Demographic and clinical information for patients with SCD who developed hematologic malignancies after allogeneic HCT
Patient No. . | SCD type . | Age at HCT, y/sex . | SCD comorbidities . | HCT type . | TBI dose, cGy . | PC . | PT-Cy dose, mg/kg . | Cytos pre-HCT . | Day of graft failure . | Malignancy . | Time of malignancy dx post-HCT, y . | Cytos and bone marrow blasts at malignancy dx . | DMC at dx . | DLC at dx . | Current status . |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | HbSS | 37/male | Recurrent VOC Chronic pain | HLA matched | 300 | No | 0 | Normal | 183 | MDS | 2.5 | Complex <5% | 0 | 0 | Dec |
2 | HbSS | 19/male | Priapism ACS | HLA matched | 300 | No | 0 | Normal | N/A | CML | 3.5 | 46XY, t(2, 9, 22), BCR/ABL1 p210 fusion <5% | 39 | 59 | Alive |
3 | HbS-β0thal | 53/male | TRV 3.2 m/s | HLA matched | 300 | No | 0 | ND | N/A | MCL | 9 | Monosomy 13, 11q deletion and t(11;14) <5% | 89 | 73 | Alive |
4 | HbSS | 34/male | TRV 2.5 m/s Priapism ACS Recurrent VOC | HLA matched | 300 | Yes | 0 | Normal | 74 | AML | 0.33 | Complex 15%-20% | 16 | 18 | Dec |
5 | HbSS | 39/female | Silent infarct ACS TRV 2.8 m/s SCD-associated liver disease | HLA matched | 300 | Yes | 0 | Normal | N/A | T-cell ALL | 3 | 46XX, t(9:22) [18]/46,XY[2] BCR/ABL1 p190 fusion 93% | 30 | 25 | Alive |
6 | HbSS | 37/male | Stroke CRI Recurrent VOC | Haplo | 400 | No | 100 | Normal | 73 | MDS | 2 | Complex <5% | 0 | 0 | Dec |
7 | HbSS | 20/female | Recurrent VOC ACS SCD-associated liver disease Chronic pain | Haplo | 400 | No | 100 | Normal | 90 | AML | 5.5 | Complex 20% | 0 | 0 | Dec |
8 | HbSS | 44/female | ESRD pHTN Diastolic dysfunction | Haplo | 400 | No | 0 | Normal | 7 mo | AML | 5 | 7q deletion 10%-15% | 0 | 0 | Dec |
Patient No. . | SCD type . | Age at HCT, y/sex . | SCD comorbidities . | HCT type . | TBI dose, cGy . | PC . | PT-Cy dose, mg/kg . | Cytos pre-HCT . | Day of graft failure . | Malignancy . | Time of malignancy dx post-HCT, y . | Cytos and bone marrow blasts at malignancy dx . | DMC at dx . | DLC at dx . | Current status . |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | HbSS | 37/male | Recurrent VOC Chronic pain | HLA matched | 300 | No | 0 | Normal | 183 | MDS | 2.5 | Complex <5% | 0 | 0 | Dec |
2 | HbSS | 19/male | Priapism ACS | HLA matched | 300 | No | 0 | Normal | N/A | CML | 3.5 | 46XY, t(2, 9, 22), BCR/ABL1 p210 fusion <5% | 39 | 59 | Alive |
3 | HbS-β0thal | 53/male | TRV 3.2 m/s | HLA matched | 300 | No | 0 | ND | N/A | MCL | 9 | Monosomy 13, 11q deletion and t(11;14) <5% | 89 | 73 | Alive |
4 | HbSS | 34/male | TRV 2.5 m/s Priapism ACS Recurrent VOC | HLA matched | 300 | Yes | 0 | Normal | 74 | AML | 0.33 | Complex 15%-20% | 16 | 18 | Dec |
5 | HbSS | 39/female | Silent infarct ACS TRV 2.8 m/s SCD-associated liver disease | HLA matched | 300 | Yes | 0 | Normal | N/A | T-cell ALL | 3 | 46XX, t(9:22) [18]/46,XY[2] BCR/ABL1 p190 fusion 93% | 30 | 25 | Alive |
6 | HbSS | 37/male | Stroke CRI Recurrent VOC | Haplo | 400 | No | 100 | Normal | 73 | MDS | 2 | Complex <5% | 0 | 0 | Dec |
7 | HbSS | 20/female | Recurrent VOC ACS SCD-associated liver disease Chronic pain | Haplo | 400 | No | 100 | Normal | 90 | AML | 5.5 | Complex 20% | 0 | 0 | Dec |
8 | HbSS | 44/female | ESRD pHTN Diastolic dysfunction | Haplo | 400 | No | 0 | Normal | 7 mo | AML | 5 | 7q deletion 10%-15% | 0 | 0 | Dec |
ACS, acute chest syndrome; ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; CML, chronic myeloid leukemia; CRI, chronic renal insufficiency; Dec, deceased; DLC, donor lymphoid chimerism; DMC, donor myeloid chimerism; dx, diagnosis; ESRD, end-stage renal disease; Haplo, haploidentical; HbS-β0thal, compound heterozygosity for hemoglobin S and β 0 thalassemia; HbSS, homozygous SCD; MCL, mantle cell lymphoma; MDS, myelodysplastic syndrome; N/A, not applicable; ND, not done; pHTN, right heart catheterization-documented pulmonary hypertension; PT-Cy, posttransplant cyclophosphamide; t, translocation; TRV, tricuspid regurgitant velocity; VOC, vaso-occlusive crises.