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The association of depressive symptoms, personality traits, and sociodemographic factors with health-related quality of life and quality of life in patients with advanced-stage lung cancer: an observational multi-center cohort study

BMC Cancer volume 20, Article number: 431 (2020) Cite this article

Abstract

Background

Identification of patient-related factors associated with Health-Related Quality of Life (HRQoL) and Quality of Life (QoL) at the start of treatment may identify patients who are prone to a decrease in HRQoL and/or QoL resulting from chemotherapy. Identification of these factors may offer opportunities to enhance patient care during treatment by adapting communication strategies and directing medical and psychological interventions. The aim was to examine the association of sociodemographic factors, personality traits, and depressive symptoms with HRQoL and QoL in patients with advanced-stage lung cancer at the start of chemotherapy.

Methods

Patients (n = 151) completed the State-Trait Anxiety Inventory (trait anxiety subscale), the Neuroticism-Extraversion-Openness-Five Factor Inventory (NEO-FFI), the Center for Epidemiologic Studies Depression (CES-D), the World Health Organization Quality of Life-BREF (WHOQOL-BREF), and the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30). Simple linear regression analyses were performed to select HRQoL and QoL associated factors (a P ≤ 0.10 was used to prevent non-identification of important factors) followed by multiple linear regression analyses (P ≤ 0.05).

Results

In the multiple regression analyses, CES-D score (β = − 0.63 to − 0.53; P-values < 0.001) was most often associated with the WHOQOL-BREF domains and general facet, whereas CES-D score (β = − 0.67 to − 0.40; P-values < 0.001) and Eastern Cooperative Oncology Group (ECOG) performance status (β = − 0.30 to − 0.30; P-values < 0.001) were most often associated with the scales of the EORTC QLQ-C30. Personality traits were not related with HRQoL or QoL except for trait anxiety (Role functioning: β = 0.30; P = 0.02, Environment: β = − 0.39; P = 0.007) and conscientiousness (Physical health: β = 0.20; P-value < 0.04).

Conclusions

Higher scores on depressive symptoms and ECOG performance status were related to lower HRQoL and QoL in patients with advanced-stage non-small cell lung cancer. Supportive care interventions aimed at improvement of depressive symptoms and performance score may facilitate an increase of HRQoL and/or QoL during treatment.

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Background

Patients with advanced-stage lung cancer have a poor prognosis [1]. A 5 year survival of 6% was reported in patients with stage IV non-small cell lung cancer according to the datasets of the International Association for the Study of Lung Cancer staging project [1]. In addition, treatment may be associated with considerable side effects, which can directly influence Health-Related Quality of Life (HRQoL) [2] or even QoL in patients with metastatic cancer. Therefore, treatment goals should not be solely focused on survival benefits, but also consider the effect on patients’ HRQoL and QoL.

HRQoL focusses on health and represents the impact of disease and treatment on the feelings patients have about their functional capabilities and well-being [3]. QoL assesses patients’ feelings (i.e., satisfied or bothered) about their functioning and well-being in at least three key areas (i.e., physical, psychological and social well-being). It also evaluates a patient’s feelings related to their environment (e.g., satisfaction with living conditions) or spirituality (e.g., meaningfulness of personal life). A recent study underscores the additional value of spirituality for a patient’s well-being as it observed that better cognitive and emotional functioning was seen in cancer patients with higher spiritual well-being [4]. Patients with better global Health Status/QoL also had higher spiritual well-being. In addition, besides the additional assessment of a patient’s environment and spirituality, a QoL instrument also contains positively phrased items.

In studies that investigate new therapies in lung cancer, often HRQoL is evaluated and not QoL. These studies evaluate HRQoL to determine the impact of treatment on cancer patients’ well-being. QoL may be used in a similar manner and provides further information as it enables a more comprehensive assessment of a patients well-being than HRQoL. In a clinical setting, application of HRQoL and QoL questionnaires may be used to identify aspects of a patient’s health he/she is bothered with. For instance, it may be used to monitor the effects of treatment on a patient’s well-being. Moreover, HRQoL and QoL assessment may provide opportunities to apply interventions to improve HRQoL and QoL. Regarding the questionnaires to evaluate HRQoL and QoL in lung cancer: according to the definition of the WHO, no lung cancer specific QoL questionnaire has been developed. Some questionnaires are specifically developed for lung cancer (e.g., European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30), Functional assessment of Cancer Therapy-Lung), although they are considered as a HRQoL instrument or even a Health Status questionnaire in case of the EORTC QLQ-C30 given the emphasis on physical complaints rather than well-being.

Several factors have been associated with HRQoL in patients with lung cancer (i.e., age, performance status, gender, education, and having a spouse/partner [5,6,7]) in the past decades. In addition, in patients with cancer, depressive symptoms are negatively related with HRQoL [8, 9]. However, given that depressive symptoms also have been negatively associated with spiritual well-being [4], investigating the association between depressive symptoms and QoL may provide further information about the relation between depressive symptoms and a patient’s well-being.

Personality has been associated with depressive symptoms in chronic illnesses [10, 11] and reduced emotional HRQoL in heart failure patients [12]. In breast cancer, high scores on certain personality traits (i.e., trait anxiety and neuroticism) were associated with lower overall QoL scores over time [13]. Considering these results, the assessment of the association of personality traits with HRQoL and QoL at the start of treatment in patients with lung cancer may help identify patients who are prone to low levels of HRQoL and/or QoL. Moreover, taking knowledge of patient’s personality traits may be of importance as they are linked with coping mechanisms. It may help personalize communication strategies and the manner in which supportive care is delivered. This may be of importance to increase, for instance, treatment adherence.

However, studies that have investigated the relation between the above mentioned factors (i.e., personality, sociodemographic, clinical and psychological factors (e.g., depressive symptoms)) and HRQoL and/or QoL in patients with lung cancer are not reported. This is unfortunate since lung cancer patients are at risk to have lower scores on functioning and well-being given their disease, treatment-related adverse events, and life expectancy [14]. Moreover, a study by Temel and colleagues demonstrated that early palliative care in newly diagnosed lung cancer patients improved HRQoL and depressive symptoms at 12 and 24 weeks after treatment commenced [15]. Therefore, knowledge of which factors are associated with HRQoL and QoL prior to or at the start of treatment may be worthwhile, because these factors may require additional care in individual patients during treatment.

