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Logo of hlthqualBioMed CentralBiomed Central Web Sitesearchsubmit a manuscriptregisterthis articleHealth and Quality of Life OutcomesJournal Front Page
Health Qual Life Outcomes. 2008; 6: 66.
Published online 2008 August 25. doi:  10.1186/1477-7525-6-66
PMCID: PMC2538505

Predictors of health-related quality of life in patients with colorectal cancer



Most studies that have identified variables associated with the health-related quality of life (HRQL) of patients with colorectal cancer have been cross-sectional or included patients with other diagnoses. The objectives of this study were to identify predictors of HRQL in patients with colorectal cancer and interpret the clinical importance of the results.


We conducted a population-based longitudinal study of patients identified through three regions of the California Cancer Registry. Surveys were completed by 568 patients approximately 9 and 19 months post-diagnosis. Three HRQL outcomes from the Functional Assessment of Cancer Therapy – Colorectal (FACT-C) were evaluated: social/family well-being (SWB), emotional well-being (EWB) and the Trial Outcome Index (TOI), which is a colorectal cancer-specific summary measure of physical function and well-being. Sociodemographic, cancer/health, and healthcare variables were assessed in multivariable regression models. We computed the difference in predicted HRQL scores corresponding to a large difference in a predictor variable, defined as a 1 standard deviation difference for interval variables or the difference relative to the reference category for nominal variables. The effect of an explanatory variable on HRQL was considered clinically meaningful if the predicted score difference was at least as large as the minimally important difference.


Common predictors of better TOI, SWB and EWB were better general health and factors related to better perceived quality of cancer care. Predictor variables in addition to general health and perceived quality of care were identified only for SWB. Being married/living as married was associated with better SWB, whereas being male or of Hispanic ethnicity was associated with worse SWB. Among the sociodemographic, cancer/health, and healthcare variables evaluated, only Hispanic ethnicity had a clinically meaningful effect on an HRQL outcome.


Our findings, particularly the information on the clinical importance of predictor variables, can help clinicians identify patients who may be at risk for poor future HRQL. Potentially modifiable factors were related to perceived quality of cancer care; thus, future research should evaluate whether improving these factors improves HRQL.


Most patients with colorectal cancer survive at least five years after diagnosis [1], making health-related quality of life (HRQL) an important outcome for these patients. Patient-reported outcomes including HRQL have been used in conjunction with traditional clinical outcomes, such as treatment response rates and disease-free survival, to assess treatment efficacy in randomized clinical trials [2-4]. HRQL is also used in quality of care research [5] and is a predictor of survival of patients with colorectal cancer [6-8]. Understanding the characteristics or conditions that predict subsequent HRQL may help clinicians identify patients who are at risk for poor HRQL. Furthermore, if a characteristic or condition is modifiable, an intervention to alter it could lead to improved HRQL.

Most studies of HRQL of patients with colorectal cancer have been cross-sectional [9-11]. While cross-sectional analyses are valuable, longitudinal analyses of predictors of HRQL are needed to understand how HRQL changes over time [11]. Previous studies of HRQL that combined data from patients with colorectal cancer and patients with other diagnoses such as breast or lung cancer [12-14] may have failed to identify relationships involving disease- and treatment-related side-effects specific to patients with colorectal cancer. Furthermore, previous research tends to focus on the HRQL of cancer patients while in treatment [15] or the HRQL of cancer survivors several years post-diagnosis [16-18]. Less is known about HRQL during the period when patients have completed treatment and are transitioning to the survivorship phase. A final limitation of previous research on predictors of HRQL is that it has not considered whether the variables identified based on statistical criteria are also clinically meaningful. Therefore, our study had the following two objectives: (1) to identify variables that predict HRQL in a prospective, population-based study of patients with colorectal cancer, and (2) to interpret the regression results in the context of clinical importance.


Study population

Men and women aged 40 to 84 diagnosed with invasive (i.e., excluding in situ) colorectal cancer from April 1999 through June 2000 were identified from three of the ten regional registries that comprise the statewide population-based California Cancer Registry (CCR): Region 1 (San Jose/Monterey area), Region 3 (Sacramento area), and Region 8 (San Francisco/Oakland area) [19].

Timing of assessments

This study employed rapid case ascertainment to identify eligible patients within 3 to 6 months of diagnosis. Respondents were first assessed in an initial survey an average of 9.2 months (range 4.6 – 23.0 months; SD 2.6 months) post-diagnosis when most patients would have recovered from their cancer surgery and completed their adjuvant treatment, if any. The primary purpose of the initial survey was to assess the quality of care for colorectal cancer by hospital and patient characteristics. The initial survey, as previously described [20], was completed by 1,079 English- or Spanish-speaking respondents (response rate 72.4%).

