Retrospective Study
Copyright ©The Author(s) 2025.
World J Stem Cells. Feb 26, 2025; 17(2): 100621
Published online Feb 26, 2025. doi: 10.4252/wjsc.v17.i2.100621
Table 1 Patient characteristics, n (%)
Characteristics
Group A (n = 21)
Group B (n = 19)
Total (n = 40)
P value
Age0.03a
        < 36 months5 (23.8)14 (73.7)19 (47.5)
        ≥ 36 months16 (76.2)5 (26.3)21 (52.5)
Sex0.19
        Male15 (71.4)14 (73.7)29 (75)
        Female6 (28.6)5 (26.3)11 (25)
Diagnosis0.84
        Neuroblastoma18 (85.7)17 (89.4)35 (87.5)
        Germ cell tumor2 (9.5)0 (0)2 (5.0)
        ATRT1 (4.8)0 (0)1 (2.5)
        Medulloblastoma0 (0)1 (5.3)1 (2.5)
        Pineoblastoma0 (0)1 (5.3)1 (2.5)
Primary site0.10
        Abdomen15 (71.4)15 (79.0)30 (75.0)
        Mediastinum4 (19.0)2 (10.5)6 (15.00)
        Testis1 (4.8)0 (0)1 (2.5)
        Central nervous system1 (4.8)2 (10.5)3 (7.5)
LDH at diagnosis0.02a
        < 1000 U/L18 (85.7)13 (68.4)31 (77.5)
        ≥ 1000 U/L3 (14.3)6 (31.6)9 (22.5)
No. of chemotherapy cycles before HDCT0.72
        ≤ 8 cycles4 (19.0)1 (5.3)5 (12.5)
        ≥ 9 cycles17 (81.0)18 (94.7)35 (87.5)
Bone marrow metastasis0.08
        Negative9 (42.9)8 (42.1)17 (42.5)
        Positive12 (57.1)11 (57.9)23 (57.5)
No. of metastasized organs0.67
        1-26 (28.6)6 (31.6)12 (30.0)
        ≥ 315 (71.4)13 (68.4)28 (70.0)
Table 2 Univariable analysis of 35 pediatric patients with high-risk neuroblastoma, n (%)
CharacteristicsTotal (n = 35)3-year OS
3-year EFS
mean ± SD
χ2
P value
mean ± SD
χ2
P value
Age
        < 36 months10 (28.6)100100
        ≥ 36 months25 (71.4)55.4 ± 12.24.850.03a51.3 ± 12.04.850.03a
Sex
        Male26 (74.3)71.8 ± 10.567.9 ± 10.7
        Female9 (25.7)57.1 ± 18.70.370.5457.1 ± 18.71.70.36
LDH
        < 1000 U/L25 (71.4)82.0 ± 8.177.4 ± 8.9
        ≥ 1000 U/L10 (28.6)30.0 ± 22.64.320.04a30.0 ± 22.63.150.08
MYCN
        Non-amplified23 (65.7)62.4 ± 14.057.9 ± 13.7
        Amplified5 (14.3)100100
        Unknown7 (20.0)57.1 ± 18.72.720.1057.1 ± 18.72.430.12
NSE
        < 200 ng/mL10 (28.6)70.0 ± 14.570.0 ± 14.5
        ≥ 200 ng/mL21 (60.0)68.8 ± 14.863.7 ± 14.5
        Unknown4 (11.4)50.0 ± 25.00.120.7350.0 ± 25.00.190.66
Table 3 Toxicity in patients with solid tumors who underwent tandem autologous stem cell transplantation, n (%)
ParameterFirst ASCT
Second ASCT
Group A (n = 21)
Group B (n = 19)
Group A (n = 21)
Group B (n = 19)
Hematologic toxicity
Fever (BT ≥ 38.0 °C)17 (81.1)18 (94.7)17 (80.1)16 (84.2)
Septicemia2 (9.5)1 (5.3)0 (0)0 (0)
Non-hematologic toxicity
Mucositis1 (4.8)3 (15.8)2 (9.5)5 (26.3)
Vomiting14 (66.7)16 (84.2)12 (57.1)11 (57.9)
Diarrhea10 (47.6)13 (68.4)10 (47.6)11 (57.9)
Elevated liver enzymes4 (19.0)4 (21.1)1 (4.7)4 (21.1)
Renal insufficiency0 (0)1 (5.3)0 (0)1 (5.3)
Hypokalemia5 (23.8)10 (52.6)2 (9.5)4 (21.1)
Hypomagnesemia8 (38.0)6 (31.6)7 (33.3)2 (10.5)
Hepatic VOD0 (0)0 (0)0 (0)3 (15.8)
Myocarditis2 (9.5)1 (5.3)0 (0)0 (0)
Treatment-related mortality00