Contemplating on these considerations, we aimed to evaluate to which extent depressive symptoms and personality traits solely and among variables related with HRQoL (i.e., age, performance status, gender, education, and having a spouse/partner [5,6,7]) are associated with HRQoL and QoL in patients with advanced-stage lung cancer prior to or at the start of treatment. We expected depressive symptoms to be associated with lower scores on HRQoL [8, 9] and QoL. In addition, we estimated neuroticism and trait anxiety to be associated with decreased HRQoL and QoL scores [13].

Methods

Study population

PERSONAL is a prospective observational multi-center cohort study of patients with stage IIIB or IV non-squamous non-small cell lung cancer and unresectable mesothelioma receiving pemetrexed. The present study is part of PERSONAL. PERSONAL aims to study the pharmacokinetic and pharmacologic effects of pemetrexed. In addition, patient reported outcomes are measured. Patients were recruited from October 2012 to November 2014 from three teaching hospitals (Erasmus University Medical Center, Amphia Hospital and Sint Franciscus Gasthuis hospital) and a regional hospital (Bravis hospital). Patients were enrolled if they met the following criteria: they were aged 18 years or older, had a cytological or histological confirmed diagnosis of stage IIIB or IV non-squamous non-small cell lung cancer or unresectable malignant pleural mesothelioma, and started treatment with pemetrexed in combination with cisplatin or carboplatin as either first line or with pemetrexed monotherapy as second line. Patients were excluded if they were not able to read Dutch or could not complete the questionnaires because of a physical or mental condition. Eligibility was checked by two physicians dedicated to the project. Informed consent was obtained from all individual participants included in the study. All procedures were in accordance with the ethical standards of the institutional review board of the Erasmus University Medical Center in Rotterdam, The Netherlands (approval number MEC-2012-232) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Procedures

All questionnaires were administered during consultations or by mail and completed after diagnosis and just before or at the first day of the first cycle of chemotherapy. Patients were asked once to complete the questionnaires and not repeatedly to prevent that they could feel obliged to comply to the researchers’ request. In addition, we collected sociodemographic information (i.e., age, gender, educational level, ethnicity, employment, partner status) and clinical information (i.e., cancer stage, type of tumour, line of therapy, and the Eastern Cooperative Oncology Group (ECOG) performance status) from the hospital electronic information records and during regular consultations.

Study measures

Quality of life

The World Health Organization Quality of Life-BREF questionnaire (WHOQOL-BREF) is a cross-cultural and generic QoL instrument [16]. The WHOQOL-BREF comprises 24 items divided over four domains plus two general facet items describing overall QoL and general health. Items are scored on a Likert-scale from one (worst QoL) to five (best QoL). The domains represent physical health (seven items), psychological health (six items), social relationships (three items) and environment (eight items). Examples of items are: How satisfied are you with your capacity for work? (physical health); How safe do you feel in your daily life? (psychological health); How satisfied are you with your personal relationships? (social relationships); How satisfied are you with your transport? (environment). WHOQOL-BREF domains are scored on a 4–20 scale and the general facet on a 2–10 scale with higher scores indicating better QoL [16, 17]. The WHOQOL-BREF has satisfactory psychometric properties in patients with lung cancer [18], chronic diseases and other cancer types [16], except for the social relationships domain (i.e., relatively low Cronbach’s alpha < 0.70).

Health-related quality of life

The European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire-Core 30 (EORTC-QLQ-C30) is a cancer specific HRQoL instrument originally developed in patients with lung cancer [19]. It consists of 30 items and incorporates a global Health Status/QoL scale, five functional scales and 13 items assessing symptoms or problems. The functional scales represent physical functioning (five items), cognitive functioning (two items), emotional functioning (four items), role functioning (two items), and social functioning (two items). Examples of items are: Do you have trouble taking a long walk? (physical functioning); Have you had difficulty remembering things? (cognitive functioning); Did you feel depressed? (emotional functioning); Has your physical condition or medical treatment interfered with your family life? (role functioning); Has your physical condition or medical treatment interfered with your social activities? (social functioning). EORTC QLQ-C30 domains are scored on a 0–100 scale, with higher scores on the functional scales being indicative of better HRQoL, whereas higher scores on the symptom scales represent worse symptoms [19]. The EORTC has demonstrated acceptable psychometric properties [20].

Personality traits

The State-Trait Anxiety Inventory (STAI) questionnaire assesses state and trait anxiety [21]. We used the 10-item STAI trait anxiety subscale (short version), which was developed in women suspected with breast cancer and breast cancer survivors [22]. Trait anxiety refers to the tendency to respond to threatening situations with increased anxiety intensity [13]. It is considered to be a personality factor. Items are scored on a four-point scale ranging from one (almost never) to four (almost always). An example of an item is: I worry too much over something that really doesn’t matter. A score of ≥ 22 is indicative for high trait anxiety [22]. The original Dutch translation of the STAI [21, 23] and the 10-item subscale itself [22] have good psychometric properties.

The 60-item Neuroticism-Extraversion-Openness-Five Factor Inventory questionnaire (NEO-FFI) assesses personality based on the Five Factor Model [24,25,26]. It describes neuroticism, extraversion, openness to experience, agreeableness, and conscientiousness. Neuroticism measures emotional stability. Extraversion assesses the level to which orientation, energy and attention are focused on the outside world instead of the inner world. Openness reflects to an open attitude towards experiences, beliefs and, people. Agreeableness relates to a person’s level of being empathic, cooperative, and considerate. Conscientiousness refers to the level of being careful, diligent, and orderly. Items are scored on a five-point scale with scores ranging from one (totally disagree) to five (totally agree). Examples of items are: I often feel inferior to others (neuroticism); I laugh easily (extraversion); Once I find the right way to do something, I stick to it (openness); I try to be courteous to everyone I meet (agreeableness); I keep my belongings clean and neat (conscientiousness). The NEO-FFI has good psychometric properties in patients with multiple sclerosis [27] and has been used in patients with cancer [28, 29]. For this study the raw scores of the NEO-FFI domains were used.

