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. 2019 Nov 20;29(2):347–355. doi: 10.1002/pon.5259

Coping strategies of patients with advanced lung or colorectal cancer in six European countries: Insights from the ACTION Study

Lea J Jabbarian 1,, Ida J Korfage 1, Branka Červ 2, Johannes JM van Delden 3, Luc Deliens 4,5, Guido Miccinesi 6, Sheila Payne 7, Anna Thit Johnsen 8,9, Mariëtte N Verkissen 4, Andrew Wilcock 10, Agnes van der Heide 1, Judith AC Rietjens 1; on behalf of the ACTION consortium
PMCID: PMC7028098  PMID: 31663183

Abstract

Objective

Even when medical treatments are limited, supporting patients’ coping strategies could improve their quality of life. Greater understanding of patients’ coping strategies, and influencing factors, can aid developing such support. We examined the prevalence of coping strategies and associated variables.

Methods

We used sociodemographic and baseline data from the ACTION trial, including measures of Denial, Acceptance, and Problem‐focused coping (COPE; Brief COPE inventory), of patients with advanced cancer from six European countries. Clinicians provided clinical information. Linear mixed models with clustering at hospital level were used.

Results

Data from 675 patients with stage III/IV lung (342, 51%) or stage IV colorectal (333, 49%) cancer were used; mean age 66 (10 SD) years. Overall, patients scored low on Denial and high on Acceptance and Problem‐focused coping. Older age was associated with higher scores on Denial than younger age (β = 0.05; CI[0.023; 0.074]), and patients from Italy (β = 1.57 CI[0.760; 2.388]) and Denmark (β = 1.82 CI[0.881; 2.750]) scored higher on Denial than patients in other countries.

Conclusions

Patients with advanced cancer predominantly used Acceptance and Problem‐focused coping, and Denial to a lesser extent. Since the studied coping strategies of patients with advanced cancer vary between subpopulations, we recommend taking these factors into account when developing tailored interventions to support patients’ coping strategies.

Keywords: advanced cancer, cancer, coping, oncology, end of life, psychology, support, tailoring

1. BACKGROUND

Patients diagnosed with advanced, incurable cancer commonly experience physical and psychological symptom burden.1, 2 When the disease has progressed to a point where curative treatments are unavailable, patients can particularly benefit from interventions aimed at improving quality of life.2

One way of assisting patients in the last phase of their lives is by supporting adaptive coping strategies. Coping strategies are distinct, ever changing cognitive, emotional and behavioral efforts to manage a (health) threat.3 For instance, when using denial, patients reduce the impact of their advanced disease by thinking that it is not real.4 Acceptance includes actively dealing with the advanced disease without unnecessary attempts to change the circumstances.5 Problem‐focused coping extends this towards a behavioral approach, for example, through taking actions to improve their way of living with their advanced disease.4 The use of coping strategies can vary between patients, situations, and over time.4 Different coping strategies may be used simultaneously or alternately.6 Whether a certain coping strategy is adaptive or not depends on the individual patient and situational context.4, 7, 8

Evidently, the way patients cope with their advanced disease impacts physical and psychological outcomes, such as quality of life and depressive symptoms.2 Since coping strategies are modifiable,4 supporting and encouraging adaptive coping strategies can contribute to the well‐being of patients, also when their disease has reached an advanced, incurable stage.9 Therefore, coping support is incorporated into interventions for patients with advanced cancer.10, 11 Coping strategies can also be used to tailor interventions. For instance, a trial compared a generic pain management program for older adults to programs matched to patients’ initial tendency towards either problem‐focused or emotion‐focused coping. Patients with problem‐focused coping were provided with specific instructions for relaxation and problem‐solving activities, patients with emotion‐focused coping received specific information on seeking support and expressing hope. The tailored interventions were more successful in reducing pain and symptoms of anxiety.12

The relevance of assessing and responding to coping needs throughout the disease trajectory of patients has been confirmed and recognized by numerous professional organizations, such as the American Society of Clinical Oncology13 and the National Institute for Clinical Excellence in the United Kingdom.14 Research in this area has mainly focused on patients in earlier stages of cancer.15, 16, 17 It is unclear if the findings in these patients are generalizable to patients with advanced cancer who face specific challenges, such as preparatory grief18 and increased existential distress.19

Given the importance of the sociocultural context for the appraisal of a (health) threat, it is not surprising that coping strategies have been found to differ among people with different socio‐cultural characteristics. For instance, younger people tend to use more active, problem‐focused coping than older people,20 and Korean Americans and Filipino Americans seemed to use more religious coping and escape avoidance than Caucasian Americans.21, 22 It is however unknown to what extent sociodemographic and clinical variables relate to the coping strategies of patients with advanced cancer. Detailed insights into coping strategies of patients with advanced cancer can inform both, the design of interventions delivering coping support and the evaluation and improvement of existing interventions by tailoring them to patients’ individual coping strategies.

