Treatment and outcome of Philadelphia chromosome-positive acute lymphoblastic leukemia in adults after relapse.
Adult
Antibodies, Monoclonal
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Drug Resistance, Neoplasm
Fusion Proteins, bcr-abl
/ genetics
Humans
Immunotherapy
/ methods
Mutation
Philadelphia Chromosome
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ drug therapy
Protein Kinase Inhibitors
/ administration & dosage
Recurrence
Acute lymphoblastic leukemia
CAR-Ts
Philadelphia chromosome
blinatumomab
inotuzumab ozogamicin
Journal
Expert review of anticancer therapy
ISSN: 1744-8328
Titre abrégé: Expert Rev Anticancer Ther
Pays: England
ID NLM: 101123358
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
pubmed:
6
10
2020
medline:
15
4
2021
entrez:
5
10
2020
Statut:
ppublish
Résumé
Despite the significant progress that has been made over the last years in the front-line treatment of Philadelphia (Ph) chromosome-positive acute lymphoblastic leukemia (ALL), relapses are frequent and their treatment remains a challenge, especially among patients with resistant This manuscript reviews available data for the treatment of adult patients with relapsed/refractory Ph-positive ALL, with a focus on the role of tyrosine kinase inhibitors (TKIs), monoclonal antibodies, and immunotherapy. Although a majority of patients with first relapsed Ph-positive ALL respond to subsequent salvage chemotherapy plus TKI combination, their outcomes remain poor. The main predictor of survival is the achievement of major molecular response anytime during the morphological response. More treatment strategies to improve survival are under investigation. Monoclonal antibodies and bispecific antibody constructs hold considerable promise in improving the outcomes of patients with relapsed ALL including Ph-positive ALL.
Identifiants
pubmed: 33016157
doi: 10.1080/14737140.2020.1832890
doi:
Substances chimiques
Antibodies, Monoclonal
0
BCR-ABL1 fusion protein, human
0
Protein Kinase Inhibitors
0
Fusion Proteins, bcr-abl
EC 2.7.10.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM