Psychiatric disorders are common in oncology and palliative care. Of considerable interest has been their contribution to the onset of cancer, its management, disease progression and mortality. If the clinical goal is to facilitate adaptation and sustain quality of life in the face of oncological illnesses, psychiatrists need to be able to discuss with patients their concerns about the aetiology of cancer and the contribution of lifestyle habits, stress, social support, depression and socioeconomic factors. In this article, we review the evidence that personality, stress, life events and social support are associated with the development of cancer and also review the psychosocial factors associated with cancer progression and mortality. We begin with review of the prevalence of psychiatric disorders in patients with cancer to establish the context in which the psychiatrist might meet such a patient.
Prevalence of psychiatric disorder
A cancer diagnosis is commonly perceived as dire and threatening. Not surprisingly, comorbid psychiatric disorders are prevalent. Although the now old study by the Psychosocial Collaborative Oncology Group (PSYCOG) in the USA recorded that 89% of cancer patients with psychiatric disorders had no pre-cancer history of mental illness (Reference Derogatis, Morrow and FettingDerogatis 1983), not until recent years have epidemiological studies updated our understanding of this morbidity. Reference Vehling, Koch and LadehoffVehling et al (2012) applied meta-analytical methods to find an 11% (95% CI 8.1–15.1) prevalence of affective disorders and a 10% (95% CI 6.9–14.8) prevalence of anxiety disorders from structured psychiatric interviews in oncology, while in palliative care, Reference Mitchell, Chan and BhattiMitchell et al (2011) recorded even higher rates of depression, at 16.5% (95% CI 13.1–20.3). Structured psychiatric interviews offer more conservative prevalence rates than self-report measures, as in the latter adjustment disorders are more readily misclassified as clinical depression.
A methodologically rigorous epidemiological study from five cancer centres in Germany used a proportionally stratified random sample based on the nationwide incidence of all cancer diagnoses (Reference Mehnert, Koch and SchulzMehnert 2012a). With a participation rate of 68%, 4200 patients were initially screened and 2143 (53%) were then randomly assigned and interviewed using the oncology-specific adaptation of the Composite International Diagnostic Interview (CIDI-O). The most common mental disorders were anxiety disorders (4-week prevalence: 13.5%, 12-month prevalence: 18.5%), followed by affective disorders (4-week prevalence: 8.5%, 12-month prevalence: 15.6%) and somatoform disorders (4-week prevalence: 5.6%, 12-month prevalence: 10.3%) (Reference Mehnert, Faller and HärterMehnert 2012b). Using self-report measures, 23.9% of the participants had moderate to severe depression (Patient Health Questionnaire-9, PHQ-9) and 14.2% had moderate to severe levels of generalised anxiety disorder (Generalised Anxiety Disorder, GAD-7). Of interest, substance use disorders had a 4-week prevalence of 5.5% and a 12-month prevalence of 9.5%, whereas post-traumatic stress disorder (PTSD) was less prominent, with a 4-week prevalence of 2.5% and a 12-month prevalence of 3.2%. A recent meta-analysis of 25 studies (4189 participants) of cancer-related PTSD identified 9 studies that used a structured diagnostic interview to reveal a 5.1% rate of PTSD in advanced disease (Reference Abbey, Thompson and HickishAbbey 2015).
These data, both meta-analytical and epidemiological, present targets for service delivery, which will be dependent on appropriate staffing of cancer centres and related psychosocial supportive care programmes. Programmes the world over fall well short of the optimal recognition and treatment of this level of psychiatric disorder. Fresh key performance indicators are thus called for to pursue such targets for care delivery.
Let us turn to factors that patients worry might have been a cause of their cancer.
Personality
The existence of a ‘cancer-prone personality’ has been much debated through the decades (e.g. Reference TemoshokTemoshok 1987). Shaffer’s 35-year follow-up of a longitudinal study of medical students who were given Rorschach tests identified that cancer was 15 times more frequent in individuals who were loners, non-aggressive or emotionally repressed (Reference Shaffer, Graves and SwankShaffer 1987). Such interpretations were quite subjective. This sort of study, together with the body of work on alexithymia, had raised support for a cancer-prone personality, dubbed type C (Reference Grossarth-Maticek, Eysenck and VetterGrossarth-Maticek 1988). However, many of the studies that explored this had methodological difficulties associated with being retrospective and involving older cohorts of patients.