Depressive symptoms

The Center for Epidemiologic Studies Depression Scale (CES-D) is a 20-item questionnaire which evaluates depressive symptoms [30]. We used the 16-item version of the CES-D, in which the four positively formulated items of the original CES-D are removed [31, 32] since they lacked validity and did not correspond well with the definition of depressive symptoms. Items are scored on a four-point scale with scores ranging from zero (rarely) to three (mostly). An example of an item is: I felt that people dislike me. The CES-D has good psychometric properties in cancer patients [31, 33, 34].

Statistics

Patient characteristics between patients who completed the questionnaires and those who did not were compared with Fisher’s exact test and the independent T-test.

Given the sample size of 151 patients, simple linear regression analyses were performed as a minimal sample size of 50 + 8 m (in which m is the number of predictors) is recommended [35]. Analyses were conducted for sociodemographic variables (i.e., age, gender, ethnicity, education, employment, partner status), ECOG performance status, CES-D score, STAI Trait subscale score, and NEO-FFI subscale scores to identify possible factors associated with the WHOQOL-BREF domains and EORTC QLQ-C30 scales. To prevent non-identification of important variables by using a more strict alpha of ≤ 0.05, variables with an alpha of ≤ 0.10 were selected as possible predictors [36, 37].

With the variables associated with the WHOQOL-BREF domains and EORTC QLQ-C30 scales according to the simple linear regression analyses, multiple linear regression analyses were performed. An alpha of ≤ 0.05 was used to identify significant factors in the multiple linear regression analyses.

To contribute to statistical power several actions were taken. Firstly, a priori hypotheses were formulated according to the literature that we aimed to test in a homogenous patient population to minimise variability in the outcome measure of interest. Secondly, a recommended rule of thumb was used to calculate sample size [35] and patients were encouraged by the investigators to complete questionnaires to minimise the number of dropouts. Lastly, to minimise the risk for a type I error we applied Benjamini-Hochberg correction to adjust for multiple analyses.

Furthermore, to confirm that the results of our multivariable analyses were supported by sufficient statistical power, we performed a post-hoc power-analysis. Given an alpha of 0.05, a total of no more than nine factors for each multivariable model, and 151 patients, we were able to find an effect size (i.e., partial R2) of 3.98%. This means that the analyses were sufficiently powered to detect factors able to explain at least 3.98% variation in a HRQoL/QoL domain/scale score.

All analyses were performed using IBM SPSS Statistics for Windows version 21.0.

Results

Patient characteristics

Figure 1 demonstrates the selection of patients. In total, 151 patients were used for analyses with the WHOQOL-BREF and 150 patients for analyses with the EORTC QLQ-C30. 89% of patients completed all domains of all questionnaires. Table 1 summarizes the patient characteristics of the included patients and the 26 patients who did not complete any of the questionnaires. In general, reasons for non-completion of questionnaires were related to the stress patients experienced resulting from a diagnosis of advanced-stage lung cancer, the near start of chemotherapy, and a poor prognosis. These patients did not differ from the 151 included patients according to the age, gender, ethnicity, employment, partner status, cancer stage, tumour type, and line of therapy, except for performance status. The proportion of patients with a performance status of two or higher was larger in the patients that were not available for the analyses than the included patients. WHOQOL-BREF domain scores, EORTC QLQ-C30 scale score, personality scale scores and CES-D scores are summarized in Table 2.

Fig. 1
figure 1

Selection of patients. Abbreviations: N, number of patients; WHOQOL-BREF, World Health Organization Quality of Life-BREF questionnaire; EORTC QLQ-C30, European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30

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Table 1 Characteristics of study population
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Table 2 WHOQOL-BREF, EORT QLQ-C30, NEO-FFI, CES-D, and STAI trait scale/domain scores
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Linear regression analyses

Results of the simple linear regression analyses for each of the HRQoL and QoL domains/scales are demonstrated in Table 3 (see also Online Resource 1). Table 4 demonstrates the multiple linear regression analyses for the WHOQOL-BREF domains and general facet. After Benjamini-Hochberg correction, CES-D score was negatively associated with the general facet and with the physical and psychological health domains. For the EORTC QLQ-C30 scale scores, CES-D score was negatively associated with the functioning scales and the global Health Status/QoL score (Table 5). All of the standardized betas for the significant associations between CES-D score and the domains/scales of the WHOQOL-BREF and EORTC QLQ-C30 were larger than 0.40. After Benjamini-Hochberg correction, ECOG performance status was negatively associated with the physical and role functioning scale scores of the EORTC QLQ-C30 and with the physical health domain of the WHOQOL-BREF. For the NEO-FFI personality traits, only a positive association between the conscientiousness scale and the physical health domain of the WHOQOL-BREF was observed. Trait anxiety was negatively associated with environment (WHOQOL-BREF) and positively with role functioning (EORTC QLQ-C30). For the WHOQOL-BREF explained variances ranged from 0.20 to 0.55 and for the EORTC QLQ-C30 from 0.36 to 0.66.

Table 3 Results of the univariable regression analyses with the WHOQOL-BREF and EORTC QLQ-C30 domains/scales as dependent variables
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Table 4 Results of the multivariable regression analyses for the WHOQOL-BREF (p < 0.05)
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Table 5 Results of the multivariable regression analyses for the EORTC QLQ-C30 (p < 0.05)
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Discussion

Due to a diagnosis of cancer and potential treatment-related side effects advanced-stage lung cancer patients are at risk to experience a decrease in HRQoL and QoL after they start with treatment. Physicians are aware of this [38] and try to optimize HRQoL and QoL. Evaluation of factors associated with HRQoL and QoL at the start of treatment may provide opportunities to prevent further deterioration of those areas of HRQoL and/or QoL that are related to these factors. To our knowledge, this prospective multi-centre observational study is the first that aimed to investigate if personality traits, depressive symptoms, and sociodemographic factors are associated with HRQoL and QoL in patients with advanced-stage lung cancer prior to or at the start of treatment. Considering that HRQoL merely reflects those components of QoL that are influenced by treatment and disease [3], we choose to include a QoL measure (i.e., WHOQOL-BREF) as well since this offers additional information describing patients’ feelings about their environment and spirituality/existentiality. We observed that higher levels of depressive symptoms were associated with decreased HRQoL and QoL except for social relationships and environment. Given the associations with both HRQoL and QoL and the fact that depressive symptoms are common [1, 2], our results emphasize the importance of physicians’ awareness for depressive symptoms in patients with advanced-stage lung cancer.

