This article has Open Peer Review reports available.
Complementary and alternative medicine use in oncology: A questionnaire survey of patients and health care professionals
© Chang et al; licensee BioMed Central Ltd. 2011
Received: 14 June 2010
Accepted: 24 May 2011
Published: 24 May 2011
We aimed to investigate the prevalence and predictors of Complementary and Alternative Medicine (CAM) use among cancer patients and non-cancer volunteers, and to assess the knowledge of and attitudes toward CAM use in oncology among health care professionals.
This is a cross-sectional questionnaire survey conducted in a single institution in Ireland. Survey was performed in outpatient and inpatient settings involving cancer patients and non-cancer volunteers. Clinicians and allied health care professionals were asked to complete a different questionnaire.
In 676 participants including 219 cancer patients; 301 non-cancer volunteers and 156 health care professionals, the overall prevalence of CAM use was 32.5% (29.1%, 30.9% and 39.7% respectively in the three study cohorts). Female gender (p < 0.001), younger age (p = 0.004), higher educational background (p < 0.001), higher annual household income (p = 0.001), private health insurance (p = 0.001) and non-Christian (p < 0.001) were factors associated with more likely CAM use. Multivariate analysis identified female gender (p < 0.001), non-Christian (p = 0.001) and private health insurance (p = 0.015) as independent predictors of CAM use. Most health care professionals thought they did not have adequate knowledge (58.8%) nor were up to date with the best evidence (79.2%) on CAM use in oncology. Health care professionals who used CAM were more likely to recommend it to patients (p < 0.001).
This study demonstrates a similarly high prevalence of CAM use among oncology health care professionals, cancer and non cancer patients. Patients are more likely to disclose CAM usage if they are specifically asked. Health care professionals are interested to learn more about various CAM therapies and have poor evidence-based knowledge on specific oncology treatments. There is a need for further training to meet to the escalation of CAM use among patients and to raise awareness of potential benefits and risks associated with these therapies.
Complementary and Alternative Medicine (CAM) is 'a comprehensive term used to refer both to traditional medical systems such as traditional Chinese medicine, Indian ayurveda and Arabic unani medicine, and to various forms of indigenous medicine' . The use of CAM has gained enormous popularity among the general public and numerous surveys have reported particularly high prevalence of use in cancer patients [2–5]. Previous studies demonstrated that patients were using CAM without obtaining enough information regarding these therapies . Documented figures of up to 60% of these patients did not disclose their CAM usage to the doctors, and most cited reason was that their doctors did not ask them [4, 5]. These findings highlighted the lack of awareness of CAM usage among health care professionals. This could have important oncologic implications due to potential drug-herb-vitamin interactions. For example, shark cartilage has been found to have no effect on tumour growth in clinical trials, but caused severe gastrointestinal toxicity [6, 7]. More importantly, St. John's Wort was associated with significantly reduced plasma levels of SN-38, the active metabolite of chemotherapeutic agent, Irinotecan . The majority of novel anticancer treatments are studied in advanced cancer patients and this cohort has been shown to use CAM more frequently . This can be a confounding factor potentially leading to under- or over-estimated drug levels, toxicity, side effect profiles, drug-herb-vitamin interactions and unreliable clinical trial data .
Previous surveys in cancer patients have mainly focused on the prevalence and predictors of CAM usage [2–5, 9]. In Ireland, the prevalence of CAM use in oncology has been reported in a selected cohort of patients with head and neck cancer . Few studies have assessed the attitudes and perceptions of health care professionals toward CAM use in oncology. Richardson et al reported negative perceptions on CAM by clinical oncologists and Hyodo et al reported discrepant views on CAM between oncologist and cancer patients [12, 13]. Risberg et al investigated oncology professionals' knowledge of and attitudes toward CAM in a group of oncologists, nurses, clerks and interventional radiographers . However, the study cohorts did not represent all the members of the current multidisciplinary team. Furthermore, these studies did not assess patients and health care professionals' attitudes and perceptions simultaneously [13, 14], which may enable better understanding of the interactions between the two parties. Lastly, health care professionals' knowledge of the use of CAM therapies in specific cancer-related clinical conditions has not previously been investigated.
