Table 1.

Characteristics of patients with SCD developing therapy-related myeloid malignancy after allogeneic hematopoietic cell transplantation at the National Institutes of Health Clinical Center

Patient IDSCD complicationsAge at AlloHCT, yDonor typeTime from transplant to graft rejectionTime from transplant to myeloid malignancy, yCytogenetics at myeloid malignancy diagnosisTP53 mutation and VAF at myeloid malignancy diagnosis
Stroke, CRI, recurrent VOC 37 Haplo 73 d Complex c.524G>A, 72.4% in bone marrow 
Recurrent VOC, chronic pain 37 HLA-matched 6 mo 2.5 Complex* c.658T>C, 4.5% in bone marrow 
ESRD, pHTN, diastolic dysfunction 44 Haplo 7 mo 7q deletion N/A 
Patient IDSCD complicationsAge at AlloHCT, yDonor typeTime from transplant to graft rejectionTime from transplant to myeloid malignancy, yCytogenetics at myeloid malignancy diagnosisTP53 mutation and VAF at myeloid malignancy diagnosis
Stroke, CRI, recurrent VOC 37 Haplo 73 d Complex c.524G>A, 72.4% in bone marrow 
Recurrent VOC, chronic pain 37 HLA-matched 6 mo 2.5 Complex* c.658T>C, 4.5% in bone marrow 
ESRD, pHTN, diastolic dysfunction 44 Haplo 7 mo 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).

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