- Open Access
Can changes in health related quality of life scores predict survival in stages III and IV colorectal cancer?
© Braun et al; licensee BioMed Central Ltd. 2011
- Received: 18 June 2011
- Accepted: 3 August 2011
- Published: 3 August 2011
Several studies have demonstrated the predictive significance on survival of baseline quality of life (QoL) in colorectal cancer (CRC) with little information on the impact of changes in QoL scores on prognosis in CRC. We investigated whether changes in QoL during treatment could predict survival in CRC.
We evaluated 396 stages III-IV CRC patients available for a minimum follow-up of 3 months. QoL was evaluated at baseline and after 3 months of treatment using EORTC QLQ-C30. Cox regression evaluated the prognostic significance of baseline, 3-month and changes in QoL scores after adjusting for age, gender and stage at diagnosis.
After adjusting for covariates, every 10-point increase in both baseline appetite loss and global QoL score was associated with a 7% increased risk of death with HR = 1.07 (95% CI, 1.01-1.14; P = 0.02) and (HR = 0.93 (95% CI, 0.87-0.98; P = 0.01) respectively. A lower risk of death was associated with a 10-point improvement in physical function at 3 months (HR, 0.86; 95% CI, 0.78-0.94; P = 0.001). Surprisingly, a higher risk of death was associated with a 10-point improvement in social function at 3 months (HR, 1.08; 95% CI, 1.02-1.13; P = 0.008).
This study provides preliminary evidence to indicate that CRC patients whose physical function improves within 3 months of treatment have a significantly increased probability of survival. These findings should be used in clinical practice to systematically address QoL-related problems of CRC patients throughout their treatment course.
- Appetite Loss
- Prior Treatment History
Quality of life (QoL) is a multidimensional construct. A growing consensus among health care providers and researchers is that treatment efficacy should be judged by effects on both quantity and quality of life; this has led to the inclusion of QoL assessment as a primary endpoint in cancer clinical trials along with traditional endpoints of tumor response and survival. There is general agreement in the medical and scientific research community that patients are the best source of information regarding their QoL. Consequently, the use of self-reported QoL assessment has become a valuable tool for both clinical practice and research. There are extensive data in the literature demonstrating that pretreatment/baseline QoL can predict survival in several different types of cancers independent of the extent of the disease and other clinical prognostic factors [1–10], however, evidence is only beginning to emerge regarding the prognostic significance of changes in QoL scores in cancer [11–15].
Advanced stage colorectal cancer (CRC) is associated with significant morbidity, which when coupled with the adverse effects of cancer treatment, can further deteriorate patient QoL. A few studies have evaluated the relationship between pretreatment QoL and survival in CRC [7, 16–19]. However, to the best of our knowledge, there is no study in the literature investigating the prognostic significance of changes in QoL scores in CRC. In the current study, we investigated whether pretreatment QoL parameters as well as changes in QoL scores from baseline until 3 months after treatment could predict survival in patients with stages III-IV CRC.
We examined 396 histologically confirmed stages III and IV colorectal cancer patients treated at Cancer Treatment Centers of America® at Midwestern (MRMC) and Southwestern (SRMC) Regional Medical Centers between January 2001 and December 2009. None of these patients had received any treatment at our hospitals when contacted to participate in this investigation. The inclusion criteria for participation in this study were a histological diagnosis of stage III or IV colorectal cancer and the ability to read English. Patients were excluded if they were unable to give informed consent or were unable to understand or cooperate with study conditions.
A trained clinical coordinator was responsible for determining eligibility, describing the study, and obtaining informed consent. All patients were assured that refusal to participate would not affect their future care in any way. Patients who chose to participate were presented with the QoL questionnaire at their initial/baseline visit and instructed to return their completed questionnaires to the clinical coordinator within 24 hours. Thus, patients completed baseline QoL questionnaires prior to receiving therapy at our facility. Following the completion of the baseline questionnaire, all patients were treated with an integrative model combining surgery, radiation and chemotherapy as appropriate, plus complementary therapy consisting primarily of nutritional, psychosocial, and spiritual support, naturopathic supplements, pain management, and physical therapy/rehabilitation.
Additional data recorded for this study included age at diagnosis, gender, stage of disease at diagnosis (III versus IV) and prior treatment history (previously treated versus newly diagnosed). The only follow-up information required was the date of death or the date of last contact/last known to be alive, obtained from the tumor registries at MRMC and SRMC. This study was approved by the Institutional Review Board at Cancer Treatment Centers of America®.