The aims of this study were therefore to a) investigate the interest and prevalence of CAM use among cancer patients attending a tertiary referral centre in Ireland; b) determine factors associated with CAM usage; (c) assess communications between health care professionals and patients by obtaining opinions and experience from both parties; and (d) investigate health care professionals' knowledge of and attitudes toward CAM.
This was a single centre cross-sectional survey. Participants were recruited between July and August 2008. Three study cohorts were included in this study, namely cancer patients, non-cancer volunteers and health care professionals. The study was granted approval by the Clinical Research Ethics Committee of the University College Hospital Galway. Patients and volunteers were accrued after explanation of the nature of the survey both in verbal and written format, followed by verbal consent. Cancer patients and non-cancer volunteers were identified from the outpatient clinics, inpatient wards, oncology day ward and radiotherapy department. Cancer patients were patients who have been diagnosed with any cancer in the past. Non-cancer volunteers were patients who were on the wards or attending outpatient clinic for reasons other than cancer, or visitors. Thirty-six consultants across 13 specialties (breast and endocrine surgery; general and gastrointestinal surgery; plastics and reconstructive surgery; urology; head and neck surgery; obstetrics and gynaecology; medical oncology; radiation oncology; dermatology; respiratory medicine; palliative medicine; neurology and haematology) gave permission to have their patients recruited in this study. The study was coordinated by a postgraduate researcher and a medical student undertaking summer research project. Nurses at each study location assisted with the accrual process.
Health care professionals consisted of doctors, nurses, physiotherapists, pharmacists, speech and language, and occupational therapists. All of these health care professionals are involved in the care of cancer patients. Doctors and nurses were asked to complete the questionnaire at various locations within the hospital. For other allied health care professionals, questionnaires were distributed to the corresponding departments.
We utilised a modified version of a previously published questionnaire validated in Japan . Prior to the commencement of the survey, the questionnaire was distributed to all participating consultants for review. The structure was further modified and questions reworded according to consultants' feedback. The anonymised questionnaire collected data on sociodemographics; use of CAM and specific details such as types of CAM, expectations and reasons for use; cancer-related characteristics and treatment (Additional files 1 and 2). The questionnaire also incorporated Hospital Anxiety and Depression Scale (HADS) which is a validated brief 14-item scoring system to assess emotional state . Data was also collected on the location of consultation, stage of cancer and a simplified Karnofsky performance status score.
The questionnaire distributed to health care professionals was composed of questions regarding their specialties and positions; use of CAM; attitudes towards CAM and previous experience during consultations. Five quiz-like questions regarding the use of CAM in specific cancer-related scenarios were incorporated to determine if health care professionals were up to date with the best available evidence (Additional files 1 and 2). The 'correct' answers to these questions were based on level 1a evidence [16–20].
Statistical analysis was performed using SPSS 15.0 software (Chicago, IL, USA). Univariate comparison of variables was assessed using χ2 test for nominal or ordinal data; Student's t-test and Mann-Whitney U test were used for parametric and non-parametric continuous data respectively. Multivariate analysis was performed using binary logistic regression with forward conditional method. Variables that were significant on univariate analyses were entered into the regression model. A p value of less than 0.05 was considered statistically significant for all tests.
Characteristics of Participants
Characteristics of patient participants
Number of Participants
Number of CAM Users (%)
p value (χ2)
52.5 ± 16.9
49.1 ± 15.5
Annual household income
€20 000 - €49 999
€50 000 - €99 999
26 (36.6) 52 (21.5)
Public Medical Card
Private Health Insurance
Head & Neck
High anxiety score (≥11)
Low anxiety score (<11)
High depression score (≥11)
Low depression score (<11)
80 - 100
50 - 70
0 - 40
Characteristics of health care professional participants
Number of Participants
Number of CAM Users (%)
p value (χ2)
31.1 ± 7.3
33.3 ± 8.6
Types of CAM Use
Types of CAM used
Types of CAM Used
Number of Users (%)
Chinese herbal medicine
Others (Neuro Linguistic Programming)
Predictors of CAM Use
Univariate and multivariate analyses of factors predictive of CAM use
Multivariate Binary Logistic Regression
95% Confidence Interval
Higher educational background
Higher annual household income
Private health insurance
In the cancer patient cohort, patients who received hormonal therapy were more likely to use CAM (p = 0.016). Interestingly, no association was found between CAM use and cancer stage, and Karnofsky performance status score.
