Loss of CD22 expression and expansion of a CD22dim subpopulation in adults with relapsed/refractory B-lymphoblastic leukaemia after treatment with Inotuzumab-Ozogamicin

Autor: Walter Fiedler, Stefan Schwartz, Jochim Reinert, Klaus Wethmar, Matthias Stelljes, Antonia Beitzen-Heineke
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
Oncology
Male
medicine.medical_treatment
Sialic Acid Binding Ig-like Lectin 2
Inotuzumab-Ozogamicin
0302 clinical medicine
Antineoplastic Agents
Immunological

Recurrence
hemic and lymphatic diseases
Antibodies
Bispecific

Antineoplastic Combined Chemotherapy Protocols
Medicine
Treatment Failure
Aged
80 and over

B-Lymphocytes
Hematology
biology
medicine.diagnostic_test
CD22
Hematopoietic Stem Cell Transplantation
B-ALL
General Medicine
Middle Aged
Sorafenib
Allografts
Flow Cytometry
030220 oncology & carcinogenesis
Imatinib Mesylate
Original Article
Female
Immunotherapy
Antibody
After treatment
medicine.drug
Adult
medicine.medical_specialty
Flow cytometry
Immunophenotyping
03 medical and health sciences
Young Adult
Refractory
Internal medicine
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Humans
Inotuzumab Ozogamicin
Inotuzumab ozogamicin
Salvage Therapy
business.industry
Lymphocyte Subsets
Clone Cells
030104 developmental biology
biology.protein
business
Zdroj: Annals of Hematology
ISSN: 1432-0584
0939-5555
Popis: Treatment options for relapsed or refractory B-lymphoblastic leukaemia (r/r B-ALL) are limited and the prognosis of these patients remains dismal, but novel immunotherapeutic options such as the anti-CD22 antibody–drug-conjugate Inotuzumab-Ozogamicin (InO) have improved outcomes in these patients. Flow cytometry is essential to assess antigen-expression prior to treatment initiation of antigen-directed immunotherapies. Here, we present flow cytometric and clinical data of three adult patients with r/r B-ALL who failed treatment with InO associated with reduced or lost antigen-expression. In addition, we present comparative data on two different diagnostic CD22-specific antibody clones that exhibit significant differences in staining intensities.
Databáze: OpenAIRE