MEASUREMENT OF QUALITY-OF-LIFE IN PATIENTS WITH LUNG-CANCER IN MULTICENTER TRIALS OF NEW THERAPIES - PSYCHOMETRIC ASSESSMENT OF THE LUNG-CANCER-SYMPTOM-SCALE
Pj. Hollen et al., MEASUREMENT OF QUALITY-OF-LIFE IN PATIENTS WITH LUNG-CANCER IN MULTICENTER TRIALS OF NEW THERAPIES - PSYCHOMETRIC ASSESSMENT OF THE LUNG-CANCER-SYMPTOM-SCALE, Cancer, 73(8), 1994, pp. 2087-2098
Background. This study continued the development and psychometric test
ing of the Lung Cancer Symptom Scale (LCSS), a disease- and site-speci
fic instrument primarily measuring the physical and functional dimensi
ons of quality of life for individuals with lung cancer. The instrumen
t contains two scales, one for patients and a counterpart for health p
rofessionals as observers. Methods. Feasibility, reliability, construc
t validity, and criterion-related validity were evaluated with 207 pat
ients with non-small cell lung cancer (NSCLC) from six cancer centers.
Within an interview with an observer, patients completed part of a ba
ttery of instruments by self-report and were interviewed for the remai
ning measures. Observers also completed measures after the interview.
Results. Feasibility, reliability, and validity were well supported fo
r this lung cancer population. Feasibility was demonstrated by patient
and staff compliance in completion at all six cancer centers. Interna
l consistency was good, with coefficient alphas of 0.82 for the patien
t scale and 0.75 for the observer scale. Construct validity was suppor
ted by 1. contrasted groups approach: regression lines (with 95% confi
dence bands) were obtained between the Karnofsky performance scale (KP
S) and each of the two LCSS scales; 2. as a refinement, relationship t
esting: significant correlations between the LCSS and KPS for each ite
m (except hemoptysis for the patient scale); and 3. multitrait-multime
thod approach: good reliability (alphas ranging from 0.75 to 0.93), go
od convergent validity for the two LCSS scales (r = 0.77), and a good
discriminant validity pattern from the Brief Symptom Inventory (BSI).
Criterion-related validity with relevant gold standard measures (Ameri
can Thoracic Society Questionnaire [ATS] and McGill Pain questionnaire
, KPS, Profiles of Mood States [POMS], and Sickness Impact Profile [SI
P]) was supported with significant correlations (0.40-0.67 for the LCS
S patient scale; 0.54-0.65 for the LCSS observer scale). Conclusions.
These psychometric properties demonstrate that the LCSS patient and ob
server scales are feasible, reliable, and valid quality of life measur
es that are ready for research and clinical use with lung cancer popul
ations.