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. Author manuscript; available in PMC: 2017 Nov 28.
Published in final edited form as: Biol Blood Marrow Transplant. 2016 Apr 7;22(7):1337–1340. doi: 10.1016/j.bbmt.2016.03.032

Table 1.

Demographics and Disease Characteristics for HSCT Recipients with TMA

Treated with Eculizumab (n = 39) Not Treated (n = 30) P
Median age, yr (IQR)     5.3 (3.6–11.1)     8.3 (3.3–13.8)   .56
Male      17 (56.7%)      26 (66.7%)   .46
Race 1.00
 White      22 (73.3%)      29 (74.4%)
 Non-white        8 (26.7%)      10 (25.6%)
Diagnosis   .41
 Bone marrow failure        9 (30%)      15 (38.5%)
 Immune deficiency      13 (43.3%)      17 (43.5%)
 Malignancy        4 (13.3%)        6 (15.4%)
 Benign hematology, genetic/metabolic        4 (13.3%)        1 (2.6%)
Donor type   .031
 Related        5 (16.7%)      10 (25.6%)
 Unrelated      20 (66.7%)      29 (74.4%)
 Autologous        5 (16.7%)        0 (0%)
Stem cell source   .52
 Bone marrow      24 (80%)      26 (66.7%)
 Peripheral blood        5 (16.7%)      10 (25.6%)
 Cord blood        1 (3.3%)        3 (7.7%)
HLA match   .59
 Matched 16/25 (64%)      28 (72%)
 Mismatched   9/25 (36%)      11 (28%)
Conditioning regimen   .63
 Myeloablative      18 (60%)      20 (51.3%)
 Reduced intensity      12 (40%)      19 (48.7%)
Calcineurin inhibitor for GVDH prophylaxis 25/25 (100%) 37/39 (95%)   .52
GVHD, grades III–IV 15/25 (60%) 10/39 (26%)   .1
TMA diagnosis, median days after HSCT (IQR)      28 (13.8–48.5)      32 (17–43)   .41
Meningococcal meningitis        0 (0%)        0 (0%) 1.00
Bacteremia      10 (33%)      11 (28%)   .79
Fungemia        2 (3.3%)        0 (0%)   .19
Cytomegalovirus viremia        7 (23%)        7 (18%)   .76
Epstein-Barr virus viremia      11 (36.6%)        4 (10.3%)   .02

IQR indicates interquartile range.