QoL was assessed at baseline and after 3 months of treatment using the European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30), which emphasizes a patient's capacity to fulfill the activities of daily living. The EORTC QLQ-C30 is a 30-item cancer specific questionnaire that incorporates five functioning scales (physical, role, cognition, emotional, and social), eight symptom scales (fatigue, pain, and nausea/vomiting, dyspnea, insomnia, loss of appetite, constipation, diarrhea, financial problems), financial well-being scale and a global scale (based on two items: global health and global QoL). The raw scores are linearly transformed to give standard scores in the range of 0-100 for each of the functioning and symptom scales. Higher scores in the global and functioning scales and lower scores in the symptom scales indicate better QoL. A difference of 5-10 points in the scores represents a small change, 10-20 points a moderate change and greater than 20 points a large, clinically significant change from the patient's perspective . This instrument has been extensively tested for reliability and validity [21–23].
Patient survival was the primary end point and defined as the time interval between the date of first patient visit to the hospital and the date of death from any cause or the date of last contact/last known to be alive. Two separate analyses were performed. First, the relationship between baseline QoL and patient survival was investigated for 396 patients. Second, the relationship between change in QoL scores between baseline and 3 months and survival was assessed for the same patient cohort. Change scores were calculated by subtracting baseline from 3-month QoL scores. The overall survival was calculated using the Kaplan-Meier method. Clinical and QoL variables were evaluated using univariate Cox proportional hazards models to determine which parameters showed individual prognostic value for survival. Multivariate Cox proportional hazards models were then performed to evaluate the joint prognostic significance of all QoL and clinical factors.
In order to minimize instability of the final multivariate model resulting from high multicollinearity, global QoL was evaluated separately because it is most highly correlated with all other variables on the EORTC QLQ-C30 questionnaire, and also because it is difficult to interpret and manipulate clinically . Each EORTC QLQ-C30 scale was treated as a continuous variable for the purpose of Cox regression analyses. The effect of QoL parameters on patient survival was expressed as hazard ratios (HRs) with 95% confidence intervals (CIs). Changes of 10 or more points on a 0 to100 scale are considered clinically relevant , so we present HRs for a 10-point change on the continuous QoL variables. An effect was considered to be statistically significant if the p value was less than or equal to 0.05. All statistical tests were two sided. All data were analyzed using SPSS version 17.0 (SPSS, Chicago, IL, USA).
Cox regression with time-invariant covariates assumes that the ratio of hazards for any two groups remains constant in proportion over time. We checked this assumption by first examining log-minus-log plots for the categorical predictors and then fitting a Cox regression with a time-varying covariate for each predictor in turn. Potential multicollinearity was assessed using multiple approaches. Large values (above 0.75) of Pearson's correlation coefficients were used as an initial screen for pairs of QoL variables, with one member of the pair not entered into the multivariate model (the measure that was more meaningful or actionable was retained). As a second check, the variance inflation factor (VIF) was used with the final model to verify that multicollinearity was not significantly influencing model coefficients [25, 26]. Finally, the possible influence of sample bias and multicollinearity on the results was investigated using a bootstrap re-sampling procedure. We generated 500 samples, each the same size as the original data set, by random selection with replacement. Cox regression was then run separately on these 500 samples to obtain robust estimates of the standard errors of coefficients, and hence the p values and confidence intervals of the model coefficients .
