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. 2022 Jan 10;12:378. doi: 10.1038/s41598-021-04296-3

Table 1.

Patient and treatment characteristics.

Characteristic Tumour burden* P value
Low High
Patient No 33 45 NA
Age Median (Range) 32 (10,73) 30 (9,68) 0.4283
Sex Male, n (%) 15 (45.45) 23 (51.11) 0.6531
Medical history Ph+, n (%) 9 (23.27) 5 (11.11) 0.0799
 ≥ 6 months, n (%) 26 (78.79) 28 (62.22) 0.1415
Pre-chemotherapy ≥ 3 times, n (%) 25 (75.76) 30 (66.67) 0.4563
Pre-HSCT, n (%) 11 (33.33) 8 (17.78) 0.1811
Relapse, n (%) 28 (84.85) 29 (64.44) 0.0695
Tumour burden evaluation time Before FC, n (%) 25 (75.76) 32 (71.11) 0.7972
After FC, n (%) 8 (24.24) 13 (28.89)
TP53 mutation Yes, n (%) 1 (3.03) 2 (4.44)  > 0.9999
Cytogenetic risk Poor, n (%) 11 (33.33) 13 (28.89) 0.8046

Ph+ , Philadelphia chromosome-positive; Pre-HSCT, previous haematopoietic stem cell transplantation; TP53, tumor protein P53; FC, fludarabine and cyclophosphamide.

*A high tumor burden was defined as a bone marrow blast level of 5% or more, and a low disease burden was defined as a bone marrow blast level of less than 5%. Minimal residual disease was assessed by multiparameter flow cytometry25, and a negative minimal residual disease status was defined as a bone marrow blast level of less than 0.01%.