A long-term survivor of congenital KMT2A-R B-lymphoblastic leukemia with persistently positive bone marrow MRD and multiple CNS relapses

Here we describe the case of an infant incidentally diagnosed with congenital KMT2A-rearranged (KMT2A-r) B-cell ALL on Day of Life 4. He received the first dose of intrathecal methotrexate on DOL 5, and induction systemic therapy on DOL 6. He demonstrated morphologic remission at the end of induction but had positive bone marrow. Minimal residual disease (MRD) was 1.4%. He experienced isolated CNS disease after consolidation and immunotherapy. At 8 months of age he underwent hematopoietic stem cell transplantation (HSCT). At 14 months of age he had medullary and CNS relapse, and at 16 months of age underwent CD19 CAR-T therapy. At 6 years of age he remains in remission with tolerable developmental delays and a good quality of life.

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Publication Details

Journal
BMC Pediatrics
Published
2025-02-28
DOI
https://doi.org/10.1186/s12887-024-05093-3
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
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article

A long-term survivor of congenital KMT2A-R B-lymphoblastic leukemia with persistently positive bone marrow MRD and multiple CNS relapses

Sazan Rasul, Taxiarhia J Arabatzis, Biren Desai, Girmay H. Tekle-Yohannes et al.
BMC Pediatrics
Acute Lymphoblastic Leukemia research
article

A long-term survivor of congenital KMT2A-R B-lymphoblastic leukemia with persistently positive bone marrow MRD and multiple CNS relapses

Sazan Rasul, Taxiarhia J Arabatzis, Biren Desai, Girmay H. Tekle-Yohannes, Michal A. Miller, Sandra Baril
article en

Abstract

Here we describe the case of an infant incidentally diagnosed with congenital KMT2A-rearranged (KMT2A-r) B-cell ALL on Day of Life 4. He received the first dose of intrathecal methotrexate on DOL 5, and induction systemic therapy on DOL 6. He demonstrated morphologic remission at the end of induction but had positive bone marrow. Minimal residual disease (MRD) was 1.4%. He experienced isolated CNS disease after consolidation and immunotherapy. At 8 months of age he underwent hematopoietic stem cell transplantation (HSCT). At 14 months of age he had medullary and CNS relapse, and at 16 months of age underwent CD19 CAR-T therapy. At 6 years of age he remains in remission with tolerable developmental delays and a good quality of life.

BMC PediatricsVol. 25(1)
Geisinger Medical Center (US)
Zero hunger
Openalex Percentile: Top 95%
Acute Lymphoblastic Leukemia research
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