Patients were eligible for participation in the follow-up survey if they completed the initial survey and were English-speaking. A total of 830 English-speaking respondents in the initial survey were invited to participate in the follow-up survey an average of 19.1 months (range 13.0 – 31.8 months; SD 2.7 months) after diagnosis when most patients would be in a relatively stable disease state. The average time between the initial and follow-up surveys was 10.2 months (range 4.7 – 17.4 months; SD 1.8 months). Data for both the initial and follow-up surveys were collected predominantly via telephone by trained interviewers from the California Public Health Institute's Survey Research Group. Some patients were surveyed through a mailed, self-administered questionnaire, particularly patients who were hearing-impaired or not successfully contacted by telephone. Institutional review boards of the California Department of Health Services, Public Health Institute, Harvard Medical School, and the Northern California Cancer Center approved the study protocols for the initial and follow-up surveys. Participant consent was obtained prior to conducting the surveys.


HRQL was measured in the initial and follow-up surveys with the Functional Assessment of Cancer Therapy-Colorectal (FACT-C) [21]. The FACT-C is a valid and reliable measure of HRQL and includes five subscales: Physical Well-Being (PWB, 7-items), Functional Well-Being (FWB, 7-items), Social/family Well-Being (SWB, 7-items), Emotional Well-Being (EWB, 6-items), and the Colorectal Cancer Subscale (CCS, 7-items), which measures concerns specific to colorectal cancer patients such as appetite and bowel control [21]. The FACT-C was scored as described in the documentation for the instrument, with higher scores indicating better HRQL [22]. The Trial Outcome Index (TOI), derived as the sum of the PWB, FWB, and CCS subscales, is a summary measure of physical function and well-being in colorectal cancer patients that is useful as a patient-reported outcome in pharmacologic interventions [21]. The TOI and the remaining two subscales, SWB and EWB, were the HRQL outcomes evaluated in this study.

Patients' perceived quality of cancer care was measured using 31 items obtained from the Picker Institute of Boston, Massachusetts [20,23,24] that measure problems associated with six aspects of cancer care: psychosocial care, access to cancer care, treatment information, health information, confidence in providers, and coordination of care. Two items measuring patients' perceptions of how well healthcare providers controlled their pain/discomfort and nausea/vomiting were also included. Higher scores indicate greater perceived problems with care.

Limitations due to each of 14 comorbid conditions were measured in the initial survey and scored as 0 if the condition was not present, 1 if the condition was present but did not limit the patient, or 2 if the condition was present and limited the patient. Scores were summed to create a comorbidity index (range 0 to 28) [12,25]. General health was measured with a single item from the Medical Outcomes Study 36-item Short form (SF-36) health survey [26]. Bowel function and overall bowel problems were measured with items from the Prostate Cancer Outcomes Study [27]. Respondents who had a colostomy at the time of the interviews were not asked these bowel-related items, including 131 (12.1%) of 1,079 patients in the initial survey and 54 (9.5%) of 568 patients in the follow-up survey.

Sociodemographic information collected via survey included race/ethnicity, education, household income, financial difficulty due to cancer, occupational status, marital status, and number of persons living in the household. Gender, age at diagnosis and stage at diagnosis were obtained from the CCR. Neighborhood socioeconomic status (SES) was calculated based on 2000 U.S. Census data using methods described in Yost et al. [28].

Data analyses

Non-response bias

To assess potential non-response bias, characteristics of eligible patients who did not participate in the follow-up survey were compared to those of patients who did using standard statistical tests for continuous and categorical data. All candidate predictor variables for the longitudinal analyses were measured either at the time of diagnosis or during the initial survey.

Regression models

Because previous studies of predictors of HRQL are inconclusive [11-13,17,29-31], we adopted an exploratory approach to identify variables predictive of HRQL at the follow-up survey. The range of time since diagnosis for the initial survey (4.6 – 23.0 months) overlapped with that for the follow-up survey (13.0 – 31.8 months). Therefore, we created non-overlapping time periods for each survey centered around the means (i.e., 9 months for initial survey and 19 months for the follow-up survey). The time period for the initial survey was restricted from 4 to less than 14 months post-diagnosis and the time period for the follow-up survey was restricted from 14 to less than 24 months post-diagnosis. The regression analyses were restricted to participants who completed their initial and follow-up surveys within these ranges. This resulted in the exclusion of 43 participants who were missing data for time since diagnosis for either the initial or follow-up survey and 29 participants who were outside of the restricted time frames. Following these exclusions, the mean times since diagnosis for the 496 respondents were 8.6 months (range 4.6–13.9, SD 1.7) for the initial survey and 18.8 months (range 14.0–24.0, SD 2.1) for the follow-up survey.