The Danish Cancer Society conducted a cohort study of 1031 individuals, who completed the Eysenck Personality Inventory (EPI) in 1976, alongside their history of smoking, alcohol and related parameters. Extraversion had been postulated to increase the risk of smoking and cancer, but at 20-year follow-up, no significant increase in cancer occurrence was evident (Reference Schapiro, Ross-Petersen and SælanSchapiro 2001). A larger prospective cohort of 59548 Swedish and Finnish twins completed the EPI, among whom 4631 cases of cancer had developed by 30-year follow-up (Reference Nakaya, Bidstrup and Saito-NakayaNakaya 2010). In multivariate analyses, neither extraversion nor neuroticism were associated with cancer in this study. A recent meta-analysis of eight prospective studies, involving 42000 participants, again failed to find any association between personality traits and cancer incidence or mortality (Reference Jokela, Batty and HintaJokela 2014).
A particularly problematic outcome from such a construct as the cancer-prone personality is the likelihood that patients will blame themselves and feel guilty for the development of their cancer. Most psycho-oncologists are sceptical about the validity of such a personality type. We do well to remember the history of psychiatry and early descriptors of personality that were proposed to cause illnesses such as tuberculosis, tertiary syphilis or peptic ulcer before the bacteriological aetiology of these diseases was recognised.
Lifestyle habits
Although the data regarding a cancer-prone personality are questionable, personality traits such as sensation-seeking and impulsivity may predispose to early risky behaviour (Reference Zuckerman and KuhlmanZuckerman 2000). With continued exposure, early behavioural experimentation can develop into maladaptive lifestyle habits such as smoking, alcohol consumption, lack of exercise and obesity, all of which are linked to both cancer incidence and the quality of life of patients with cancer.
Exercise
Multiple studies have demonstrated that physical activity has a convincing protective role against colon cancer and a probable protective role against breast and endometrial malignancies (Reference Kruk and CzerniakKruk 2013). Physical activity of 30–60 min per day has been shown in epidemiological studies to reduce rates of colon cancer in men and women by 30–40% and breast cancer in women by 20–30% compared with inactive people (Reference LeeLee 2003). Meta-analyses based on 60 studies of exercise prescribed after treatment for breast cancer showed moderate reductions of fatigue and cancer-specific concerns (Reference Speck, Courneya and MasseSpeck 2010).
The well-established positive effect of physical activity on mood extends to affective disorders in patients with cancer, as demonstrated by a meta-analysis of 15 randomised controlled trials among cancer survivors which showed a modest reduction in depressive symptoms (−0.22; 95% CI −0.43 to −0.09), particularly when exercise was performed under supervision (Reference Craft, van Iterson and HelenowskiCraft 2011).
Several mechanisms have been proposed to underlie the benefits of physical activity in the context of cancer, including changes in endogenous sexual and metabolic hormone levels, reduction of systemic inflammation and improved immune function. Perhaps most significant, however, is the protective effect afforded by decreased central obesity (Reference Friedenreich and OrensteinFriedenreich 2002; Reference Kruk and CzerniakKruk 2013).
Obesity
Obesity has been consistently shown to increase the risk of developing endometrial cancer, breast cancer in postmenopausal women and renal cell carcinoma (Reference CarrollCarroll 1998). It has also been shown to contribute to the progression of precancerous changes into hepatocellular, pancreatic and prostate malignancies (Reference CarrollCarroll 1998; Reference Li, Yeung and HassanLi 2009). Population studies of more than 28 000 people (1965–1993) linked to the cancer registry in Sweden revealed a 33% excess incidence of cancer in obese individuals (Reference Wolk, Gridley and SvenssonWolk 2001). Proposed underlying mechanisms include inflammatory adipokine activity, insulin resistance and changes in steroid hormone activity (Reference Calle and KaaksCalle 2004; Reference RedingerRedinger 2007). Incidentally, chronic inflammation has also been implicated in the development of depressive disorder (Reference Haroon, Raison and MillerHaroon 2012), which may contribute to the increased risk of depression in obese people as well as depression being found to be predictive of obesity (Reference Luppino, De Wit and BouvyLuppino 2010).
