Predictive validity of five comorbidity indices in prostate carcinoma patients treated with curative intent

被引:38
作者
Boulos, DL
Groome, PA
Brundage, MD
Siemens, DR
Mackillop, WJ
Heaton, JPW
Schulze, KM
Rohland, SL
机构
[1] Queens Univ, Div Canc Care & Epidemiol, Queens Canc Res Inst, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Urol, Kingston, ON K7L 3N6, Canada
关键词
survival rate; comorbidity; health status indicators; predictive value of tests; reproducibility of results; prostatic neoplasms;
D O I
10.1002/cncr.21813
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Comorbidity is important to consider in clinical research on curative prostate carcinoma because of the role of competing risks. Five chart-based comorbidity indices were assessed for their ability to predict survival. METHODS. This was a case-cohort study of prostate carcinoma patient cohort treated with curative intent in Toronto and Southeast Cancer Care Ontario regions between 1990 and 1996; the subcohort was drawn from these men, whereas cases were cohort members who died from causes other than prostate carcinoma. Comorbidity data were obtained from medical charts (269 subjects). Vital status, age, area of residence, and socioeconomic status information were available. Predictive validity was quantified by the percent variance explained (PVE) over and above age using proportional hazards modeling. RESULTS. The Chronic Disease Score (CDS) (PVE = 11.3%; 95% confidence interval [95% CI], 3.5-22.8%), Index of Coexistent Disease (ICED) (PVE = 9.0%; 95% Cl, 2.9-17.9%), Cumulative Illness Rating Scale (CIRS) (PVE = 7.2%; 95% CI, 1.4-17.1%), Kaplan-Feinstein Index (PVE = 4.9%; 95% CI, 0.6-12.8%), and Charlson Index (PVE = 3.8%; 95% CI, 0.3-10.9%) each explained some outcome variability beyond age. PVE differences among indices were not statistically significant. A comorbidity identified at the time of cancer diagnosis was the cause of death in 59.2% of cases (75% for cardiac or vascular causes). CONCLUSIONS. The better-performing, more comprehensive indices (CDS, ICED, and CIRS) would be useful in measuring and controlling for comorbidity in this setting. The CDS was easiest to apply and explained the most outcome variability.
引用
收藏
页码:1804 / 1814
页数:11
相关论文
共 45 条
[1]  
Agresti A., 1990, Analysis of categorical data
[2]   The impact of co-morbidity on life expectancy among men with localized prostate cancer [J].
Albertsen, PC ;
Fryback, DG ;
Storer, BE ;
Kolon, TF ;
Fine, J .
JOURNAL OF UROLOGY, 1996, 156 (01) :127-132
[3]   LONG-TERM SURVIVAL AMONG MEN WITH CONSERVATIVELY TREATED LOCALIZED PROSTATE-CANCER [J].
ALBERTSEN, PC ;
FRYBACK, DG ;
STORER, BE ;
KOLON, TF ;
FINE, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (08) :626-631
[4]   ROBUST VARIANCE-ESTIMATION FOR THE CASE-COHORT DESIGN [J].
BARLOW, WE .
BIOMETRICS, 1994, 50 (04) :1064-1072
[5]   Analysis of case-cohort designs [J].
Barlow, WE ;
Ichikawa, L ;
Rosner, D ;
Izumi, S .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1999, 52 (12) :1165-1172
[6]   Impact of comorbidity on survival after surgical resection in patients with stage I non-small cell lung cancer [J].
Battafarano, RJ ;
Piccirillo, JF ;
Meyers, BF ;
Hsu, HS ;
Guthrie, TJ ;
Cooper, JD ;
Patterson, GA .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2002, 123 (02) :280-287
[7]  
*BRIT COL CANC AG, CANC MAN MAN
[8]   A NEW METHOD OF CLASSIFYING PROGNOSTIC CO-MORBIDITY IN LONGITUDINAL-STUDIES - DEVELOPMENT AND VALIDATION [J].
CHARLSON, ME ;
POMPEI, P ;
ALES, KL ;
MACKENZIE, CR .
JOURNAL OF CHRONIC DISEASES, 1987, 40 (05) :373-383
[9]   ADAPTING A CLINICAL COMORBIDITY INDEX FOR USE WITH ICD-9-CM ADMINISTRATIVE DATABASES [J].
DEYO, RA ;
CHERKIN, DC ;
CIOL, MA .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1992, 45 (06) :613-619
[10]   A VALIDATION OF THE FUNCTIONAL INDEPENDENCE MEASUREMENT AND ITS PERFORMANCE AMONG REHABILITATION INPATIENTS [J].
DODDS, TA ;
MARTIN, DP ;
STOLOV, WC ;
DEYO, RA .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1993, 74 (05) :531-536