Compared to a recent study in Dutch patients with lung cancer, we observed a lower general health/QoL score (i.e., facet score of 7.0 (SD 1.4) versus 5.8 (SD 1.7) in this study) [39]. Probably this is due to the inclusion of solely patients with locally-advanced and metastatic lung cancer in our study whereas the referred study included patients with all stages of lung cancer with stage I and II comprising 45% of the study population. However, this difference in QoL underscores the need for the development of interventions to improve QoL in patients with advanced-stage lung cancer. In patients with breast and prostate cancer, it was reported that an easy-to-use well-being intervention (i.e., recording of positive experiences in a diary, listening to a mindfulness CD, planning a pleasurable activity) could positively influence overall QoL (i.e., facet score WHOQOL-BREF) [40]. Moreover, in a study with Iranian breast cancer patients an intervention of eight mindfulness group-based training sessions resulted in improved overall QoL and less depressive symptoms, anxiety, and stress compared to the control group [41]. Regarding HRQoL, a Cochrane review reported that exercise training resulted in improved global HRQoL although this was not observed for physical functioning. Also the risk of bias in all six included studies was high and the quality of evidence for the outcomes was low [42]. In another study, Nabilone, a synthetic cannabinoid used to improve caloric intake, resulted in improved aspects of HRQoL (i.e., role functioning, emotional functioning, and social functioning) [43]. Unfortunately, all of the mentioned studies are hampered by their design and relatively small sample sizes, although their results suggest that the development of interventions to improve HRQoL and QoL could be beneficial for patients with advanced-stage cancer. Therefore, randomized studies with larger patient populations are needed that could further develop and test the additional value of interventions designed to improve HRQoL and QoL. Such studies should particularly aim their proposed interventions at improving performance status and depressive symptoms as, according to our results, these factors contribute the most to HRQoL and QoL.

In the present study CES-D score was related to all HRQoL scales and QoL domains, except the WHOQOL-BREF domains social relationships and environment. Previousy, the CES-D score has been related with HRQoL and QoL in breast cancer [44, 45]. In the study by Hyphantis and colleagues, amongst others, age, stage of cancer, levels of anxiety, depressive symptoms, and use of repression were related with QoL [45]. In line with the results of the present study, they did not observe a relationship between social relationships and CES-D score. However, in another study in lung cancer patients significant depressive symptoms were associated with decreased QoL, including social relationships and environment [46]. Reasons for this may be related to differences in patient characteristics or the relatively large time since diagnosis (i.e., at least 20 months) that patients completed the questionnaires compared to our study. In our study, patients were at the start or prior to treatment whereas in the study by Gu et al. patients already received treatment for some time [46]. Treatment may have had an impact on the relation between depressive symptoms and QoL.

NEO-FFI personality traits were not associated with HRQoL and QoL in this study, except for conscientiousness. Trait anxiety was associated with only two HRQoL and QoL scales/domains, namely role functioning and environment. Considering that CES-D score was associated with almost all HRQoL and QoL scales/domains, we hypothesized whether the absent effect of personality traits on HRQoL and QoL was influenced by CES-D score. Therefore, new analyses were performed without CES-D score. For the WHOQOL-BREF, trait anxiety was associated with not only the environment domain, but also with physical and psychological health. Instead of an association with role functioning, trait anxiety was associated with the EORTC QLQ-C30 scales emotional functioning and social functioning. Previously, similar results have been observed. In a study with Turkish colorectal patients that received chemotherapy, patients with low trait anxiety (scale score < 45) had better HRQoL for all EORTC QLQ-C30 functioning scales and the global QoL/HS scale [47]. Another study in women under follow-up for breast cancer observed that the level of anxiety according to the total STAI score was related with the emotional functioning scale of the EORTC QLQ-C30 [48]. As such, our observations and the results of these studies emphasize the importance of trait anxiety as a factor associated with HRQoL and QoL, especially in the absence of depressive symptoms and may provide professionals opportunities to personalize the way they provide supportive care (e.g., by adapting communication strategies, stimulating effective coping mechanisms). Given that neuroticism has been linked with depressive symptoms in patients with lung cancer [49], we expected that the effect of neuroticism was masked by CES-D score. However, after removal of CES-D score from the models, neuroticism was not associated with any HRQoL scale or QoL domain. Furthermore, none of the other NEO-FFI personality traits were associated with HRQoL and QoL. In contrast, type D personality has previously been related with decreased HRQoL in patients with cancer [50, 51]. Given that in the past type D personality has been positively correlated with neuroticism and negatively with extraversion in healthy individuals [52, 53], it remains unclear why neuroticism or extraversion were not related with HRQoL or QoL in the present study. A reason for this may be that type D personality is more related with HRQoL and QoL than the NEO-FFI personality traits as was observed in female patients with ulcerative colitis [53]. Unfortunately, other studies that could further elucidate this lack of significance between NEO-FFI personality traits and HRQoL and QoL in cancer patients have not been reported. Therefore, the effect of personality traits according to the NEO-FFI on HRQoL and QoL remains unclear in patients with lung cancer.

We observed an unexpected result during the multiple regression analyses. First, the direction of the beta of the STAI trait scale in the analysis with role functioning as dependent variable was positive. This is in contrast with previous results. In a study with patients with chronic diseases trait anxiety was negatively associated with role physical and role emotional score of the Short-Form 36, a HRQoL questionnaire [54]. Moreover, in colorectal survivors anxiety was significantly associated with lower role functioning over time [55]. To analyse whether this finding was due to multi-collinearity, we correlated the STAI trait scale with the other variables that were associated with role functioning (i.e., CES-D score and ECOG performance status). We observed a strong and positive correlation with CES-D score. This could indicate that the effect of trait anxiety is explained by CES-D score. Second, we observed an, at first glance, unexpected negative direction of the beta of partner status in the analysis with social functioning as dependent variable. However, in a study with advanced-stage cancer patients a similar result was observed [5]. Another study reported also lower social functioning in married/cohabited patients [6]. Moreover, as only weak correlations were observed between partner status and ECOG performance status, CES-D score and age, indications for multi-collinearity were not found.

