Clinical Outcome and Molecular Profile in Patients with DDX41 Mutation Hot-Spots

<b>Background/Objectives:</b><i>DDX41</i>, DEAD-box RNA helicase 41 gene located on chromosome 5q25.3, is one of the most mutated genes in patients with germline predisposition to myeloid neoplasms. Germline and somatic mutations often have different locations and patterns of mutation, with some hotspots displaying diversity based on ethnicity. We aimed to explore clinical outcomes in patients with various <i>DDX41</i> hot-spot mutations. <b>Methods</b>: This was a retrospective study of patients at Mayo Clinic with <i>DDX41</i> mutation identified through Next Generation Sequencing (NGS) between 2018 and 2024. We completed unadjusted comparisons using continuous or categorical variables, and survival rates were assessed using the Kaplan-Meier method and cox regression analysis. <b>Results</b>: Overall survival appears to be higher in those with p.M1| when compared to p.Asp140GlyFs*2 and p.Arg525His, with comparable survival between p.Arg525His and p.Asp140GlyFs*2. Among males with p.M1| who underwent bone marrow transplant, those who underwent bone marrow transplant appeared to have lower survival rates, although not statistically significant. Our study was limited by a small sample size, therefore limiting our ability to reach significance. <b>Conclusions</b>: Our findings suggest potential implications for clinical outcomes based on <i>DDX41</i> mutation hot-spots.

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Journal
Hematology Reports
Published
2025-05-08
DOI
https://doi.org/10.3390/hematolrep17030026
Citations
1
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
1.82
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article

Clinical Outcome and Molecular Profile in Patients with DDX41 Mutation Hot-Spots

Antoine N. Saliba, Cecilia Y. Arana Yi, Aref Al‐Kali, Abhishek Avinash Mangaonkar et al.
1 citations
Hematology Reports
Genetics and Neurodevelopmental Disorders
1.82
article

Clinical Outcome and Molecular Profile in Patients with DDX41 Mutation Hot-Spots

Antoine N. Saliba, Cecilia Y. Arana Yi, Aref Al‐Kali, Abhishek Avinash Mangaonkar, Mithun Vinod Shah, Dragan Jevremović, Rong He, James M. Foran, Nadia Toumeh, Hassan B. Alkhateeb, Mehrdad Hefazi, Mrinal M. Patnaik, Ahmad Nanaa, William J. Hogan, Yazan Jabban, David S. Viswanatha
article en
1 citations

Abstract

<b>Background/Objectives:</b><i>DDX41</i>, DEAD-box RNA helicase 41 gene located on chromosome 5q25.3, is one of the most mutated genes in patients with germline predisposition to myeloid neoplasms. Germline and somatic mutations often have different locations and patterns of mutation, with some hotspots displaying diversity based on ethnicity. We aimed to explore clinical outcomes in patients with various <i>DDX41</i> hot-spot mutations. <b>Methods</b>: This was a retrospective study of patients at Mayo Clinic with <i>DDX41</i> mutation identified through Next Generation Sequencing (NGS) between 2018 and 2024. We completed unadjusted comparisons using continuous or categorical variables, and survival rates were assessed using the Kaplan-Meier method and cox regression analysis. <b>Results</b>: Overall survival appears to be higher in those with p.M1| when compared to p.Asp140GlyFs*2 and p.Arg525His, with comparable survival between p.Arg525His and p.Asp140GlyFs*2. Among males with p.M1| who underwent bone marrow transplant, those who underwent bone marrow transplant appeared to have lower survival rates, although not statistically significant. Our study was limited by a small sample size, therefore limiting our ability to reach significance. <b>Conclusions</b>: Our findings suggest potential implications for clinical outcomes based on <i>DDX41</i> mutation hot-spots.

Hematology ReportsVol. 17(3)
Mayo Clinic (US), John H. Stroger, Jr. Hospital of Cook County (US), WinnMed (US), Mayo Clinic in Arizona (US), Mayo Clinic in Florida (US)
Openalex Percentile: Top 16%
Genetics and Neurodevelopmental Disorders
1.82
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