| Literature DB >> 29966470 |
M Kathiravan1, Minu Singh1, Prateek Bhatia1, Amita Trehan1, Neelam Varma2, Manupdesh Singh Sachdeva2, Deepak Bansal1, Richa Jain1, Shano Naseem2.
Abstract
Considering conflicting data on CDKN2A/B deletion in ALL, this study to assess its prognostic significance as an independent marker in a total of 96 pediatric B and T-ALL cases was planned. The overall frequency of CDKN2A/B deletion was 44% (n = 43) with 36% (30/83) in B-ALL and 100% (13/13) in T-ALL. CDKN2A/B deletion was significantly associated with high WBC count (p = .002) and National Cancer Institute risk (p = .01) in B-ALL. Importantly, CDKN2A/B deletion cases had poor EFS of 42% at 28 months compared to EFS of 90% in rest (p = .0004). Further, relapse free survival was only 56% for cases with CDKN2A/B deletions (n = 25), compared to 100% in control group (p = .001). Moreover, CDKN2A/B deletion was the only risk factor associated with early relapse (p = .01) compared to IKZF1 deletion (p = .73) or occurrence of BCR-ABL1 fusion transcript (p = .26). Thus our study data highlights potential prognostic role of CDKN2A/B deletions in early disease stratification in pediatric B-ALL.Entities:
Keywords: Acute lymphoblastic leukemia; BCP-ALL; CDKN2A/B; MLPA; copy number abnormality; minimal residual disease
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Year: 2018 PMID: 29966470 DOI: 10.1080/10428194.2018.1482542
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022