Separate linear regression analyses [32] were conducted for each of the three HRQL outcomes measured at the follow-up survey using the following candidate predictor variables. Initial HRQL: TOI, SWB or EWB measured at the initial survey. Sociodemographic: age at diagnosis, gender, race/ethnicity, marital status (married/living as married vs. not married), education (high school or less vs. technical school or some college, college or higher), occupational status (working vs. not working), number in household, neighborhood SES (standardized principal component score [28]), financial problems due to cancer, and household income (missing, <$25,000, $25,000–$50,000 vs. $50,000+). Household income was not reported by 58 (10.2%) respondents. Rather than exclude these respondents from the analyses, "missing" income was treated as a separate income category. Cancer/health: stage at diagnosis (Stage I/II/III vs. Stage IV), general health, colostomy (yes/no), history of radiation therapy (yes/no), history of chemotherapy (yes/no), currently receiving chemotherapy at the time of the initial survey (yes/no), comorbidity index, bowel function, overall bowel problems, family history of colorectal cancer (yes/no), time since diagnosis, and site (colon vs. rectum). Healthcare: type of health insurance [Medicare, other/none (e.g., Medicaid, other government-provided, uninsured) vs. commercial (e.g., HMO, PPO, private)], six domains of perceived quality of care, control of pain and discomfort (definitely vs. somewhat/not at all) and control of nausea and vomiting (definitely vs. somewhat/not at all).

Variables associated with HRQL were selected in two stages. First, follow-up HRQL was regressed on initial HRQL plus one other candidate variable. Candidate variables that had a significant relationship with follow-up HRQL by a liberal (p < 0.25) criterion were identified [33]. These variables were then combined into a multivariable model. Backward elimination with a criterion of p < 0.05 for retention was used to select a final model. We also conducted forward and stepwise regression to determine whether the same model was identified. Multicollinearity in the final models was assessed with the variance inflation factor (VIF). To facilitate interpretation of our regression results, we report squared semi-partial correlations (sr2) in addition to p-values. Because the sr2 expresses the unique variance in the dependent variable explained by a predictor variable, it is a useful measure of the importance of a predictor [34].

Meaningful effects

We assessed the clinical meaningfulness of each predictor variable [35,36]. For interval variables (e.g., age), we computed the difference in predicted HRQL scores corresponding to a large difference in a predictor variable, defined as a 1 SD difference [37], where the SD was based on the data for the 496 respondents evaluated in the regression analyses. For nominal variables (e.g., race/ethnicity), we computed the difference in the predicted HRQL score relative to the reference category. The effect of an explanatory variable on follow-up HRQL was considered meaningful if the corresponding predicted score difference was at least as large as the minimally important difference (MID), which we defined as the smallest difference in HRQL scores that patients perceive as important, and thus might lead a clinician to consider changing the patient's management [38]. MIDs have been determined for the TOI (4–6 points) [39] and the SWB and EWB subscales (2–3 points) [40]. We used the lower bounds of these ranges to identify clinically meaningful effects as an indication of the potential prognostic impact of predictor variables. We also computed the percent of patients whose HRQL improved or declined more than the lower bound of the MID range.


Sample characteristics

Of the 830 English-speaking patients invited to participate in the follow-up study, 26 were ineligible because they had died. Follow-up surveys were completed by 568 (70.6%) of the 804 eligible patients. Of the 236 patients who did not participate in the follow-up study, 28 were either hearing or mentally impaired or too ill to participate, 79 refused, and 129 were not successfully contacted.

Table Table11 summarizes the characteristic at the time of diagnosis or at the time of the initial survey for the 496 participants of the follow-up survey with non-overlapping survey periods who were evaluated in this study. Characteristics for all 568 respondents and the 236 non-respondents of the follow-up survey are also described in Table Table1.1. Non-respondents were significantly more likely to be non-white, unmarried, with low income, more financial problems due to cancer, longer time since diagnosis, have more perceived problems with access to care, confidence in providers, and coordination of care, and more perceived problems with control of pain/discomfort. They were significantly less likely to be on chemotherapy at the time of the initial survey. HRQL scores measured in the initial survey were lower for non-respondents than for respondents of the follow-up survey. Cronbach's alpha, a measure of reliability, was acceptable (≥0.70) in both the initial and follow-up surveys, respectively, for the TOI scale (0.90, 0.90) and the SWB (0.74, 0.77) and EWB (0.74, 0.76) subscales. The 95% confidence intervals around the initial scores for SWB (22.9, 23.7) and EWB (20.1, 20.7) for the 568 respondents did not contain the general U.S. population norms of 19.1 and 19.9 for the SWB and EWB, respectively [41], nor did they contain the norms for colon cancer patients of 22.0 and 19.8, respectively [22]. This indicates that the respondents had significantly higher scores for these domains than the norms. There are no general or cancer-specific norms for the TOI.

Table 1
Characteristics of follow-up survey respondents and non-respondents at the time of diagnosis or the initial survey

Clinically meaningful change in HRQL

The percent of patients with a clinically meaningful decline in EWB scores from the initial to follow-up survey was exactly the same as the percent with a clinically meaningful improvement (Table (Table2).2). Slightly more patients had a meaningful improvement than decline in TOI scores, but fewer patients had a meaningful improvement than decline in SWB scores. EWB scores were the most stable, with 47.6% of patients experiencing a change less than the MID. The magnitude of the average decline in scores was slightly larger than that of the average improvement for all three HRQL outcomes.

