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Articles

Clinicopathologic and genetic evaluation of B-lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 (iAMP21) in adult patients

, , , , , , & ORCID Icon show all
Pages 3200-3207 | Received 29 Mar 2022, Accepted 03 Aug 2022, Published online: 22 Aug 2022
 

Abstract

Intrachromosomal amplification of chromosome 21 (iAMP21) defines a rare provisional entity of B-cell acute lymphoblastic leukemia (B-ALL) in the current WHO classification and has been described as specific for pediatric patients with a median age at diagnosis of 9–10 years. We report two adult cases of B-ALL with iAMP21, one 31-year-old woman and one 40-year-old man, identified by karyotyping and next generation sequencing (NGS), with fluorescence in situ hybridization (FISH) pattern meeting diagnostic criteria for iAMP21. Both patients were treated on high-risk chemotherapeutic regimen followed by stem cell transplant. In contrast to reported high relapse rate within the first three years in pediatric population, our adult patients are alive in remission, with the interval from diagnosis to last follow up of 2.95 and 3.96 years. Our cases illustrate the importance of screening for iAMP21 in adult population when ETV6-RUNX1 FISH testing is not routinely performed for adult patients.

Acknowledgments

The authors thank the staff of the cytogenetics and molecular diagnostics laboratories for their technical expertise.

Author contributions

Contribution: M.S. undertook concept and design; S.D., J.A. and J.M. provided study materials; M.S. and T.Z. collected and assembled data; M.S. and T.Z. undertook data analysis and clinical interpretation; M.S. and T.Z. wrote the manuscript; X.L., J.G., A.B., and P.J. reviewed the manuscript and provided constructive critics, and all authors edited the article and provided final approval.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was partially supported by National Institute of Diabetes and Digestive and Kidney Disease (NIDDK) grant R01DK124220 (P.J.), National Heart, Lung, and Blood Institute (NHLBI) grant R01HL148012 (P.J.), R01HL150729 (P.J.).

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