| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5527787 | Leukemia Research | 2017 | 8 Pages |
â¢CD200 over-expression is associated with poor prognosis in AML.â¢In CN AML, CD200 correlated with lower rates of CR and shorter DFS and OS.â¢Cases with high CD200 expression displayed worse outcomes.â¢CD200 overexpression is associated with poor prognosis also in FLT3-/NPM1+ CN AML.
Overexpression of CD200, a trans-membrane protein belonging to the immunoglobulin superfamily, has been associated with poor prognosis in patients with acute myeloid leukemia (AML). As few data are available in the subset of cytogenetically-normal (CN) AML, we retrospectively evaluated the correlations between CD200 expression and response to therapy in a series of 139 adults with CN-AML.CD200 was expressed in 67/139 (48%) cases; 18 of them (28%) expressed CD200 at high intensity. No differences in CD200 expression rate were observed according to age, WBC count, type of leukemia, FLT3 or NMP1 mutation, and CD56 expression. A higher incidence of CD200 expression was observed in CD34+ cases (PÂ <Â 0.0001) and in BCL2+ patients (PÂ =Â 0.04).Complete remission (CR) was evaluable achieved in 98 patients (70%): 56/71 (79%) in CD200- and 47/67 (63%) in CD200+ patients (PÂ =Â 0.03), with a lower CR rate in patients with high CD200 intensity (9/18, 50%). CD200 expression had a negative impact on long-term outcome. CD200 expression, per se, did not impact on disease-free survival (DFS), but cases with high CD200 expression had a lower 3-year DFS compared to CD200-negative and low-expressing ones (0% vs 65% vs 68%, PÂ =Â 0.019). Three-year overall survival (OS) was 51% in CD200- and 27% in CD200+ patients (PÂ =Â 0.01), with a significant difference among cases with low or high CD200 expression (35% vs 0%, PÂ =Â 0.001). CD200 high expression defined a group with very poor DFS and OS also among the 37 FLT3-/NPM1+: 3-year DFS and OS were 88% and 60% in CD200-, 50% and 32% in CD200 low and 0% and 0% in CD200 high patients, respectively (PÂ =Â 0.01 for DFS and PÂ =Â 0.05 for OS).Our data suggest a negative impact of CD200 expression in CN-AML, with a further worsening in high-expressing cases, also in the subset of FLT3-/NPM1+ patients.
