Table 2.

ORR stratified by GVHD and patient characteristics

Itacitinib (n = 70)Systemic corticosteroids (n = 140)P value
GVHD characteristics    
GVHD grade    
Grade I 11/12 (92%) 19/25 (76%) .39 
Grade II/III 51/58 (90%) 101/115 (88%) 
Target organ involvement    
LGI ± Other 18/21 (86%) 36/42 (86%) 
Skin 1/2 ± UGI 15/16 (94%) 24/30 (80%) .39 
Skin 3 ± UGI 26/28 (93%) 51/56 (91%) 
UGI Only 3/5 (60%) 9/12 (75%) .60 
Days between HCT and start of systemic treatment     
≤40 23/26 (88%) 73/85 (86%) 
>40 39/44 (89%) 47/55 (85%) .77 
Patient characteristics    
Age, y    
<60 31/34 (91%) 66/77 (86%) .55 
≥60 31/36 (86%) 54/63 (86%) 
Donor type    
Related 23/28 (82%) 53/61 (87%) .54 
Unrelated 39/42 (93%) 67/79 (85%) .26 
Stem cell source    
Bone marrow 10/10 (100%) 33/35 (94%) 
Peripheral blood 52/60 (87%) 87/105 (83%) .66 
HLA match    
Matched 44/50 (88%) 77/90 (86%) .80 
Mismatched 4/5 (80%) 15/17 (88%) 
Haploidentical 14/15 (93%) 28/33 (85%) .65 
Conditioning intensity    
Myeloablative 29/33 (88%) 59/68 (87%) 
Non-myeloablative/reduced intensity 33/37 (89%) 61/72 (85%) .77 
GVHD prophylaxis    
CNI based 29/33 (88%) 71/82 (87%) 
Cyclophosphamide based 32/35 (91%) 47/55 (85%) .52 
Other 1/2 (50%) 2/3 (67%) 
Itacitinib (n = 70)Systemic corticosteroids (n = 140)P value
GVHD characteristics    
GVHD grade    
Grade I 11/12 (92%) 19/25 (76%) .39 
Grade II/III 51/58 (90%) 101/115 (88%) 
Target organ involvement    
LGI ± Other 18/21 (86%) 36/42 (86%) 
Skin 1/2 ± UGI 15/16 (94%) 24/30 (80%) .39 
Skin 3 ± UGI 26/28 (93%) 51/56 (91%) 
UGI Only 3/5 (60%) 9/12 (75%) .60 
Days between HCT and start of systemic treatment     
≤40 23/26 (88%) 73/85 (86%) 
>40 39/44 (89%) 47/55 (85%) .77 
Patient characteristics    
Age, y    
<60 31/34 (91%) 66/77 (86%) .55 
≥60 31/36 (86%) 54/63 (86%) 
Donor type    
Related 23/28 (82%) 53/61 (87%) .54 
Unrelated 39/42 (93%) 67/79 (85%) .26 
Stem cell source    
Bone marrow 10/10 (100%) 33/35 (94%) 
Peripheral blood 52/60 (87%) 87/105 (83%) .66 
HLA match    
Matched 44/50 (88%) 77/90 (86%) .80 
Mismatched 4/5 (80%) 15/17 (88%) 
Haploidentical 14/15 (93%) 28/33 (85%) .65 
Conditioning intensity    
Myeloablative 29/33 (88%) 59/68 (87%) 
Non-myeloablative/reduced intensity 33/37 (89%) 61/72 (85%) .77 
GVHD prophylaxis    
CNI based 29/33 (88%) 71/82 (87%) 
Cyclophosphamide based 32/35 (91%) 47/55 (85%) .52 
Other 1/2 (50%) 2/3 (67%) 

Denominators reflect the number of patients within each subgroup of each GVHD or patient characteristic. Numerators reflect the number of patients who had a complete response (CR) or partial response (PR) to treatment within each subgroup.

HCT, hematopoietic cell transplantation; LGI, lower gastrointestinal; UGI, upper gastrointestinal.

The median number of days from HCT to start of systemic treatment for the entire cohort (n = 210) was 40 days.

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