Table 1.
Patient ID | SCD complications | Age at AlloHCT, y | Donor type | Time from transplant to graft rejection | Time from transplant to myeloid malignancy, y | Cytogenetics at myeloid malignancy diagnosis | TP53 mutation and VAF at myeloid malignancy diagnosis |
---|---|---|---|---|---|---|---|
1 | Stroke, CRI, recurrent VOC | 37 | Haplo | 73 d | 2 | Complex | c.524G>A, 72.4% in bone marrow |
2 | Recurrent VOC, chronic pain | 37 | HLA-matched | 6 mo | 2.5 | Complex* | c.658T>C, 4.5% in bone marrow |
3 | ESRD, pHTN, diastolic dysfunction | 44 | Haplo | 7 mo | 5 | 7q deletion | N/A |
A total of 76 patients received AlloHCT for HbSS at this center; myeloid malignancy was only seen within those who did not engraft
CRI, chronic renal insufficiency; ESRD, end-stage renal disease; Haplo, haploidentical donor; N/A, not available; pHTN; pulmonary hypertension.
Patient 2 had complex cytogenetics at graft rejection 2 years before formal myeloid malignancy diagnosis (no aspirate collected at a later point).