Attitudes and Perceptions Toward CAM
Among 155 CAM users, reasons for using CAM were: 72 (51.1%) recommended by family or friends; 42 (29.8%) own will, 12 (8.5%) media influence and 6 (4.3%) recommended by doctor. Among the non-cancer volunteers, CAM users expected CAM to improve immune function (n = 79, 61.7%), general wellbeing (n = 20, 15.7%) and a small proportion expected CAM to prevent cancer (n = 8, 6.3%). On the other hand, the cancer patient cohort used CAM with the expectations that it would cure cancer (n = 1, 0.7%), halt cancer progression (n = 1, 0.7%), improve symptoms (n = 6, 4.1%), and 6 patients used it as a complementary to conventional treatments. When asked if they thought CAM was effective, the majority of CAM users (n = 93, 66.5%) either agreed or strongly agreed. Only 4 participants reported negative effects from CAM use (one constipation and diarrhoea; one drowsiness; one cough, sweating and weight gain; one urinary incontinence).
In 359 non-users, reasons for not using CAM were reported to be: did not have enough information about it (n = 150, 50.2%), no interest (n = 64, 21.4%), did not believe in it (n = 38, 12.7%), never needed it (n = 14, 4.7%), too expensive (n = 12, 4%), happy with conventional medicine (n = 5, 1.7%) and heard bad comments about it (n = 4, 1.3%). Interestingly, 151 (46.6%) of the non-users would like to learn more about CAM.
Among health care professionals, there was a significant association between CAM use and professions (p = 0.050). The prevalence of CAM use was the highest among pharmacist (4/5, 80%), followed by nurses (30/61, 49.2%), physiotherapists (10/27, 37.0%), and the least prevalent among doctors (17/59, 28.8%). Longer duration since qualification was associated with higher likelihood of CAM usage (p = 0.007). There was a high level of interest among health care professionals with 110 (75.3%) wanting to learn more about CAM.
Communications Between Health Care Professionals and Patients
In 155 CAM users, 43 (30.1%) voluntarily reported CAM use to their doctors. The doctors' response was reported to be: encouraged to continue (n = 16, 37.2%), advised to stop (n = 7, 16.3%), neither discouraged nor encouraged (n = 20, 46.5%), and doctor did not know about CAM (n = 4, 2.8%). Among patients who did not report CAM use voluntarily, only 8 were asked about its use by their doctors. The majority of patients did not mention CAM use because the doctor never asked (n = 47, 34.6%), some thought that the doctor would not understand (n = 5, 3.7%), or would disapprove (n = 8, 5.9%).
From the health care professionals perspective, when asked about their responses to patients regarding CAM use, 26 (17.2%) reported that they would encourage to continue, 5 (3.3%) advise to stop, 92 (60.9%) neither discourage nor encourage. Of these, 58 (38.2%) have been asked about CAM during consultations in the previous 6 months. A large proportion of health care professionals (n = 68, 45.9%) thought they would ask patients about CAM use, while 57 (38.8%) would recommend CAM to patients. Health care professionals who used CAM were more likely to recommend CAM to their patients (p = 0.001).
Health Care Professionals' Knowledge on CAM
Health care professionals were asked to self-rate their knowledge on CAM. With regards to having adequate knowledge, 1 strongly agreed, 22 (14.4%) agreed, 40 (26.1%) undecided, 62 (40.5%) disagreed and 28 (18.3%) strongly disagreed. When asked if they were up to date with the best available evidence on CAM use, none strongly agreed, 5 agreed, 27 (17.5%) undecided, 83 (53.9%) disagreed and 39 (25.3%) strongly disagreed.
Distribution of answers provided by health care professionals on evidence-based practices of CAM in cancer
Numbers of Answers (%)
There is evidence that acupuncture is effective in reducing first day vomiting after chemotherapy.
There is evidence that Chinese herbs decrease side-effects in patients treated with chemotherapy.
There is evidence to support recommending antioxidant vitamins such as α-tocopherol, beta-carotene or retinol to prevent lung cancer.
There is evidence to support the use of oral fish oil for the management of cancer cachexia.
There is evidence that ginger has a potential role as an antiemetic herbal remedy.
In this study, we surveyed the prevalence of CAM use in three distinctive populations and investigated the prevalence, predictive factors, knowledge of and attitudes toward CAM use. The communication on CAM between health care professionals and cancer patients was explored.