Baseline characteristics of 396 colorectal cancer patients
Age at Diagnosis (years)
■ Newly diagnosed
■ Previously treated
Stage at Diagnosis
■ Stage III
■ Stage IV
Baseline Characteristics and Associated HRs for Death
HR (95% CI)
Age at Diagnosis (years) used as continuous variable*
1.08 (0.94 - 1.21)
Gender (male as reference)
0.83 (0.63 - 1.1)
Treatment History (newly diagnosed as reference)
2.6 (1.9 - 3.6)
Stage at Diagnosis (stage III as reference)
1.4 (1.1 - 1.9)
Association between Baseline QoL and Survival
Baseline QoL Measures and Associated HRs for Death
QoL Score Mean (SD)
HR (95% CI)
HR (95% CI)
General Quality of Life
0.92 (0.87 - 0.98)
0.93 (0.87 - 0.98)
0.96 (0.89 - 1.02)
1.08 (0.97 - 1.20)
0.97 (0.92 - 1.02)
1.0 (0.94 - 1.06)
1.01 (0.92 - 1.09)
0.99 (0.94 - 1.05)
1.02 (0.93 - 1.12)
0.96 (0.91 - 1.0)
0.93 (0.86 - 1.01)
1.04 (0.99 - 1.08)
1.01 (0.90 - 1.11)
0.99 (0.93 - 1.05)
0.95 (0.87 - 1.03)
1.03 (0.99 - 1.08)
1.02 (0.95 - 1.08)
1.06 (1.01 - 1.11)
1.05 (0.99 - 1.12)
1.03 (0.99 - 1.07)
1.04 (0.99 - 1.10)
1.05 (1.0 - 1.09)
1.07 (1.01 - 1.14)
0.96 (0.91 - 1.02)
0.94 (0.88 - 1.00)
1.07 (1.02 - 1.12)
1.01 (0.95 - 1.07)
0.99 (0.95 - 1.03)
0.98 (0.92 - 1.03)
Bootstrap Multivariate HRs for Baseline QoL Measures
HR (95% CI)
General Quality of Life
0.93 (0.87 - 0.98)
1.08 (0.97 - 1.22)
1.01 (0.92 - 1.10)
1.02 (0.93 - 1.13)
0.93 (0.83 - 1.02)
1.01 (0.90 - 1.10)
0.95 (0.83 - 1.05)
1.02 (0.95 - 1.09)
1.05 (0.99 - 1.13)
1.04 (0.99 - 1.12)
1.07 (1.0 - 1.16)
0.94 (0.85 - 1.01)
1.01 (0.94 - 1.09)
0.98 (0.91 - 1.05)
Association between Changes in QoL and Survival
Change in QoL Measures and Associated HRs for Death
QoL Change Mean (SD)
HR (95% CI)
HR (95% CI)
General Quality of Life
1.00 (0.95 - 1.04)
0.99 (0.95 - 1.04)
0.96 (0.91 - 1.01)
0.86 (0.78 - 0.94)
1.02 (0.99 - 1.05)
1.00 (0.96 - 1.04)
1.01 (0.95 - 1.07)
1.01 (0.96 - 1.05)
0.99 (0.92 - 1.06)
1.03 (1.00 - 1.07)
1.08 (1.02 - 1.13)
0.99 (0.95 - 1.02)
0.98 (0.90 - 1.05)
1.01 (0.97 - 1.06)
1.03 (0.97 - 1.09)
1.00 (0.96 - 1.03)
1.01 (0.96 - 1.07)
0.98 (0.94 - 1.02)
0.98 (0.93 - 1.03)
1.00 (0.97 - 1.04)
1.0 (0.95 - 1.04)
0.98 (0.95 - 1.02)
0.96 (0.91 - 1.01)
1.02 (0.99 - 1.06)
1.02 (0.98 - 1.07)
0.99 (0.94 - 1.03)
1.02 (0.98 - 1.07)
1.00 (0.97 - 1.04)
1.01 (0.97 - 1.04)
Bootstrap Multivariate HRs for Change in QoL Measures
HR (95% CI)
General Quality of Life
0.99 (0.94 - 1.05)
0.86 (0.75 - 0.95)
1.01 (0.95 - 1.09)
0.99 (0.91 - 1.06)
1.08 (1.02 - 1.14)
0.98 (0.89 - 1.06)
1.03 (0.95 - 1.10)
1.01 (0.94 - 1.07)
0.98 (0.91 - 1.05)
1.0 (0.95 - 1.05)
0.96 (0.90 - 1.02)
1.02 (0.98 - 1.08)
1.02 (0.98 - 1.09)
1.01 (0.96 - 1.05)
The current study was undertaken to investigate whether baseline QoL as well as changes in QoL after 3 months of treatment could predict survival in stages III and IV CRC. We chose EORTC QLQ-C30 as a valid and a reliable tool to assess patient QoL. The EORTC QLQ-C30 concentrates on a patients' ability to fulfill the activities of daily life justifying its use in clinical trials investigating new drugs or novel combinations of agents. Clinical practitioners and investigators need to know what happens to a patient's capacity to fulfill the activities of daily life at work and in the home. Consequently, this instrument has an extensive physical functioning scale coupled with a comprehensive symptom inventory.
There are three key findings of our study. First, appetite loss and global health at baseline provides prognostic information for survival after adjusting for the effects of age, gender, treatment history, tumor stage and other QoL variables. Second, improvement in physical function at 3 months is an indicator of improved patient survival after adjusting for other covariates. Third, contrary to what one might predict, improvement in social function at 3 months is independently associated with a worse survival.