Some limitations of this study have to be addressed. First, because of the cross-sectional nature of our data, we cannot conclude whether depressive symptoms are a cause of decreased HRQoL and QoL or a consequence, or whether both depressive symptoms and HRQoL and QoL are caused by a third variable. Therefore, ideally, our findings should be cross validated in another study as the observed results may merely describe idiosyncrasies of the data at hand. Second, the relatively small number of patients may have influenced our results. This could have resulted in the non-identification of variables associated with HRQoL and QoL. For this reason, the 10 patients with mesothelioma (i.e., 6.6% of the total patient population) were also used for the analysis. Given that the mesothelioma patients received the same chemotherapy as the other patients, we did not expect differences in terms of number and severity of adverse events between the mesothelioma and the lung cancer patients. Moreover, prognosis in patients with mesothelioma is also limited. Therefore, considering these similarities it was expected that the use of the data of the 10 patients for our analyses would not interfere with the observations of this study. To verify this assumption, the multivariable analyses were rerun without the 10 mesothelioma patients. After Benjamini-Hochberg correction, we observed the same results except that conscientiousness was no longer identified as a predictor of physical health. Third, there is a potential response bias in that possibly the most optimistic of patients or those who had a caregiver who could help with the survey were the ones who returned the questionnaires. Fourth, we related the total CES-D score with HRQoL and QoL. Given that the CES-D contains some items that may demonstrate an overlap with the domains/scales of the WHOQOL-BREF and EORTC QLQ-C30, this could partly explain the observed associations between CES-D score and these domains/scales. However, it was previously demonstrated that just low to moderate correlations exist between the CES-D and the WHOQOL-BREF [56]. Moreover, in the same article results of a Rasch-analysis were reported that demonstrated that just 11 items of the WHOQOL-BREF demonstrated differential item functioning regarding the presence of depression meaning that at a same level of QoL patients with a depression scored these 11 items differently than those without a depression. Removing these 11 items from our analyses would hamper comparing our results with other studies as most studies in cancer do not use an adapted version of the WHOQOL-BREF. In addition, given that the constructs of these questionnaires differ, this also contributes to their utility apart from each other. Fifth, the CES-D also contains some items that demonstrate an overlap with physical symptoms of cancer patients. In potential, this could also partly explain the observed associations between CES-D score and HRQoL and QoL. However, in a study evidence for removing somatic items from the CES-D in cancer patients could not be confirmed (1). In addition, the definition of depressive symptoms includes symptoms like weight loss and fatigue besides symptoms associated with a negative affect. Moreover, to not include the scores of the somatic items in the total CES-D score, would hamper comparing our results with other studies as many studies in cancer exploring depressive symptoms use a total CES-D score.

This study has some strengths too. We are the first to investigate the association between sociodemographic variables, clinical variables, depressive symptoms, and personality traits with both HRQoL and QoL. Moreover, although our sample size was relatively small, we describe results of a prospective study with a homogeneous patient population. Also the application of well-recognized standardized questionnaires, the multi-center prospective design of this study, and the inclusion of patients that resemble clinical practice strengthen our findings.

Conclusions

In conclusion, our results demonstrated that health care professionals are recommended to have high awareness during consultations for patients with depressive symptoms and those with an ECOG performance status of two or higher at the start of treatment. This is of importance as these factors may indicate low levels of HRQoL and QoL of patients. Moreover, merely assessing HRQoL and QoL and not depressive symptoms or performance status may be insufficient. For instance if psychological health is low, one has to further investigate if this is caused by anxiety or depressive symptoms or another reason given that treatment may differ according to the cause of the low psychological health. Therefore screening for the presence of these two factors before treatment is initiated (e.g., by means of an e-tool that screens for depressive symptoms, consequently reporting performance status during consultations) may be worthwhile. Additional care (e.g., referral to a psychologist, physiotherapist, medication, etc) aimed at improving these factors can then be provided.

Availability of data and materials

The data that support the findings of this study are not publicly available due to them containing information that could compromise research participant privacy/consent but are strictly available from the corresponding author on reasonable request.

Abbreviations

HRQoL:

Health-Related Quality of Life

QoL:

Quality of Life

NEO-FFI:

Neuroticism-Extraversion-Openness-Five Factor Inventory

CES-D:

Center for Epidemiologic Studies Depression

WHOQOL-BREF:

World Health Organization Quality of Life-BREF

EORTC QLQ-C30:

European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30

ECOG:

Eastern Cooperative Oncology Group

STAI:

State-Trait Anxiety Inventory

SD:

Standard deviation

IQR:

Interquartile range

CI:

Confidence interval

n:

Number of patients

B:

Unstandardized beta

SE:

Standard error

β:

Standardized beta

R2 :

Explained varriance

References

  1. Chansky K, Detterbeck FC, Nicholson AG, Rusch VW, Vallieres E, Groome P, Kennedy C, Krasnik M, Peake M, Shemanski L, Bolejack V, Crowley JJ, Asamura H, Rami-Porta R, Staging I, Prognostic Factors Committee AB, Participating I. The IASLC lung Cancer Staging project: external validation of the revision of the TNM stage groupings in the eighth edition of the TNM classification of lung Cancer. J Thoracic Oncol. 2017;12(7):1109–21. https://doi.org/10.1016/j.jtho.2017.04.011.

    Article  Google Scholar 

  2. Al-Batran SE, Hozaeel W, Tauchert FK, Hofheinz RD, Hinke A, Windemuth-Kieselbach C, Hubner A, Burmester M, Koenigsmann M, Wiegand J, Zur Hausen G, Linsse B, Kuhl R, Pauligk C, Arbeitsgemeinschaft Internistische O. The impact of docetaxel-related toxicities on health-related quality of life in patients with metastatic cancer (QoliTax). Ann Oncol. 2015;26(6):1244–8. https://doi.org/10.1093/annonc/mdv129.

    Article  PubMed  Google Scholar 

  3. De Vries JDOBL. The choice determines the success. Nederlands tijdschrift voor Orthopaedie. 2014;21(2):39–42.

    Google Scholar 

  4. Chaar EA, Hallit S, Hajj A, Aaraj R, Kattan J, Jabbour H, Khabbaz LR. Evaluating the impact of spirituality on the quality of life, anxiety, and depression among patients with cancer: an observational transversal study. Support Care Cancer. 2018;26(8):2581–90. https://doi.org/10.1007/s00520-018-4089-1.

