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The study aimed at evaluating the prevalence of IDH1 and IDH2 mutations in Indian AML patients and ascertaining its impact on the treatment outcomes. A retrospective cohort study was carried out from 2019 to 2023, where 100 AML patients were tested for the presence of IDH mutations. The clinical and laboratory parameters of the patients were analysed and compared with an age matched control group of IDH1/2 negative AML patients. Treatment outcome was also compared between the groups and overall survival (OS) was calculated with subgroup analysis of intensive chemotherapy vs. Hypomethylating agent (HMA) and Venetoclax therapy in the IDH1/2 mutated group. A total of 26 (26%) patients tested positive for IDH mutations (19 for IDH1 and, 6 for IDH2, and one for both). Coexistence of IDH mutation with NPM1 mutation was observed in 7 patients (26.9%) while 3 patients (11.5%) showed positivity for FLT3 mutations. Sixteen patients opted for therapy at our centre; of which 62.5% received intensive chemotherapy and 37.5% received hypomethylating agents and venetoclax. Relapse was seen in 31.2% vs. 18.7% and mean OS was 1.6 years vs. 2.5 years in the IDHmut vs. the control arm. Overall mortality was 37.5% in IDHmut as compared to 25% in the control arm. The study thus higlights that IDHmut AML patients had a higher relapse and poorer survival outcome when compared to the IDH negative control group.
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http://dx.doi.org/10.1007/s12288-024-01855-2 | DOI Listing |
Blood Adv
September 2025
AP-HP, Hôpital Saint Louis and University of Paris, INSERM U944 and THEMA insitute, Paris, France.
Germline DDX41 mutations (DDX41mut) are identified in approximately 5% of myeloid malignancies with excess of blasts, representing a distinct MDS/AML entity. The disease is associated with better outcomes compared to DDX41 wild-type (DDX41WT), but patients who do not undergo allogeneic hematopoietic stem cell transplantation (HSCT) may experience late relapse. Due to the recent identification of DDX41mut, data on post-HSCT outcomes remain limited.
View Article and Find Full Text PDFBackground: Nucleophosmin 1 (NPM1) mutations represent one of the most frequent genetic alterations in acute myeloid leukemia (AML). However, the prognostic significance of concurrent molecular abnormalities and clinical features in NPM1-mutated AML remains to be fully elucidated.
Methods: We retrospectively analyzed 73 adult AML patients with NPM1 mutations.
Background: This study aimed to identify the diagnostic and prognostic ability of serum miR-411-3p in patients with acute myeloid leukemia (AML).
Methods: Blood samples were collected from 60 AML patients and 60 healthy controls to measure serum miR-411-3p and thereafter discuss its potential clinical value.
Results: Serum miR-411-3p was decreased in AML patients and was even lower in those with M4/M5 subtypes or high white blood cell count or adverse cytogenetic risk.
Background: Angioimmunoblastic T-cell lymphoma (AITL) is a rare and aggressive form of peripheral T-cell lymphoma, accounting for 1 - 2% of non-Hodgkin lymphomas. Diagnosis is challenging, and there is no established standard first-line treatment. This case report highlights a rare progression from AITL to therapy-related acute myeloid leukemia (AML-pCT) following cytotoxic chemotherapy.
View Article and Find Full Text PDFBackground: This study aims to gain further insights into the characteristics of the rare subtype of acute myeloid leukemia (AML) with BCR∷ABL by analyzing laboratory detection results of various gene mutations, such as NPM1.
Methods: Laboratory detection results of multiple gene missense mutations, including NPM1, were analyzed in a case of primary AML with BCR∷ABL.
Results: The patient exhibited morphological features of acute leukemia in the bone marrow.