AI Article Synopsis

  • The treatment of adults with Philadelphia-negative acute lymphoblastic leukaemia (ALL) hinges on various risk factors, with minimal residual disease (MRD) emerging as a significant indicator of relapse risk.
  • A study analyzing 132 patients showed that an MRD level greater than or equal to 0.1% after treatment induction is a strong predictor for relapse, particularly for both standard and high-risk groups.
  • Combining MRD status with traditional risk assessments can help identify low-risk patients, suggesting that MRD evaluation post-induction should be integrated into treatment planning for adult ALL.

Article Abstract

The treatment of adults with Philadelphia-negative acute lymphoblastic leukaemia (ALL) depends on the presence of risk factors including age, white blood cell count, immunophenotype and time to complete remission. In recent years, status of minimal residual disease (MRD) has been postulated as an additional risk criterion. This study prospectively evaluated the significance of MRD. Patients were treated with a uniform Polish Adult Leukemia Group (PALG) 4-2002 protocol. MRD status was assessed after induction and consolidation by multiparametric flow cytometry. Out of 132 patients included (age, 17-60 years), 116 patients were suitable for analysis. MRD level >/=0.1% of bone marrow cells after induction was found to be a strong and independent predictor for relapse in the whole study population (P < 0.0001), as well as in the standard risk (SR, P = 0.0003) and high-risk (P = 0.008) groups. The impact of MRD after consolidation on outcome was not significant. The combination of MRD status with conventional risk stratification system identified a subgroup of patients allocated to the SR group with MRD <0.1% after induction who had a very low risk of relapse of 9% at 3 years as opposed to 71% in the remaining subjects (P = 0.001). We conclude that MRD evaluation after induction should be considered with conventional risk criteria for treatment decisions in adult ALL.

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Source
http://dx.doi.org/10.1111/j.1365-2141.2008.07185.xDOI Listing

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