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. 2021 Dec 13;5(23):5420–5428. doi: 10.1182/bloodadvances.2021005507

Table 2.

Clinical characteristics and NUDT15 variants in primary ALL cases

Case n Primary
cancer
Risk group Genetic subtypes of primary ALL SMN subtype Interval, y* Cytogenetics of tMDS/AML NUDT15 genotype 6-MP dose, mg/m2
1 BCP-ALL HR MDS 10 Normal karyotype WT 48
2 BCP-ALL IR Bladder cancer 24 HT 60
3 BCP-ALL HR ETV6-RUNX1 AML 3 MLL rearrangement HT 32
4 BCP-ALL HR AML 30 45,X,-X,
t(8;16;21)(q22;p11.2;q22)
HT 70
5 BCP-ALL IR t(1;19) BCC 25 WT 47
6 BCP-ALL HR ES 9 WT NA
7 BCP-ALL HR FUS-ERG AML 3 NA WT 16.6
8 BCP-ALL SR AML 8 MLL rearrangement WT 85
9 BCP-ALL SR Neurilemmoma 12 WT 68
10 T-ALL SR AML 2 Normal karyotype WT 115
11 BCP-ALL IR MDS 4 46,XX, add(3)(q26), −7, +mar HT 60
12 BCP-ALL HR AML 4 Normal karyotype HT 38
13 BCP-ALL HR MLL-AF4 OS 8 HT 37
14 BCP-ALL SR ETV6-RUNX1 MDS 1 46,XX t(5;12;17)(q35;p13;q12) WT 27

BCP-ALL, B-cell precursor ALL; BCC, basal cell carcinoma; ES, Ewing sarcoma; HR, high risk; HT, heterozygous type; IR, intermediate risk; MDS, myelodysplastic syndrome; NA, not available; OS, osteosarcoma; SR, standard risk; T-ALL, T-cell precursor ALL; WT, wild type.

*

Time from primary cancer to SMN.

HT indicates heterozygous for rs116855232.