We aimed to (1) characterize the prevalence of denial, acceptance, and problem‐focused coping among patients with advanced lung or colorectal cancer and (2) identify sociodemographic and clinical characteristics associated with the use of these coping strategies, including a comparison between countries.

2. METHODS

We used the sociodemographic and baseline data of patients of the ACTION trial, a cluster randomized trial investigating the effects of an advance care planning intervention compared to care as usual. We included only patients from the care‐as‐usual arm of this cluster‐randomized trial to avoid potential selection bias. Patients were recruited in outpatient pulmonology and oncology departments in academic and nonacademic hospitals in Belgium, Denmark, Italy, the Netherlands, Slovenia, and the United Kingdom, between June 2015 and May 2017 (see Box 1 for the inclusion and exclusion criteria).23 Written informed consent was obtained. Research ethics committees of the participating countries approved the trial.

Box 1. Inclusion and Exclusion Criteria for the ACTION trial.

Inclusion criteria
  1. Histologically confirmed diagnosis of:
  1. Lung cancer:
  • Small cell – extensive disease/ Stage III or IV*
  • Non‐small cell – stage III or IV*
  • Colorectal cancer: Stage IV or metachronous metastases*,
*according to the 7th edition of TNM classification and staging system
  • Written informed consent to participate,
  • WHO performance status of 0‐3
Exclusion criteria:
  1. Age <18 years,
  2. Unable to provide consent,
  3. Unable to complete questionnaire in country's language,
  4. Less than 3 months anticipated life expectancy,
  5. Taking part in a research study that is evaluating palliative care services or communication strategies.

2.1. Measures

2.1.1. Sociodemographic and clinical variables

Patients provided information about their age, educational level, gender, living situation, and religion. Their healthcare providers registered type and stage of the disease and the time since diagnosis of the primary tumor and current stage of the disease, and on current treatment and performance status according to the World Health Organization (WHO) scale (0‐fully active to 3‐capable of only limited self‐care).24

2.1.2. Coping

We measured patients’ coping strategies with the subscales Denial and Acceptance of the COPE Inventory and the subscales Planning and Active coping of the Brief COPE.7, 25 Patients were asked to rate the items according to the best description of how they had been coping with their disease during the past two months. Items were rated on a four‐point Likert scale from 1 (“I don't do this at all”), 2 (“I do this a little bit”), 3 (“I do this a medium amount”), to 4 (“I do this a lot”).

Following questionnaire instructions, we confirmed the subscales of the underlying coping strategies,7 by conducting a principal components analysis with the 12 selected items of the questionnaires. The analysis identified three distinct factors, each with eigenvalues above 1. The analysis confirmed the two subscales Denial and Acceptance.7 The subscales Active coping and Planning of the Brief COPE loaded on the same factor, in accordance with the structure of the questionnaire as described by the developers.25 We therefore combined Active coping and Planning, and, following previous research,26 labeled the resulting subscale “Problem‐focused coping” (see Box 2 for an overview of the subscales and included questions). For detailed psychometric information see Table S1. We summed the responses per subscale to create subscale sum scores. This resulted in a range of 4 to 16 for each subscale. Higher scores indicate more use of that particular coping strategy.

Table 1.

Sociodemographic and clinical characteristics

Belgium

(n = 135)

Denmark

(n = 68)

Italy

(n = 139)

Netherlands

(n = 168)

Slovenia

(n = 25)

United Kingdom

(n = 140)

Total

(N = 675)

Age (years), mean (SD) 65.3 (9.5) 65.5 (9.0) 65.5 (9.6) 65.4 (8.1) 71.1 (9.5) 68.4 (11.0) 66.2 (9.6)
Years of education, mean (SD) 13.9 (4.4) 13.5 (5.9) 11.4 (5.2) 13.2 (3.7) 9.9 (3.3) 13.5 (4.7) 12.9 (4.7)
Gender (male), n (%) 91 (67.4) 35 (51.5) 90 (64.7) 111 (66.1) 10 (40.0) 70 (50.4) 407 (60.4)
Living with a spouse, n (%) 106 (79.1) 55 (80.9) 99 (73.9) 129 (78.2) 15 (62.5) 93 (69.9) 497 (75.5)
Having children, n (%) 114 (85.1) 62 (91.2) 118 (86.8) 146 (86.9) 21 (84.0) 60 (44.1) 583 (87.3)
Religion, n (%)
Not specified 31 (23.8) 9 (13.6) 16 (11.7) 17 (10.1) 2 (8.0) 18 (13.2) 93 (14.0)
Not religious 30 (23.1) 38 (57.6) 24 (17.5) 76 (45.2) 2 (8.0) 58 (42.6) 228 (34.4)
Religious 69 (53.1) 19 (28.8) 97 (70.8) 75 (44.6) 21 (84.0) 60 (44.1) 341 (51.5)
Diagnosis, n (%)
Lung cancer stage III/IV 79 (58.5) 34 (50.0) 71 (51.1) 76 (45.2) 0 (0.0) 82 (58.6) 342 (50.7)
Colorectal cancer stage IV 56 (41.5) 34 (50.0) 68 (48.9) 92 (54.8) 25 (100) 58 (41.4) 333 (49.3)