Smoking
Smoking is another lifestyle habit that has long been associated with cancer incidence. In comparison to cigarette smoking, the carcinogenic effects of smokeless tobacco use have received little attention. In recent years, however, numerous studies have emerged from the Indian subcontinent highlighting the increased risk of cancer in those who chew paan and gutka (areca nut and betel quid) (Reference Critchley and UnalCritchley 2003). Similarly, shisha smoking is emerging as a significant global public health problem (Reference Shishani, Roll and ArmstrongShishani 2012). Although these practices are socially perceived to be less harmful than cigarette smoking, they have been directly linked to both lung and head and neck malignancies (Reference Javed, Chotai and MehmoodJaved 2010; Reference MaziakMaziak 2013). The paucity of data and lack of methodological rigour applied to this area of research needs to be addressed in order to manage the growing global burden of tobacco-related disease and inform policy regarding the regulation of such substances (Reference Changrani and GanyChangrani 2005).
Hospital admission can be utilised as a window of opportunity to improve the lifestyle of patients (Box 1). Counselling to quit that is delivered to smokers in association with an admission to hospital has been shown in meta-analyses to be effective (Reference Freund, Campbell and PaulFreund 2009; Reference Parsons and DaleyParsons 2010). Smoking is three times more prevalent among people with mental illnesses, and smoking cessation is particularly important, given the risks of vascular and cardiac disease, alongside cancer. With some eight or more sessions, 20% of smokers are able to cease (Reference Burkhalter, Springer and ChhabraBurkhalter 2005). This outcome is clearly dependent on the stage of motivation of the patient. Motivational counselling alone has limited efficacy (d = 0.11; 95% CI −0.05 to 0.27) (Reference Burke, Arkowitz and MencholaBurke 2003) in helping patients stop smoking, unless supplemented by nicotine replacement therapies (OR = 2.37; 95% CI 1.12–5.13) and medications such as varenicline (OR = 2.41; 95% CI 1.91–3.12) and buproprion (OR = 2.07; 95% CI 1.73–2.55) (Reference Eisenberg, Filion and YavinEisenberg 2008). The concept of a ‘teachable moment’ in a person who is approaching surgery or attending their dentist has been useful in helping to recognise when people may be influenced to stop smoking (Reference McBride and OstroffMcBride 2003). Public health initiatives, including television advertisements that promote awareness of the dangers of tobacco in all forms and of the need to quit, are certainly fundamental and vital for community well-being (Reference Wakefield, Spittal and DurkinWakefield 2011).
BOX 1 The stigma of smoking
John was just 50 when his non-small cell lung cancer was diagnosed. He had smoked since 15 years of age and talked of his sense that relatives and friends thought ‘We told you so’. As his cancer was metastatic to bones and brain at diagnosis, his prognosis was fairly grim despite recent advances such as cetuximab. His wife worked, but his two adolescent sons were still completing high school, hoping to go on to university. Loss of the father and his income would be a severe blow for his family. This saddened John and caused him significant embarrassment. He had so intended to be a good provider. He felt deep regret for the many years of excuses he made about his nicotine dependence and his inability to quit smoking. A course of varenicline and some nicotine replacement therapy had assisted his easy withdrawal. Now acceptance of the consequences of his lifestyle choices was a bitter pill. He felt too awkward about his predicament to be able to easily share how he felt about this with his physicians. Facilitating a conversation with his sons about his regret at smoking helped John feel he was both educating and advising them to not make the mistakes of his own youth.
Alcohol and substance misuse
Alcohol is a well-established risk factor for the development of oropharyngeal, laryngeal and oesophageal cancers, contributing to up to 80% of cases (Reference Morris-BrownMorris-Brown 2005). Although the precise mechanisms by which alcohol exerts its carcinogenic effect have not been fully elucidated, the genotoxic effect of acetaldehyde as it is metabolised from ethanol has been strongly implicated (Reference Yokoyama and OmoriYokoyama 2005; Reference Poschl and SeitzPoschl 2004). There is also moderate evidence to suggest that alcohol serves as a solvent for other carcinogens (Reference Boffetta and HashibeBoffetta 2006), which is particularly significant as the habits of both smoking and drinking are often combined.
Marijuana use has been linked to lung cancer in a manner similar to smoking, although studies are often methodologically confounded and results are contradictory (Reference Hashibea, Straifa and TashkinHashibea 2005). Needle sharing in intravenous substance misuse leads to hepatitis infections that are strongly associated with the subsequent development of hepatocellular cancer (Reference Lok, Seeff and MorganLok 2009) (Box 2).