One of the strengths of this study is the recruitment process. Participants were approached and invited to complete the questionnaires, instead of using mailed-questionnaire method. With the assistance of nurse coordinators, the response rate of our study was 100% among patients who were invited to participate. This eradicates selection bias inherently associated with most mail-based study design as patients who use CAM are more inclined to participate. One might argue that the prevalence rate of CAM use in this study may not be a true reflection of the entire population as participants were accrued from the hospital setting. However, the prevalence rate reported here is in keeping with previous large scale population surveys [2, 21–23]. Furthermore, patients (cancer or non-cancer) and visitors included in this study are a representative group of individuals that hospital-based health care workers interact with on a daily basis and are therefore clinically relevant.
In our study, the prevalence of CAM use is high in all groups of participants, intriguingly, the highest among health care professionals. This would reflect the growing rates of CAM use and it is an encouraging finding as CAM becomes more acceptable in the society. There is no difference in CAM use between cancer patients and non-cancer volunteers, which is not consistent with previous reports [5, 22–26]. This may be explained by the inclusion of patients suffering from chronic disorders other than cancer in the non-cancer volunteer cohort. Factors associated with increased CAM use such as female gender, younger age, higher socioeconomic status and private health insurance shown in our study are consistent with previous data [4, 5, 27, 28]. Interestingly, patients with higher anxiety or depression score, more advanced disease stage and poorer performance status are not more likely to use CAM. Kristoffersen et al previously reported higher prevalence of CAM use among cancer patients with poorer prognosis . The authors suggested that this may be due to patients resorting to non-conventional therapy when less hope of cure is given by the physicians. In contrast, other studies have demonstrated that CAM use is not associated with more advanced disease stage [29–31]. This may be related to the complexity of underlying psychological and behavioural mechanisms influencing the use of CAM in cancer patients such as attitude, family support and coping behaviour as have been shown by previous reports [32, 33].
The most commonly used CAM is orally ingested agents such as natural supplements, vitamins, green tea and herbal remedies. This further highlights the importance of documentation of the intake of these substances as part of routine clerking and assessment of patients in order to avoid potential drug-herb-vitamin interactions particularly in patients undergoing chemo- or hormonal therapy. As demonstrated by our study, most patients do not inform their doctors about CAM use, mainly because the doctors never ask, or are perceived to be lack of CAM knowledge or disapproving. Therefore the initiatives to elicit CAM usage through history taking may be effective in obtaining such information.
There are numerous reports expressing communication gaps between health care professionals and patients on CAM. This is possibly related to the suboptimal evidence-based knowledge on these therapies but none of these studies had addressed this in detail [4, 5, 28, 34–36]. To our knowledge, this is the first study that includes both health care professionals' attitudes toward CAM use in oncology and an assessment of their knowledge on these therapies. There is a significant discrepancy comparing patients and health care professionals' reported experience toward CAM. While only 8 of 155 CAM users were asked by their doctors about CAM use, a much higher proportion (45.9%) of health care professionals thought they would ask patients about its use. Similarly, only 17.2% of health care professionals would encourage patients to continue CAM, which is markedly different from experience reported by patients that 37.2% of doctors encouraged them to continue CAM when consulted.
When asked about their knowledge on CAM, the majority of health care professionals thought they did not have adequate knowledge (58.8%) nor were up to date with the best available evidence (79.2%) on CAM use. This is evident from answers provided by health care professionals to the five evidence-based CAM questions. Up to 80% were unsure of the roles of the aforementioned CAM practices in cancer-related scenarios, thereby not being able to advise patients regarding the benefits, limitations and even potential harms.
The findings of this study have major implications for undergraduate education. We demonstrated a high prevalence of CAM use in our study population consisting of cancer and non-cancer patients as well as health care workers. Despite the lack of awareness and knowledge on CAM, health care professionals expressed a high level of interest in CAM education. Until recently few allopathic medical students worldwide would have been exposed to the teaching of CAM. In recognition of the growing needs for medical graduates that have at least basic understanding of CAM in order to make appropriate referrals as part of integration of CAM into conventional medicine; several countries have incorporated CAM into undergraduate curricula such as the United States of America (USA), Finland, Germany, Japan, Canada, the Netherlands and Switzerland. Notably in Finland acupuncture has been part of the undergraduate curriculum since 1975. According to the worldwide review on CAM published by the World Health Organization, the majority of medical schools in the USA offer courses on CAM. Since 1997, primary care physicians have been encouraged to attend courses that enable them to incorporate homeopathy into practices. In Germany, medical schools are required to test students' knowledge of CAM. In Australia, acupuncturists form a part of the multidisciplinary management of patients in the public health sector. The British Medical Association recommends incorporating CAM into undergraduate curriculum and making accredited postgraduate training available . University of Southampton commenced education on CAM as part of the Special Study Module (SSM) out of students' request . As part of the Professionalism curriculum, CAM SSM has been made available at the National University of Ireland Galway for the last 2 years. The potential for incorporating CAM as part of a compulsory undergraduate curriculum remains to be evaluated.