Table 2
Clinically meaningful change in HRQL* from the initial to follow-up surveys

Prognostic impact on patient-reported HRQL

Predictors of follow-up TOI scores

In addition to initial TOI scores, two variables were retained as predictors of follow-up TOI following backward elimination (Table (Table3),3), accounting for 43.9% of the variance. Forward and stepwise selection identified the same model. No sociodemographic variables were retained. One cancer/health-related variable, general health, was retained. The Treatment Information problem score from the Picker Institute measure was the only healthcare variable retained. Only initial TOI was a clinically meaningful predictor of follow-up TOI, with a 1 SD increase (12.7 points) in initial TOI scores corresponding to a 6.4 point increase in follow-up TOI scores. Initial TOI accounted for the largest proportion of variance, as indicated by the sr2. The p-value, sr2 and effect on follow-up TOI indicated that general health had a greater prognostic impact than Treatment Information. All VIFs were less than 2.0 indicating there was no multicolinearity among the predictors.

Table 3
Predictors of follow-up TOI

Predictors of follow-up SWB scores

Backward selection identified a model with six statistically significant predictors of follow-up SWB explaining a total of 39.3% of the variance (Table (Table4),4), including initial SWB, three sociodemographic indicators (gender, race/ethnicity, marital status), one cancer/health-related indicator (general health), and one healthcare measure (problems with control of pain/discomfort). Forward and stepwise selection yielded a slightly different model that did not include gender and marital status. We report the model identified using backward selection as it had a larger adjusted R2 (39.3 vs. 38.1). Both initial SWB and Hispanic ethnicity were clinically meaningful predictors of follow-up SWB. Hispanic ethnicity also had a larger sr2 relative to the other sociodemographic, cancer/health and healthcare variables.

Table 4
Predictors of follow-up SWB

Predictors of follow-up EWB scores

Predictors of EWB at the follow-up survey included initial EWB, general health and control of nausea/vomiting, explaining 36.5% of the variance (Table (Table5).5). Backward, forward and stepwise selection all identified the same model. After initial EWB, general health had the largest sr2, while problems with control of nausea/vomiting had the largest prognostic impact as indicated by the size of the effect on follow-up EWB. Initial EWB was the only meaningful predictor of follow-up EWB.

Table 5
Predictors of follow-up EWB


Exploratory longitudinal analyses were conducted to evaluate the relationship between three HRQL outcomes and sociodemographic, cancer/health, and healthcare variables in a population-based sample of patients with colorectal cancer. General health was the only variable common to all three outcomes, although each model also contained a quality of care variable: Perceived problems with Treatment Information was a predictor of follow-up TOI, perceived problems with control of pain/discomfort predicted follow-up SWB and perceived problems with control of nausea/vomiting was a predictor of follow-up EWB.

Rather than relying solely on statistical measures such as p-values and sr2 to interpret the results of the regression analyses, we also used clinical meaningfulness of the effect of a predictor variable on the HRQL outcome. For follow-up TOI, both initial TOI and general health were highly statistically significant predictors (p < 0.001). The sr2 for general health was smaller than that for initial TOI, but even with this information, it may still not be intuitive to some clinicians or researchers whether to consider general health as an important predictor. By considering the clinical importance of these variables, we showed that even a large (1 SD) difference in the general health score would not have a clinically meaningful effect on follow-up TOI scores. This information may help clinicians and researchers understand the results regardless of their familiarity with regression modeling or the FACT-C instrument.

Perceived problems with Treatment Information was also retained in the model for follow-up TOI. A measure of perceived quality of treatment information is not commonly included in studies aimed at identifying predictors of HRQL. That this variable was identified in our study as a significant predictor of HRQL over other commonly evaluated variables such as gender, age, and comorbidities [12,17,30] warrants the addition of perceived quality of treatment information to the list of candidate variables in future research of HRQL predictors.

Relative to non-Hispanic White participants, Hispanic participants had significantly lower follow-up SWB. Wan et al. [14] also observed significantly lower SWB scores among Hispanic cancer patients relative to White patients. Both initial SWB and Hispanic ethnicity were highly significantly related to follow-up SWB (p < 0.001). The sr2 for Hispanic ethnicity was much smaller than that for initial SWB suggesting that Hispanic ethnicity was the less influential predictor of the two. However, by considering clinical importance, we obtained a slightly different interpretation; that the two variables had comparable clinically meaningful effects on follow-up SWB.

The relationship between gender and the social domain of HRQL may depend on how the domain is measured. For example, as measured in the present study with the FACT-C, men had worse initial SWB (data not shown) and follow-up SWB than women. Normative data for the SWB in both the general U.S. population and cancer patients also show lower average scores for men than women [41]. However, several studies have evaluated the relationship between gender and social functioning as measured by the EORTC QLQ-C30 in cancer patients and reported no differences [31,42,43].

