[Contribution of radioimmunotherapy to the treatment of lymphoma]

Ann Pharm Fr. 2008 Nov-Dec;66(5-6):300-8. doi: 10.1016/j.pharma.2008.09.003. Epub 2008 Nov 8.
[Article in French]

Abstract

Radioimmunotherapy (RIT) is an emerging treatment option for non-Hodgkin's lymphoma. Only Zevalin (Bayer Schering Pharma) radiolabeled with yttrium 90 ((90)Y) is approved in France for the treatment of adult patients with rituximab relapsed or refractory CD20+ follicular B-cell non-Hodgkin's lymphoma. This radioimmunotherapeutic agent consists of ibritumomab, a murine anti-CD20 monoclonal antibody, conjugated to the metal chelator tiuxetan for retention of the beta emitter (90)Y. This review presents the concept of RIT. The pharmacological characteristics of [(90)Y]-ibritumomab tiuxetan, the specificity of its preparation and its special precautions for use will be described. The other radionuclides and antibodies in development will also be mentioned.

Publication types

  • Review

MeSH terms

  • Adult
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal / pharmacokinetics
  • Antibodies, Monoclonal / therapeutic use*
  • Antigens, CD20 / immunology
  • Chelating Agents / administration & dosage
  • Clinical Trials, Phase III as Topic
  • Drug Delivery Systems
  • Female
  • Hematologic Diseases / chemically induced
  • Humans
  • Lymphoma, B-Cell / radiotherapy*
  • Male
  • Multicenter Studies as Topic
  • Pregnancy
  • Pregnancy Complications, Neoplastic / radiotherapy
  • Radioimmunotherapy* / adverse effects
  • Randomized Controlled Trials as Topic
  • Tissue Distribution
  • Yttrium Radioisotopes / adverse effects
  • Yttrium Radioisotopes / pharmacokinetics
  • Yttrium Radioisotopes / therapeutic use*

Substances

  • Antibodies, Monoclonal
  • Antigens, CD20
  • Chelating Agents
  • Yttrium Radioisotopes
  • ibritumomab tiuxetan