Table 1 Clinico-pathological characteristics of the samples used for UTUC PDX.

From: Modeling biological and genetic diversity in upper tract urothelial carcinoma with patient derived xenografts

Variable

PDX growth (N = 17)

No PDX growth (N = 17)

P-value

Median age at surgery, years (IQR)

69.6 (65.7–75.7)

65.6 (60.0–75.3)

0.390

Gender

  

1.000

 Male

11 (64.7)

11 (64.7)

 

 Female

6 (35.3)

6 (35.3)

 

Lynch syndrome/MSI-H

  

0.166

 Yes

4 (23.5)

1 (5.9)

 

 No

12 (70.6)

16 (94.1)

 

 Not tested

1 (5.9)

0 (0)

 

Smoking status

  

0.039

 Current/former

10 (58.8)

16 (94.1)

 

 Never

7 (41.2)

1 (5.9)

 

Prior history of urothelial cancer

  

1.000

 Yes

5 (29.4)

6 (35.3)

 

 No

12 (70.6)

11 (64.7)

 

Location of primary tumor

  

1.000

 Renal pelvis

15 (88.2)

14 (82.4)

 

 Ureter

2 (11.8)

3 (17.6)

 

Specimen type

  

0.6a

 Primary

14 (82.4)

16 (94.1)

 

 Lymph node

1 (5.9)

0 (0)

 

 Distant metastasis

2 (11.8)

0 (0)

 

 Endoscopic biopsy

0 (0)

1 (5.9)

 

Grade

  

0.480

 Low

2 (11.8)

0 (0)

 

 High

15 (88.2)

17 (100)

 

pT stage

  

0.166

 <pT2 (non-invasive)

5 (29.4)

10 (58.8)

 

 ≥pT2 (invasive)

12 (70.6)

7 (41.2)

 

pN stage

  

0.460

 pN0

10 (58.8)

13 (70.5)

 

 pN+

5 (29.4)

2 (11.8)

 

 pNx

2 (11.8)

2 (11.8)

 

Prior chemotherapy

  

0.688

 Yes

3 (17.6)

5 (29.4)

 

 No

14 (82.4)

12 (70.6)

 
  1. Two-sided P-values were obtained using Wilcoxon-rank sum for continuous and Fisher’s exact test for categorical variables.
  2. aSpecimen type was dichotomized as primary vs all others for this comparison.