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J Oncol Pract. 2013 January; 9(1): 34–41.
Published online 2012 October 2. doi:  10.1200/JOP.2012.000634
PMCID: PMC3545661

Prevalence and Correlates of Postdiagnosis Initiation of Complementary and Alternative Medicine Among Patients at a Comprehensive Cancer Center

Abstract

Purpose:

Patients with cancer increasingly use complementary and alternative medicine (CAM) in conjunction with conventional oncology treatments. Previous studies have not investigated postdiagnosis initiation of CAM therapies or independent correlates of use of individual CAM modalities. The purpose of this study was to determine the prevalence and correlates of individual CAM modalities initiated after cancer diagnosis.

Methods:

A cross-sectional survey was conducted of a random sample of adults with a cancer diagnosis (N = 1,228) seeking care at a National Cancer Institute–designated comprehensive cancer center within a 12-month period.

Results:

The majority of patients were female (64.7%), white (86.9%), and married (72.8%).Three-quarters (75.2%) used at least one CAM modality, and 57.6% of those using CAM initiated use after cancer diagnosis. For all CAM therapies combined, women were 1.7 times more likely than men to initiate any CAM therapy after cancer diagnosis. However, when CAM modalities were differentiated by type, men and women were equally likely to initiate all therapies except for psychotherapy and mind-body approaches. Postdiagnosis initiation of every CAM modality, except mind-body therapies, differed by cancer type.

Conclusion:

A significant proportion of patients initiated CAM use after diagnosis. However, specific type of CAM initiated varied by demographics and cancer type, suggesting there is not a “typology” of CAM user. Optimal comprehensive cancer treatment, palliation, and survivorship care will require patient and provider education regarding CAM use by modality type; improved provider-patient communication regarding potential benefits, limitations, and risks; and institutional policies to support integrated conventional and CAM treatment.

Introduction

Individuals diagnosed with cancer are among those whose use of complementary and alternative medicine (CAM) has increased over the past 25 years in the United States.18 Studies have shown that as many as 91% of individuals undergoing cancer treatment use some form of CAM,9 and individuals with a previous or current cancer diagnosis are more likely to use CAM than the general population.10 The most common reasons for using CAM include seeking a cure or reducing risk of recurrence7,11; mitigating chemotherapy and radiation adverse effects9,12,13; and improving overall health, quality of life, and well-being.14 Among patients undergoing traditional cancer treatments, the most popular CAM modalities include special diets, dietary supplements/botanicals, mind-body techniques, and movement-physical therapy (PT).9,1417

The efficacy of some CAM therapies for cancer treatment and palliation has been documented.13,18,19 Chinese herbal medications are associated with reduced treatment adverse effects, increased quality of life, and improved survival rates across cancer sites.20 Estrogenic botanical supplements have been associated with better quality of life in patients with breast cancer.21 Massage therapy has been shown to reduce lymphedema in breast and gynecologic cancers,22 and decrease pain and improve mood in patients with advanced cancers.23 Randomized trials have shown acupuncture reduces the number and severity of hot flashes in women with breast cancer24 and men with prostate cancer.25,26

Despite the documented benefits of some CAM therapies, risks to patient safety exist. Drug-supplement interactions have been documented with chemotherapies.12,17 St John's wort reduces plasma levels of the active metabolites of three chemotherapy agents: irinotecan, imatinib mesylate, and docetaxel.2730 Acupuncture and intensive manipulative therapies are not advisable in patients with bleeding disorders.13 Macrobiotic-type diets that limit calorically dense foods may cause cachexia in some patients.31 Certain patients also may be at increased risk for rare events associated with massage, including internal hemorrhage, fractures, and infection.32

The majority of individuals diagnosed with cancer continue to use conventional medical therapies alongside CAM therapies.3,8,9,11,12,33,34 However, many patients fail to disclose CAM use to their oncologists,7,9,33,35,36 limiting the oncologist's ability to discuss benefits, limitations, and potential risks of the modalities used. We conducted a survey to evaluate how adults receiving treatment at a comprehensive cancer center (CCC) use CAM, with a specific focus on describing patients who initiate CAM after diagnosis. To our knowledge, this is one of the first studies to report incident use of CAM after diagnosis. Study outcomes might facilitate the development of interventions to enhance patient-provider communication about the benefits, limitations, and risks of CAM therapies during cancer treatment, especially during the vulnerable period immediately after diagnosis. Findings might also lay the groundwork for developing models of integrated CAM and traditional medicine for comprehensive cancer treatment, palliation, and survivorship care.

