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. Author manuscript; available in PMC: 2019 Mar 13.
Published in final edited form as: N Engl J Med. 2018 Sep 13;379(11):1028–1041. doi: 10.1056/NEJMoa1804714

Table 1.

Characteristics of the Patients at Initial Banking and Univariate Associations with Disease Progression.*

Variable All Patients (N = 86) Disease Progression (N = 35) No Disease Progression (N = 51) Disease Progression or Death (N = 60) Disease Progression Disease Progression or Death
Hazard Ratio (95% CI) P Value Hazard Ratio (95% CI) P Value
number of patients
Age at transplantation
 ≤60 yr 48 16 32 28 1.60 (0.83–3.08) 0.16 1.77 (1.05–2.97) 0.03
 >60 yr 38 19 19 32
IPSS-R score
 Very low 1 0 1 0 1.55 (1.04–2.30) 0.03 1.20 (0.92–1.57) 0.18
 Low 14 4 10 7
 Intermediate 13 3 10 9
 High 30 11 19 21
 Very high 19 12 7 15
 Missing data 9 5 4 8
Type of MDS
 Primary MDS 40 15 25 23
 Therapy-related MDS 25 11 14 18 1.19 (0.56–2.55) 0.65 1.48 (0.80–2.76) 0.22
 Secondary AML§ 21 9 12 19 1.08 (0.48–2.45) 0.85 1.98 (1.07–3.64) 0.03
Poor-risk gene or pathway
 RAS pathway 14 7 7 11 0.99 (0.51–1.92) 0.97 1.03 (0.54–2.00) 0.92
TP53 16 11 5 14 2.77 (1.41–5.44) 0.003 1.98 (1.09–3.63) 0.03
RUNX1 17 9 8 11 1.67 (0.79–3.56) 0.18 0.98 (0.51–1.88) 0.94
ASXL1 19 8 11 13 1.21 (0.55–2.64) 0.64 1.13 (0.61–2.10) 0.70
Conditioning regimen
 Myeloablative 50 15 35 34 0.40 (0.21–0.78) 0.007 0.73 (0.44–1.22) 0.23
 Reduced intensity 36 20 16 26
Day 30 variant allele frequency
 <0.5% 54 14 40 33 3.65 (1.88–7.09) <0.001 2.07 (1.24–3.46) 0.005
 ≥0.5% 32 21 11 27
Day 100 variant allele frequency in 58 patients
 <0.5% 40 9 31 21 6.04 (2.53–14.44) <0.001 2.46 (1.24–4.88) 0.01
 ≥0.5% 18 13 5 14
 NA 28 13 15 25
*

AML denotes acute myeloid leukemia, CI confidence interval, IPSS-R Revised International Prognostic Scoring System, MDS myelodysplastic syndrome, and NA not applicable.

The P value was calculated with the use of the Fine–Gray subdistribution hazard model and Gray’s test.

The P value was calculated with the use of the Cox proportional-hazards model and chi-square test.

§

Three patients received a diagnosis of therapy-related MDS but were found to have secondary AML before transplantation.

Not all patients had a mutation in one of these genes or pathways.