Table 1.

Univariate analysis comparing ICH patients in the derivation cohort who survived or died within 30 days of ICH diagnosis

Alive (n = 45)Dead (n = 25)P*
Demographic features 
 Age, range, y 29 (4-57) 37 (12-54) .038 
 Male sex 27 (60%) 21 (84%) .102 
Clinical features related to allo-HSCT 
 Primary disease   .655 
  AML 13 (28.9%) 7 (28.0%)  
  ALL 15 (33.3%) 8 (32.0%)  
  CML 2 (4.4%) 0 (0.0%)  
  MDS 6 (13.3%) 6 (24.0%)  
  AA 5 (11.1%) 1 (4.0%)  
  Others 4 (8.9%) 3 (12.0%)  
 Disease status   .022 
  Standard risk 38 (84.4%) 15 (60.0%)  
  High risk 7 (15.6%) 10 (40.0%)  
 Time from diagnosis to HSCT, range, d 227 (29-5992) 208 (75-1750) .637 
 No. of transplantation   .091 
  1 44 (97.8%) 22 (88.0%)  
  2 1 (2.2%) 3 (12.0%)  
 Type of transplantation   .031 
  Haplo-identical 40 (88.9%) 17 (68.0%)  
  HLA match 5 (11.1%) 8 (32.0%)  
 Donor–patient sex   .611 
  Match 26 (57.8%) 16 (64.0%)  
  Mismatch 19 (42.2%) 9 (36.0%)  
 ABO type   .372 
  Match 23 (51.1%) 10 (40.0%)  
  Mismatch 22 (48.9%) 15 (60.0%)  
 Stem cell source   .463 
  PB + BM 39 (86.7%) 20 (80.0%)  
  PB 6 (13.3%) 5 (20.0%)  
 WBC engraftment, range, d 14 (10-22) 14 (9-27) [n = 24] .909 
 Delayed PLT engraftment (> 30 d) 22 (48.9%) 12 (48.0%) .943 
 History of acute GVHD   .638 
  None 16 (35.6%) 7 (28.0%)  
  I-II 22 (48.9%) 12 (48.0%)  
  III-IV 7 (15.6%) 6 (24.0%)  
 History of chronic GVHD   .592 
  None 38 (84.4%) 20 (80.0%)  
  Limited 1 (2.2%) 0 (0.0%)  
  Extensive 6 (13.3%) 5 (20.0%)  
 History of TMA 4 (8.9%) 5 (20.0%) .183 
 History of DIC 3 (6.7%) 4 (16.0%) .212 
 Systemic infection 35 (77.8%) 20 (80.0%) .828 
Clinical features related to ICH 
 Time from HSCT to ICH, range, d 131 (14-1472) 119 (21-944) .686 
 Bleeding site   .505 
  IP 27 (60.0%) 18 (72.0%)  
  SAH 5 (11.1%) 4 (16.0%)  
  SD 5 (11.1%) 2 (8.0%)  
  ED 2 (4.4%) 0 (0.0%)  
  Multiple 6 (13.3%) 1 (4.0%)  
 IVH 4 (8.9%) 6 (24.0%) .083 
 Preexisting CNS events 20 (44.4%) 7 (28.0%) .176 
 Hypertension 6 (13.3%) 4 (16.0%) .760 
 Diabetes 1 (2.2%) 2 (8.0%) .253 
Laboratory features 
 WBC count (×109/L) 3.44 (1.31-14.11) 2.11 (0.20-18.15) .025 
 RBC count (×1012/L) 2.77 (1.57-4.53) 2.28 (1.73-3.36) .007 
 Hemoglobin, g/dL 90.20 (2.29-152.00) 73.00 (63.00-113.00) .008 
 Platelet count (×109/L) 55.0 (9.0-249.0) 24.0 (2.0-74.0) <.001 
 PT, s 11.80 (9.30-17.50) 13.60 (10.00-20.20) .045 
 INR 1.07 (0.87-1.54) 1.22 (0.96-1.84) .033 
 Fibrinogen, mg/dL 304.0 (101.0-550.0) 319.0 (106.0-598.0) .408 
 LDH, U/L 341.0 (155.0-1416.0) 507.0 (118.0-1500.0) .038 
 Urea, mmol/L 5.22 (1.12-21.12) 7.78 (3.14-90.18) .006 
 Creatinine, µmol/L 51.0 (21.0-137.0) 70.0 (22.0-143.0) .013 
 Albumin, g/L 36.5 (28.6-45.0) 31.9 (21.3-47.1) .001 
 Bilirubin, µmol/L 16.2 (2.0-341.1) 40.6 (6.9-652.3) .001 
 Cholesterol, mmol/L 4.49 (1.88-8.97) [n = 40] 3.78 (1.14-16.44) [n = 24] .560 
 Triglyceride, mmol/L 2.75 (1.29-9.89) [n = 40] 2.50 (0.83-11.32) [n = 24] .501 
Alive (n = 45)Dead (n = 25)P*
Demographic features 
 Age, range, y 29 (4-57) 37 (12-54) .038 
 Male sex 27 (60%) 21 (84%) .102 
Clinical features related to allo-HSCT 
 Primary disease   .655 
  AML 13 (28.9%) 7 (28.0%)  
  ALL 15 (33.3%) 8 (32.0%)  
  CML 2 (4.4%) 0 (0.0%)  
  MDS 6 (13.3%) 6 (24.0%)  
  AA 5 (11.1%) 1 (4.0%)  
  Others 4 (8.9%) 3 (12.0%)  
 Disease status   .022 
  Standard risk 38 (84.4%) 15 (60.0%)  
  High risk 7 (15.6%) 10 (40.0%)  