    Article  PubMed  Google Scholar 

  5. Jordhoy MS, Fayers P, Loge JH, Saltnes T, Ahlner-Elmqvist M, Kaasa S. Quality of life in advanced cancer patients: the impact of sociodemographic and medical characteristics. Br J Cancer. 2001;85(10):1478–85. https://doi.org/10.1054/bjoc.2001.2116.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Lundh Hagelin C, Seiger A, Furst CJ. Quality of life in terminal care--with special reference to age, gender and marital status. Support Care Cancer. 2006;14(4):320–8. https://doi.org/10.1007/s00520-005-0886-4.

    Article  CAS  PubMed  Google Scholar 

  7. Zimmermann C, Burman D, Swami N, Krzyzanowska MK, Leighl N, Moore M, Rodin G, Tannock I. Determinants of quality of life in patients with advanced cancer. Support Care Cancer. 2011;19(5):621–9. https://doi.org/10.1007/s00520-010-0866-1.

    Article  PubMed  Google Scholar 

  8. Skarstein J, Aass N, Fossa SD, Skovlund E, Dahl AA. Anxiety and depression in cancer patients: relation between the hospital anxiety and depression scale and the European Organization for Research and Treatment of Cancer Core quality of life questionnaire. J Psychosom Res. 2000;49(1):27–34.

    Article  CAS  PubMed  Google Scholar 

  9. Mystakidou K, Tsilika E, Parpa E, Katsouda E, Galanos A, Vlahos L. Assessment of anxiety and depression in advanced cancer patients and their relationship with quality of life. Qual Life Res. 2005;14(8):1825–33. https://doi.org/10.1007/s11136-005-4324-3.

    Article  CAS  PubMed  Google Scholar 

  10. Brouwers C, Kupper N, Pelle AJ, Szabo BM, Westerhuis BL, Denollet J. Depressive symptoms in outpatients with heart failure: importance of inflammatory biomarkers, disease severity and personality. Psychol Health. 2014;29(5):564–82. https://doi.org/10.1080/08870446.2013.869813.

    Article  PubMed  Google Scholar 

  11. de Voogd JN, Wempe JB, Postema K, van Sonderen E, Ranchor AV, Coyne JC, Sanderman R. More evidence that depressive symptoms predict mortality in COPD patients: is type D personality an alternative explanation? Ann Behav Med. 2009;38(2):86–93. https://doi.org/10.1007/s12160-009-9105-8.

    Article  PubMed  Google Scholar 

  12. Pedersen SS, Herrmann-Lingen C, de Jonge P, Scherer M. Type D personality is a predictor of poor emotional quality of life in primary care heart failure patients independent of depressive symptoms and New York heart association functional class. J Behav Med. 2010;33(1):72–80. https://doi.org/10.1007/s10865-009-9236-1.

    Article  PubMed  Google Scholar 

  13. van der Steeg AF, De Vries J, Roukema JA. Anxious personality and breast cancer: possible negative impact on quality of life after breast-conserving therapy. World J Surg. 2010;34(7):1453–60. https://doi.org/10.1007/s00268-010-0526-0.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Hollen PJ, Gralla RJ, Kris MG, Eberly SW, Cox C. Normative data and trends in quality of life from the lung Cancer symptom scale (LCSS). Support Care Cancer. 1999;7(3):140–8.

    Article  CAS  PubMed  Google Scholar 

  15. Temel JS, Greer JA, El-Jawahri A, Pirl WF, Park ER, Jackson VA, Back AL, Kamdar M, Jacobsen J, Chittenden EH, Rinaldi SP, Gallagher ER, Eusebio JR, Li Z, Muzikansky A, Ryan DP. Effects of early integrated palliative Care in Patients with Lung and GI Cancer: a randomized clinical trial. J Clin Oncol. 2017;35(8):834–41. https://doi.org/10.1200/JCO.2016.70.5046.

    Article  PubMed  Google Scholar 

  16. Skevington SM, Lotfy M, O'Connell KA, Group W. The World Health Organization's WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. A report from the WHOQOL group. Qual Life Res. 2004;13(2):299–310.

    Article  CAS  PubMed  Google Scholar 

  17. The WHOQOL Group. Development of the World Health Organization WHOQOL-BREF quality of life assessment. Psychol Med. 1998;28(3):551–8.

  18. Lin CY, Yang SC, Lai WW, Su WC, Wang JD. Rasch models suggested the satisfactory psychometric properties of the World Health Organization quality of life-brief among lung cancer patients. J Health Psychol. 2015. https://doi.org/10.1177/1359105315603474.

  19. Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, Filiberti A, Flechtner H, Fleishman SB, de Haes JC, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85(5):365–76.

    Article  CAS  PubMed  Google Scholar 

  20. Luckett T, King MT, Butow PN, Oguchi M, Rankin N, Price MA, Hackl NA, Heading G. Choosing between the EORTC QLQ-C30 and FACT-G for measuring health-related quality of life in cancer clinical research: issues, evidence and recommendations. Ann Oncol. 2011;22(10):2179–90. https://doi.org/10.1093/annonc/mdq721.

    Article  CAS  PubMed  Google Scholar 

  21. Spielberger CD, Gorsuch RL, Lushene RE. STAI manual for the state-trait anxiety inventory. Palo Alto CA: Consulting Psychologists Press; 1970.

    Google Scholar 

  22. De Vries J, Van Heck GL. Development of a short version of the Dutch version of the Spielberger STAI trait anxiety scale in women suspected of breast cancer and breast cancer survivors. J Clin Psychol Med Settings. 2013;20(2):215–26. https://doi.org/10.1007/s10880-012-9325-0.

    Article  PubMed  Google Scholar 

  23. Van Der Ploeg HM, Defares PB, Spielberger CD. Handleiding bij de Zelf-Beoordelings Vragenlijst, ZBV: Een Nederlandstalige Bewerking van de Spielberger State-Trait Anxiety Inventory, STAI-DY. Lisse: Swets & Zeitlinger; 1980.

    Google Scholar 

  24. Costa PT, McCrae, R.R. (1989) The NEO-PI/ FFI manual supplement. Odessa, Florida: Psychological Assessment Resources Inc.

