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Table 2 Distribution of clinical pathological variables among 78 1p-intact neuroblastoma cases with and without mutational variants

From: Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma

Variable

Neuroblastoma candidate gene variant present (n (%))

Neuroblastoma candidate genes variant absent (n (%))

Chi-square

P-value

Gender (n = 78)

Male

26 (57.8)

18 (54.5)

0.081

0.776

Female

19 (42.2)

15 (45.5)

INPC histology (n = 78)

FH

18 (40.0)

19 (57.6)

2.359

0.125

UH

27 (60.0)

14 (42.4)

Treatment status (n = 78)

Pre-chemotherapy

4 (8.9)

5 (15.2)

0.732

0.392

Post-chemotherapy/ relapse

41 (91.1)

28 (84.8)

Specimen site (n = 78)

Primary tumor

40 (88.9)

32 (97.0)

5.165

0.076

Metastatic tumor

5 (11.1)

-

Both

-

1 (3.0)

MYCN status (n = 78)

Amplified

9 (20.0)

6 (18.2)

0.041

0.840

Non-amplified

36 (80.0)

27 (81.8)

11q status (n = 76)

Deleted

7 (36.8)

12 (21.1)

4.017

0.045

Not deleted

12 (63.2)

45 (78.9)

Metastatic status (n = 76)

Metastatic

34 (75.6)

19 (61.3)

1.770

0.183

Localized

11 (24.4)

12 (38.7)

COG risk (n = 75)

High

40 (88.9)

22 (73.3)

3.040

0.081

Low/intermediate

5 (11.1)

8 (26.7)

  1. INPC International Neuroblastoma Pathology Classification, FH Favorable histology, UH Unfavorable histology, COG Children’s Oncology Group