Antibody treatment in multiple myeloma.
ADP-ribosyl Cyclase 1
/ antagonists & inhibitors
Animals
Antibodies, Bispecific
/ adverse effects
Antineoplastic Agents, Immunological
/ adverse effects
B-Cell Maturation Antigen
/ antagonists & inhibitors
Humans
Immunoconjugates
/ adverse effects
Multiple Myeloma
/ drug therapy
Signaling Lymphocytic Activation Molecule Family
/ antagonists & inhibitors
Journal
Clinical advances in hematology & oncology : H&O
ISSN: 1543-0790
Titre abrégé: Clin Adv Hematol Oncol
Pays: United States
ID NLM: 101167661
Informations de publication
Date de publication:
Mar 2021
Mar 2021
Historique:
entrez:
19
3
2021
pubmed:
20
3
2021
medline:
3
6
2021
Statut:
ppublish
Résumé
Antibody therapy, which has become a critical option in the treatment of multiple myeloma (MM), includes monoclonal antibodies, antibody-drug conjugates, and bispecific antibodies. Anti-CD38 and anti-SLAMF7 monoclonal antibodies were the first to enter the MM portfolio as treatment options for relapsed/ refractory MM. More recently, daratumumab has become important in the treatment of newly diagnosed MM, and a subcutaneous formulation has been approved. BCMA-targeted antibody-drug conjugates and bispecific antibodies, which are the newest antibody therapies to be investigated, provide additional therapeutic options for patients with heavily pretreated MM. This article reviews how antibody therapy has influenced the treatment of MM, describes the unique adverse event profiles of each relevant drug class, and explains how to incorporate antibody therapy into practice.
Substances chimiques
Antibodies, Bispecific
0
Antineoplastic Agents, Immunological
0
B-Cell Maturation Antigen
0
Immunoconjugates
0
SLAMF7 protein, human
0
Signaling Lymphocytic Activation Molecule Family
0
TNFRSF17 protein, human
0
ADP-ribosyl Cyclase 1
EC 3.2.2.6
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM