Figure 2.
Figure 2. Persistence of BCR/ABL+ cells with CFC and LTCIC capacity in CML patients in CCR with imatinib mesylate treatment. CD34+ cells were plated in CFC (committed progenitor, n = 15) and LTCIC (primitive progenitor, n = 13) assays, and the resulting colonies were harvested and analyzed for BCR/ABL+ cells by FISH as shown in the bottom half of the figure. Results from the first sample studied are shown and represent the percentage of BCR/ABL+ cells in colonies resulting from CFC and LTCIC assays. The percentage of CD34+ cells (n = 15) that were BCR/ABL+ is shown for comparison. A percentage less than or equal to 6% of cells with a BCR/ABL fusion signal is considered within background limits and is shown by the horizontal line. CD34+ cells from 4 patients, CFCs from 4 patients, and LTCICs from 3 patients were BCR/ABL– by FISH.

Persistence ofBCR/ABL+cells with CFC and LTCIC capacity in CML patients in CCR with imatinib mesylate treatment. CD34+ cells were plated in CFC (committed progenitor, n = 15) and LTCIC (primitive progenitor, n = 13) assays, and the resulting colonies were harvested and analyzed for BCR/ABL+ cells by FISH as shown in the bottom half of the figure. Results from the first sample studied are shown and represent the percentage of BCR/ABL+ cells in colonies resulting from CFC and LTCIC assays. The percentage of CD34+ cells (n = 15) that were BCR/ABL+ is shown for comparison. A percentage less than or equal to 6% of cells with a BCR/ABL fusion signal is considered within background limits and is shown by the horizontal line. CD34+ cells from 4 patients, CFCs from 4 patients, and LTCICs from 3 patients were BCR/ABL by FISH.

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