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Table 1 Clinicopathological characteristics and KRAS and BRAF mutations in LGSC

From: Low frequency of BRAF and KRAS mutations in Chinese patients with low-grade serous carcinoma of the ovary

Clinicopathological

characteristics

KRAS/BRAF gene

P-value

Mutation

(n = 11)

Wild-type

(n = 21)

Age (years)

  

0.106

  < 45

1 (9.10%)

9 (42.86%)

 

  ≥ 45

10 (90.90%)

12 (57.14%)

 

FIGO stage

  

1.000

 I/II

3 (27.27%)

7 (33.33%)

 

 III/IV

8 (72.73%)

14 (66.67%)

 

CA125 (U/ml)

  

1.000

  ≤ 35 U/mL

0 (0.00%)

1 (4.76%)

 

  > 35 U/mL

11 (100.00%)

20 (95.24%)

 

Tumor size(cm)

  

0.442

  < 10

5 (45.45%)

6 (28.57%)

 

  ≥ 10

6 (54.55%)

15 (71.43%)

 

Laterality

  

0.053

 Unilateral

7 (63.64%)

5 (23.81%)

 

 Bilateral

4 (36.36%)

16 (76.19%)

 

Cytology

  

0.703

 Negative

8 (72.73%)

13 (61.90%)

 

 Positive

3 (27.27%)

8 (38.10%)

 

Ascites

  

0.441

 Absent

2 (18.18%)

7 (33.33%)

 

 Present

9 (81.82%)

14 (66.67%)

 

Ovarian surface involvement

  

0.815

 No

3 (27.27%)

8 (38.10%)

 

 Yes

7 (63.64%)

11 (52.38%)

 

 Unknown

1 (9.10%)

2 (9.52%)

 

Metastases

  

1.000

 No

3 (27.27%)

7 (33.33%)

 

 Yes

8 (72.73%)

14 (66.67%)

 

Lymph node involvement

  

0.392

 No

1 (9.10%)

1 (4.76%)

 

 Yes

2 (18.18%)

1 (4.76%)

 

 Unknown

8 (72.73%)

19 (90.48%)