Figure 1.
Figure 1. Molecular monitoring can detect residual disease during many years of imatinib therapy. There are an estimated 1012 leukemic cells present at diagnosis of CML. The Philadelphia chromosome remains detectable by cytogenetic analysis until the leukemic cells decline by approximately 2 logs, which occurs at an estimated median of 6 months of imatinib. Therefore, the Philadelphia chromosome may never be detectable beyond 6 months in a substantial number of patients. However, we have found that BCR-ABL1 transcripts remain detectable in approximately half of the patients for 6 years and molecular monitoring continues to track the leukemic cell decline. The limit of detection of BCR-ABL1 by RQ-PCR is reached when the leukemic cells decline approximately 4.5-5 logs.

Molecular monitoring can detect residual disease during many years of imatinib therapy. There are an estimated 1012 leukemic cells present at diagnosis of CML. The Philadelphia chromosome remains detectable by cytogenetic analysis until the leukemic cells decline by approximately 2 logs, which occurs at an estimated median of 6 months of imatinib. Therefore, the Philadelphia chromosome may never be detectable beyond 6 months in a substantial number of patients. However, we have found that BCR-ABL1 transcripts remain detectable in approximately half of the patients for 6 years and molecular monitoring continues to track the leukemic cell decline. The limit of detection of BCR-ABL1 by RQ-PCR is reached when the leukemic cells decline approximately 4.5-5 logs.

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