  25. Costa PT, McCrae, R.R. (1992) Revised NEO personality inventory (NEO-PI-R) and the five factor inventory (NEO-FFI): professional manual. Odessa, Florida: Psychological Assessment Resources Inc.

  26. Hoekstra HA, Ormel J, De Fruyt F. NEO-PI-R/NEO-FFI Big Five Persoonlijkheidsvragenlijst: Handleiding. Lisse, Nederland: Harcourt Assessment; 2003.

    Google Scholar 

  27. Schwartz ES, Chapman BP, Duberstein PR, Weinstock-Guttman B, Benedict RH. The NEO-FFI in multiple sclerosis: internal consistency, factorial validity, and correspondence between self and informant reports. Assessment. 2011;18(1):39–49. https://doi.org/10.1177/1073191110368482.

    Article  PubMed  Google Scholar 

  28. Lima MP, Machado WL, Irigaray TQ. Predictive factors of treatment adherence in cancer outpatients. Psycho-oncology. 2018;27(12):2823–8. https://doi.org/10.1002/pon.4897.

    Article  PubMed  Google Scholar 

  29. Morgan S, Cooper B, Paul S, Hammer MJ, Conley YP, Levine JD, Miaskowski C, Dunn LB. Association of Personality Profiles with depressive, anxiety, and Cancer-related symptoms in patients undergoing chemotherapy. Personal Individ Differ. 2017;117:130–8. https://doi.org/10.1016/j.paid.2017.05.039.

    Article  Google Scholar 

  30. Radloff LS. The CES-D scale: a self-report depression scale for research in the general population. Appl Psychol Measures. 1977;1:385–401.

    Article  Google Scholar 

  31. Schroevers MJ, Sanderman R, van Sonderen E, Ranchor AV. The evaluation of the Center for Epidemiologic Studies Depression (CES-D) scale: depressed and positive affect in cancer patients and healthy reference subjects. Qual Life Res. 2000;9(9):1015–29.

    Article  CAS  PubMed  Google Scholar 

  32. Hanewald GJFP (1987) CES-D. De Nederlandse versie. Een onderzoek naar de betrouwbaarheid en de validiteit. Amsterdam, Vakgroep klinische Psychologie, Universiteit van Amsterdam, interne publikatie.

  33. Vodermaier A, Linden W, Siu C. Screening for emotional distress in cancer patients: a systematic review of assessment instruments. J Natl Cancer Inst. 2009;101(21):1464–88. https://doi.org/10.1093/jnci/djp336.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Hann D, Winter K, Jacobsen P. Measurement of depressive symptoms in cancer patients: evaluation of the Center for Epidemiological Studies Depression Scale (CES-D). J Psychosom Res. 1999;46(5):437–43. https://doi.org/10.1016/s0022-3999(99)00004-5.

    Article  CAS  PubMed  Google Scholar 

  35. Green SB. How many subjects does it take to do a regression analysis? Multivar Behav Res. 1991;26(3):499–510.

    Article  CAS  Google Scholar 

  36. Hosmer DW, Lemeshow S. Applied survival analysis: regression modeling of time to event data. New York: Wiley; 1999.

    Google Scholar 

  37. Hosmer DW, Lemeshow S. Applied logistic regression. New York: Wiley; 2000.

    Book  Google Scholar 

  38. Hamann HA, Lee JW, Schiller JH, Horn L, Wagner LI, Chang VT, Fisch MJ. Clinician perceptions of care difficulty, quality of life, and symptom reports for lung cancer patients: an analysis from the symptom outcomes and practice patterns (SOAPP) study. J Thoracic Oncol. 2013;8(12):1474–83. https://doi.org/10.1097/01.JTO.0000437501.83763.5d.

    Article  Google Scholar 

  39. van Montfort E, de Vries J, Arts R, Aerts JG, Kloover JS, Traa MJ. The relation between psychological profiles and quality of life in patients with lung cancer. Support Care Cancer. 2020;28(3):1359–67. https://doi.org/10.1007/s00520-019-04923-w.

    Article  PubMed  Google Scholar 

  40. Ramachandra P, Booth S, Pieters T, Vrotsou K, Huppert FA. A brief self-administered psychological intervention to improve well-being in patients with cancer: results from a feasibility study. Psycho-oncology. 2009;18(12):1323–6. https://doi.org/10.1002/pon.1516.

    Article  PubMed  Google Scholar 

  41. Pouy S, Attari Peikani F, Nourmohammadi H, Sanei P, Tarjoman A, Borji M (2018) Investigating the effect of mindfulness-based training on psychological status and quality of life in patients with breast Cancer. Asian Pacific journal of cancer prevention : APJCP 19 (7):1993-1998. Doi:10.22034/APJCP.2018.19.7.1993.

  42. Peddle-McIntyre CJ, Singh F, Thomas R, Newton RU, Galvao DA, Cavalheri V. Exercise training for advanced lung cancer. Cochrane Database Syst Rev. 2019;2:CD012685. https://doi.org/10.1002/14651858.CD012685.pub2.

    Article  PubMed  Google Scholar 

  43. Turcott JG, Del Rocio Guillen Nunez M, Flores-Estrada D, Onate-Ocana LF, Zatarain-Barron ZL, Barron F, Arrieta O. The effect of nabilone on appetite, nutritional status, and quality of life in lung cancer patients: a randomized, double-blind clinical trial. Support Care Cancer. 2018;26(9):3029–38. https://doi.org/10.1007/s00520-018-4154-9.

    Article  PubMed  Google Scholar 

  44. Ha EH, Cho YK. The mediating effects of self-esteem and optimism on the relationship between quality of life and depressive symptoms of breast Cancer patients. Psychiatry Investig. 2014;11(4):437–45. https://doi.org/10.4306/pi.2014.11.4.437.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Hyphantis T, Almyroudi A, Paika V, Degner LF, Carvalho AF, Pavlidis N. Anxiety, depression and defense mechanisms associated with treatment decisional preferences and quality of life in non-metastatic breast cancer: a 1-year prospective study. Psycho-oncology. 2013;22(11):2470–7. https://doi.org/10.1002/pon.3308.