Although the association between being married/living as married and having better physical and psychological well-being is well established, the link between marital status and SWB is less clear [44]. We found that married/living as married persons had better SWB as measured by the FACT-C, which is predominantly a measure of social support and contains items such as "I get emotional support from my family" and "I feel close to my partner (or the person who is my main support)." It is reasonable to expect married/living as married persons to answer these questions more favorably.

Initial EWB was the only meaningful predictor of follow-up EWB. After initial EWB, general health was the strongest predictor based on the p-value and sr2, but problems with control of nausea and vomiting was the strongest predictor based on the effect on follow-up EWB score. Thus, by considering clinical importance, we obtained a slightly different interpretation of the importance of these two predictors.

The measures of perceived quality of care (problems with Treatment Information, control of pain/discomfort, control of nausea/vomiting) are the only predictors of HRQL in our study that are potentially modifiable. These variables are not typically included as predictors of HRQL in multivariable regression analyses, yet they were more clinically meaningful predictors of the HRQL outcomes than some more commonly evaluated predictors, including gender, marital status and general health. Additional research is needed to better understand the association between factors related to perceived quality of care at the time of cancer treatment and HRQL at some follow-up assessment. Furthermore, as these are potentially modifiable variables, intervention studies could explore methods for improving certain aspects of quality of care to determine whether those changes lead to improved HRQL.

While only a few of the statistically significant predictors individually met our criteria for clinical importance, in combination they may identify patients at high risk for poor HRQL. For example, unmarried male patients with worse general health and more perceived problems with control of pain/discomfort may have meaningfully lower average follow-up SWB scores (i.e., at least 2 points lower) than married female patients with better general health and fewer perceived problems with control of pain/discomfort even after adjusting for initial SWB. Initial HRQL was consistently the strongest predictor of follow-up HRQL; therefore, clinicians could identify patients at risk for poor future HRQL by routinely assessing HRQL in clinical practice [45].

A strength of our study is that the respondents were identified through a population-based cancer registry and were therefore representative of English-speaking colorectal cancer patients in California. A potential limitation of our study is possible non-response bias in the follow-up sample. The follow-up respondents and non-respondents differed significantly on a number of variables that may be related to follow-up HRQL, which limits the generalizability of our results. In particular, non-respondents had significantly lower initial HRQL than respondents and therefore likely had lower follow-up HRQL. Nonresponse might also have affected the selection and estimated prognostic impact of predictors of HRQL. Another potential limitation is that there may be other variables predictive of follow-up HRQL that were not considered in this analysis. Variables such as spiritual well-being [14,46], optimism [47], and sexual dysfunction [10] have been shown to be related to HRQL. However, these topics were not measured in the initial survey. The follow-up survey did not measure whether the respondents had experienced a recurrence or whether they were undergoing any adjuvant treatment for either their primary or a recurrent cancer, which could have affected their follow-up HRQL [29,48,49]. Because of inconclusive results in the literature regarding variables that predict HRQL in colorectal patients, we adopted an exploratory approach and evaluated a large number of variables, including variables rarely, if ever, evaluated previously in this population as potential predictors, such as perceived quality of cancer care. Thus, another potential limitation of our study is an inflated type I error. The predictors of HRQL in patients with colorectal cancer may differ from those in patients with other types of cancer. Furthermore, the predictors of HRQL may vary based on how HRQL is measured.


We identified sociodemographic, clinical, and healthcare variables that predict HRQL as measured by the FACT-C. The most consistent finding was that patients with poor general health and problems with certain domains of perceived quality of cancer care may be at risk for poor HRQL. Other characteristics that might identify at-risk patients were specific to each HRQL outcome and included being male, unmarried or Hispanic. Computing the clinical importance of the effect on the HRQL outcome helped to interpret the impact of specific statistically significant predictors. As the only potentially modifiable variables identified in our study were related to perceived quality of cancer care, future research should evaluate whether interventions aimed at improving these variables enhances subsequent HRQL.

List of abbreviations

HRQL: Health-related quality of life; FACT-C: Functional Assessment of Cancer Therapy-Colorectal; PWB: Physical well-being; EWB: Emotional well-being; SWB: Social/family well-being, FWB: Functional well-being; TOI: Trial outcome index; CCR: California Cancer Registry; SD: Standard deviation; HMO: Health maintenance organization; PPO: Preferred provider organization; VIF: Variance inflation factor.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

KJY, AMZ, JZA, and DWW made substantial contributions to the study concept and design, EAH and AMZ provided guidance on the statistical analysis, KJY conducted the statistical analysis, interpreted the results and drafted the manuscript, EAH, AMZ, JZA, and DWW participated in critical revisions of the manuscript for important intellectual content. All authors read and approved the final manuscript.