Years since diagnosis,

mean (SD)

1.5 (1.7) 2.7 (3.2) 2.0 (3.5) 1.9 (1.9) 2.3 (2.4) 0.9 (1.4) 1.7 (2.4)

Years since diagnosis

current stage, mean (SD)

1.1 (1.4) 1.6 (2.2) 0.8 (1.1) 1.2 (1.4) 1.3 (1.9) 0.4 (0.7) 1.0 (1.4)

Current systemic treatment,

n (%)

126 (96.2) 68 (100.0) 135 (97.1) 144 (86.2) 8 (53.3) 115 (87.8) 596 (91.6)
WHO performance status, n (%)
3 0 (0.0) 0 (0.0) 0 (0.0) 2 (1.2) 1 (4.0) 5 (3.6) 8 (1.2)
2 7 (5.5) 1 (1.5) 2 (1.4) 12 (7.1) 13 (52.0) 20 (14.3) 55 (8.3)
1 56 (44.1) 40 (58.8) 65 (47.1) 122 (72.6) 10 (40.0) 49 (35.0) 342 (51.4)
0 64 (50.4) 27 (39.7) 71 (51.4) 32 (19.0) 1 (4.0) 66 (47.1) 261 (39.2)

SD = standard deviation

Includes chemotherapy, immunotherapy, targeted therapy; treatments were not mutually exclusive.

Missings total: Age (n = 6), Education (n = 89), Gender (n = 1), Living with a spouse (n = 15), Having children (n = 6), Religion (n = 13), Years since diagnosis (n = 1), Years since diagnosis current stage (n = 6), Systemic treatment (n = 24), WHO performance status (n = 9).

Box 2. Overview of the Subscales and items of the COPE and the brief COPE after the Principal Component Analysis.
Denial
  1. I act as though this hasn't even happened.
  2. I say to myself “this isn't real”
  3. I pretend that this hasn't really happened to me.
  4. I refuse to believe that this happened to me.
Acceptance:
  1. I accept the reality of the fact that this has happened to me.
  2. I learn to live with my situation.
  3. I get used to the idea that this has happened to me.
  4. I accept that this has happened to me and that it can't be changed.
Problem‐focused coping
  1. I concentrate my efforts on doing something about my situation.
  2. I take action to try to make my situation better.
  3. I try to come up with a strategy about what to do in my situation.
  4. I think hard about what steps to take in my situation.

2.2. Statistical methods

Missing items are common in palliative care trials.27 Given the low percentage of missing items (<5%) in our study, we carried out a complete case analysis by including only data of patients with full responses on all items of the three respective coping subscales.

We used SPSS 24 for the analyses. We summarized patients’ sociodemographic and clinical characteristics with means and standard deviations for continuous variables and counts and percentages for categorical variables. The distribution of scores on the coping subscales is presented with mean sum scores and standard deviations. Pearson correlation coefficients describe the linear correlation between coping strategies.

Multivariate multilevel regression models were used to analyze associations between coping strategies and sociodemographic and clinical variables. This type of model allows accounting for clustering at the hospital level and thus for nonindependency of observations.28 For inclusion numbers per hospital, see Table S2. The variable Country was included as a confounder. First, bivariate multilevel models were used to test associations between each sociodemographic and clinical variable and the distinct coping strategies. A significance level of p < 0.20 was used to select variables for the final model.29 For the final multivariate model, the significance level was set at p < 0.05. The Benjamini‐Hochberg procedure was used to account for the false discovery rate.30 Betas, 95% confidence intervals and Benjamini‐Hochberg p‐values are reported.

Table 2.

