<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>100(11)</volume><submitter>Reinert J</submitter><funding>Universitätsklinikum Hamburg-Eppendorf (UKE)</funding><pubmed_abstract>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.</pubmed_abstract><journal>Annals of hematology</journal><pagination>2727-2732</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8510963</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Loss of CD22 expression and expansion of a CD22&lt;sup>dim&lt;/sup> subpopulation in adults with relapsed/refractory B-lymphoblastic leukaemia after treatment with Inotuzumab-Ozogamicin.</pubmed_title><pmcid>PMC8510963</pmcid><pubmed_authors>Schwartz S</pubmed_authors><pubmed_authors>Reinert J</pubmed_authors><pubmed_authors>Beitzen-Heineke A</pubmed_authors><pubmed_authors>Fiedler W</pubmed_authors><pubmed_authors>Wethmar K</pubmed_authors><pubmed_authors>Stelljes M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Loss of CD22 expression and expansion of a CD22&lt;sup>dim&lt;/sup> subpopulation in adults with relapsed/refractory B-lymphoblastic leukaemia after treatment with Inotuzumab-Ozogamicin.</name><description>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.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-04T12:22:49.735Z</modification><creation>2025-02-19T01:26:16.169Z</creation></dates><accession>S-EPMC8510963</accession><cross_references><pubmed>34331563</pubmed><doi>10.1007/s00277-021-04601-0</doi></cross_references></HashMap>