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. 2016 Jan 4;127(10):1269–1275. doi: 10.1182/blood-2015-10-674242

Table 3.

Factors predictive of EFS including the type of BCR-ABL transcripts

N Events Log-rank HR 95% CI HR P value
Univariate*
 TKI type
  Imatinib 400 69 21 0.013
  Imatinib 800 199 38 0.58 (0.34-0.99) .045
  Dasatinib 104 7 0.28 (0.12-0.67) .004
  Nilotinib 108 11 0.45 (0.22-0.95) .035
 Transcript type
  e13a2 199 40 0.091
  e14a2 196 24 0.57 (0.35-0.95) .032
  Both 85 13 0.74 (0.40-1.39) .355
 Splenomegaly (≥10 cm)
  No 453 68 0.012
  Yes 27 9 2.38 (1.19-4.77) .014
Multivariate
 TKI type
  Imatinib 400 69 21
  Imatinib 800 199 38 0.55 (0.32-0.94) .030
  Dasatinib 104 7 0.28 (0.12-0.67) .004
  Nilotinib 108 11 0.44 (0.21-0.92) .029
 Transcript type
  e13a2 199 40
  e14a2 196 24 0.59 (0.36-0.98) .043
  Both 85 13 0.80 (0.43-1.50) .489
 Splenomegaly (≥10 cm)
  No 453 68
  Yes 27 9 2.18 (1.07-4.44) .031
*

White blood cell count, age, Sokal score, hemoglobin, platelet count, peripheral blood blasts, and serum lactate dehydrogenase are not significant (P = not significant; data not shown).

Imatinib 400 is the reference for comparison with the other 3 TKI modalities.

e13a2 is the reference for comparison with e14a2 and both (coexpressed transcripts).