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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2020 Feb 14;26(6):1137–1143. doi: 10.1016/j.bbmt.2020.02.006

Table 3.

A Cox regression model was fitted for all eligible patients to evaluate the impact of main effect on overall survival since 30-d post relapse, while controlling for other risk factors.

Cox Model Estimates (N=215)
Parameter N (N Event) HR (%95 CI) P-value Overall P-value
Disease status prior to HCT
 CP1 (reference) 69 (22) 1.00 <.001
 AP 35 (16) 1.60 (0.83, 3.09) 0.157
 BP 25 (21) 5.51 (2.93, 10.37) <.001
 CP2+ 52 (31) 2.64 (1.46, 4.79) 0.001
 Hematologic CR 34 (18) 1.90 (0.94, 3.86) 0.075
Main effect
 TKI + DLI (reference) 48 (24) 1.00 0.011
 DLI but no TKI 39 (24) 2.28 (1.23, 4.24) 0.009
 TKI but no DLI 128 (60) 1.06 (0.65, 1.72) 0.813
Post-HCT maintenance TKI Therapy
 Yes (reference) 58 (20) 1.00 0.007
 No 157 (88) 2.00 (1.21, 3.31) 0.007
Year of Transplant
 2002–2007 (reference) 110 (49) 1.00 0.026
 2008–2014 105 (59) 1.68 (1.06, 2.64) 0.026
*

In addition, the other variables we considered but were not selected are age group, gender, country, KPS, ATG/Alemtuzumab, time from transplant to relapse, TBI given, conditioning intensity, recipient CMV status, donor type, graft source, GVHD Prophylaxis and GVHD prior to the landmark analysis.