Patient mean sum scores (SD) on coping subscales by sociodemographic and clinical characteristics

Denial

(n = 655)

Acceptance

(n = 659)

Problem‐focused

(n = 643)

Mean Sum Score (SD) 6.6 (3.1) 12.6 (2.7) 12.2 (2.9)
Age in years
18‐64 6.1 (2.8) 12.6 (2.9) 12.6 (2.7)
65‐79 6.9 (3.2) 12.6 (2.5) 12.0 (2.8)
≥80 7.3 (3.9) 13.3 (3.0) 11.5 (3.6)
Years of education
0‐4 6.4 (2.8) 12.5 (2.2) 10.4 (3.3)
5‐12 7.0 (3.3) 12.3 (2.8) 12.2 (2.8)
≥13 6.1 (2.8) 12.9 (2.5) 12.3 (2.9)
Gender
Male 6.6 (3.1) 12.5 (2.7) 12.0 (3.0)
Female 6.6 (3.2) 12.8 (2.8) 12.6 (2.7)
Living with a spouse
Yes 6.6 (3.0) 12.6 (2,7) 12.2 (2.8)
No 6.7 (3.5) 12.6 (2.6) 12.1 (3.1)
Having children
Yes 6.7 (3.2) 12.6 (2.7) 12.2 (2.9)
No 5.8 (2.5) 12.8 (2.7) 12.4 (2.9)
Religion
Not specified 6.5 (3.0) 12.0 (2.9) 11.7 (3.0)
Not religious 6.3 (3.1) 12.7 (2.7) 12.2 (2.9)
Religious 6.9 (3.1) 12.7 (2.6) 12.5 (2.8)
Diagnosis
Lung cancer stage III/IV 6.7 (3.1) 12.4 (2.6) 12.1 (2.8)
Colorectal cancer stage IV 6.6 (3.1) 12.8 (2.8) 12.3 (3.0)
Years since diagnosis
≤1 year 6.5 (3.0) 12.7 (2.7) 12.3 (2.8)
> 1 year 6.5 (3.1) 12.8 (2.8) 12.4 (3.1)

Years since diagnosis

current stage

≤0.5 year 6.5 (3.0) 12.6 (2.6) 12.4 (2.6)
>0.5 year 6.7 (3.3) 12.7 (2.7) 12.0 (3.1)
Current systemic treatment 6.6 (3.1) 12.6 (2.6) 12.2 (2.8)
WHO performance status
3 5.8 (2.4) 13.4 (2.1) 11.3 (1.9)
2 7.2 (3.6) 12.5 (2.8) 11.8 (2.9)
1 6.6 (3.1) 12.3 (2.7) 12.2 (2.8)
0 6.6 (3.0) 12.9 (2.7) 12.4 (3.1)
Country of residence
Belgium 6.5 (2.9) 11.7 (2.8) 10.4 (3.0)
Denmark 7.6 (3.5) 13.3 (2.4) 12.6 (2.9)
Italy 7.5 (3.1) 12.5 (2.5) 12.8 (2.3)
Netherlands 6.0 (2.9) 12.5 (2.6) 13.0 (2.4)
Slovenia 7.3 (3.5) 12.6 (2.5) 12.4 (2.6)
United Kingdom 6.1 (3.0) 13.4 (2.8) 12.2 (3.2)

Range for coping strategies is 4‐16 (higher scores indicate greater use of coping strategy).

Includes chemotherapy, immunotherapy, targeted therapy; treatments were not mutually exclusive.

Missings range: Age (5‐6), Education (n = 79‐89), Gender (n = 1), Living with a spouse (n = 14‐15), Children (n = 6), Religion (n = 12‐13), Time since diagnosis (n = 1), Time since diagnosis current stage (n = 6), Systemic treatment (n = 20‐23), WHO performance status (n = 8‐9).

3. RESULTS

The analyses included 675 patients enrolled in the control arm of the ACTION trial. Numbers of patients per country ranged from n = 25 (Slovenia) to n = 168 (the Netherlands, Table 1). Patients’ average age was 66 (SD 9.6) years, the majority of patients were male (60%). Most of the patients were living with a partner (76%) and had children (87%), half of them described themselves as being religious (52%). Half of the population was diagnosed with lung cancer stage III or IV (51%). On average, patients were diagnosed with their primary tumor 1.7 years prior to inclusion (2.4 SD). Most patients received systemic antitumor treatment (92%) at time of inclusion.

3.1. Prevalence of coping strategies

Patients scored low on Denial (mean sum score 6.6 (SD 3.1) and high on Acceptance and Problem‐focused coping (mean sum score 12.6 [SD 2.7] and 12.2 [SD 2.9], respectively; Table 2). Higher scores on Acceptance were correlated with higher scores on Problem‐focused coping (r = 0.36; p < 0.001), higher scores on Problem‐focused coping were correlated with higher scores on Denial (r = 0.11; p < 0.001). Denial and Acceptance were not correlated (r = 0.04; p = 0.267).

