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. 2018 Dec 20;33(3):686–695. doi: 10.1038/s41375-018-0302-y

Table 3.

Impact of risk factors in different time periods after alloHCT

Time-period/population 0–2 years, all patients 2–10 years, 2-year LM population 5–10 years, 5-year LM population
Risk factor HR (95% CI) p-value HR (95% CI) p-value HR (95% CI) p-value
Patient sex
 Male 1 1 1
 Female 0.9 (0.9–1.0) 0.2 0.9 (0.7–1.0) 0.1 0.7 (0.5–1.0) 0.04
Age at alloHCT (per decade) 1.1 (1.1–1.2) <0.001 1.2 (1.1–1.3) <0.001 1.3 (1.1–1.6) 0.001
Year of alloHCT (per 5 years) 0.8 (0.8–0.9) <0.001 1.2 (1.0–1.4) 0.02 1.4 (1.0–2.0) 0.06
MDS subtype
 MDS w/o EB 1 1 1
 MDS with EB 1.2 (1.1–1.4) <0.001 1.9 (1.4–2.4) <0.001 2.3 (1.3–4.0) 0.003
 sAML 1.4 (1.2–1.5) <0.001 2.1 (1.6–2.8) <0.001 2.0 (1.2–3.6) 0.01
Donor match
 HLA-identical sibling 1 1 1
 Other donor 1.2 (1.1–1.3) <0.001 1.1 (0.9–1.3) 0.3 1.1 (0.8–1.6) 0.5
Conditioning
 Myeloablative 1 1 1
 Reduced intensity 0.9 (0.9–1.0) 0.1 0.8 (0.7–1.0) 0.02 0.8 (0.5–1.1) 0.2
 Previous relapse NA 5.1 (4.2–6.1) <0.001 5.0 (3.5–7.2) <0.001

Cox models for excess mortality in defined time periods for patients alive at different landmarks.

LM landmark, HR hazard ratio, CI confidence interval, NA not applicable. Patients with missing information for conditioning were kept in the analysis in a separate category (not shown)