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Detection of a GLIS3 fusion in an infant with AML refractory to chemotherapy

Title: Detection of a GLIS3 fusion in an infant with AML refractory to chemotherapy
Authors: Smith, Stephen M; Lee, Alex; Tong, Schuyler; Leung, Stanley; Hongo, Henry; Rivera, Jose; Sweet-Cordero, Alejandro; Michlitsch, Jennifer; Stieglitz, Elliot
Source: Molecular Case Studies, vol 8, iss 5
Publisher Information: eScholarship, University of California
Publication Year: 2022
Collection: University of California: eScholarship
Subject Terms: Biomedical and Clinical Sciences; Cardiovascular Medicine and Haematology; Oncology and Carcinogenesis; Stem Cell Research; Human Genome; Pediatric; Hematology; Childhood Leukemia; Cancer Genomics; Rare Diseases; Biotechnology; Orphan Drug; Transplantation; Stem Cell Research - Nonembryonic - Human; Genetics; Pediatric Cancer; Cancer; Good Health and Well Being; acute myeloid leukemia; hematological neoplasm; Pharmacology and pharmaceutical sciences
Subject Geographic: mcs.a006220
Description: Infants diagnosed with acute myeloid leukemia (AML) frequently harbor cytogenetically cryptic fusions involving KMT2A, NUP98 or GLIS2. Those with AML driven specifically by CBFA2T3::GLIS2 fusions have a dismal prognosis and are currently risk-stratified to receive hematopoietic stem cell transplantation (HSCT) in first remission. Here we report an infant with AML who was refractory to multiple lines of chemotherapy but lacked an identifiable fusion despite cytogenetic, fluorescence in situ hybridization (FISH) and targeted next generation sequencing (NGS) testing. Research-grade RNASeq from a relapse sample revealed in-frame CBFA2T3::GLIS3 and GLIS3::CBFA2T3 fusions. A patient-derived xenograft (PDX) generated from this patient has a short latency period and represents a strategy to test novel agents that may be effective in this aggressive subtype of AML. This report describes the first case of AML with a CBFA2T3::GLIS3 fusion and highlights the need for unbiased NGS testing including RNASeq at diagnosis, as patients with CBFA2T3::GLIS3 fusions should be considered for HSCT in first remission.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: qt82d0n4h0; https://escholarship.org/uc/item/82d0n4h0; https://escholarship.org/content/qt82d0n4h0/qt82d0n4h0.pdf
DOI: 10.1101/mcs.a006220
Availability: https://escholarship.org/uc/item/82d0n4h0; https://escholarship.org/content/qt82d0n4h0/qt82d0n4h0.pdf; https://doi.org/10.1101/mcs.a006220
Rights: CC-BY-NC
Accession Number: edsbas.A0073E5
Database: BASE