3.2. Multilevel models

3.2.1. Denial and sociodemographic and clinical variables

For Denial (n = 655), bivariate multilevel models showed significant associations (p < 0.20) with age, years of education, having children, years since the diagnosis of the primary tumor, and country of residence (Table S3). These variables were included in the final multivariate model (Table 3), which showed that older age was associated with higher scores on Denial than younger age (β = 0.05; 95% CI[0.023;0.074], p = 0.010), and patients in Italy (β = 1.57; 95% CI[0.760; 2.388]; p = 0.010) and Denmark (β = 1.82; 95% CI[0.881; 2.750]; p = 0.010) scored higher than patients in other countries.

Table 3.

Multivariate multilevel analyses of coping strategies

Denial

(n = 655)

Acceptance

(n = 659)

Problem‐focused

(n = 643)

β 95% CI p β 95% CI p β 95% CI p
Explanatory Variables
Age .049 .023, .074 .010* −.016 −.041, .010 .0.324
Years of education −.042 −.095, .012 .233 .053 .005, .100 .143 .038 −.012, .088 ..233
Gender NA NA .296
Male −.324 −.808, .158
Female Ref
Having children .204 NA NA
Yes .673 −.065, 1.410
No Ref
Religion NA .351 .351
Not specified −.550 −1.230, .127 −.387 −1.100, .326
Not religious −.083 −.585, .418 −.400 −.926, .130
Religious Ref Ref
Diagnosis NA .517 NA
Lung cancer stage III/IV −.181 −.667, .304
Colorectal cancer stage IV Ref
Years since diagnosis .041 −.058, .140 .496 .017 −.090, .124 .772 −.014 −.107, .079 .772
Years since diagnosis current stage NA .156 −.030, .343 .211 NA
WHO performance status NA .204 .057
3 .882 −1.258, 3.022 −1.542 −3.816, .732 .183
2 −.542 −1.523, .438 −1.335 −2.330, −.340 .009*
1 −.591 −1.093, −.088 −.748 −1.268, −.228 .005*
0 Ref Ref
Country of residence .010 .204 .204
Netherlands .081 −.661, .823 .831 −.842 −1.897, .213 1.281 −.558, 3.120
Belgium .689 −.108, 1.486 .090 −1.881 −2.990, −.772 −1.679 −3.677, .319
Slovenia 1.072 −.360, 2.499 .141 −.795 −2.334, .744 .798 −1.657, 3.253
Italy 1.574 .760, 2.388 <.001 −.662 −1.770, .447 .518 −1.480, 2.517
Denmark 1.812 .881, 2.750 <.001 −.186 −1.561, 1.190 .530 −1.936, 3.000
United Kingdom Ref Ref Ref
*

p < 0.05

3.2.2. Acceptance and sociodemographic and clinical variables

Bivariate multilevel models for Acceptance (n = 659) showed significant associations (p < 0.20) with years of education, being religious or not, primary diagnosis, years since diagnosis of the primary tumor and diagnosis of the current stage, WHO performance status, and country of residence (Table S3). These variables were included in the final multivariate model (Table 3), which showed no significant associations.

3.2.3. Problem‐focused coping and sociodemographic and clinical variables

For Problem‐focused coping (n = 643), bivariate multilevel models showed significant associations (p < 0.20) with age, years of education, gender, being religious or not, years since diagnosis of the primary tumor, WHO performance status, and country of residence (Table S3). These variables were included in the final multivariate model (Table 3). The association between the WHO status and Problem‐focused coping was borderline significant (p = 0.057) with patients with a WHO status of 1 (β=−0.75; 95% CI[−1.268; −0.228]) or 2 (β=−1.33; 95% CI [−2.330; 0.340], ie, somewhat restricted in activities) scoring lower on Problem‐focused coping than patients with a WHO status of 0 (ie, fully active).

4. CONCLUSIONS

Patients with advanced lung or colorectal cancer predominantly used Acceptance and Problem‐focused coping. The coping strategies were associated with sociodemographic and clinical characteristics.

Our findings that patients scored low on the use of Denial and high on Acceptance and Problem‐focused coping aligns with observations in patients with early stage cancer,31 patients recently diagnosed with incurable cancer2 and cancer survivors.32 Our results show that higher scores on Acceptance were correlated with higher scores on Problem‐focused coping. Endler and colleagues observed that patients with acute health problems predominantly used one coping strategy, in an effort to soothe their symptoms.6 Contrarily, patients with chronic health problems relied on more than one coping strategy, possibly because they have to adjust their life styles to a new situation.6 A similar challenge might be faced by patients with advanced cancer. Seemingly contradictory coping strategies Denial and Problem‐focused coping were positively correlated, be it only weakly. Denial includes pretending that the disease is not real while Problem‐focused coping concerns taking action to make a situation better.4 Possibly, both mechanisms are used to distract oneself from the actual situation. Denial itself has been association with negative and positive outcomes. One study in the United States of America showed that patients with asthma who scored high on denial tended to disregard symptoms of breathing difficulty, resulting in a higher rate of hospitalizations.33 Yet, in a study with patients with lung cancer, high scores on denial were related to a better overall perception of health and less pain.8