This work was supported by grants from the Surveillance, Epidemiology and End Results Special Study program (NO1-PC-65107), and the Agency for Healthcare Research and Quality and the National Cancer Institute (R01 HS09869, U01 CA93324). The authors would like to thank William Wright for his guidance on study design and the following individuals for assistance with data collection and database management: Mark Allen, Gretchen Agha, Craig Grilley, Scott Riddle, Bonnie Davis, Ann Hitchcock and staff of the California Public Health Institute Survey Research Group. We also thank David Eton for his thoughtful review and comments.


  • American Cancer Society Cancer Facts and Figures, 2007. Atlanta, GA, American Cancer Society; 2007.
  • Storniolo AM, Enas NH, Brown CA, Voi M, Rothenberg ML, Schilsky R. An investigational new drug treatment program for patients with gemcitabine: results for over 3000 patients with pancreatic carcinoma. Cancer. 1999;85:1261–1268. doi: 10.1002/(SICI)1097-0142(19990315)85:6<1261::AID-CNCR7>3.0.CO;2-T. [PubMed] [Cross Ref]
  • Passik SD, Kirsh KL. The importance of quality-of-life endpoints in clinical trials to the practicing oncologist. Hematol Oncol Clin North Am. 2000;14:877–886. doi: 10.1016/S0889-8588(05)70316-6. [PubMed] [Cross Ref]
  • Hahn EA, Glendenning GA, Sorensen MV, Hudgens SA, Druker BJ, Guilhot F, Larson RA, O'Brien SG, Dobrez DG, Hensley ML, Cella D. Quality of life in patients with newly diagnosed chronic phase chronic myeloid leukemia on imatinib versus interferon alfa plus low-dose cytarabine: results from the IRIS Study. J Clin Oncol. 2003;21:2138–2146. doi: 10.1200/JCO.2003.12.154. [PubMed] [Cross Ref]
  • Treurniet HF, Essink-Bot ML, Mackenbach JP, van der Maas PJ. Health-related quality of life: an indicator of quality of care? Qual Life Res. 1997;6:363–369. doi: 10.1023/A:1018435427116. [PubMed] [Cross Ref]
  • Maisey NR, Norman A, Watson M, Allen MJ, Hill ME, Cunningham D. Baseline quality of life predicts survival in patients with advanced colorectal cancer. Eur J Cancer. 2002;38:1351–1357. doi: 10.1016/S0959-8049(02)00098-9. [PubMed] [Cross Ref]
  • Camilleri-Brennan J, Steele RJ. Prospective analysis of quality of life and survival following mesorectal excision for rectal cancer. Br J Surg. 2001;88:1617–1622. doi: 10.1046/j.0007-1323.2001.01933.x. [PubMed] [Cross Ref]
  • Efficace F, Innominato PF, Bjarnason G, Coens C, Humblet Y, Tumolo S, Genet D, Tampellini M, Bottomley A, Garufi C, Focan C, Giacchetti S, Levi F. Validation of patient's self-reported social functioning as an independent prognostic factor for survival in metastatic colorectal cancer patients: results of an international study by the Chronotherapy Group of the European Organisation for Research and Treatment of Cancer. J Clin Oncol. 2008;26:2020–2026. doi: 10.1200/JCO.2007.12.3117. [PubMed] [Cross Ref]
  • Sprangers MA, Taal BG, Aaronson NK, te Velde A. Quality of life in colorectal cancer. Stoma vs. nonstoma patients. Dis Colon Rectum. 1995;38:361–369. doi: 10.1007/BF02054222. [PubMed] [Cross Ref]
  • Camilleri-Brennan J, Steele RJ. Quality of life after treatment for rectal cancer. Br J Surg. 1998;85:1036–1043. doi: 10.1046/j.1365-2168.1998.00808.x. [PubMed] [Cross Ref]
  • Dunn J, Lynch B, Aitken J, Leggett B, Pakenham K, Newman B. Quality of life and colorectal cancer: a review. Aust N Z J Public Health. 2003;27:41–53. doi: 10.1111/j.1467-842X.2003.tb00378.x. [PubMed] [Cross Ref]
  • Schag CA, Ganz PA, Wing DS, Sim MS, Lee JJ. Quality of life in adult survivors of lung, colon and prostate cancer. Qual Life Res. 1994;3:127–141. doi: 10.1007/BF00435256. [PubMed] [Cross Ref]
  • Rustoen T, Moum T, Wiklund I, Hanestad BR. Quality of life in newly diagnosed cancer patients. J Adv Nurs. 1999;29:490–498. doi: 10.1046/j.1365-2648.1999.00912.x. [PubMed] [Cross Ref]
