Evidence map›Paper›PMID 40889038›Full record

ArticleBlood research2025

RUNX1 alterations and survival outcomes in AML: leukocyte dynamics and thrombocytosis insights from an Indonesian cohort.

Ikhwan Rinaldi, Elly Yanah Arwanih, Kevin Winston, Farida Farah Adibah, Yuli Maulidiya Shufiyani, Rafida Amalia Salma

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Article in Blood research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ikhwan RinaldiDivision of Hematology and Medical Oncology, Faculty of Medicine, Department of Internal Medicine, Cipto Mangunkusumo National General Hospital, Universitas Indonesia, Jakarta, Indonesia. ikhwanrinaldi@gmail.com.
Elly Yanah ArwanihDivision of Hematology and Medical Oncology, Faculty of Medicine, Department of Internal Medicine, Cipto Mangunkusumo National General Hospital, Universitas Indonesia, Jakarta, Indonesia.
Kevin WinstonFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Farida Farah AdibahFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Yuli Maulidiya ShufiyaniFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Rafida Amalia SalmaFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.

Funding

Universitas Indonesia NKB-168/UN2.RST/HKP.05.00/2022
6 · The paper itself

Abstract

purposeAcute myeloid leukemia (AML) is a heterogeneous hematologic malignancy with varying prognostic outcomes. This study aimed to observe potential patterns or association between RUNX1 mutations and clinical features of AML patients, including hyperleukocytosis, thrombocytosis, and 12-month survival outcomes.

methodsA prospective cohort study involving 38 patients diagnosed with de novo AML was conducted at the RSUPN Dr. Cipto Mangunkusumo and Dharmais Cancer Hospital between 2022 and 2023. Patients were followed up for 12 months, and RUNX1 mutations within exons 4, 5, 7, and 8 were detected using polymerase chain reaction (PCR)-Sanger sequencing.

resultsThis study found RUNX1 mutations in 18.4% of the patients, predominantly in exons 4 and 5. Significant differences in leukocyte counts were observed between patients with and without RUNX1 mutations (p = 0.004). However, no significant association was observed between RUNX1 mutations and hyperleukocytosis or thrombocytosis. Survival analysis revealed that Individuals with RUNX1 mutations had notably lower survival rates (hazard ratio = 6.024, p = 0.014, 95% CI = 1.436-25.279).

conclusionIn conclusion, RUNX1 mutations may be associated with poor survival outcomes in Indonesian AML patients. Further studies involving larger cohorts and comprehensive molecular analyses are required to confirm the prognostic significance of these findings.

Indexed as

AMLCohort studyHyperleukocytosisPrognosisRUNX1 mutation analysis

Identifiers

PMID40889038
PMCPMC12401826

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