We found that older age was associated with higher scores on Denial than younger age. It has been hypothesized that older patients use “threat minimization” more, which includes keeping feelings to oneself and avoiding emotional distress by trying to forget.34 Patients in Italy and Denmark scored higher on Denial than patients in other countries. A review about culture and end‐of‐life care suggested a general reluctance to talk about death, as well as a trend towards partial/no disclosure of patients’ diagnosis and prognosis in Italy and Norway (a Scandinavian country with supposedly cultural resemblance to Denmark).35 This tendency was related to respect for privacy and/or to a strong death taboo,35 which might facilitate Denial as a way of pretending that the disease is not real. We also found borderline significant results that patients with a worse WHO performance status scored lower on Problem‐focused coping than patients who were fully active. The behavioral efforts often required for Problem‐focused coping might become more challenging with declining physical abilities.

4.1. Clinical implications

As Walshe et al stressed,11 a major conceptual issue in current interventions is that they largely ignore coping strategies of patients with advanced cancer, which might worsen their psychological experience.11 The clinical use of our results are twofold: (1) through tailoring interventions and framing discussions according to patients’ coping strategies and (2) through offering adequate coping support where needed. For instance, patients with a better WHO performance status might benefit from interventions activating their skills and confidence to manage their disease, acknowledging their tendency towards problem‐focused coping. For older patients, we advise to consider their tendency towards denial and adapt, for instance, information provision through carefully considering the detail of their information.36

Addressing coping strategies and providing support, eg, as an element of a palliative care intervention for patients with advanced cancer, is associated with improved quality of life.9 Our findings might help to decide which coping strategies to include in such interventions. Interestingly, our study showed that patients tend to use acceptance and problem‐focused coping more than denial. Referring to the approach‐avoidance dimension,37 we observed a higher tendency towards approach‐oriented coping than avoidance‐oriented coping. Early palliative care has been found to increase patients’ use of approach‐oriented coping strategies, leading to higher quality of life and lower depressive symptoms.9 Generic interventions offering approach‐oriented coping support might thus not be beneficial for most patients, instead interventions should focus on encouraging and building on pre‐existing strategies. To identify these pre‐existing strategies, as well as individual needs of patients, assessing coping strategies might be a useful approach. The Mental Adjustment to Cancer (MAC) scales is specifically developed for and widely used in cancer and palliative care settings and has shown good measurement properties.38, 39

4.2. Strengths

This paper presents unique data of patients with an advanced stage of two common cancer types in six European countries. We were able to collect detailed sociodemographic and clinical information, which allowed a thorough analysis of coping strategies.

4.3. Study limitations and recommendations

To minimize questionnaire burden, we restricted the assessment to three coping strategies. Future research should include additional coping strategies, such as spirituality or seeking social support, which might give more information about cultural sensitivity and relevance of coping strategies. In this study, we focused on patients with advanced lung or colorectal cancer. Replication of these findings in patients with other oncologic diagnoses and advanced diseases is recommended. Since we observed patients using a combination of different coping strategies, we recommend to investigate which combinations of coping strategies are beneficial for patients, and how these combinations might develop over time and between countries. Given that coping strategies are context‐dependent, it would be informative to determine which coping strategies were used to deal with which specific challenge. One should note that some beta weights as well as the differences between the mean sum scores were small, and replication of our findings is therefore desirable.

4.4. Conclusion

We investigated the prevalence of coping strategies and associated sociodemographic and clinical characteristics in patients with advanced cancer in six European countries. We found that patients with advanced cancer predominantly use Acceptance and Problem‐focused coping and use different strategies simultaneously. Denial was used less often. Being aware of the variance in the use of coping strategies can help healthcare professionals to fine‐tune their care. Interventions should be tailored to patients’ coping strategies.

CONFLICT OF INTEREST

None declared.

Supporting information

Table S1. Psychometric information for the coping scales

Table S2. Inclusion numbers per hospital

Table S3. Bivariate multilevel analysis of the association between sociodemographic characteristics, clinical characteristics and country of residence, and coping strategies (online only)

ACKNOWLEDGEMENTS

This publication is based on the ACTION project (Advance care planning—an innovative palliative care intervention to improve quality of life in oncology), conducted by a collaboration of research teams from the Netherlands, Denmark, Belgium, Slovenia, the United Kingdom, and Italy. The ACTION trial was supported by the European Union's 7th Framework Programme for Research and Technological Development (FP7) (Proposal No: 602541‐2).

