Skip to main content

Table 1 Demographic and clinical characteristics of 76 treated patients

From: Molecular profiling of advanced malignancies guides first-line N-of-1 treatments in the I-PREDICT treatment-naïve study

Characteristics

All treated patients

[N = 76]

Matching Score

P-values

≥ 60%

[N = 27]

1-59%

[N = 27]

Unmatched

[N = 22]

≥ 60%

vs.

1–59%

≥ 60%

vs.

unmatched

1–59%

vs.

unmatched

Age, years*

 Median (range)

63.0 (22.5-92.7)

63.5 (36.4-82.6)

62.3 (35.7-92.7)

63.4 (22.5-86.4)

0.82

0.92

0.85

 ≥ 63

38 (50%)

14 (51.9%)

13 (48.1%)

11 (50.0%)

> 0.99

> 0.99

> 0.99

 < 63

38 (50%)

13 (48.1%)

14 (51.9%)

11 (50.0%)

--

--

--

Gender

 Women

40 (52.6%)

14 (51.9%)

14 (51.9%)

12 (54.5%)

> 0.99

> 0.99

> 0.99

 Men

36 (47.4%)

13 (48.1%)

13 (48.1%)

10 (45.5%)

--

--

--

Ethnicity

 Caucasian

45 (59.2%)

15 (55.6%)

19 (70.4%)

11 (50.0%)

0.40

0.78

0.24

 Hispanic

15 (19.7%)

6 (22.2%)

6 (22.2%)

3 (13.6%)

> 0.99

0.49

0.49

 Asian

9 (11.8%)

4 (14.8%)

2 (7.4%)

3 (13.6%)

0.67

> 0.99

0.65

 African American

3 (3.9%)

2 (7.4%)

0 (0.0%)

1 (4.5%)

0.49

> 0.99

0.45

 Others

4 (5.3%)

0 (0.0%)

0 (0.0%)

4 (18.2%)

--

0.04

0.04

Tumor type

 Gastrointestinal, non-colorectal

12 (15.8%)

4 (14.8%)

3 (11.1%)

5 (22.7%)

> 0.99

0.71

0.44

 Carcinoma of unknown primary

10 (13.2%)

6 (22.2%)

3 (11.1%)

1 (4.5%)

0.47

0.11

0.62

 Hepatobiliary

9 (11.8%)

4 (14.8%)

4 (14.8%)

1 (4.5%)

> 0.99

0.36

0.36

 Colorectal

7 (9.2%)

3 (11.1%)

3 (11.1%)

1 (4.5%)

> 0.99

0.62

0.62

 Pancreatic

7 (9.2%)

1 (3.7%)

2 (7.4%)

4 (18.2%)

> 0.99

0.16

0.39

 Head and neck

5 (6.6%)

2 (7.4%)

2 (7.4%)

1 (4.5%)

> 0.99

> 0.99

> 0.99

 Appendiceal

4 (5.3%)

2 (7.4%)

0 (0.0%)

2 (9.1%)

0.49

> 0.99

0.20

 Gynecologic

4 (5.3%)

0 (0.0%)

2 (7.4%)

2 (9.1%)

0.49

0.20

> 0.99

 Breast

3 (3.9%)

1 (3.7%)

2 (7.4%)

0 (0.0%)

> 0.99

> 0.99

0.50

 Lung, non-small cell

3 (3.9%)

2 (7.4%)

1 (3.7%)

0 (0.0%)

> 0.99

0.50

> 0.99

 Genitourinary

2 (2.6%)

0 (0.0%)

0 (0.0%)

2 (9.1%)

--

0.20

0.20

 Skin/melanoma

2 (2.6%)

1 (3.7%)

1 (3.7%)

0 (0.0%)

> 0.99

> 0.99

> 0.99

 Others

8 (10.5%)

1 (3.7%)

4 (14.8%)

3 (13.6%)

0.35

0.31

> 0.99

Number of genomic alterations per patient

 Median (range)

5 (0-15)

5 (1-15)

6 (0-11)

4.5 (0-11)

0.11

0.59

0.42

Number of drugs administered

 ≥ 2 drugs

62 (81.6%)

25 (92.6%)

20 (74.1%)

17 (77.3%)

0.14

0.22

> 0.99

 Single drug

14 (18.4%)

2 (7.4%)

7 (25.9%)

5 (22.7%)

--

--

--

  1. *Age at date of treatment start
  2. Neuroendocrine tumor (N = 2), adrenocortical carcinoma (N = 1), Erdheim-Chester disease (N = 1), Ewing's sarcoma (N = 1), myxofibrosarcoma (N = 1), perivascular epithelioid cell neoplasm (N = 1), and pleomorphic sarcoma (N = 1)
  3. Variants of unknown significance were excluded. Two pathogenic variants in the same gene were counted as two alterations