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letter
. 2013 Jun 25;109(2):497–501. doi: 10.1038/bjc.2013.312

Table 1. Associations of TERT mutation status with clinical and pathological parameters in conjunctival melanoma.

Parameter Level TERT wild-type (n=26) TERT mutant (n=12) P-value
Median age (years)
 
67.2
73.3
0.72a
Sex
Female
15
6
1.00
 
Male
10
5
 
Sites of involvementb        
Bulbar No 11 8 0.13
  Yes 12 2  
Caruncle No 20 5 0.043
  Yes 2 4  
Fornix No 16 6 1.00
  Yes 6 2  
Sclera No 23 9 0.51
  Yes 1 1  
Palpebra No 19 6 0.32
  Yes 3 3  
Multifocal No 16 4 0.14
 
Yes
7
6
 
Clinical stage Ia 5 1 0.20
  Ib 7 1  
  IIa 0 1  
  IIb 6 2  
  IIc 0 2  
  IId 1 0  
  IIIa 1 1  
 
IIIb
3
2
 
Pathological stage I 1 0 0.19
  Ia 5 2  
  Ib 3 0  
  Ic 3 0  
  IIa 4 1  
  IIb 1 0  
  IIc 1 4  
 
III
4
3
 
Associated lesion PAM 15 6 0.47
  Naevus 3 1  
 
De novo
5
1
 
Cell type Mixed 13 3 0.22
  Spindle 3 3  
 
Epithelioid
3
3
 
Pigmentation Yes 20 8 0.52
 
No
1
1
 
NRAS mutation No 24 9 0.30
 
Yes
2
3
 
BRAF mutation No 20 8 0.69
 
Yes
6
4
 
Disease-free survival
1.25 (0.47–3.35)c
24d
18d
0.65e
Overall survival 1.92 (0.60–6.08)c NRd 89d 0.27e

Abbreviations: NR=not reached; PAM=primary acquired melanosis.

P-values are derived from χ2 or Fisher's exact tests, as appropriate, unless otherwise specified.

Clinical and pathological stage is according to the American Joint Committee on Cancer staging system for conjunctival melanoma, 7th edition.

Note: The sum of the numbers of cases for individual parameters may not equal the total number of cases because data for some parameters was not available in all cases.

a

Kruskal–Wallis test.

b

Sites of involvement refer to structures affected by the tumour, either primarily or secondarily. Only tumours of conjunctival origin were included in the study.

c

Hazard ratio (95% confidence interval for hazard ratio).

d

Estimates of median survival (in months), derived from Kaplan–Meier method.

e

P-values, derived from univariate Cox regression analysis.