Table 1.
Characteristics and results of qualitative studies on stigma and nihilism in lung cancer
| Study | Design (Level of evidence) | Participants | Aim of interview | Study factor | Results |
|---|---|---|---|---|---|
| Chapple 2004a & b, UK |
Home interview (Level III) |
Lung cancer patients |
Lung cancer patients’ experience of lung cancer including their perceptions, how others reacted to the diagnosis and financial issues |
Stigma |
Some participants perceived lung cancer as being viewed in the broader society as a self-inflicted disease resulting from smoking and leading to a horrible death. One participant noted that the stigma applied to all lung cancer patients; smokers and non-smokers. As a result of the smoking related stigma it was thought that lung cancer research and screening was neglected. |
| N = 45 |
The press was criticised for blaming lung cancer patients in particular for their disease. |
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| NSCLC, SCLC and mesothelioma; All stages. |
Medical and treatment outcomes |
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| Recruited through general practices, nurses, oncologists, chest physicians and support groups and through study website. |
Smoking related stigma was thought to be a reason for lung cancer symptoms not being taken as seriously as those for other cancers leading to delays in diagnosis. |
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|
Psychosocial outcomes | |||||
| Stigma was perceived to result in social isolation, and deterred support group participation (1 participant) and seeking financial relief (1 participant). | |||||
| Conlon 2010, USA |
Interview, (Level III) |
Oncology social workers |
Social workers’ perceptions of the lung cancer experience |
Stigma |
Smoking stigma |
| N = 18 |
Lung cancer was always associated with smoking and patients often reported stigma, guilt, blame and shame. Smoking stigma was seen as a reason why support, funding and advocacy for lung cancer were lower. |
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| Recruited from 17 cancer hospitals in 13 states with experience with approximately 25,000 lung cancer patients. |
Division between lung cancer patient smokers and non-smokers. |
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|
Poor prognosis stigma | |||||
| Patient reported lung cancer stigmatised as being mostly fatal. | |||||
|
Psychosocial outcomes | |||||
| Patients reported smoking stigma sometimes resulted in reluctance to tell others that they have lung cancer. | |||||
|
Psychosocial outcomes | |||||
| Poor prognosis stigma potentially led to difficulties attending support groups. | |||||
| Corner 2005 & 2006, UK |
Semi-structured interviews with a time-line prompt mostly in home and often with a relative present (Level III) |
Patients recently (<3 months) diagnosed with lung cancer |
To explore delays in lung cancer diagnosis |
Stigma |
Medical and treatment outcomes |
| All experienced symptoms for 4 months or more prior to visiting doctor |
Factors potentially leading to delay in seeking medical treatment included expectation and fear that smokers would be denied treatment (reported by 1 participant who was a smoker) |
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| N = 22; 12 men, 10 women | |||||
| Median age = 68 years | |||||
| 15/22 inoperable disease | |||||
| 1/22 never smoker | |||||
| Recruited from 2 hospital outpatient clinics. | |||||
| Leydon 2003, UK |
Telephone and face-to-face semi-structured interviews (Level IV) |
Cancer patients diagnosed < 2 years ago with a focus on those of lower SES |
Perceptions of cancer diagnostic process |
Lung cancer specific fear |
Medical and treatment outcomes |
| N = 17; 5 men, 12 women |
Lung cancer viewed as fatal (by 1 participant). This theme was reported as arising in the context of potential barriers to seeing a doctor |
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| Included 2 lung cancer patients; a 67 year old male and a 59 year old female. | |||||
| Recruited through cancer support community organisations. | |||||
| Sharf 2005 USA, Texas |
Interview with guiding questions (Level III) |
Patients with NSCLC or a suspicious pulmonary mass who refused or did not follow-up for physician-recommended treatment (N = 7) or invasive investigation (N = 2). |
Reasons for declining physician-recommended treatment or follow–up options |
Nihilism |
Medical and treatment outcomes |
| 100% male, 89% white |
Reasons reported included the view that lung cancer treatments were futile (5 participants). |
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| Identified at multidisciplinary pulmonary conferences and review of pathology reports at a university affiliated Veterans Affairs hospital. | |||||
| 9/31 eligible patients interviewed | |||||
| 2 with history of depression | |||||
| Tod 2008, UK |
Semi-structured home interviews with partner or a friend participating at the request of 12 participants (Level III) |
Lung cancer patients |
Factors influencing delay in reporting symptoms (patient delay) |
Stigma |
Medical and treatment outcomes |
| N = 20; 12 men, 8 women. |
Nihilism |
Factors identified that might result in patient delay in consulting a doctor about their symptoms included the stigma that it was caused by smoking and fear. |
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| 18 diagnosed in past 6 months | |||||
| 3 non smokers; 9 previous smokers. | |||||
| Recruited from deprived health district by a respiratory physician and lung cancer nurse specialists. | |||||
| Tod 2010 UK | 3 focus groups, (Level III) | Focus group 1; 6 community pharmacists (50% female) |
Factors influencing delay in reporting symptoms (patient delay) | Stigma |
Medical and treatment outcomes |
| Focus group 2: 6 clinical nurse specialists (100% female) |
Factors identified that might result in lung cancer patient delay in consulting a doctor about their symptoms included fear of negative evaluation and expectation of denial of treatment especially for smokers. | ||||
| Focus group 3: 2 practice nurses (100% female) | |||||
| Recruited an area with high levels of lung cancer and smoking and a history of heavy industry |
NSCLC = Non small cell lung cancer; SCLC = Small cell lung cancer.