Our finding of improvement in physical function scores correlating with better survival in CRC is consistent with recent studies in esophagogastric and head and neck cancer patients (HNC) [11, 13]. In patients with localized HNC, Meyer F et al. found that at 1 year after treatment, the HR associated with a positive physical function change of 10 points was 0.75 (95% CI, 0.68 to 0.83). After physical function was taken into account, no other QoL variable was associated with survival . In patients with esophagogastric cancer, a 10-point change in physical function (hazard ratio [HR], 0.85; 95% CI, 0.76 to 0.96; P = .007), pain (HR, 1.20; 95% CI, 1.09 to 1.33; P < .001), and fatigue (HR, 1.16; 95% CI, 1.04 to 1.30; P = .009) scores were each associated with better survival .
An explanation for the unexpected association of an increase in the social function scale score and decreased patient survival cannot be elucidated from this study. Multicollinearity does not seem to explain this counterintuitive finding. It is relevant to note, however, that the two questions that comprise this scale query both the effects of physical condition and medical treatment on social function. Thus, both factors contribute to the overall social function scale score but are expected to be weighted differently at each assessment point for any individual patient. Since this function is reported as a single score, it is impossible to delineate the impact of each factor on the change score. Nevertheless, it is reasonable to speculate that change in the social function score that is caused primarily by the effects of medical treatment would be of lower prognostic value than changes in physical condition. This hypothesis is testable and worth further investigation. Our unexpected finding regarding the social function scale stands in contrast with the finding reported by Efficace et al. in advanced CRC, where a 9% decrease in patient's hazard of death was found for any 10-point increase in the social functioning score. In that study, social functioning was concluded to be a prognostic measure of survival beyond a number of previously known biomedical parameters . This finding was further validated in an independent sample of metastatic CRC patients by the same research group .
The results of this study have important implications for both clinical and research practices. They suggest that baseline QoL should be considered when planning treatment and regular QoL assessment performed during the course of treatment. Furthermore, interventions aimed at improving specific QoL parameters should be applied when indicated. The utility of this approach to patient management, based on the findings described in this study, would be validated definitively if interventions that enhance specific QoL parameters are shown to enhance survival.
Thus, the findings reported here suggest that QoL monitoring, coupled with treatment to improve appetite loss, global health and physical function when indicated, should be investigated in prospective studies in CRC. Positive effects on survival as a consequence of interventions designed specifically to improve patient symptoms and QoL independent of tumor therapy would go a long way towards establishing causative relationships between specific QoL parameters and disease control. Although some progress has been made with respect to the treatment of appetite loss and physical function in cancer patients, clinical effectiveness is inconsistent and unpredictable. And there are at present no effective means to address more complex QoL factors such as global health. This challenges the cancer research enterprise to develop greater understanding of the complex physiology responsible for all aspects of QoL, and to use this information to develop more effective and predictable methods to favorably modulate this critical aspect of patient health and wellness.
Several limitations of this study require careful acknowledgment. Our study, because of its retrospective nature, relies on data not collected to test a specific hypothesis. As a result, we could not control for certain factors in our analyses that could influence survival such as treatment received at our institution, medical co-morbidities, socioeconomic factors, support system, exercise and educational level. The patient cohort was limited only to those patients who were English speakers and therefore is not representative of the complete spectrum of colorectal cancer patients. Moreover, this study does not reveal a causative relationship between QoL and survival. Rather, patient QoL was found to act as a surrogate for otherwise undetected prognostic factors . QoL scores were assessed over a three month interval only which may not be sufficient time for score changes to develop in other QoL parameters that may be prognostic of survival. We did not control for the multiple comparisons made in this study, but this is acceptable for hypothesis-generating studies .
This study also has several strengths, including no missing data on any EORTC QLQ-C30 variables for the entire study sample; a homogeneous population of patients with advanced CRC (stages III and IV) at presentation to our hospitals; the use of a valid and reliable QoL instrument; the availability of clinical parameters in nearly all patients; and availability of mature and reliable survival data. As is the case for all exploratory retrospective studies, the most important outcome that can be achieved is the development of a hypothesis suggested by the results. As a consequence of this study, we hypothesize that the parameters of physical function, appetite loss, and global health are independent determinants of survival in colorectal cancer, and should be regularly assessed and when indicated, targeted for intervention.
This exploratory study provides preliminary evidence to indicate that CRC patients whose physical function improves within 3 months of treatment have a significantly increased probability of survival. These findings should be used in clinical practice to systematically address QoL-related problems of CRC patients throughout their treatment course.
This study was funded by Cancer Treatment Centers of America®. We thank Norine Oplt and Carol Wages for providing us with reliable and updated survival data. Finally, we thank all our patients and their families.
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