 Time from diagnosis to HSCT, range, d 227 (29-5992) 208 (75-1750) .637 
 No. of transplantation   .091 
  1 44 (97.8%) 22 (88.0%)  
  2 1 (2.2%) 3 (12.0%)  
 Type of transplantation   .031 
  Haplo-identical 40 (88.9%) 17 (68.0%)  
  HLA match 5 (11.1%) 8 (32.0%)  
 Donor–patient sex   .611 
  Match 26 (57.8%) 16 (64.0%)  
  Mismatch 19 (42.2%) 9 (36.0%)  
 ABO type   .372 
  Match 23 (51.1%) 10 (40.0%)  
  Mismatch 22 (48.9%) 15 (60.0%)  
 Stem cell source   .463 
  PB + BM 39 (86.7%) 20 (80.0%)  
  PB 6 (13.3%) 5 (20.0%)  
 WBC engraftment, range, d 14 (10-22) 14 (9-27) [n = 24] .909 
 Delayed PLT engraftment (> 30 d) 22 (48.9%) 12 (48.0%) .943 
 History of acute GVHD   .638 
  None 16 (35.6%) 7 (28.0%)  
  I-II 22 (48.9%) 12 (48.0%)  
  III-IV 7 (15.6%) 6 (24.0%)  
 History of chronic GVHD   .592 
  None 38 (84.4%) 20 (80.0%)  
  Limited 1 (2.2%) 0 (0.0%)  
  Extensive 6 (13.3%) 5 (20.0%)  
 History of TMA 4 (8.9%) 5 (20.0%) .183 
 History of DIC 3 (6.7%) 4 (16.0%) .212 
 Systemic infection 35 (77.8%) 20 (80.0%) .828 
Clinical features related to ICH 
 Time from HSCT to ICH, range, d 131 (14-1472) 119 (21-944) .686 
 Bleeding site   .505 
  IP 27 (60.0%) 18 (72.0%)  
  SAH 5 (11.1%) 4 (16.0%)  
  SD 5 (11.1%) 2 (8.0%)  
  ED 2 (4.4%) 0 (0.0%)  
  Multiple 6 (13.3%) 1 (4.0%)  
 IVH 4 (8.9%) 6 (24.0%) .083 
 Preexisting CNS events 20 (44.4%) 7 (28.0%) .176 
 Hypertension 6 (13.3%) 4 (16.0%) .760 
 Diabetes 1 (2.2%) 2 (8.0%) .253 
Laboratory features 
 WBC count (×109/L) 3.44 (1.31-14.11) 2.11 (0.20-18.15) .025 
 RBC count (×1012/L) 2.77 (1.57-4.53) 2.28 (1.73-3.36) .007 
 Hemoglobin, g/dL 90.20 (2.29-152.00) 73.00 (63.00-113.00) .008 
 Platelet count (×109/L) 55.0 (9.0-249.0) 24.0 (2.0-74.0) <.001 
 PT, s 11.80 (9.30-17.50) 13.60 (10.00-20.20) .045 
 INR 1.07 (0.87-1.54) 1.22 (0.96-1.84) .033 
 Fibrinogen, mg/dL 304.0 (101.0-550.0) 319.0 (106.0-598.0) .408 
 LDH, U/L 341.0 (155.0-1416.0) 507.0 (118.0-1500.0) .038 
 Urea, mmol/L 5.22 (1.12-21.12) 7.78 (3.14-90.18) .006 
 Creatinine, µmol/L 51.0 (21.0-137.0) 70.0 (22.0-143.0) .013 
 Albumin, g/L 36.5 (28.6-45.0) 31.9 (21.3-47.1) .001 
 Bilirubin, µmol/L 16.2 (2.0-341.1) 40.6 (6.9-652.3) .001 
 Cholesterol, mmol/L 4.49 (1.88-8.97) [n = 40] 3.78 (1.14-16.44) [n = 24] .560 
 Triglyceride, mmol/L 2.75 (1.29-9.89) [n = 40] 2.50 (0.83-11.32) [n = 24] .501 

Laboratory data proximate to the time of ICH diagnosis are reported. AA, aplastic anemia; ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; BM, bone marrow; CML , chronic myelogenous leukemia; DIC, disseminated intravascular coagulation; HLA, human leukocyte antigen; MDS, myelodysplastic syndrome; PB, peripheral blood; PLT, platelet; PT, prothrombin time; RBC, red blood cell; TMA, thrombotic microangiopathy.

*

For continuous variables, median and range are displayed, and the nonparametric Mann-Whitney test was used for calculating the P value. For categorical variables, number and percentage of total patients are displayed, and the χ2 test was used for significance calculation.

Others include lymphoma, acute mixed-lineage leukemia, lymphoma, chronic lymphocytic leukemia, and Epstein-Barr virus–associated hemophagocytic lymphohistiocytosis.

CNS diseases diagnosed before ICH diagnosis, including CNS leukemia, CNS infections, reversible posterior leukoencephalopathy syndrome, and ischemic stroke.

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