The trial is registered in the “international standard randomised controlled trial number” registry (ISRCTN63110516).

We thank all participating patients, hospital staff, and the Advisory Board for their valuable contribution to this project. We thank Bud Hammes and Linda Briggs for their advice throughout the project.

This study has been presented as part of a Plenary session at the World Conference of the European Association for Palliative Care (May 23‐24, 2019).

Jabbarian LJ, Korfage IJ, Červ B, et al. Coping strategies of patients with advanced lung or colorectal cancer in six European countries: Insights from the ACTION Study. Psycho‐Oncology. 2020;29:347–355. 10.1002/pon.5259

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

REFERENCES

  • 1. Singer S, Das‐Munshi J, Brahler E. Prevalence of mental health conditions in cancer patients in acute care‐‐a meta‐analysis. Ann Oncol. 2010;21(5):925‐930. [DOI] [PubMed] [Google Scholar]
  • 2. Nipp RD, El‐Jawahri A, Fishbein JN, et al. The relationship between coping strategies, quality of life, and mood in patients with incurable cancer. Cancer. 2016;122(13):2110‐2116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Lazarus RS, Folkman S. Stress, Appraisal, and Coping. New York, NY: Springer; 1984. [Google Scholar]
  • 4. Lazarus RS. Coping theory and research: past, present, and future. Psychosom Med. 1993;55:234‐249. [DOI] [PubMed] [Google Scholar]
  • 5. Fletcher L, Hayes SC. Relational frame theory, acceptance and commitment therapy, and a functional analytic definition of mindfulness. J Ration Emotive Cogn Behav Ther. 2005;23(4):315‐336. [Google Scholar]
  • 6. Endler NS, Kocovski NL, Macrodimitris SD. Coping, efficacy, and perceived control in acute vs chronic illnesses. Pers Individ Differ. 2001;30:617‐625. [Google Scholar]
  • 7. Carver CS, Scheier MF, Weintraub JK. Assessing coping strategies: a theoretically based approach. J Pers Soc Psychol. 1989;56(2):267‐283. [DOI] [PubMed] [Google Scholar]
  • 8. Vos MS, Putter H, van Houwelingen HC, de Haes HCJM. Denial and physical outcomes in lung cancer patients, a longitudinal study. Lung Cancer. 2010;67(2):237‐243. [DOI] [PubMed] [Google Scholar]
  • 9. Greer JA, Jacobs JM, El‐Jawahri A, et al. Role of patient coping strategies in understanding the effects of early palliative care on quality of life and mood. J Clin Oncol. 2018;36(1):53‐60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. von Heymann‐Horan AB, Puggaard LB, Nissen KG, et al. Dyadic psychological intervention for patients with cancer and caregivers in home‐based specialized palliative care: the Domus model. Palliat Support Care. 2017;1‐9. [DOI] [PubMed] [Google Scholar]
  • 11. Walshe C, Roberts D, Appleton L, et al. Coping well with advanced cancer: aserial qualitative interview study with patients and family carers. PLoS ONE. 2017;12(1):e0169071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Fry PS, Wong PTP. Pain management training in the elderly: matching interventions with subjects' coping styles. Stress Health. 1991;7(2):93‐98. [Google Scholar]
  • 13. Ferrell BR, Temel JS, Temin S, et al. Integration of palliative care into standard oncology care: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2017;35(1):96‐112. [DOI] [PubMed] [Google Scholar]
  • 14. National Institute for Clinical Execellence . Improving supportive and palliative care for adults with cancer ‐ the manual. London, UK: NHS; 2004. [Google Scholar]
  • 15. Dempster M, Howell D, McCorry NK. Illness perceptions and coping in physical health conditions: a meta‐analysis. J Psychosom Res. 2015;79(6):506‐513. [DOI] [PubMed] [Google Scholar]
  • 16. Pascoe EC, Edvardsson D. Psychological characteristics and traits for finding benefit from prostate cancer: correlates and predictors. Cancer Nurs. 2016;39(6):446‐454. [DOI] [PubMed] [Google Scholar]
  • 17. Stanton AL, Rowland JH, Ganz PA. Life after diagnosis and treatment of cancer in adulthood: contributions from psychosocial oncology research. Am Psychol. 2015;70(2):159‐174. [DOI] [PubMed] [Google Scholar]
  • 18. Periyakoil VS, Kraemer HC, Noda A, et al. The development and initial validation of the Terminally Ill Grief or Depression Scale (TIGDS). Int J Methods Psychiatr Res. 2005;14(4):202‐212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Kissane DW, Clarke DM, Street AF. Demoralization syndrome‐‐a relevant psychiatric diagnosis for palliative care. J Palliat Care. 2001;17(1):12‐21. [PubMed] [Google Scholar]
