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Table 1 Sociodemographic and clinical characteristics of the sample

From: Quality of Life in Spanish advanced non-small-cell lung cancer patients: determinants of global QL and survival analyses

Characteristics

No

Percentage

Mean

SD

Present age (range 40–81)

66.1

9.9

 ≥66 years old

24

61.5

  

Gender

 Female

4

10.3

  

 Male

35

89.7

  

Marital status

 Single

1

2.5

  

 Married

36

92.3

  

 Widowed

2

5.2

  

Limiting comorbidity

19

48.7

  

Performance status (range 60–90)a

79.1

8.9

 60–80

26

66.7

  

 90

13

33.3

  

Stage

 IV

35

89.7

  

 III-B

4

10.3

  

Histological types

 Adenocarcinoma

18

46.2

  

 Large-cell carcinoma

1

2.5

  

 Squamous cell carcinoma

19

48.8

  

 Adenosquamous carcinoma

1

2.5

  

Chemotherapy

 Carboplatin doublet

29

74.4

  

 Cisplatin doublet

10

25.6

  

Morphine

29

74.4

  

2nd assessment

 Performance status (range 30–100)

  

70.5

17.4

Treatment response

 Progressive disease

17

43.6

  

 Stable disease

14

35.9

  

 Partial response

8

20.5

  

Toxicity

 Neutropenia

2

5.2

  

 Thrombopenia

2

5.2

  

 Vomiting

1

2.6

  

 Fatigue

1

2.6

  

3rd assessment

 Performance status (range 50–90)

  

76.8

12.1

Treatment response 3rd assessment

 Progression

7

36.8

  

 No changes

12

63.2

  

Chemotherapy cycles received (range 1–14) median 4

5.2

 

 Platin doublet

33

15.4

  

 Platin doublet + maintenance treatment

6

84.6

  

CT from 3 to 2 weeks

3

7.7

  

Time-to-disease progression

 Range 0.93–17.23; median 5.20

  

5.98

4.54

Survival

 Range 2.20–44.63; median 7.45

  

10.99

8.92

  1. aThe median of the Performance status in the first measurement is presented as scores did not follow a normal distribution
  2. Treatment response 2nd, 3rd assessments: treatment response at second and third assessment points
  3. Toxicity: ≥3 values
  4. Chemotherapy cycles received by those who completed the third assessments
  5. CT from 3 to 2 weeks: patients whose CT changed from being administered every 3 weeks to every 2 weeks
  6. Time to progression and survival in months