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Comprehensive Protocol to Sample and Process Bone Marrow for Measuring Measurable Residual Disease and Leukemic Stem Cells in Acute Myeloid Leukemia
Published on: March 5, 2018
Current survival measures reliably reflect modern sequential treatment in CML: correlation with prognostic
Tomas Pavlik1, Eva Janousova, Jiri Mayer
1Institute of Biostatistics and Analyses, Masaryk University, Brno, Czech Republic.
Early BCR-ABL1 transcript levels in chronic myeloid leukemia (CML) patients treated with imatinib predict long-term outcomes. Patients with low BCR-ABL1 transcripts at 3 months show better survival, aiding early risk stratification.
Area of Science:
- Hematology
- Oncology
- Clinical Research
Background:
- Chronic myeloid leukemia (CML) management relies on prognostic scores and response monitoring.
- Imatinib therapy has revolutionized CML treatment, necessitating refined prognostic tools.
Purpose of the Study:
- To evaluate the prognostic value of established scores (Sokal, Euro, EUTOS) and early treatment response markers.
- To assess the predictive power of BCR-ABL1 transcript levels and complete cytogenetic response (CCgR) at 3 months for survival outcomes.
Main Methods:
- Analysis of data from 723 chronic phase CML patients.
- Comparison of prognostic scores, BCR-ABL1 levels, and CCgR achievement.
- Evaluation using current cumulative incidence (CCI), current leukemia-free survival (CLFS), and overall survival.
Main Results:
- BCR-ABL1 transcript levels at 3 months significantly predicted 5-year CCI, with levels ≤10% associated with 94.3% CCI versus >10% with 57.1% (P=0.005).
- Early BCR-ABL1 levels effectively identified patients with poorer outcomes on imatinib.
- CLFS was not significantly impacted by the evaluated prognostic factors once CCgR was achieved.
Conclusions:
- BCR-ABL1 transcript levels at 3 months are a crucial early predictor of imatinib therapy response and long-term survival in CML.
- Achieving CCgR indicates a favorable prognosis, regardless of initial risk stratification.
- This finding supports early identification of high-risk CML patients for intensified monitoring or alternative therapies.
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