Abstract
The biology and outcome of adult t(4;11)(q21;q23)/MLL-AFF1 acute lymphoblastic leukemia are poorly understood. We describe the outcome and delineate prognostic factors and optimal post-remission therapy in 85 consecutive patients (median age 38 years) treated uniformly in the prospective trial UKALLXII/ECOG2993. The immunophenotype of this leukemia was pro-B (CD10(NEG)). Immaturity was further suggested by high expression of the stem-cell antigens, CD133 and CD135, although CD34 expression was significantly lower than in t(4; 11)negative patients. Complete remission was achieved in 77 (93%) patients but only 35% survived 5 years (95% CI: 25-45%); the relapse rate was 45% (95% CI: 33-58%). Thirty-one patients underwent allogeneic transplantation in first remission (15 sibling donors and 16 unrelated donors): with 5-year survival rates of 56% and 67% respectively, only 2/31 patients relapsed. This compares with a 24% survival rate and 59% relapse rate in 46 patients who received post-remission chemotherapy. A major determinant of outcome was age with 71% of patients aged
| Original language | English |
|---|---|
| Pages (from-to) | 945-952 |
| Number of pages | 8 |
| Journal | Haematologica |
| Volume | 98 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Jun 2013 |
Keywords
- MINIMAL-RESIDUAL-DISEASE
- GENE REARRANGEMENTS
- COMPLETE REMISSION
- REDUCED-INTENSITY
- TRANSPLANTATION
- EXPRESSION
- TRANSLOCATIONS
- ABNORMALITIES
- CHEMOTHERAPY
- CHILDHOOD
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