Table 1

Characteristics associated with the first BCR-ABL1 rise

Clinical context at the time of the BCR-ABL1 riseNo. of patientsNo. of patients with a riseDoubling timeFirst fold riseMeasurement interval, dBCR-ABL1% IS before the riseBCR-ABL1% IS after the rise
Relapse directly into BC 12 12 9.0 (6.1-17.6) 71 (18-631) 68 (29-84) 0.64 (0.13-9.9) 81 (19.6-175) 
BCR-ABL1 mutation and CP maintained 30 29 48 (17.3-143) 3.6 (2.1-19) 85 (37-305) 0.16 (0.003-7.2) 1.2 (0.03-64) 
Imatinib discontinuation after ≥ 2 y of CMR 36 17 9.0 (6.9-26.5) 9.5 (2.2-22.1) 33 (14-63) 0.006* (0.001-0.03) 0.07 (0.007-0.48) 
Complete dose interruption 12 12 9.4 (4.2-17.6) 10.5 (2.5-2400) 28 (7-93) 0.08 (0.01-4.7) 4.0 (0.15-48) 
Partial dose interruption 34 27 37 (11.6-104) 7.6 (2.1-234) 84 (36-339) 0.21 (0.01-9.9) 3.3 (0.05-68) 
Clinical context at the time of the BCR-ABL1 riseNo. of patientsNo. of patients with a riseDoubling timeFirst fold riseMeasurement interval, dBCR-ABL1% IS before the riseBCR-ABL1% IS after the rise
Relapse directly into BC 12 12 9.0 (6.1-17.6) 71 (18-631) 68 (29-84) 0.64 (0.13-9.9) 81 (19.6-175) 
BCR-ABL1 mutation and CP maintained 30 29 48 (17.3-143) 3.6 (2.1-19) 85 (37-305) 0.16 (0.003-7.2) 1.2 (0.03-64) 
Imatinib discontinuation after ≥ 2 y of CMR 36 17 9.0 (6.9-26.5) 9.5 (2.2-22.1) 33 (14-63) 0.006* (0.001-0.03) 0.07 (0.007-0.48) 
Complete dose interruption 12 12 9.4 (4.2-17.6) 10.5 (2.5-2400) 28 (7-93) 0.08 (0.01-4.7) 4.0 (0.15-48) 
Partial dose interruption 34 27 37 (11.6-104) 7.6 (2.1-234) 84 (36-339) 0.21 (0.01-9.9) 3.3 (0.05-68) 

Data are median (range).

*

The BCR-ABL1 values for these patients represent the first positive value before the rise.

The 34 patients had 43 dose interruptions. One of the 34 patients also had a complete interruption and overlaps both the complete and partial interruption groups (45 patients in total with at least 1 interruption).

A rise occurred for 31 of the 43 partial interruptions, and the median doubling time was calculated for these 31 intervals.

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