Nevertheless there are some limitations to our study. The survey was carried out in a single institution involving generally defined populations of cancer patients, non-cancer volunteers and health care professionals. While further studies may be warranted to investigate the attitudes toward CAM in more specifically defined populations, the present study produced useful information on the overall prevalence of CAM use. The non-cancer volunteer cohort was accrued from the hospital environment, which may not be truly reflective of the general population. Furthermore, the questionnaire used in this study did not address the use of CAM within a specific time period or specifically in relation to cancer.
This survey demonstrates a high prevalence of CAM use among patients and health care professionals. Increased awareness of CAM use and potential drug-herb-vitamin interactions is critical for optimal patient care in oncology. The incorporation of CAM education into undergraduate medical curriculum may improve health care professionals' knowledge on CAM, thereby improving doctor-patient communication.
- World Health Organization: WHO traditional medicine strategy 2002-2005. [http://apps.who.int/medicinedocs/en/d/Js2297e/]
- Eisenberg DM, Kessler RC, Foster C, Norlock FE, Calkins DR, Delbanco TL: Unconventional medicine in the United States. N Engl J Med. 1993, 328: 246-252. 10.1056/NEJM199301283280406.View ArticlePubMedGoogle Scholar
- Eisenberg DM, Davis RB, Ettner SL, Appel S, Wilkey S, Van Rompay M, Kessler RC: Trends in alternative medicine use in the United States, 1990-1997: Results of a follow-up national survey. JAMA. 1998, 280: 1569-1575. 10.1001/jama.280.18.1569.View ArticlePubMedGoogle Scholar
- Richardson MA, Sanders T, Palmer JL, Greisinger A, Singletary SE: Complementary/alternative medicine use in a comprehensive cancer center and the implications for oncology. J Clin Oncol. 2000, 18: 2505-2514.PubMedGoogle Scholar
- Hyodo I, Amano N, Eguchi K, Narabayashi M, Imanishi J, Hirai M, Nakano T, Takashima S: Nationwide survey on complementary and alternative medicine in cancer patients in Japan. J Clin Oncol. 2005, 23: 2645-2654.View ArticlePubMedGoogle Scholar
- Miller DR, Anderson GT, Stark JJ, Granick JL, Richardson D: Phase I/II trial of the safety and efficacy of shark cartilage in the treatment of advanced cancer. J Clin Oncol. 1998, 16: 3649-3655.PubMedGoogle Scholar
- Loprinzi CL, Levitt R, Barton DL, Sloan JA, Atherton PJ, Smith DJ, Dakhil SR, Moore DF, Krook JE, Rowland KM, Mazurczak MA, Berg AR, Kim GP, North Central cancer Treatment Group: Evaluation of shark cartilage in patients with advanced cancer: a North Central Cancer Treatment group trial. Cancer. 2005, 104: 176-182. 10.1002/cncr.21107.View ArticlePubMedGoogle Scholar
- Mathijssen RH, Verweij J, de Bruijn P, Loos WJ, Sparreboom A: Effects of St. John's wort on irinotecan metabolism: St. John's Wort--More implications for cancer patients. J Natl Cancer Inst. 2002, 94: 1247-1249.View ArticlePubMedGoogle Scholar
- Kristoffersen AE, Fonnebo V, Norheim AJ: Do cancer patients with a poor prognosis use complementary and alternative medicine more often than others?. J Altern Complement Med. 2009, 15: 1115-1120. 10.1089/acm.2009.0083.View ArticleGoogle Scholar
- Hlubocky FJ, Ratain MJ, Wen M, Daugherty CK: Complementary and alternative medicine among advanced cancer patients enrolled on phase I trials: a study of prognosis, quality of life, and preferences for decision making. J Clin Oncol. 2007, 25: 548-554. 10.1200/JCO.2005.03.9800.View ArticlePubMedGoogle Scholar
