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Table 4 Clinical characteristics of patients whose tumors acquired CDKN2A deletions at recurrence/progression

From: Characterizing temporal genomic heterogeneity in pediatric low-grade gliomas

Patient ID #

Age at diagnosis (years)

Sex

Tumor Pathologic classification

Tumor location

Metastatic disease at diagnosis

Extent of surgery #1

Time to first progression (months)

Time to surgery #2 (months)

Treatment received between diagnosis and gain of CDKN2A deletion

Current status (months from diagnosis to last follow-up)

1

5

F

Pilocytic astrocytoma

Diencephalic (hypothalamic/optic pathway)

No

STR

20

26

Chemotherapy (carboplatin, temozolomide)

Alive (104)

2

12

M

Pilocytic astrocytoma

Diencephalic (hypothalamic/optic pathway)

No

STR

2

27

Irradiation photon (50.4 Gy)]

Alive (116)

4

0.8

F

Pilomyxoid astrocytoma

Diencephalic (hypothalamic)

No

Biopsy

3.5

7

Chemotherapy (carboplatin/vincristine, vinblastine, temozolomide, trametinib), additional debulking surgery

Alive (58)

15

1

M

Pilocytic astrocytoma

Posterior fossa

No

STR

19

19

Surgery only

Alive (93)

18

5

M

Pilocytic astrocytoma

Posterior fossa

No

STR

17

17

Surgery only

Alive (182)

26

15

M

Pilocytic astrocytoma

Cerebrum (Right temporal-parietal)

No

STR (biopsy, then STR 1 week later)

5.5

5.5

Surgery only

Deceased (91; Drug overdose, unrelated to disease)

41

0.4

F

Desmoplastic infantile ganglioglioma

Cerebrum (Right frontal)

No

STR

4

8

Chemotherapy (carboplatin/vincristine)

Alive (94)