B-Cell, Diffuse / therapy*
  • Receptors, Antigen, T-Cell / immunology

Substances

  • Antibodies, Bispecific
  • Antibodies, Monoclonal
  • Antigens, CD19
  • Antineoplastic Agents
  • Immunoconjugates
  • Receptors, Antigen, T-Cell