NUP98 rearranged acute myeloid leukemia: An initial experience

Background: Nucleoporin 98 ( NUP98 ) rearranged acute myeloid leukemia (AML) is a distinct category in the World Health Organization classification and is classified as an adverse risk in the 2022 European Leukemia NET Risk Stratification. These are distinct subtypes of AML, affecting both pediatric and adult AML cases, with dismal outcomes despite transplantation. Due to the rarity of occurrence, limited evidence is available, except for anecdotal cases and small series, and none yet from India. Methods: This is a single-center experience with 16 NUP98 rearranged AML from India. Clinicopathologic, immunophenotypic, and genomic details were retrieved from the medical record archives of the hospital. Results: Sixteen patients with NUP98 rearranged AML were included in the study, of which 14 were adults and two were pediatric. The median age of the adult AML patients was 27 years (range: 21–34 years). The majority of cases were M5 (7/16, 44%), followed by M1 and M4 in 4 (31%) and 5 (25%) cases, respectively. Among the 16 patients, all had nuclear receptor binding SET domain protein 1 ( NSD1) as their partner. Twelve (75%) patients harbored concurrent Fms-like tyrosine kinase 3 internal tandem duplication ( FLT 3-ITD) mutations and 56% had a pathogenic missense or truncating variant in Wilms tumor 1 ( WT1) gene. Other common concomitant genomic alterations included ten-eleven translocation 2 ( TET2) (25%), Proto-Oncogene, GTPase , ( NRAS) (19%), neurofibromin 1 ( NF1) (13%), DNA methyltransferase 3 alpha ( DNMT3A) (13%), and cohesin complex component (RAD21 ) (6%) in descending order. The median time to detection of NUP98 rearrangement was 3.3 days, and hence, induction was based on genomic findings. None of the patients achieved complete response (CR) and none underwent transplantation. Conclusion: This is a single-center experience of NUP98 rearranged AML from India, possibly the largest reported so far from the peninsula. NUP98 rearranged AML have been described to follow an aggressive and tumultuous disease course with non-achievement of CR despite intensive chemotherapy.

Authors

Institutions

Publication Details

Journal
International Journal of Molecular and Immuno Oncology
Published
2025-11-24
DOI
https://doi.org/10.25259/ijmio_3_2025
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

NUP98 rearranged acute myeloid leukemia: An initial experience

Swati Bhayana, Sunisha Arora, Sohini Chakraborty, Anusha Swaminathan et al.
International Journal of Molecular and Immuno Oncology
Acute Myeloid Leukemia Research
article

NUP98 rearranged acute myeloid leukemia: An initial experience

Swati Bhayana, Sunisha Arora, Sohini Chakraborty, Anusha Swaminathan, Nikhil Kumar, Arun Danewa, Chitresh Yadav, Shrinidhi Nathany, Neha Rastogi, Rahul Bhargava, Vikas Dua
article en

Abstract

Background: Nucleoporin 98 ( NUP98 ) rearranged acute myeloid leukemia (AML) is a distinct category in the World Health Organization classification and is classified as an adverse risk in the 2022 European Leukemia NET Risk Stratification. These are distinct subtypes of AML, affecting both pediatric and adult AML cases, with dismal outcomes despite transplantation. Due to the rarity of occurrence, limited evidence is available, except for anecdotal cases and small series, and none yet from India. Methods: This is a single-center experience with 16 NUP98 rearranged AML from India. Clinicopathologic, immunophenotypic, and genomic details were retrieved from the medical record archives of the hospital. Results: Sixteen patients with NUP98 rearranged AML were included in the study, of which 14 were adults and two were pediatric. The median age of the adult AML patients was 27 years (range: 21–34 years). The majority of cases were M5 (7/16, 44%), followed by M1 and M4 in 4 (31%) and 5 (25%) cases, respectively. Among the 16 patients, all had nuclear receptor binding SET domain protein 1 ( NSD1) as their partner. Twelve (75%) patients harbored concurrent Fms-like tyrosine kinase 3 internal tandem duplication ( FLT 3-ITD) mutations and 56% had a pathogenic missense or truncating variant in Wilms tumor 1 ( WT1) gene. Other common concomitant genomic alterations included ten-eleven translocation 2 ( TET2) (25%), Proto-Oncogene, GTPase , ( NRAS) (19%), neurofibromin 1 ( NF1) (13%), DNA methyltransferase 3 alpha ( DNMT3A) (13%), and cohesin complex component (RAD21 ) (6%) in descending order. The median time to detection of NUP98 rearrangement was 3.3 days, and hence, induction was based on genomic findings. None of the patients achieved complete response (CR) and none underwent transplantation. Conclusion: This is a single-center experience of NUP98 rearranged AML from India, possibly the largest reported so far from the peninsula. NUP98 rearranged AML have been described to follow an aggressive and tumultuous disease course with non-achievement of CR despite intensive chemotherapy.

International Journal of Molecular and Immuno OncologyVol. 10
Fortis Memorial Research Institute (IN)
Openalex Percentile: Top 53%
Acute Myeloid Leukemia Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.