  • Wan GJ, Counte MA, Cella DF, Hernande L, Deasy S, Shiomoto G. An analysis of the impact of demographic, clinical and social factors on health-related quality of life. Value in Health. 1999;2:308–318. doi: 10.1046/j.1524-4733.1999.24006.x. [PubMed] [Cross Ref]
  • Holloway S, Sarosi G, Kim L, Nwariaku F, O'Keefe G, Hynan L, Jones C, Anthony T. Health-related quality of life and postoperative length of stay for patients with colorectal cancer. J Surg Res. 2002;108:273–278. doi: 10.1006/jsre.2002.6549. [PubMed] [Cross Ref]
  • Trentham-Dietz A, Remington PL, Moinpour CM, Hampton JM, Sapp AL, Newcomb PA. Health-related quality of life in female long-term colorectal cancer survivors. Oncologist. 2003;8:342–349. doi: 10.1634/theoncologist.8-4-342. [PubMed] [Cross Ref]
  • Ramsey SD, Berry K, Moinpour C, Giedzinska A, Andersen MR. Quality of life in long term survivors of colorectal cancer. Am J Gastroenterol. 2002;97:1228–1234. doi: 10.1111/j.1572-0241.2002.05694.x. [PubMed] [Cross Ref]
  • Anthony T, Jones C, Antoine J, Sivess-Franks S, Turnage R. The effect of treatment for colorectal cancer on long-term health-related quality of life. Ann Surg Oncol. 2001;8:44–49. doi: 10.1007/s10434-001-0044-2. [PubMed] [Cross Ref]
  • Kwong S, Perkins CI, Morris CR, Cohen R, Allen M, Wright WE. Cancer in California: 1988-1999. Sacramento, CA, California Department of Health Services, Cancer Surveillance Section; 2001.
  • Ayanian JZ, Zaslavsky AM, Guadagnoli E, Fuchs CS, Yost KJ, Creech CM, Cress RD, O'Conner LC, West DW, Wright WE. Patients' perceptions of quality of care for colorectal cancer by race, ethnicity, and language. J Clin Oncol. 2005;23:6576–6586. doi: 10.1200/JCO.2005.06.102. [PubMed] [Cross Ref]
  • Ward WL, Hahn WA, Mo F, Hernandez L, Tulsky DS, Cella D. Reliability and validity of the Functional Assessment of Cancer Therapy-Colorectal (FACT-C) quality of life instrument. Qual Life Res. 1999;8:181–195. doi: 10.1023/A:1008821826499. [PubMed] [Cross Ref]
  • Cella D. Manual of the Functional Assessment of Chronic Illness Therapy (FACIT Scales) - Version 4.1. Evanston, IL, Center on Outcomes, Research & Education (CORE), Evanston Northwestern Healthcare and Northwestern University; 2004.
  • Cleary PD, Edgman-Levitan S. Health care quality. Incorporating consumer perspectives. JAMA. 1997;278:1608–1612. doi: 10.1001/jama.278.19.1608. [PubMed] [Cross Ref]
  • Cleary PD, McNeil BJ. Patient satisfaction as an indicator of quality care. Inquiry. 1988;25:25–36. [PubMed]
  • Kaplan MH, Feinstein AR. The importance of classifying initial co-morbidity in evaluating the outcome of diabetes mellitus. J Chronic Dis. 1974;27:387–404. doi: 10.1016/0021-9681(74)90017-4. [PubMed] [Cross Ref]
  • Ware JE, Snow KK, Kosinski M. SF-36 Health Survey: Manual and Interpretation Guide. Lincoln, RI, QualityMetric Incorporated; 2000.
  • Potosky AL, Harlan LC, Stanford JL, Gilliland FD, Hamilton AS, Albertsen PC, Eley JW, Liff JM, Deapen D, Stephenson RA, Legler J, Ferrans CE, Talcott JA, Litwin MS. Prostate cancer practice patterns and quality of life: the Prostate Cancer Outcomes Study. J Natl Cancer Inst. 1999;91:1719–1724. doi: 10.1093/jnci/91.20.1719. [PubMed] [Cross Ref]
  • Yost K, Perkins C, Cohen R, Morris C, Wright WE. Socioeconomic status and breast cancer incidence in California for different race/ethnic groups. Cancer Causes Control. 2001;12:703–711. doi: 10.1023/A:1011240019516. [PubMed] [Cross Ref]
  • Parker PA, Baile WF, De Moor C, Cohen L. Psychosocial and demographic predictors of quality of life in a large sample of cancer patients. Psychooncology. 2003;12:183–193. doi: 10.1002/pon.635. [PubMed] [Cross Ref]
  • Ramsey SD, Andersen MR, Etzioni R, Moinpour C, Peacock S, Potosky A, Urban N. Quality of life in survivors of colorectal carcinoma. Cancer. 2000;88:1294–1303. doi: 10.1002/(SICI)1097-0142(20000315)88:6<1294::AID-CNCR4>3.0.CO;2-M. [PubMed] [Cross Ref]
  • Mosconi P, Apolone G, Barni S, Secondino S, Sbanotto A, Filiberti A. Quality of life in breast and colon cancer long-term survivors: an assessment with the EORTC QLQ-C30 and SF-36 questionnaires. Tumori. 2002;88:110–116. [PubMed]
