The prognostic significance of minimal residual disease in adult Egyptian patients with precursor acute lymphoblastic leukemia

• Published in: Journal of Egyptian National Cancer Institute Vol. 25; no. 3; pp. 135 - 142
• Main Authors: Samra, Mohamed A., Mahmoud, Hossam K., Abdelhamid, Thoraya M., El Sharkawy, Nahla M., Elnahass, Yasser H., Elgammal, Mossaad, Abdelfattah, Rafaat M, Eid, Salem, Ghaleb, Fayek M., Kamel, Azza M.
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Elsevier B.V 01.09.2013; Cairo University, National Cancer Institute
• Subjects: Adolescent; Adult; Adult ALL; Disease-Free Survival; Egypt - epidemiology; Female; Flowcytometry; Humans; Leukemia; Male; Middle Aged; Minimal residual disease; Neoplasm, Residual; Patients; Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality; Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy; Prognosis; Risk Factors; Survival Analysis; Young Adult; المرضى; سرطان الدم; Egypt; Flowcytometry; Minimal residual disease; Adult ALL
• ISSN: 1110-0362; 1687-9996; 2589-0409
• DOI: 10.1016/j.jnci.2013.05.004

Minimal residual disease (MRD) studies in adult acute lymphoblastic leukemia (ALL) give highly significant prognostic information superior to other standard criteria as age, gender and total leucocytic count (TLC) in distinguishing patients at high and low risk of relapse. We aimed to determine the value of MRD monitoring by flowcytometry (FCM) in predicting outcome in adult Precursor ALL patients. 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). Study included 57 adult ALL patients (44 males and 13 females) with a median age of 22years (18–49). DFS showed no significant difference with age, gender and initial TLC (p=0.838, 0.888 and 0.743, respectively). Cumulative DFS at 2years was 34% for B-lineage ALL (n: 35) and 57% for T-lineage ALL (n: 18) (p=0.057). Cumulative DFS at 2years was 7% for MRD1 positive (high risk, HR) versus 57% for MRD1 negative patients (Low risk, LR) (p<0.001). Cumulative DFS at 2years was 29% for HR patients (n: 26) versus 55% for LR (n: 27) according to GMALL classification (p=0.064). Cumulative OS did not differ according to age, gender and TLC (p=0.526, 0.594 and 0.513, respectively). Cumulative OS at 2years was 36% for B ALL (n: 39) versus 77% for TALL (n: 18) (p=0.016) and was 49% for Philadelphia chromosome (Ph) negative patients versus 0% for Ph-positive patients (p<0.001). Regarding MRD1, OS at 2years was 18% for MRD1 HR (n: 17) versus 65% for MRD1 LR (n: 38) (p<0.001). OS was 35% for high-risk patients (n: 30) and 62% for low-risk patients (n: 27) classified according to GMALL risk stratification (p=0.017). 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.