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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2019 May 31;25(9):1744–1755. doi: 10.1016/j.bbmt.2019.05.019

Table 3:

Multivariate Outcomes in Myeloablative Related and Unrelated Donor Transplant

Tac+MTX CSA+MMF CSA+MTX Tac+MMF
Matched Related donor (MRD) HR (95% CI), P-value
aGVHD grade 2–4 Ref (1.00) 1.65 (1.24–2.20) P<0.001 1.17 (1.04–1.33) P=0.010 1.05 (0.83–1.34) P=0.661
aGVHD grade 3–4 1.92 (1.31–2.83) P<0.001 1.13 (0.92–1.37) P=0.283 1.19 (0.85–1.66) P=0.319
cGVHD* <5 months 1.34 (0.83–2.17) P=0.233 1.41 (1.20–1.67) P<0.001 1.28 (0.94-.74) P=0.119
cGVHD* ≥5 months 0.56 (0.34–0.95) P=0.030 0.74 (0.65–0.85) P<0.001 0.92 (0.71–1.19) P=0.512
TRM* <5 months 4.03 (2.61–6.23) P<0.001 2.29 (1.78–2.95) P<0.001 1.17 (0.71–1.94) P=0.537
TRM* ≥5 months 1.38 (0.78–2.44) P=0.275 0.83 (0.67–1.03) P=0.095 0.90 (0.59–1.36) P=0.609
Relapse 1.43 (1.05–1.93) P=0.022 0.86 (0.74–0.98) P=0.029 0.92 (0.73–1.14) P=0.444
OS* <5 months 2.31 (1.73–3.09) P<0.001 1.27 (1.10–1.48) P=0.002 1.05 (0.81–1.37) P=0.704
OS* ≥5 months 0.94 (0.62–1.43) P=0.767 0.74 (0.64–0.87) P<0.001 0.92 (0.70–1.20) P=0.530
Unrelated donor (URD) HR (95% CI), P-value
aGVHD, grade 2–4 Ref (1.00) 1.49 (1.08–2.07) P=0.016 1.00 (0.90–1.12) P=0.961 1.14 (0.99–1.32) P=0.066
aGVHD, grade 3–4 2.31 (1.57–3.42) P<0.001 1.02 (0.87–1.20) P=0.806 1.26 (1.02–1.56) P=0.030
cGVHD* <4 months 1.54 (0.79–2.98) P=0.203 1.62 (1.35–1.93) P<0.001 1.34 (1.04–1.73) P=0.022
cGVHD* ≥4 months 0.92 (0.52–1.63) P=0.779 0.85 (0.74–0.98) P=0.025 1.47 (1.24–1.75) P<0.001
TRM* <4 months 3.09 (2.00–4.77) P<0.001 1.24 (1.02–1.51) P=0.030 1.02 (0.77–1.36) P=0.896
TRM* ≥4 months 0.89 (0.42–1.90) P=0.763 1.00 (0.84–1.20) P=0.979 1.45 (1.16–1.81) P=0.001
Relapse 0.81 (0.50–1.32) P=0.398 0.97 (0.85–1.12) P=0.699 0.93 (0.78–1.12) P=0.449
OS* <4 months 2.36 (1.67–3.35) P<0.001 1.23 (1.08–1.41) P=0.002 1.20 (1.01–1.44) P=0.044
OS* ≥4 months 1.10 (0.64–1.89) P=0.730 0.91 (0.79–1.05) P=0.221 1.34 (1.12–1.61) P=0.001
*

Given differential effects over time (non-proportional hazards), models were constructed breaking the post-transplant time course into 2 periods, using the maximized partial likelihood method to find the most appropriate breakpoint.