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Inotuzumab ozogamicin in B-cell acute lymphoblastic leukemias and non-Hodgkin's lymphomas.

AbstractINTRODUCTION:
The expression profile of the CD22 antigen and its role in B-cell function make it an important target in B-cell leukemias and lymphomas. Inotuzumab ozogamicin (IO), a humanized monoclonal antibody targeting CD22, is one of the most promising monoclonal antibodies for the treatment of relapsed/refractory B-cell acute lymphoblastic leukemia (ALL).
AREAS COVERED:
This article reviews the current literature of IO in adult leukemias and lymphomas.
EXPERT OPINION:
Single-agent IO has demonstrated activity in patients with relapsed B-cell ALL and non-Hodgkin lymphoma (NHL). It has also demonstrated favorable early results when combined with chemotherapy in older patients with ALL. There is potential for IO to be combined with other targeted therapies under development for these diseases; data are still early and further studies of IO are warranted. While the pivotal randomized study of IO for relapsed NHL versus physician's choice did not show a statistically significant advantage in response rate, the results of the pivotal study in ALL are not yet available.
AuthorsMaro Ohanian, Hagop Kantarjian, Daniel Guy, Deborah Thomas, Elias Jabbour, Susan O'Brien
JournalExpert opinion on biological therapy (Expert Opin Biol Ther) Vol. 15 Issue 4 Pg. 601-11 (Apr 2015) ISSN: 1744-7682 [Electronic] England
PMID25775418 (Publication Type: Journal Article, Review)
Chemical References
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Sialic Acid Binding Ig-like Lectin 2
  • Inotuzumab Ozogamicin
Topics
  • Acute Disease
  • Animals
  • Antibodies, Monoclonal (pharmacology, therapeutic use)
  • Antibodies, Monoclonal, Humanized (pharmacology, therapeutic use)
  • B-Lymphocytes (drug effects, immunology, metabolism)
  • Humans
  • Inotuzumab Ozogamicin
  • Leukemia, B-Cell (drug therapy, immunology, metabolism)
  • Lymphoma, Non-Hodgkin (drug therapy, immunology, metabolism)
  • Sialic Acid Binding Ig-like Lectin 2 (antagonists & inhibitors, biosynthesis)

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