Baseline patient characteristics
Characteristic . | Number of patients, n = 39 (%) . |
---|---|
Age (y), median (range) | 62 (25-77) |
Female | 21 (53.8) |
Median time from HCT to study entry (range), mo | 43 (6-173) |
ECOG performance status | |
0 | 1 (2.6) |
1 | 27 (69.2) |
2 | 11 (28.2) |
Indication for transplant | |
AML | 18 (46.2) |
MDS | 8 (20.5) |
ALL | 5 (12.8) |
CML | 2 (5.1) |
MPD | 2 (5.1) |
MPN with fibrosis | 2 (5.1) |
Myelofibrosis | 1 (2.6) |
NHL | 1 (2.6) |
Stem cell source | |
Bone marrow | 4 (10.3) |
Peripheral blood stem cell | 35 (89.7) |
Conditioning intensity | |
Myeloablative | 24 (61.5) |
Nonmyeloablative | 14 (35.9) |
Unknown | 1 (2.6) |
HLA matching (A, B, C, and DRB1) | |
Matched related | 15 (38.4) |
Matched unrelated | 22 (56.4) |
Mismatched related | 1 (2.6) |
Mismatched unrelated | 1 (2.6) |
Baseline NIH cGVHD severity score | |
Mild | 0 (0) |
Moderate | 18 (46.2) |
Severe | 21 (53.8) |
Organs involved | |
Number of organs involved, median (range) | 3 (2-7) |
≥4 organs involved | 19 (48.7) |
Skin | 33 (84.6) |
Mouth | 17 (43.5) |
Eyes | 28 (71.7) |
GI | 6 (15.3) |
Liver | 9 (23.1) |
Lung | 22 (56.4) |
Joints | 32 (82.1) |
Prior systemic therapy for cGVHD | |
Prior lines of therapy, median (range) | 3 (1-8) |
Corticosteroid (prednisone, methylprednisolone) | 39 (100) |
Tacrolimus | 24 (61.5) |
Mycophenolate mofetil | 15 (38.5) |
Sirolimus | 11 (28.2) |
Cyclosporine | 2 (5.1) |
Rituximab | 10 (25.6) |
Ruxolitinib | 7 (17.9) |
Ibrutinib | 4 (10.3) |
Aldesleukin | 7 (17.9) |
Characteristic . | Number of patients, n = 39 (%) . |
---|---|
Age (y), median (range) | 62 (25-77) |
Female | 21 (53.8) |
Median time from HCT to study entry (range), mo | 43 (6-173) |
ECOG performance status | |
0 | 1 (2.6) |
1 | 27 (69.2) |
2 | 11 (28.2) |
Indication for transplant | |
AML | 18 (46.2) |
MDS | 8 (20.5) |
ALL | 5 (12.8) |
CML | 2 (5.1) |
MPD | 2 (5.1) |
MPN with fibrosis | 2 (5.1) |
Myelofibrosis | 1 (2.6) |
NHL | 1 (2.6) |
Stem cell source | |
Bone marrow | 4 (10.3) |
Peripheral blood stem cell | 35 (89.7) |
Conditioning intensity | |
Myeloablative | 24 (61.5) |
Nonmyeloablative | 14 (35.9) |
Unknown | 1 (2.6) |
HLA matching (A, B, C, and DRB1) | |
Matched related | 15 (38.4) |
Matched unrelated | 22 (56.4) |
Mismatched related | 1 (2.6) |
Mismatched unrelated | 1 (2.6) |
Baseline NIH cGVHD severity score | |
Mild | 0 (0) |
Moderate | 18 (46.2) |
Severe | 21 (53.8) |
Organs involved | |
Number of organs involved, median (range) | 3 (2-7) |
≥4 organs involved | 19 (48.7) |
Skin | 33 (84.6) |
Mouth | 17 (43.5) |
Eyes | 28 (71.7) |
GI | 6 (15.3) |
Liver | 9 (23.1) |
Lung | 22 (56.4) |
Joints | 32 (82.1) |
Prior systemic therapy for cGVHD | |
Prior lines of therapy, median (range) | 3 (1-8) |
Corticosteroid (prednisone, methylprednisolone) | 39 (100) |
Tacrolimus | 24 (61.5) |
Mycophenolate mofetil | 15 (38.5) |
Sirolimus | 11 (28.2) |
Cyclosporine | 2 (5.1) |
Rituximab | 10 (25.6) |
Ruxolitinib | 7 (17.9) |
Ibrutinib | 4 (10.3) |
Aldesleukin | 7 (17.9) |
Baseline patient characteristics of the 39 patients enrolled in the trial including key transplant, cGVHD, and immunosuppressant management features.
ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; CML, chronic myeloid leukemia; ECOG, Eastern Cooperative Oncology Group; HCT, hematopoietic cell transplant; MDS, myelodysplastic syndrome; MPD, myeloproliferative disorder; MPN, myeloproliferative neoplasm; NHL, non-Hodgkin lymphoma.