[HTML][HTML] Biologic and therapeutic implications of genomic alterations in acute lymphoblastic leukemia

I Iacobucci, S Kimura, CG Mullighan - Journal of clinical medicine, 2021 - mdpi.com
Acute lymphoblastic leukemia (ALL) is the most successful paradigm of how risk-adapted
therapy and detailed understanding of the genetic alterations driving leukemogenesis and …

The genomic landscape of pediatric acute lymphoblastic leukemia and precision medicine opportunities

TH Tran, SP Hunger - Seminars in cancer biology, 2022 - Elsevier
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer and constitutes
approximately 25% of cancer diagnoses among children under the age of 15 (Howlader et …

[HTML][HTML] Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domains

HS Kuehn, IS Sakovich, JE Niemela… - The Journal of …, 2024 - Am Soc Clin Investig
AIOLOS, also known as IKZF3, is a transcription factor that is highly expressed in the
lymphoid lineage and is critical for lymphocyte differentiation and development. Here, we …

[HTML][HTML] Molecular profiling and clinical implications of patients with acute myeloid leukemia and extramedullary manifestations

JN Eckardt, F Stölzel, D Kunadt, C Röllig… - Journal of Hematology & …, 2022 - Springer
Background Extramedullary manifestations (EM) are rare in acute myeloid leukemia (AML)
and their impact on clinical outcomes is controversially discussed. Methods We …

Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001

TH Tran, S Langlois, C Meloche, M Caron… - Blood …, 2022 - ashpublications.org
The molecular hallmark of childhood acute lymphoblastic leukemia (ALL) is characterized by
recurrent, prognostic genetic alterations, many of which are cryptic by conventional …

IKAROS-associated diseases in 2020: genotypes, phenotypes, and outcomes in primary immune deficiency/inborn errors of immunity

HS Kuehn, CJ Nunes-Santos… - Journal of Clinical …, 2021 - Springer
IKAROS, encoded by IKZF1, is a zinc finger transcription factor and a critical regulator of
hematopoiesis. Mutations in IKZF1 have been implicated in immune deficiency …

[HTML][HTML] Mutated IKZF1 is an independent marker of adverse risk in acute myeloid leukemia

JN Eckardt, S Stasik, C Röllig, A Petzold, T Sauer… - Leukemia, 2023 - nature.com
Genetic lesions of IKZF1 are frequent events and well-established markers of adverse risk in
acute lymphoblastic leukemia. However, their function in the pathophysiology and impact on …

Prognostic significance of IKZF1 deletions and IKZF1plus profile in children with B‐cell precursor acute lymphoblastic leukemia treated according to the ALL‐IC BFM …

M Braun, A Pastorczak, Ł Sędek, J Taha… - Hematological …, 2022 - Wiley Online Library
The strongest predictors of outcome in pediatric B‐cell precursor acute lymphoblastic
leukemia (BCP‐ALL) are minimal residual disease (MRD) and specific molecular …

[HTML][HTML] Prediction of complete remission and survival in acute myeloid leukemia using supervised machine learning

JN Eckardt, C Röllig, K Metzeler, M Kramer… - …, 2023 - ncbi.nlm.nih.gov
Achievement of complete remission signifies a crucial milestone in the therapy of acute
myeloid leukemia (AML) while refractory disease is associated with dismal outcomes …

Allogeneic hematopoietic stem cell transplantation overcome the poor prognosis of patients with IKZF1plus CD20–a very high-risk subtype in B-cell acute …

B Tang, Z Cai, Z Wang, D Lin, X He, Q Li… - Bone Marrow …, 2022 - nature.com
Genetic deletions of IKZF1 (IKZF1 del) and IKZF1 del plus other mutations (IKZF1 plus) have
been identified in B-cell acute lymphoblastic leukemia (B-ALL) with a poor prognosis …