MicroRNA-92a as a marker of treatment response and survival in adult acute myeloid leukemia patients

Leuk Lymphoma. 2020 Oct;61(10):2475-2481. doi: 10.1080/10428194.2020.1775218. Epub 2020 Jun 14.

Abstract

This prospective study assessed circulating miR-92a levels in acute myeloid leukemia (AML) at diagnosis and after induction therapy and followed patients for a maximum of 30 months. The study included 63 consecutive adult AML patients. Circulating miR-92a levels were assessed using real-time polymerase chain reaction (RT-PCR). There was significant rise of miR-92a expression after induction (median (range): 0.297 (0.001-3.438)) in comparison to the reported levels at diagnosis (median (range): 0.236 (0.001-3.305)). Post-induction levels of miR-92a are significantly higher in patients who achieved CR in comparison to patients without CR (median (range): 0.408 (0.017-3.438) vs. 0.01 (0.001-1.010), p<.001). Cox hazard regression analysis identified miR-92a as a significant predictor of OS and DFS in univariate and multivariate analyses. In conclusion, baseline circulating miR-92a in AML patients may be a useful prognostic marker of treatment response and survival over 2.5 years follow up.

Keywords: Acute myeloid leukemia; miR-92a; micro-RNAs.

MeSH terms

  • Adult
  • Biomarkers, Tumor / genetics
  • Humans
  • Leukemia, Myeloid, Acute* / diagnosis
  • Leukemia, Myeloid, Acute* / drug therapy
  • Leukemia, Myeloid, Acute* / genetics
  • MicroRNAs* / genetics
  • Prognosis
  • Prospective Studies
  • Real-Time Polymerase Chain Reaction

Substances

  • Biomarkers, Tumor
  • MicroRNAs