- Amin M, Glynn F, Rowley S, O'Leary G, O'Dwyer T, Timon C, Kinsella J: Complementary medicine use in patients with head and neck cancer in Ireland. Eur Arch Otorhinolaryngol. 2010, 267: 1291-1297. 10.1007/s00405-010-1223-1.View ArticlePubMedGoogle Scholar
- Richardson MA, Masse LC, Nanny K, Sanders C: Discrepant views of oncologists and cancer patients on complementary/alternative medicine. Support Care Cancer. 2004, 12: 797-804. 10.1007/s00520-004-0677-3.View ArticlePubMedGoogle Scholar
- Hyodo I, Eguchi K, Nishina T, Endo H, Tanimizu M, Mikami I, Takashima S, Imanishi J: Perceptions and attitudes of clinical oncologists on complementary and alternative medicine. Cancer. 2003, 97: 2861-2868. 10.1002/cncr.11402.View ArticlePubMedGoogle Scholar
- Risberg T, Kolstad A, Bremnes Y, Holte H, Wist EA, Mella O, Klepp O, Wilsgaard T, Cassileth BR: Knowledge of and attitudes toward complementary and alternative therapies: a national multicentre study of oncology professionals in Norway. Eur J Cancer. 2004, 40: 529-535. 10.1016/j.ejca.2003.11.011.View ArticlePubMedGoogle Scholar
- Hyodo I, Eguchi K, Takigawa N, Segawa Y, Hosokawa Y, Kamejima K, Inoue R: Psychological impact of informed consent in hospitalized cancer patients: A sequential study of anxiety and depression using the hospital anxiety and depression scale. Support Care Cancer. 1999, 7: 396-399. 10.1007/s005200050299.View ArticlePubMedGoogle Scholar
- Ezzo J, Vickers A, Richardson MA, Allen C, Dibble SL, Issell B, Lao L, Pearl M, Ramirez G, Roscoe JA, Shen J, Shivnan JC, Streitberger K, Treish I, Zhang G: Acupuncture-Point stimulation for chemotherapy-induced nausea and vomiting. J Clin Oncol. 2005, 23: 7188-7198. 10.1200/JCO.2005.06.028.View ArticlePubMedGoogle Scholar
- Taixiang W, Munro AJ, Guanjian L: Chinese medical herbs for chemotherapy side effects in colorectal cancer patients. Cochrane Database of Systematic Reviews. 2005, 1: CD004540-PubMedGoogle Scholar
- Caraballoso M, Sacristan M, Serra C, Bonfill X: Drugs for preventing lung cancer in healthy people. Cochrane Database of Systematic Reviews. 2003, 2: CD002141-PubMedGoogle Scholar
- Dewey A, Baughan C, Dean T, Higgins B, Johnson I: Eicosapentaenoic acid (EPA, an omega-3 fatty acid from fish oils) for the treatment of cancer cachexia. Cochrane Database of Systematic Reviews. 2007, 1: CD004597-PubMedGoogle Scholar
- Ernst E, Pittler MH: Efficacy of ginger for nausea and vomiting: a systematic review of randomized clinical trials. British Journal of Anaesthesia. 2007, 84: 367-371.View ArticleGoogle Scholar
- Fisher P, Ward A: Complementary medicine in Europe. BMJ. 1994, 309: 107-111.View ArticlePubMedPubMed CentralGoogle Scholar
- MacLennan AH, Wilson DH, Taylor AW: Prevalence and cost of alternative medicine in Australia. Lancet. 1996, 347: 569-573. 10.1016/S0140-6736(96)91271-4.View ArticlePubMedGoogle Scholar
- Fox P, Coughlan B, Butler M, Kelleher C: Complementary alternative medicine (CAM) use in Ireland: a secondary analysis of SLAN data. Complement Ther Med. 2010, 18: 95-103. 10.1016/j.ctim.2010.02.001.View ArticlePubMedGoogle Scholar
- Rees RW, Feigal I, Vickers A, Zollman C, McGurk R, Smith C: Prevalence of complementary therapy use by women with breast cancer: a population-based survey. Eur J Cancer. 2000, 36: 1359-1364. 10.1016/S0959-8049(00)00099-X.View ArticlePubMedGoogle Scholar
