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Related Experiment Video

Updated: Jul 4, 2026

Constructing and Visualizing Models using Mime-based Machine-learning Framework
06:19

Constructing and Visualizing Models using Mime-based Machine-learning Framework

Published on: July 22, 2025

Risk Prognostication After Hypomethylating Agents Combined With Venetoclax in AML: The PRISM Risk Model.

Curtis A Lachowiez1, Joshua F Zeidner2, Jad Othman3,4,5

  • 1Oregon Health and Science University, Portland, OR.

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|July 2, 2026
PubMed
Summary
This summary is machine-generated.

A new Prognostic Risk Integration for Survival Modeling (PRISM) score accurately predicts survival for acute myeloid leukemia (AML) patients on venetoclax-based therapy. This tool improves risk stratification beyond current methods for personalized treatment decisions.

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Last Updated: Jul 4, 2026

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06:19

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Published on: July 22, 2025

Area of Science:

  • Hematology
  • Oncology
  • Genomics

Background:

  • Risk stratification for acute myeloid leukemia (AML) patients receiving lower-intensity venetoclax-based therapy is currently suboptimal.
  • There is a need for improved prognostic models that integrate diverse patient data.

Purpose of the Study:

  • To develop and validate a prognostic model, the Prognostic Risk Integration for Survival Modeling (PRISM) score, for AML patients treated with hypomethylating agents plus venetoclax (HMA + VEN).
  • To integrate clinical, cytogenetic, and molecular features for enhanced survival risk stratification.

Main Methods:

  • A multinational dataset of 2,092 adults with newly diagnosed AML treated with HMA + VEN was assembled.
  • Elastic Net and Ridge regression were used to develop the PRISM score, which was validated in internal and external cohorts.
  • The PRISM score was compared against the existing 4-gene classifier.

Main Results:

  • The PRISM model integrated 17 clinical and genomic variables and showed a linear association with overall survival (OS).
  • PRISM-3 risk categories (low, moderate, high) consistently stratified survival across all validation cohorts (P < .001).
  • PRISM-3 demonstrated significantly better discrimination than the 4-gene classifier in validation cohorts (C-index 0.63-0.65 vs. 0.59-0.61; P < .05).

Conclusions:

  • PRISM is a validated prognostic model that enhances survival risk stratification for AML patients on HMA + VEN therapy.
  • The PRISM score supports individualized, risk-adapted clinical decision-making.
  • The PRISM model is publicly accessible at prism-aml.com for clinical use.