Background
Mini
mal residual disease (MRD) studies in adult acute ly
mphoblastic leuke
mia (ALL) give highly significant prognostic infor
mation superior to other standard criteria as age, gender and total leucocytic count (TLC) in distinguishing patients at high and low risk of r
elapse.
Objectives
We aimed to determine the value of MRD monitoring by flowcytometry (FCM) in predicting outcome in adult Precursor ALL patients.
Patients and methods
Bone marrow (BM) samples were analyzed by 4-color FCM collected at diagnosis and after induction therapy (MRD1) to correlate MRD positivity with disease free survival (DFS) and overall survival (OS).
Results
Study included 57 adult ALL patients (44 males and 13 females) with a median age of 22 years (18-49). DFS showed no significant difference with age, gender and initial TLC (m>pm> = 0.838, 0.888 and 0.743, respectively). Cumulative DFS at 2 years was 34 % for B-lineage ALL (m>nm>: 35) and 57 % for T-lineage ALL (m>nm>: 18) (m>pm> = 0.057). Cumulative DFS at 2 years was 7 % for MRD1 positive (high risk, HR) versus 57 % for MRD1 negative patients (Low risk, LR) (m>pm> < 0.001). Cumulative DFS at 2 years was 29 % for HR patients (m>nm>: 26) versus 55 % for LR (m>nm>: 27) according to GMALL classification (m>pm> = 0.064). Cumulative OS did not differ according to age, gender and TLC (m>pm> = 0.526, 0.594 and 0.513, respectively). Cumulative OS at 2 years was 36 % for B ALL (m>nm>: 39) versus 77 % for TALL (m>nm>: 18) (m>pm> = 0.016) and was 49 % for Philadelphia chromosome (Ph) negative patients versus 0 % for Ph-positive patients (m>pm> < 0.001). Regarding MRD1, OS at 2 years was 18 % for MRD1 HR (m>nm>: 17) versus 65 % for MRD1 LR (m>nm>: 38) (m>pm> < 0.001). OS was 35 % for high-risk patients (m>nm>: 30) and 62 % for low-risk patients (m>nm>: 27) classified according to GMALL risk stratification (m>pm> = 0.017).
Conclusion
MRD by FCM is a strong independent predictor of outcome in terms of DFS and OS and is a powerful informative parameter in guiding individual treatment in ALL patients.