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Table 2 Clinicopathological features for patients after re-evaluation

From: Supratentorial CNS-PNETs in children; a Swedish population-based study with molecular re-evaluation and long-term follow-up

 

HGG (n = 25)

AT/RT (n = 8)

CNS NB-FOXR2 (n = 7)

ETMR (n = 6)

EPN (n = 6)

OTHER (n = 14)

Age at diagnosis, median (years)

12.7

2.6

5.3

2.8

5.9

3.3

Gender

      

 Male

12 (48%)

4 (50%)

3 (43%)

6 (100%)

3 (50%)

9 (64%)

 Female

13 (52%)

4 (50%)

4 (57%)

¨

3 (50%)

5 (36%)

Location of primary tumor

      

Hemisphere

18 (72%)

7 (88%)

7 (100%)

5 (83%)

6 (100%)

9 (64%)

Central/Midline

7 (28%)

1 (12%)

¨

1 (17%)

¨

2 (14%)

Details unknown

     

3 (22%)

Metastatic status

      

M0

24 (96%)

7 (88%)

6 (86%)

6 (100%)

6 (100%)

13 (93%)

M1-3

1 (4%)

¨

1 (14%)

¨

¨

1 (7%)

Details unknown

 

1 (12%)

    

Tumor resection

      

GTR

8 (32%)

3 (38%)

5 (71%)

2 (33%)

4 (67%)

7 (50%)

Partial resection

9 (36%)

1 (12%)

2 (29%)

1 (17%)

1 (17%)

2 (14%)

Biopsy

4 (16%)

     

Details unknown

4 (16%)

4 (50%)

 

3 (50%)

1 (17%)

5 (36%)

Radiotherapy received

      

Yes

19 (76%)

2 (25%)

7 (100%)

1 (17%)

5 (83%)

7 (50%)

No

6 (20%)

6 (75%)

¨

5 (83%)

1 (17%)

7 (50%)

Chemotherapy received

      

Yes

21 (84%)

8 (100%)

7 (100%)

5 (83%)

6 (100%)

12 (85%)

No

3 (12%)

¨

¨

1 (17%)

¨

2 (15%)

High-dose chemotherapy with stemcell rescue

¨

1 (12%)

2 (29%)

2 (33%)

¨

2 (14%)

Details unknown

1 (4%)

¨

¨

¨

¨

¨

Survival data

      

5-year progression free survival

17% ± 17%

25% ± 37%

100%

17% ± 48%

83% ± 21%

36% ± 27%

5-year overall survival

20% ± 16%

25% ± 27%

100%

33% ± 35%

100%

50% ± 26%

  1. HGG, High-grade glioma; AT/RT, atypical teratoid rhabdoid tumour; EPN, ependymoma