Table 1 Patient Demographics and Baseline Clinical Characteristics.

From: Disease progression, hospital readmissions, and clinical outcomes for patients with steroid-refractory acute graft-versus-host disease: A multicenter, retrospective study

 

Steroid-Refractory Acute GVHD (n = 113)

Steroid-Dependent Acute GVHD (n = 55)

Total Population(N = 168)

Age, y, mean (SD)

53.6 (13.2)

57.3 (10.5)

54.8 (12.5)

Age groups, y, n (%)

<18

3 (2.7)

0

3 (1.8)

18–40

19 (16.8)

4 (7.3)

23 (13.7)

>40

91 (80.5)

51 (92.7)

142 (84.5)

Male, n (%)

69 (61.1)

38 (69.1)

107 (63.7)

Race, n (%)

White

96 (85.0)

50 (90.9)

146 (86.9)

Black

4 (3.5)

3 (5.5)

7 (4.2)

Other

5 (4.4)

1 (1.8)

6 (3.6)

Unknown

7 (6.2)

0

7 (4.2)

Insurance status at transplant,* n (%)

Private or group health insurance

77 (68.1)

38 (69.1)

115 (68.5)

Medicare

32 (28.3)

16 (29.1)

48 (28.6)

Medicaid

10 (8.8)

1 (1.8)

11 (6.5)

Other

7 (6.2)

3 (5.5)

10 (6.0)

Underlying malignancy, n (%)

Acute myeloid leukemia

40 (35.4)

19 (34.5)

59 (35.1)

Myelodysplastic syndrome

22 (19.5)

10 (18.2)

32 (19.0)

Acute lymphoid leukemia

18 (15.9)

9 (16.4)

27 (16.1)

Chronic myeloid leukemia

8 (7.1)

4 (7.3)

12 (7.1)

Multiple myeloma

8 (7.1)

3 (5.5)

11 (6.5)

Non-Hodgkin lymphoma

6 (5.3)

5 (9.1)

11 (6.5)

Other

11 (9.7)

5 (9.1)

16 (9.5)

Remission status of primary disease at transplant, n (%)

Complete remission

74 (65.5)

33 (60.0)

107 (63.7)

Stable disease

16 (14.2)

9 (16.4)

25 (14.9)

Partial remission

11 (9.7)

7 (12.7)

18 (10.7)

Progressive disease

5 (4.4)

4 (7.3)

9 (5.4)

Not assessed

7 (6.2)

2 (3.6)

9 (5.4)

HCT Comorbidity Index at transplant, n (%)

Low risk (0)

16 (14.2)

7 (12.7)

23 (13.7)

Intermediate risk (1–2)

31 (27.4)

18 (32.7)

49 (29.2)

High risk (≥3)

63 (55.8)

26 (47.3)

89 (53.0)

Unknown

3 (2.7)

4 (7.3)

7 (4.2)

Year of transplant, n (%)

2014

29 (25.7)

14 (25.5)

43 (25.6)

2015

63 (55.8)

29 (52.7)

92 (54.8)

2016

21 (18.6)

12 (21.8)

33 (19.6)

Transplant setting, n (%)

Inpatient

99 (87.6)

54 (98.2)

153 (91.1)

Outpatient

11 (9.7)

1 (1.8)

12 (7.1)

Graft source, n (%)

Peripheral blood

81 (71.7)

43 (78.2)

124 (73.8)

Umbilical cord blood

16 (14.2)

6 (10.9)

22 (13.1)

Bone marrow

12 (10.6)

6 (10.9)

18 (10.7)

Unknown

4 (3.5)

0

4 (2.4)

HLA donor type, n (%)

Matched, unrelated

61 (54.0)

25 (45.5)

86 (51.2)

Matched, related

31 (27.4)

8 (14.5)

39 (23.2)

Mismatched, unrelated

16 (14.2)

8 (14.5)

24 (14.3)

Mismatched, related

4 (3.5)

14 (25.5)

18 (10.7)

Unknown

1 (0.9)

0

1 (0.6)

Transplant conditioning regimen, n (%)

Myeloablative

58 (51.3)

14 (25.5)

72 (42.9)

Reduced intensity

27 (23.9)

26 (47.3)

53 (31.5)

Nonmyeloablative

28 (24.8)

15 (27.3)

43 (25.6)

GVHD prophylaxis therapy, n (%)

Tacrolimus-based

74 (71.8)

34 (61.8)

108 (74.0)

Methotrexate

50 (48.5)

17 (30.9)

67 (45.9)

Mycophenolate

44 (42.7)

23 (41.8)

67 (45.9)

Cyclosporine-based

28 (27.2)

7 (12.7)

35 (24.0)

Antithymocyte globulin

13 (12.6)

8 (14.5)

21 (14.4)

High-dose cyclophosphamide (posttransplant)

1 (1.0)

9 (16.4)

10 (6.8)

Sirolimus

1 (1.0)

5 (9.1)

6 (4.1)

Other

2 (1.9)

7 (12.7)

9 (6.2)

Duration of follow-up since transplant,§ d, mean (SD)

504.9 (469.3)

497.0 (472.0)

502.3 (468.8)

  1. GVHD, graft-versus-host disease; HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen.
  2. *Insurance status was not available for 1 patient (steroid refractory); 18 patients (10.7%; steroid refractory, n = 15; steroid dependent, n = 3) had multiple types of insurance coverage; 1 patient (0.6%; steroid refractory) was uninsured.
  3. Transplant setting was unknown for 3 patients (steroid refractory). Patients could receive >1 type of prophylactic therapy.
  4. §Patients were followed for ≥2 years from transplant until death or end of observation, whichever occurred first.