- Paltier O, Avitzour M, Peretz T, Cherny N, Kaduri L, Pfeffer RM, Wagner N, Soskolne V: Determinants of the use of complementary therapies by patients with cancer. J Clin Oncol. 2001, 19: 2439-2448.Google Scholar
- Malassiotis A, Fernandez-Ortega P, Pud D, Ozden G, Scott JA, Panteli V, Margulies A, Browall M, Magri M, Selvekerova S, Madsen E, Milovics L, Bruyns I, Gudmundsdottir G, Hummerston S, Ahmad AM, Platin N, Kearney N, Patiraki E: Use of complementary and alternative medicine in cancer patients: a European survey. Ann Oncol. 2005, 16: 655-663. 10.1093/annonc/mdi110.View ArticleGoogle Scholar
- Gansler T, Kaw C, Crammer C, Smith T: A population-based study of prevalence of complementary methods use by cancer survivors. Cancer. 2008, 113: 1048-1057. 10.1002/cncr.23659.View ArticlePubMedGoogle Scholar
- Corner J, Yardley J, Maher EJ, Roffe L, Young T, Maslin-Prothero S, Gwilliam C, Haviland J, Lewith G: Patterns of complementary and alternative medicine use among patients undergoing cancer treatment. Eur J Cancer Care. 2009, 18: 271-279. 10.1111/j.1365-2354.2007.00911.x.View ArticleGoogle Scholar
- Munstedt K, Kirsch K, Milch W, Sachsse S, Vahrson H: Unconventional cancer therapy: Survey of patients with gynecological malignancy. Arch Gynecol Obstet. 1996, 258: 81-88.PubMedGoogle Scholar
- Begbie SD, Kerestes ZL, Bell DR: Patterns of alternative medicine use by cancer patients. Med J Aust. 1996, 165: 545-548.PubMedGoogle Scholar
- Risberg T, Lund E, Wist E, Dahl O, Sundstrøm S, Andersen OK, Kaasa S: The use of non-proven therapy among patients treated in Norwegian oncological departments: A cross-sectional national multicenter study. Eur J Cancer. 1995, 31A: 1785-1789.View ArticlePubMedGoogle Scholar
- Hirai K, Komura K, Tokoro A, Kuromaru T, Ohshima A, Ito T, Sumiyoshi Y, Hyodo I: Psychological and behavioral mechanisms influencing the use of complementary and alternative medicine (CAM) use in cancer patients. Ann Oncol. 2008, 19: 49-55.View ArticlePubMedGoogle Scholar
- Sollner W, Maislinger S, DeVries A, Steixner E, Rumpold G, Lukas P: Use of complementary and alternative medicine by cancer patients is not associated with perceived distress or poor compliance with standard treatment but with active coping behavior. Cancer. 2000, 89: 873-880. 10.1002/1097-0142(20000815)89:4<873::AID-CNCR21>3.0.CO;2-K.View ArticlePubMedGoogle Scholar
- Gratus C, Wilson S, Greenfield SM, Damery SL, Warmington SA, Grieve R, Steven NM, Routledge P: The use of herbal medicines by people with cancer: a qualitative study. BMC Complement Altern Med. 2009, 9: 14-10.1186/1472-6882-9-14.View ArticlePubMedPubMed CentralGoogle Scholar
- Shih V, Chiang JYL, Chan A: Complementary and alternative medicine (CAM) usage in Singaporean adult cancer patients. Ann Oncol. 2009, 20: 752-757. 10.1093/annonc/mdn659.View ArticlePubMedGoogle Scholar
- Robinson A, McGrail MR: Disclosure of CAM use to medical practitioners: a review of qualitative and quantitative studies. Complement Ther Med. 2004, 12: 90-98. 10.1016/j.ctim.2004.09.006.View ArticlePubMedGoogle Scholar
- Legal status of traditional medicine and complementary/alternative medicine: a worldwide review. 2001, World Health OrganizationGoogle Scholar
- Owen DK, Lewith G, Stephens CR: Can doctors respond to patients' increasing interest in complementary and alternative medicine?. BMJ. 2001, 322: 154-158. 10.1136/bmj.322.7279.154.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/11/196/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.