Rafael Madero-Marroquin, Ryan W. Hunter, Caner Saygin, Hannah Johnston, Adam S. DuVall, Hamed Rahmani Youshanlouei, Clinton Osei, Syed Shah, Wendy Stock, Sandeep Gurbuxani, Anand A. Patel
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引用次数: 0
Abstract
Background
CD58 loss has been described as a mechanism of resistance to blinatumomab and chimeric antigen receptor T-cell therapy, functioning as a modulator of response to T-cell activation.
Methods
Using flow cytometry, we evaluated the impact of CD58 mean fluorescence intensity (MFI) on the probability of achieving measurable residual disease (MRD) negativity in patients with B-cell acute lymphoblastic leukemia treated with inotuzumab ozogamicin (InO).
Results
The odds ratio of achieving MRD negativity was 1.03 for every 1000 unit increase in CD58 MFI.
Conclusion
Our results suggest that MRD negativity rates after InO are high, regardless of the intensity of CD58 expression.