  • Neter J, Wasserman W, Kutner MH. Applied Linear Statistical Models. 3rd. Burr Ridge, IL, Richard D. Irwin, Inc.; 1990.
  • Hosmer DW, Lemishow S. Applied Logistic Regression. Second. New York, John Wiley & Sons; 2000. [PubMed]
  • Tabachnick BG, Fidell LS. Using Multivariate Statistics. Third. New York, NY, HarperCollins College Publishers; 1996. Multivariate Analysis of Variance and Covariance; pp. 375–440.
  • Martin P. Seattle Symposium on Cancer Research Outcomes: commentary on the papers by Donaldson and Moinpour and by Osoba. Med Care. 2002;40:III54–5. doi: 10.1097/00005650-200206001-00008. [PubMed] [Cross Ref]
  • McHorney CA. The potential clinical value of quality-of-life information response to Martin. Med Care. 2002;40:III56–62. [PubMed]
  • Cohen J. Statistical Power Analysis for the Behavioral Sciences. Second. Hillsdale, NJ, Lawrence Erlbaum Associates; 1988.
  • Guyatt GH, Osoba D, Wu AW, Wyrwich KW, Norman GR. Methods to explain the clinical significance of health status measures. Mayo Clin Proc. 2002;77:371–383. [PubMed]
  • Yost KJ, Cella D, Chawla A, Holmgren E, Eton DT, Ayanian JZ, West DW. Minimally important differences were estimated for the Functional Assessment of Cancer Therapy-Colorectal (FACT-C) instrument using a combination of distribution- and anchor-based approaches. J Clin Epidemiol. 2005;58:1241–1251. doi: 10.1016/j.jclinepi.2005.07.008. [PubMed] [Cross Ref]
  • Yost KJ, Sorensen MV, Hahn EA, Glendenning GA, Gnanasakthy A, Cella D. Using Multiple Anchor- and Distribution-Based Estimates to Evaluate Clinically Meaningful Change on the Functional Assessment of Cancer Therapy-Biologic Response Modifiers (FACT-BRM) Instrument. Value in Health. 2005;8:117–127. doi: 10.1111/j.1524-4733.2005.08202.x. [PubMed] [Cross Ref]
  • Brucker PS, Yost K, Cashy J, Webster K, Cella D. General population and cancer patient norms for the Functional Assessment of Cancer Therapy-General (FACT-G) Eval Health Prof. 2005;28:192–211. doi: 10.1177/0163278705275341. [PubMed] [Cross Ref]
  • Rauch P, Miny J, Conroy T, Neyton L, Guillemin F. Quality of life among disease-free survivors of rectal cancer. J Clin Oncol. 2004;22:354–360. doi: 10.1200/JCO.2004.03.137. [PubMed] [Cross Ref]
  • Schmidt CE, Bestmann B, Kuchler T, Longo WE, Rohde V, Kremer B. Gender differences in quality of life of patients with rectal cancer. A five-year prospective study. World J Surg. 2005;29:1630–1641. doi: 10.1007/s00268-005-0067-0. [PubMed] [Cross Ref]
  • Shapiro A, Keyes CLM. Marital status and social well-being: Are the married always better off? Soc Indic Res. 2007;Online
  • Detmar SB, Muller MJ, Schornagel JH, Wever LD, Aaronson NK. Health-related quality-of-life assessments and patient-physician communication: a randomized controlled trial. JAMA. 2002;288:3027–3034. doi: 10.1001/jama.288.23.3027. [PubMed] [Cross Ref]
  • Cohen SR, Mount BM, Tomas JJ, Mount LF. Existential well-being is an important determinant of quality of life. Evidence from the McGill Quality of Life Questionnaire. Cancer. 1996;77:576–586. doi: 10.1002/(SICI)1097-0142(19960201)77:3<576::AID-CNCR22>3.0.CO;2-0. [PubMed] [Cross Ref]
  • Allison PJ, Guichard C, Gilain L. A prospective investigation of dispositional optimism as a predictor of health-related quality of life in head and neck cancer patients. Qual Life Res. 2000;9:951–960. doi: 10.1023/A:1008931906253. [PubMed] [Cross Ref]
  • Schultz AA, Winstead-Fry P. Predictors of quality of life in rural patients with cancer. Cancer Nurs. 2001;24:12–19. doi: 10.1097/00002820-200102000-00002. [PubMed] [Cross Ref]
  • Padilla GV, Grant MM, Lipsett J, Anderson PR, Rhiner M, Bogen C. Health quality of life and colorectal cancer. Cancer. 1992;70:1450–1456. doi: 10.1002/1097-0142(19920901)70:3+<1450::AID-CNCR2820701537>3.0.CO;2-E. [PubMed] [Cross Ref]

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