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Table. 3. Application of multiple-hit TP53 mutation criteria in patients with TP53 mutations according to the 5th WHO classification and ICC
Multi-hit TP53 mutation 5th WHO ICC ICC 5th WHO/ICC P
(B vs. C)
P
(A vs. D)
A: MDS
(blasts<20%)
(N=116)
B: MDS
(blasts<10%)
(N=88)
C: MDS/AML (10%≤blasts<20%)
(N=28)
D: AML
(blasts≥20%)
(N=194)
Criteria for multi-hit TP53 mutation
1. 5th WHO: two or more TP53 mutations 9/116 (7.8%) 7/88 (8.0%) 2/28 (7.1%) 22/194 (11.3%) 1.000 0.309
2. 5th WHO: one TP53 mutation with 17p loss 32/115 (27.8%) 18/87 (20.7%) 14/28 (50.0%) 75/188 (39.9%) 0.003 0.033
3. 5th WHO/ICC: one TP53 mutation with VAF >50% 48/116 (41.4%) 36/88 (40.9%) 12/28 (42.9%) 83/194 (42.8%) 0.855 0.809
4. ICC: two or more TP53 mutations (each with a VAF >10%) 8/116 (6.9%) 6/88 (6.8%) 2/28 (7.1%) 17/194 (8.8%) 1.000 0.559
5. ICC: one TP53 mutation (with a VAF >10%) with 17p loss 31/115 (27.0%) 18/87 (20.7%) 13/28 (46.4%) 71/188 (37.8%) 0.008 0.053
6. ICC: one TP53 mutation (with a VAF >10%) with CK 85/113 (75.2%) 63/85 (74.1%) 22/28 (78.6%) 143/188 (76.1%) 0.636 0.869
Multi-hit TP53 mutation, N (%) according to the 5th WHO 2022 classification* 68/116 (58.6%) 49/88 (55.7%) 19/28 (67.9%) 134/194 (69.1%) 0.255 0.062
Multi-hit TP53 mutation, N (%) according to the ICC 89/116 (76.7%) 66/88 (75.0%) 23/28 (82.1%) 156/194 (80.4%) 0.436 0.44
Multi-hit TP53 mutation (excluding CK), N (%) according to the ICC 66/116 (56.9%) 48/88 (54.5%) 18/28 (64.3%) 127/194 (65.5%) 0.365 0.132
Any TP53 mutation with VAF >10% 107/116 (92.2%) 80/88 (90.9%) 27/28 (96.4%) 174/194 (89.7%) 0.685 0.455

*Corresponding to criteria 1, 2, or 3 for multi-hit TP53 mutations.

Corresponding to criteria 3, 4, 5, or 6 for multi-hit TP53 mutations.

Corresponding to criteria 3, 4, or 5 for multi-hit TP53 mutations.

Bold indicates cases that meet the multi-hit criteria for TP53-mutated MDS, MDS/AML, and AML according to the 5th WHO classification and ICC.

Abbreviations: MDS, myelodysplastic neoplasm; ICC, International Consensus Classification; VAF, variant allele frequency; CK, complex karyotype.

Ann Lab Med 2025;45:160~169 https://doi.org/10.3343/alm.2024.0351

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