Baseline patient characteristics
Characteristic . | Number of patients . |
---|---|
Total patients, n | 17 |
Median age, y (range) | 62 (27-72) |
Sex, n (%) | |
Male | 9 (53) |
Female | 8 (47) |
Diagnosis, n | |
ALL | 2 |
AML | 3 |
CML | 1 |
HL | 3 |
MDS | 2 |
Myelofibrosis | 1 |
NHL | 5 |
Stem cell donor, n (%) | |
HLA-matched sibling | 7 (41) |
HLA-matched unrelated | 9 (53) |
HLA-mismatched unrelated | 1 (6) |
Stem cell source, n (%) | |
Peripheral blood | 16 (94) |
Bone marrow | 1 (6) |
Conditioning regimen intensity, n (%) | |
NMA/RIC | 10 (59) |
Myeloablative | 7 (41) |
cGVHD presentation, n (%) | |
De novo | 15 (88) |
Progressive | 2 (12) |
NIH cGVHD severity, n (%) | |
Mild | 1 (6) |
Moderate | 6 (35) |
Severe | 10 (59) |
End-organ involvement, n (%) | |
Skin | 16 (94) |
Musculoskeletal | 16 (94) |
Ocular | 9 (53) |
Oral | 9 (53) |
Urogenital | 6 (35) |
Lung | 3 (18) |
Gastrointestinal | 2 (12) |
Liver alone | 2 (12) |
Previous or concurrent systemic cGVHD therapies, n (%) | |
Corticosteroids | 16 (94) |
Rituximab | 7 (41) |
Extracorporeal photopheresis | 6 (35) |
Mycophenolate mofetil | 4 (24) |
Tacrolimus | 4 (24) |
Imatinib | 3 (18) |
Brentuximab vedotin | 2 (12) |
Interleukin-2 | 2 (12) |
Sirolimus | 2 (12) |
Median concurrent systemic cGVHD therapies at study enrollment, n (range) | 1 (0-3) |
Concurrent systemic cGVHD therapies at study enrollment, n (%) | |
Corticosteroids | 15 (88) |
Mycophenolate mofetil | 4 (24) |
Tacrolimus | 3 (18) |
Sirolimus | 2 (12) |
Median time from HCT to enrollment, months (range) | 40 (13-121) |
Median time from cGVHD diagnosis to enrollment, months (range) | 31 (1-101) |
Characteristic . | Number of patients . |
---|---|
Total patients, n | 17 |
Median age, y (range) | 62 (27-72) |
Sex, n (%) | |
Male | 9 (53) |
Female | 8 (47) |
Diagnosis, n | |
ALL | 2 |
AML | 3 |
CML | 1 |
HL | 3 |
MDS | 2 |
Myelofibrosis | 1 |
NHL | 5 |
Stem cell donor, n (%) | |
HLA-matched sibling | 7 (41) |
HLA-matched unrelated | 9 (53) |
HLA-mismatched unrelated | 1 (6) |
Stem cell source, n (%) | |
Peripheral blood | 16 (94) |
Bone marrow | 1 (6) |
Conditioning regimen intensity, n (%) | |
NMA/RIC | 10 (59) |
Myeloablative | 7 (41) |
cGVHD presentation, n (%) | |
De novo | 15 (88) |
Progressive | 2 (12) |
NIH cGVHD severity, n (%) | |
Mild | 1 (6) |
Moderate | 6 (35) |
Severe | 10 (59) |
End-organ involvement, n (%) | |
Skin | 16 (94) |
Musculoskeletal | 16 (94) |
Ocular | 9 (53) |
Oral | 9 (53) |
Urogenital | 6 (35) |
Lung | 3 (18) |
Gastrointestinal | 2 (12) |
Liver alone | 2 (12) |
Previous or concurrent systemic cGVHD therapies, n (%) | |
Corticosteroids | 16 (94) |
Rituximab | 7 (41) |
Extracorporeal photopheresis | 6 (35) |
Mycophenolate mofetil | 4 (24) |
Tacrolimus | 4 (24) |
Imatinib | 3 (18) |
Brentuximab vedotin | 2 (12) |
Interleukin-2 | 2 (12) |
Sirolimus | 2 (12) |
Median concurrent systemic cGVHD therapies at study enrollment, n (range) | 1 (0-3) |
Concurrent systemic cGVHD therapies at study enrollment, n (%) | |
Corticosteroids | 15 (88) |
Mycophenolate mofetil | 4 (24) |
Tacrolimus | 3 (18) |
Sirolimus | 2 (12) |
Median time from HCT to enrollment, months (range) | 40 (13-121) |
Median time from cGVHD diagnosis to enrollment, months (range) | 31 (1-101) |
ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; cGVHD, chronic graft-versus-host disease; CML, chronic myeloid leukemia; HCT, hematopoietic cell transplantation; HL, Hodgkin lymphoma; HLA, human leukocyte antigen; NIH, National Institutes of Health; NMA, nonmyeloablative; RIC, reduced-intensity conditioning.