  • 20. Folkman S, Lazarus RS, Pimley S. NovacekJ. Age differences in stress and coping processes. Psychol Aging. 1987;2(2):171‐184. [DOI] [PubMed] [Google Scholar]
  • 21. Connor‐Smith JK, Flachsbart C. Relations between personality and coping: a meta‐analysis. J Pers Soc Psychol. 2007;93(6):1080‐1107. [DOI] [PubMed] [Google Scholar]
  • 22. Bjorck JP, Cuthbertson W, Thurman JW, Lee YS. Ethnicity, coping, and distress among Korean Americans, Filipino Americans, and Caucasian Americans. J Soc Psychol. 2001;141(4):421‐442. [DOI] [PubMed] [Google Scholar]
  • 23. Rietjens JAC, Korfage IJ, Dunleavy L, et al. Advance care planning‐‐a multi‐centre cluster randomised clinical trial: the research protocol of the ACTION study. BMC Cancer. 2016;16:264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Oken MM, Creech RH, Tormey DC, et al. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol. 1982;5(6):649‐655. [PubMed] [Google Scholar]
  • 25. Carver CS. You want to measure coping but your protocol's too long: consider the brief COPE. Int J Behav Med. 1997;4(1):92‐100. [DOI] [PubMed] [Google Scholar]
  • 26. Sanders SL, Bantum EO, Owen JE, Thornton AA, Stanton AL. Supportive care needs in patients with lung cancer. Psychooncology. 2010;19(5):480‐489. [DOI] [PubMed] [Google Scholar]
  • 27. Hussain JA, White IR, Langan D, et al. Missing data in randomized controlled trials testing palliative interventions pose a significant risk of bias and loss of power: a systematic review and meta‐analyses. J Clin Epidemiol. 2016;74:57‐65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Diez R. A glossary for multilevel analysis. J Epidemiol Community Health. 2002;56(8):588‐594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Mickey RM, Greenland S. The impact of confounder selection criteria on effect estimation. Am J Epidemiol. 1989;129(1):125‐137. [DOI] [PubMed] [Google Scholar]
  • 30. Benjamini Y, Hochberg Y. Controlling the false discovery rate: apractical and powerful approach to multiple testing. J Royal Stat Soc B. 1995;57(1):289‐300. [Google Scholar]
  • 31. Carver CS, Pozo C, Harris SD, et al. How coping mediates the effect of optimism on distress: a study of women with early stage breast cancer. J Pers Soc Psychol. 1993;65(2):375‐390. [DOI] [PubMed] [Google Scholar]
  • 32. Deimling GT, Wagner LJ, Bowman KF, Sterns S, Kercher K, Kahana B. Coping among older‐adult, long‐term cancer survivors. Psychooncology. 2006;15(2):143‐159. [DOI] [PubMed] [Google Scholar]
  • 33. Staudenmayer H, Kinsman RA, Dirks JF, Spector SL, Wangaard C. Medical outcome in asthmatic patients: effects of airways hyperreactivity and symptom‐focused anxiety. Psychosom Med. 1979;41(2):109‐118. [DOI] [PubMed] [Google Scholar]
  • 34. Ward SE, Leventhal H, Love R. Repression revisited tactics used in coping with a severe health threat. Pers Soc Psychol Bull. 1988;14(4):735‐746. [Google Scholar]
  • 35. Gysels M, Evans N, Menaca A, et al. Culture and end of life care: a scoping exercise in seven European countries. PLoS ONE. 2012;7(4):e34188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Vos MS, Putter H, van Houwelingen HC, de Haes HCJM. Denial and social and emotional outcomes in lung cancer patients: the protective effect of denial. Lung Cancer. 2011;72(1):119‐124. [DOI] [PubMed] [Google Scholar]
  • 37. Roth S, Cohen LJ. Approach, avoidance and coping with stress. Am Psychol. 1986;41(7):813‐819. [DOI] [PubMed] [Google Scholar]
  • 38. Greer S, Moorey S, Watson M. Patients’ adjustment to cancer: the Mental Adjustment to Cancer (MAC) scale vs clinical ratings. J Psychosom Res. 1989;33:373‐377. [DOI] [PubMed] [Google Scholar]
  • 39. Watson M, Homewood J. Mental adjustment to cancer scale: psychometric properties in a large cancer cohort. Psychooncology. 2008;17(11):1146‐1151. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Table S1. Psychometric information for the coping scales

Table S2. Inclusion numbers per hospital

Table S3. Bivariate multilevel analysis of the association between sociodemographic characteristics, clinical characteristics and country of residence, and coping strategies (online only)

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


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