BOX 2 Needle sharing and hepatoma
Susan at 45 had lived with chronic hepatitis B and C for many years, suffering the toll of what now seemed a brief phase of needle sharing in her late teens. She had had periods of treatment with interferon, liked to take ginseng herself, but knew that her liver function tests were abnormal with a cirrhotic process occurring. As more bruising occurred and ascites developed, imaging revealed a multifocal hepatocellular cancer, not deemed suitable for surgery. Treatment with sorafenib helped for a few months, but Susan felt very sad, alone, fatigued and nauseated. She wondered if further treatment was worthwhile. She had lost a lot of weight, yet her swollen belly caused discomfort and early jaundice was again apparent in her sclera. Acknowledging that she felt depressed, she asked to stop treatment so that she could die in peace. Psychotherapeutic support focused on the narrative of Susan’s life, highlighting what she had accomplished and affirming the meaningful relationships in her life.
What the literature tells us
In view of the above, if there is a role for behavioural medicine to play in decreasing the burden of disease attributable to cancer, it is these modifiable lifestyle factors that should be addressed rather than the fixed nature of personality as whole.
Stress, life events and risk of cancer development
The notion that stress might be a cause of cancer is prevalent in many societies (Reference Chida, Hamer and WardleChida 2008; Reference JohansenJohansen 2012). However, many of the studies that support this belief are weakened by methodological errors such as the retrospective attribution of a stressor as causal after the cancer has been diagnosed, or the lack of control for confounding lifestyle factors such as smoking, alcohol, obesity and exercise. (Reference Dalton, Boesen and RossDalton 2002a). Better studies have been based on the Danish Cancer Registry, established nationwide in 1943, and the Danish personal identification number, established in 1968, which permits linkage to clinical databases where lifestyle factors are recorded (Reference Thygesen and ErsbollThygesen 2011).
Studies that have made use of these Danish data and looked for a link with cancer causation include 8042 parents who had lost a child (Reference Li, Johansen and HansenLi 2002) and 11231 parents whose child was diagnosed with cancer (Reference Johansen and OlsenJohansen 1997). Neither study found an increased risk of cancer in these parents, in keeping with Ewertz’s classic bereavement study in 1986. These studies contrast, for example, with the findings of a large cohort of bereaved Israelis after the Yom Kippur War (Reference Levav, Kohn and IscovichLevav 2000), but the latter study carries a potential risk of selection bias compared with studies in which the samples were drawn from administrative registries, where the information on exposure was collected independently of any scientific hypotheses.
The US-based Nurses’ Health Study of 69886 women examined the stress of providing informal care to relatives in one large subgroup (Reference Kroenke, Hankinson and SchernhammerKroenke 2004) and the presence of job stress in another (Reference Schernhammer, Hankinsin and RosnerSchernhammer 2004): neither study found any increase in the occurrence of breast cancer in these women. A meta-analysis of 5700 incident cancer events in 116056 European men and women similarly found no association between self-reported ‘job strain’ at baseline and risk of cancer after 12 years (Reference Heikkilä, Nyberg and TheorellHeikkilä 2013).
Another type of stressor could be the diagnosis of mental illness. The Danes again examined all admissions to psychiatric wards since 1969, and from a cohort of 89491 such patients with major depression found no increased risk of cancer once smoking and alcohol were controlled for (Reference Dalton, Mellemkjaer and OlsenDalton 2002b). The diagnosis of schizophrenia as a stressor was examined in both patients and their parents, without any evidence of increased cancer risk (Reference Dalton, Munk Laursen and MellemkjaerDalton 2004, Reference Dalton, Mellemkjaer and Thomassen2005).
Such Danish data are nationwide and population-based, with extensive follow-up over long periods. The results appear relatively robust and provide empirical evidence refuting the usual assumption that stress causes cancer. Clinicians with knowledge of this are empowered to provide substantial relief to patients who otherwise jump to an unwarranted retrospective attribution of their cancer to a recent and coincidental life event.
Social support and outcome
Early epidemiological studies indicated that social isolation was as powerful a cause of mortality in the general population as were smoking and high cholesterol (Reference Goodwin, Hunt and KeyGoodwin 1987; Reference Lai, Lai and KrongradLai 1999). More recent examination of 734 889 cancer patients in the Surveillance, Epidemiology and End Results (SEER) Medicare database (2004–2008) in the USA revealed that married patients were 20% less likely than unmarried to die of their cancer (after adjusting for demographics, stage and treatment: HR = 0.80, 95% CI 0.79–0.81, P <0.001) (Reference Aizer, Chen and McCarthyAizer 2013). For the ten leading cancers that result in death, married patients were less likely to present with metastatic disease and more likely to receive definitive anti-cancer therapy. The benefit associated with marriage was greater for men than women, but remained significant for women across all of the ten cancers. Being single, separated, widowed or divorced identifies a demographic that places people at risk of social isolation; identification and referral of individuals with this characteristic to psycho-oncology services may be warranted.
