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. 2014 Jan 24;7(4):1169–1174. doi: 10.3892/ol.2014.1822

Table IV.

Characteristics of the study population.

No. Age, years Gender Immunophenotype Initial WBC, ×109/l Day 8 PB blast/μl Risk group Mean minimum WBC/μl Outcome

Day 1 Day 8
1 12 M B 81 63 HR HR 1,167 RFS
2 11 F B 581 632 HR HR 450 Relapsed
3 14 M T 279 14 HR HR 433 RFS
4 8 F B 7.2 7,684 IR HR 367 RFS
5 9 M T 430 116 HR HR 500 Relapsed
6 12 F B 8.2 1,269 IR HR 733 Relapsed
7 14 M T 1.5 0 HR HR 367 RFS
8 7 M T 259 20 HR HR 433 Relapsed
9 12 F T 147 247 HR HR 233 RFS
10 15 M T 42 0 HR HR 433 RFS
11 6 F T 11 0 HR HR 233 RFS
12a 3 F B 8.5 825 SR SR 667 RFS
13 7 F B 12 76 HR HR 300 RFS
14 11 F B 21 12,802 IR HR 200 RFS
15 13 M T 126 bND HR HR 633 Relapsed
16 10 M B 539 7 HR HR 467 RFS
17 13 M B 53 81 HR HR 200 RFS
18 6 M T 28 28 HR HR 467 RFS
19 6 M T 65 459 HR HR 300 RFS
Median 11 52.9 69.5 433
IQR 6–13 8.5–278.6 7–825 233–633
a

Patient number 12 started treatment with the TCCSG L04-16 SR protocol. Hematological remission was achieved following remission induction, but leukemic infiltration remained in the liver and frontal bone. The patient was finally stratified into high-risk group and received all courses of the ALL-BFM 95 HR protocol with the exception of the induction phase.

b

Unable to determine ‘day eight’ since prednisolone monotherapy was transiently terminated due to tumor lysis syndrome.

The peripheral blood count decreased rapidly to <1,000/μl following initiation of prednisolone. WBC, white blood cell count; PB, peripheral blood; SR, standard-risk; IR, intermediate-risk; HR, high-risk; RFS, relapse-free survival; IQR, interquartile range; ND, no data.