CD22
医学
四分位数
内科学
耐火材料(行星科学)
肿瘤科
置信区间
CD20
免疫组织化学
生物
天体生物学
作者
Chiara Sartor,Mario Arpinati,Gabriella Chirumbolo,Luca Dozza,Gianluca Cristiano,Jacopo Nanni,Giovanni Marconi,Valentina Robustelli,Ilaria Vigliotta,Sarah Parisi,Carolina Terragna,Nicoletta Testoni,Stefania Paolini,Giovanni Martinelli,Antonio Curti,Michèle Cavo,Cristina Papayannidis
摘要
Antigen-directed target therapy for B-cell acute lymphoblastic leukemia (B-ALL) is now the standard of care for relapsed/refractory (R/R) disease. A comprehensive determination of the target itself is mandatory to aid physician's choice. We determined baseline Cluster of differentiation 22 (CD22) expression percentage and fluorescent intensity on lymphoblasts of 30 patients with R/R B-ALL treated with anti-CD22 immunoconjugate drug Inotuzumab Ozogamicin (INO) and analyzed the impact of both parameters on patient outcome. Most patients (24/30, 80%) had a high leukemic blast CD22-positivity defined as ≥90%. We did not observe a benefit in terms of complete remission, overall survival (OS) and duration of response (DoR) for patients with CD22 ≥ 90% versus CD22 < 90%. Concerning CD22-FI quartile analysis we appreciated a trend for superior response rates in higher quartiles (Q2 -Q4 ) compared to Q1 and a significant benefit in terms of OS and DoR for patients with higher CD22-FI. INO demonstrates to be effective also in patients with lower CD22 expression, but therapeutical benefits are more evident in patients with higher CD22-FI. The evaluation of both CD22 percentage and CD22-FI of the leukemic blast may help physicians in therapeutic choices for R/R B-ALL patients when multiple treatment options are available, although no CD22 expression threshold can currently be identified below which INO should be considered not effective.
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