Treatment adherence
Social support has also been demonstrated to improve adherence to medical treatment. (Reference DiMatteoDiMatteo 2004a). Although non-adherence to recommended anti-cancer therapies is associated with increased mortality among patients with cancer (Reference Hershman, Shao and KushiHershman 2011), it is important to consider that non-adherence may be an informed rational decision, based on experiences of toxicity or perceived benefit (or lack thereof). Of paramount importance therefore is the provision of satisfactory explanations of treatment options and joint decision-making informed by an understanding of the patient’s attitudes and health beliefs, all of which can mediate better treatment adherence and outcome (Reference Martin, Williams and HaskardMartin 2005).
Group therapy and support groups
Group therapy is a well-established support model for cancer services. When patients come together to share distress and grief with others who have experienced a similar predicament, adaptive healing with improved coping can be promoted. Group therapy has been shown to both prevent and ameliorate clinical depression and can promote adherence to anti-cancer therapy (Reference Kissane, Grabsch and ClarkeKissane 2007). Much hope was held that cancer support groups would improve survival (Reference Spiegel, Kraemer and BloomSpiegel 1989), yet careful replication studies involving women with advanced breast cancer, powered to detect a 15% difference in survival (Reference Goodwin, Leszcz and EnnisGoodwin 2001), have failed to show this (Reference Goodwin, Leszcz and EnnisGoodwin 2001; Reference Kissane, Grabsch and ClarkeKissane 2007; Reference Spiegel, Butler and Giese-DavisSpiegel 2007). A ceiling effect may have resulted from the inclusion of married women, rather than targeting individuals at risk because of poor social support, clinical depression and unmarried status (Reference KissaneKissane 2013). Group leadership is vital to retaining the socially alienated in cancer support groups and creating an inclusive, cohesive group environment. Effective group facilitation is an expert clinical skill, necessitating staffing ratios adequate to the delivery of such services.
The development of interventions to help the leaders of community-based cancer support groups has been a welcome step forward (Reference Zordan, Butow and KirstenZordan 2012). The interventions assessed – a group leaders’ website and discussion forum, a DVD and group therapy leadership manual, and a 2-day evidence-based workshop – illustrate the sort of package needed to improve the quality of cancer support groups. A considerable training agenda exists here in many countries.
Psychosocial factors in cancer progression and mortality
Although the jury is still out regarding the role of behavioural factors in the aetiology of cancer, the evidence in favour of their effect on tumour progression is increasingly persuasive. Behavioural factors have been shown to contribute to the regulation of gene expression, immune response and the inflammatory process, highlighting the potential impact of mental state on disease progression (Reference Constanzo, Sood and LutgendorfConstanzo 2011). Equally, the inflammatory process secondary to tumour growth has been linked to the pathogenesis of depression and cancer-related fatigue (Reference Musselman, Miller and PorterMusselman 2001; Reference Jehn, Kuehnhardt and BartholomaeJehn 2006).
Depression
Depressive disorder is common among patients with cancer, yet not well recognised by busy clinicians when tears, grief and distress are normal components of the experience of diagnosis and disease progression. Screening for depression or distress can increase recognition of psychiatric disorder (Reference MitchellMitchell 2007). For example, when routine computerised out-patient screening for depression was introduced at a cancer centre in a randomised controlled trial, targeted psychosocial interventions resulted in a significant reduction in depression 6 months later (Reference McLachlan, Allenby and MatthewsMcLachlan 2001). Untreated clinical depression is strongly associated with poor adherence to anti-cancer treatments (Reference DiMatteo, Lepper and CroghanDiMatteo 2000) and shorter survival, with mortality rates in meta-analyses increased by 19% (Reference Satin, Linden and PhillipsSatin 2009) and 39% (Reference Pinquart and DubersteinPinquart 2010), depending on the studies selected.
At the primary care level, a large multi-site randomised controlled trial revealed reduced cancer mortality from screening for and treatment of depression (Reference Gallo, Bogner and MoralesGallo 2007). Among patients being treated for metastatic lung cancer, those who received early palliative care had longer survival and more effective symptom management, including reduced depression, than those receiving standard treatment (Reference Temel, Greer and MuzikanskyTemel 2010). There is no doubt that both the recognition and treatment of depression are vital (Box 3).