    Article  PubMed  Google Scholar 

  46. Gu W, Xu YM, Zhu JH, Zhong BL (2017) Depression and its impact on health-related quality of life among Chinese inpatients with lung cancer. Oncotarget 8 (62):104806-104812. Doi:https://doi.org/10.18632/oncotarget.21001.

  47. Alacacioglu A, Binicier O, Gungor O, Oztop I, Dirioz M, Yilmaz U. Quality of life, anxiety, and depression in Turkish colorectal cancer patients. Support Care Cancer. 2010;18(4):417–21. https://doi.org/10.1007/s00520-009-0679-2.

    Article  PubMed  Google Scholar 

  48. Karakoyun-Celik O, Gorken I, Sahin S, Orcin E, Alanyali H, Kinay M. Depression and anxiety levels in woman under follow-up for breast cancer: relationship to coping with cancer and quality of life. Med Oncol. 2010;27(1):108–13. https://doi.org/10.1007/s12032-009-9181-4.

    Article  PubMed  Google Scholar 

  49. Shimizu K, Nakaya N, Saito-Nakaya K, Akechi T, Yamada Y, Fujimori M, Ogawa A, Fujisawa D, Goto K, Iwasaki M, Tsugane S, Uchitomi Y. Clinical biopsychosocial risk factors for depression in lung cancer patients: a comprehensive analysis using data from the lung Cancer database project. Ann Oncol. 2012;23(8):1973–9. https://doi.org/10.1093/annonc/mds061.

    Article  CAS  PubMed  Google Scholar 

  50. Mols F, Thong MSY, de Poll-Franse LVV, Roukema JA, Denollet J. Type D (distressed) personality is associated with poor quality of life and mental health among 3080 cancer survivors. J Affect Disord. 2012;136(1–2):26–34. https://doi.org/10.1016/j.jad.2011.08.034.

    Article  PubMed  Google Scholar 

  51. Kim SR, Nho JH, Nam JH. Relationships among type-D personality, symptoms and quality of life in patients with ovarian cancer receiving chemotherapy. J Psychosom Obstet Gynaecol. 2018;39(4):289–96. https://doi.org/10.1080/0167482X.2017.1372416.

    Article  PubMed  Google Scholar 

  52. de Fruyt F, Denollet J. Type D personality: a five-factor model perspective. Psychol Health. 2002;17(5):671–83. https://doi.org/10.1080/08870440290025858.

    Article  Google Scholar 

  53. Sajadinejad MS, Molavi H, Asgari K, Kalantari M, Adibi P. Personality dimensions and type D personality in female patients with ulcerative colitis. J Res Med Sci. 2012;17(10):898–904.

    PubMed  PubMed Central  Google Scholar 

  54. Kepka S, Baumann C, Anota A, Buron G, Spitz E, Auquier P, Guillemin F, Mercier M. The relationship between traits optimism and anxiety and health-related quality of life in patients hospitalized for chronic diseases: data from the SATISQOL study. Health Qual Life Outcomes. 2013;11:134. https://doi.org/10.1186/1477-7525-11-134.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Mols F, Schoormans D, de Hingh I, Oerlemans S, Husson O. Symptoms of anxiety and depression among colorectal cancer survivors from the population-based, longitudinal PROFILES registry: prevalence, predictors, and impact on quality of life. Cancer. 2018;124(12):2621–8. https://doi.org/10.1002/cncr.31369.

    Article  PubMed  Google Scholar 

  56. da Rocha NS, Power MJ, Bushnell DM, Fleck MP. Is there a measurement overlap between depressive symptoms and quality of life? Compr Psychiatry. 2009;50(6):549–55. https://doi.org/10.1016/j.comppsych.2008.11.015.

    Article  PubMed  Google Scholar 

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Acknowledgements

Not applicable.

Funding

This study was funded by ZonMw, The Netherlands (project number: 152001017). ZonMw was not involved in the design of the study and in the collection, analysis and interpretation of data nor were they involved in the process of writing the manuscript.

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Authors and Affiliations

  1. Department of Pulmonary Diseases, Amphia Hospital, P.O. Box 90158, 4800, RK, Breda, The Netherlands

    Mark de Mol, Sabine Visser, Joachim Aerts, Nico van Walree & Huub Belderbos

  2. Department of Pulmonary Diseases, Erasmus MC Cancer Institute, P.O. Box 2040, 3000, CA, Rotterdam, The Netherlands

    Mark de Mol, Sabine Visser & Joachim Aerts

  3. Department of Epidemiology, Erasmus MC – University Medical Centre Rotterdam, P.O. Box 2040, 3000, CA, Rotterdam, The Netherlands

    Sabine Visser

  4. Department of Methodology and Statistics, Tilburg University, P.O. Box 90151, 5000, LE, Tilburg, The Netherlands

    Paul Lodder

  5. Department of Medical and Clinical Psychology, Centre of Research on Psychological and Somatic Disorders (CoRPS), Tilburg University, P.O. Box 90151, 5000, LE, Tilburg, The Netherlands

    Paul Lodder & Brenda den Oudsten

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Contributions

MdM was involved in the study design, collection, analysis and interpretation of data, and in writing of the manuscript. SV was involved in the study design and collection of data. JGJVA was involved in the study design and writing of the manuscript. PL was involved in the analysis and interpretation of data, and in writing of the manuscript. NvW was involved in writing of the manuscript. HB was involved in writing of the manuscript. BLdO was involved in the study design, analysis and interpretation of data, and in writing of the manuscript. All authors have read and approved the final version of the manuscript.

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Correspondence to Brenda den Oudsten.

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Written informed consent was obtained from all individual participants included in the study. All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This study was approved by the Institutional Review Board of the Erasmus University Medical Center in Rotterdam, the Netherlands (MEC-2012-232).

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The authors declare that they have no competing interests except J. Aerts. J. Aerts has received personal fees as a speaker for/member of the advisory board of Eli Lilly.

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de Mol, M., Visser, S., Aerts, J. et al. The association of depressive symptoms, personality traits, and sociodemographic factors with health-related quality of life and quality of life in patients with advanced-stage lung cancer: an observational multi-center cohort study. BMC Cancer 20, 431 (2020). https://doi.org/10.1186/s12885-020-06823-3

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BMC Cancer

ISSN: 1471-2407

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