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. 2021 Jan 6;56(6):1325–1334. doi: 10.1038/s41409-020-01191-9

Table 2.

Patient characteristics.

All N = 59 2yrS N = 43 2yrD N = 16 P value
Age [years]a 56 (19–78) 54 (19–75) 61 (31–78) 0.063
Sex [n]b
  Male:female 40:19 (68:32) 27:16 (63:37) 13:3 (81:19)
Disease [n]b 0.715
  Myeloidc 46 (78) 34 (79) 12 (75)
  Lymphaticd 15 (22) 9 (21) 4 (25)
Remission at alloHCT [n]b 0.591
  CR/chronic phase 27 (46) 23 (54) 4 (25)
  Not in CR 32 (54) 20 (46) 12 (75)
HLA-mismatch [n]b 0.650
  None (10/10) 36 (61) 27 (62.8) 9 (56.3)
  Mismatch (≤9/10) 23 (39) 16 (37.2) 7 (43.8)
Gender donor: recipient 0.964
  Female:male 15 (25) 11 (26) 4 (25)
  All other 44 (75) 32 (74) 12 (75)
Conditioning [n]b 0.168
  Myeloablative 15 (25.4) 12 (27.9) 3 (18.8)
   TT/BU/FLU 12 (20.3) 9 (21) 3 (18.8)
   TBI/VP16 1 (1.7) 1 (2.3) 0
   TBI/TT 1 (1.7) 1 (2.3) 0
   FLU/BU 4 1 (1.7) 1 (2.3) 0
  Reduced intensity 44 (74.6) 31 (72.1) 13 (81.2)
   FLU/BCNU/MEL 14 (23.7) 10 (23.3) 4 (25)
   FLU/BCNU/TT 1 (1.7) 1 (2.3) 0
   FLU/TT/MEL 28 (47.5) 20 (46.5) 8 (50)
   FLU/TT mod. + TREOS 1 (1.7) 0 1 (6.2)
 Time diagnosis to alloHCT [days]a 214 (51–2569) 187 (51–2569) 550 (85–1702) 0.068
 KPS [%]a 90 (70–100) 90 (70–100) 90 (70–100) 0.375
HCT-CI [n]b 0.550
  Low risk (0) 17 (29) 13 (30) 4 (25)
  Intermediate risk (1–2) 20 (34) 15 (35) 5 (31)
  High risk (≥3) 22 (37) 15 (35) 7 (44)
EBMT score [n]b 0.768
  Low risk (0–2) 7 (12) 5 (12) 2 (13)
  Intermediate risk (3–5) 36 (61) 27 (63) 9 (56)
  High risk (6–7) 16 (27) 11 (25) 5 (31)
 rDRI [n]b 0.139
  Low risk 1 (1.7) 1 (2.3) 0
  Intermediate risk 32 (54.2) 24 (55.8) 8 (50)
  High risk 18 (30.5) 16 (37.2) 2 (12.5)
  Very high risk 8 (13.6) 2 (4.7) 6 (37.5)
 rPAM score [score]a 23.9 (12.1–42.1) 22.9 (12.1–33.5) 25 (16.4–42.1) 0.192
Acute GVHD [n]b 0.687
  None 29 (49.2) 21 (48.8) 8 (50)
  Grade I 11 (18.6) 9 (20.9) 2 (12.5)
  Grade II 6 (10.2) 6 (14) 0
  Grade III 11 (18.6) 5 (11.6) 6 (37.5)
  Grade IV 2 (3.4) 2 (4.7) 0
Chronic GVHD [n]b 0.022*
  None 32 (54.2) 24 (55.8) 8 (50)
  Limited 8 (13.6) 8 (18.6) 0
  Extensive 11 (18.6) 11 (25.6) 0
  Missing datae 8 (13.6) 0 8 (50)
Causes of death [n]b
  Alive 43 (72.9) 43 (100) 0
  Relapse/progression disease 4 (6.8) 0 4 (25)
  Organ failure 1 (1.7 0 1 (6.3)
  GVHD 5 (8.5) 0 5 (31.3)
  Infection 6 (10.2) 0 6 (37.5)

2yrsS 2-year survivor, 2yrsD 2-year decedents, HLA human leukocyte antigen, TT thiotepa, BU busulfan, FLU fludarabine, TBI total body irradiation, VP16 etoposide, BCNU camustin, MEL melphalan, TREOS treosulfan, ALL acute lymphocytic leukemia, CR complete remission, KPS Karnofsky Performance Scale, HCT-CI Hematopoietic Cell Transplantation-specific Comorbidity Index, EBMT European Society for Blood and Marrow Transplantation, rDRI revised Disease Risk Index, rPAM revised Pretransplant Assessment of Mortality, GVHD graft-versus-host disease.

aMedian (range).

bpercentage of N (%).

cIncludes: acute myeloid leukemia, chronic myeloid leukemia, chronicle myelomonocytic leukemia, osteomyelofibrosis and myelodysplastic syndrome.

dIncludes: hodgkin disease, non-hodgkin lymphoma, multiple myeloma, chronic lymphatic leukemia, acute lymphatic leukemia.

ePatients had died by the time chronic GVHD can occur (100 days after alloHCT).