BOX 3 Is it grief or depression?
Mary had been shocked at her diagnosis of advanced pancreatic cancer. She was only 55 and, although one of her children had married, no grandchildren had been born. She cried freely when her oncologist suggested that her prognosis was guarded. Her fatigue had been pronounced for weeks; her sadness steadily deepened and spoilt most days. She wondered what was the point of life. Her oncologist reassured her that her distress was comprehensible: ‘Chemotherapy is important to contain disease growth. It often causes fatigue due to mild anaemia, but Mary, you will learn to cope’. As Mary struggled on, poor concentration, reduced interest and poor sleep continued to spoil her quality of life. For a time she thought, ‘I must keep trying for my family’. But her depressed mood steadily worsened until she became suicidal. Then psychiatric help was sought. Mary was treated with mirtazapine, chosen as an antidepressant to stimulate her appetite and help her sleep, while supportive psychotherapy employed activity scheduling and re-engagement with her family.
Socioeconomic disadvantage
The other major circumstance associated with shorter survival in people with cancer is socioeconomic disadvantage or social disparity. This is the case in countries both with (Reference Dalton, Ross and DuringDalton 2007; Reference Gentil-Brevet, Colonna and DanzonGentil-Brevet 2008) and without universal access to healthcare (Reference Jha, Peto and ZatonskiJha 2006; Reference Albano, Ward and JemalAlbano 2007). The health literacy of any cultural group may be central to the factors that influence their access to screening and early detection, but the complex interrelationships between the various contributory factors make understanding this difficult. Population-based data-sets measure socioeconomic status inadequately, but there can be no doubt from the evidence base that disparities exist. Policy change is needed to address educational, occupational and income-related inequalities, but also to influence housing, exposure to carcinogens and promotion of a healthy lifestyle.
Clinical perspectives
Both the prevalence of depressive disorders and the consequences of untreated depression highlight the importance of its recognition and treatment in the comprehensive care of patients with cancer. Identifying those at risk of poorer outcomes – the unmarried, socially isolated and socioeconomically deprived – is also crucial to optimise care delivery. Poor lifestyle choices may lead to shame and stigma when cancer does occur, but much can be done to reassure those inclined to attribute their cancer to stress, life events or personality.
Conclusions
Cancer competes with cardiac disease as a leading cause of death in many societies. Psycho-oncology seeks to reduce distress, depression and suffering among people with cancer and their families. Knowledge of risk factors related to the incidence and progression of cancer will help the clinician to provide appropriate guidance about issues that commonly remain a source of confusion in society.
MCQs
Select the single best option for each question stem
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1 Research shows that:
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a stress is a common cause of cancer
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b major life events are associated with the development of cancer
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c stress is not accepted as a cause of cancer
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d increased rates of cancer follow distressing bereavement
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e diagnosis of schizophrenia in a child can result in the development of cancer in the parents.
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2 As regards depression:
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a unrecognised or untreated depression is associated with shorter cancer survival
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b depression in the mentally ill is a cause of cancer
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c depression is unrelated to treatment adherence among the medically ill
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d treatment of depression has no impact on cancer survival
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e group therapy has no impact on ameliorating depression among cancer patients.
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3 In oncology and cancer care:
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a death anxiety is the basis of affective disorders in oncology
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b somatoform disorders are common because patients become hypervigilant about bodily symptoms
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c post-traumatic stress disorders are very common, given the trauma of the cancer diagnosis
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d alcohol use disorders are uncommon
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e premorbid mental disorders are more predictive of psychiatric disorders in patients with cancer than is the diagnosis of cancer itself.
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4 As regards smoking and cancer:
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a advising smokers to quit is a waste of time
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b motivational counselling is very effective in stopping smoking
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c attention to smoking status while patients are in hospital is inconsequential
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d combination pharmacotherapy and motivational counselling achieves incremental benefits in stopping smoking
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e only smoking and not alcohol ingestion is linked to causing cancer.
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5 Regarding impact on cancer:
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a the stress of being married can increase risk for cancer
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b marriage improves the cancer survival rates in men but not in women
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c group support is trendy but is an unproven cancer therapy
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d widowers do as well as married men in cancer survival outcomes
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e social isolation is associated with higher mortality.
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MCQ answers
| 1 | c | 2 | a | 3 | b | 4 | d | 5 | e |
eLetters
No eLetters have been published for this article.