Table 1 Demographic and treatment characteristics of adult survivors of childhood cancer (including glioma survivors and all cancer survivors) and siblings, divided by neurofibromatosis type 1 status.

From: Late morbidity and mortality in adult survivors of childhood glioma with neurofibromatosis type 1: report from the Childhood Cancer Survivor Study

 

Glioma survivors

All survivors

 
 

with NF1 N (%)

without NF1 N (%)

with NF1 N (%)

without NF1 N (%)

Siblings N (%)

All participants

147

2629

176

22,316

5 051

Sex

  Male

67 (46%)

1382 (53%)

83 (49%)

11,905 (53%)

2408 (48%)

  Female

80 (54%)

1247 (47%)

93 (51%)

10,411 (47%)

2643 (52%)

Race/ethnicity

  Non-Hispanic White

126 (86%)

2209 (84%)

151 (85%)

18,345 (83%)

4370 (87%)

  Non-Hispanic Black

7 (5%)

136 (5%)

7 (4%)

1385 (6%)

149 (3%)

  Hispanic

8 (5%)

174 (7%)

11 (7%)

1614 (7%)

214 (4%)

  Other

6 (4%)

110 (4%)

7 (4%)

972 (4%)

318 (6%)

Age at diagnosis

  <1 year

5 (3%)

141 (5%)

13 (7%)

1708 (7%)

 

  1–3 years

48 (33%)

545 (21%)

57 (33%)

5484 (23%)

 

  4–7 years

43 (29%)

702 (27%)

46 (27%)

4905 (26%)

 

  8–10 years

22 (15%)

400 (15%)

24 (13%)

2407 (14%)

 

  11–14 years

19 (13%)

525 (20%)

22 (12%)

3944 (18%)

 

  15–20 years

10 (7%)

316 (12%)

14 (8%)

3868 (12%)

 

Decade of diagnosis

  1970–1979

7 (5%)

512 (19%)

11 (6%)

6322 (22%)

 

  1980–1989

37 (25%)

954 (36%)

48 (28%)

9055 (37%)

 

  1990–1999

103 (70%)

1163 (44%)

117 (66%)

6939 (41%)

 

Diagnosis

  ALL

0 (0%)

0 (0%)

3 (5%)

6145 (5%)

 

  AML

0 (0%)

0 (0%)

0 (0%)

0 (0%)

 

  Other leukemia

0 (0%)

0 (0%)

1 (0.6%)

302 (0.6%)

 

  Glioma

147 (100%)

2629 (100%)

147 (81%)

2629 (81%)

 

  Medulloblastoma, PNET

0 (0%)

0 (0%)

0 (0%)

0 (0%)

 

  Hogdkin lymphoma

0 (0%)

0 (0%)

1 (0.6%)

2995 (0.6%)

 

  Non-Hodgkin lymphoma

0 (0%)

0 (0%)

1 (0.6%)

1986 (0.6%)

 

  Kidney tumors

0 (0%)

0 (0%)

4 (2%)

2155 (2%)

 

  Neuroblastoma

0 (0%)

0 (0%)

6 (3%)

1845 (3%)

 

  Soft tissue sarcoma

0 (0%)

0 (0%)

9 (5%)

1697 (5%)

 

  Ewing sarcoma

0 (0%)

0 (0%)

1 (0.6%)

713 (0.6%)

 

  Osteosarcoma

0 (0%)

0 (0%)

2 (1%)

1203 (1%)

 

  Other bone tumor

0 (0%)

0 (0%)

1 (0.6%)

97 (0.6%)

 

CNS radiation dose

  None

89 (67%)

1391 (59%)

113 (70%)

14,522 (61%)

 

  >0 to <20 Gy

0 (0%)

7 (0%)

2 (3%)

1851 (2%)

 

  20 to <30 Gy

1 (1%)

4 (0%)

1 (1%)

1579 (1%)

 

  30 to <50 Gy

6 (5%)

134 (6%)

7 (4%)

589 (6%)

 

  ≥50 Gy

37 (28%)

811 (35%)

37 (22%)

1310 (30%)

 

Chemotherapy exposure

  Vinca alkyloid

45 (32%)

402 (17%)

62 (39%)

14,617 (28%)

 

  Platinum

36 (26%)

257 (11%)

42 (24%)

1975 (12%)

 

  Alkylating agent

12 (9%)

261 (11%)

27 (19%)

9468 (20%)

 

  Anthracycline

0 (0%)

6 (0%)

14 (11%)

9758 (10%)

 

  Antimetabolite

7 (5%)

133 (5%)

14 (11%)

9009 (12%)

 

  Steroid

5 (4%)

196 (8%)

11 (8%)

9538 (13%)

 

  Epipodophyllotoxin

6 (4%)

88 (4%)

11 (9%)

3248 (7%)

 

  IT methotrexate

0 (0%)

5 (0%)

4 (5%)

6936 (6%)

 

  IV methotrexate

1 (1%)

9 (0%)

5 (4%)

4922 (5%)

 

  Other

1 (1%)

25 (1%)

1 (1%)

170 (1%)

 
  1. ALL acute lymphoblastic leukemia, AML acute myeloid leukemia, CNS central nervous system, Gy Gray, IT intrathecal, IV intravenous, NF1 neurofibromatosis type 1, PNET primitive neuroectodermal tumor.