Methods

Participants

We conducted a cross-sectional survey of adults (≥ 18 years of age) seeking care at the Cancer Institute of New Jersey, a National Cancer Institute (NCI) –designated CCC, within the 12-month period of March 1, 2004 to February 29, 2005. Children were excluded, as their CAM use may be determined by parents/guardians. Other inclusion criteria included willingness and ability to complete the study questionnaire and English literacy. There were no exclusions based on years since diagnosis or treatment status. After obtaining institutional review board approval from the University of Medicine and Dentistry of New Jersey, a potential participant list was randomly generated from an existing patient database that included patients seen for cancer, treatment, screening, and prevention at the CINJ to obtain a sample of 33% of the 9,062 cancer center patients seen that year (N = 2,777). This sample size provided adequate power to detect an effect size of 0.10 at 80% power with alpha set at 0.05 assuming a response rate (RR) of 50%. Participants were mailed a cover letter, survey, and self-addressed stamped envelope in which to return the survey. The institutional review board–approved cover letter served as the consent document and explained to potential subjects that completion and return of the survey indicated their consent to participate. To maximize the RR, a postcard was mailed 2 weeks after the survey and a second survey packet with cover letter was mailed 1 month later to all nonresponders. Respondents received a $10 voucher for a local restaurant. A total of 1,755 usable (eg, complete data, met eligibility criteria) surveys were returned (58.6% usable RR). This compares to a 51.4% RR in a similar study conducted at another NCI-designated CCC.12

Survey Instrument

The survey instrument was adapted from a tool previously used and validated with patients attending a CCC.12 To ensure readability and face validity, it was pilot tested by five nonpatient volunteers of representative sociodemographics who were employees of the school of health-related professions at UNDMJ. Survey completion time ranged from 20 to 25 minutes, and no changes to instruction or content were necessary. To assess CAM use, patients were given a list of different modalities (Appendix Table A1, online only) and asked to check whether they had ever used it, currently used it, and if they currently used it, whether they initiated use “only after diagnosis.” In addition, demographics including sex, race/ethnicity, marital status, and educational level were measured categorically and age measured continuously based on birth date. Oncologic information, including cancer site(s), cancer status (recurrence, metastases, cancer free), and treatment type(s) was measured categorically, and years since diagnosis was measured continuously based on self-reported date of diagnosis. Patients' reasons for use, perceived benefit, sources of CAM information, and decision to communicate with health care providers regarding CAM were also collected and will be reported elsewhere. To protect health information, participants' data were deidentified and only study identification numbers were used in the database and on the surveys.

Statistical Analyses

Frequency distributions (No., %) and descriptive statistics (mean, standard deviation) were used to report outcomes, and categories are reported as they appear in the survey. For inferential analyses, categories with small cell sizes were either combined or excluded from the analysis. For instance, the primary cancer diagnosis was recoded from 28 categories to represent the most prevalent cancers in the United States37: prostate, breast, lung, skin (melanoma), hematologic (leukemia, Hodgkin and non-Hodgkin lymphomas), colorectal, gynecologic (cervical, vaginal, ovarian, and uterine), and “other.” Bivariate associations between postdiagnosis CAM use and demographic and cancer type variables were assessed using χ2 analyses, and variables with statistically significant bivariate associations were included in the multivariate models specific for each of the CAM practices. Multivariate logistic regression models were used to examine the covariates of postdiagnosis CAM use within each type of CAM practice. Odds ratios and 95% CIs are reported for all independent variables categories. Statistical analyses were performed using SPSS V19.0 for Windows (Chicago, IL, SPSS) A priori alpha was set at P < .05.

Results

A total of 1,755 surveys were available for analysis, of which 1,228 (71.5%) respondents indicated a cancer diagnosis. Among those with a cancer diagnosis, 75.2% (n = 923) were currently using at least one CAM modality, and 57.6% (n = 532) of CAM users initiated use after diagnosis. Of those who initiated CAM after cancer diagnosis, 93.2% (n = 496) were still using CAM at the time of the survey.

Demographic characteristics of sample subjects are reported in Table 1. The majority of respondents were female (64.7%), white (86.9%), and married (72.8%). Only female sex (χ2 = 10.28; P = .001) and younger age group (χ2 = 29.40; P < .001) were significantly associated with current CAM use. For all types of postdiagnosis CAM combined, female sex (χ2 = 16.80; P < .001), younger age (χ2 = 37.06; P < .001) and divorced/separated/single marital status (χ2 = 10.82; P = .013) were significantly associated with initiation of CAM therapy after cancer diagnosis.

Table 1.
Current CAM Use and CAM Use Initiated After Diagnosis, by Demographic Characteristic

Table 2 presents the most frequently reported cancer diagnoses (with at least 20 respondents). Breast cancer was the most frequently reported diagnosis (n = 397, 34.4%), followed by melanoma (n = 151, 13.1%). All other diagnoses were less than 10% of the sample. Mean time since diagnosis ranged from 30.77 months for lung cancer to 88.08 months for uterine cancer. Current CAM use was similar across cancer types, ranging from 72.1% for lung cancer to 85.0% for nonmelanoma skin cancer. Postdiagnosis CAM initiation varied more across cancer diagnoses, from 53.6% for ovarian cancer to less than 20% for nonmelanoma skin cancer.

Table 2.
Most Frequent Cancer Diagnosis by Current CAM Use and Use Initiated After Diagnosis

Separate multivariate models were created for the following CAM types: special diet, psychotherapy, movement-PT, spirituality, mind-body, and dietary supplement (Table 3). For special diet use, three variables (age group, level of education, and cancer type) were bivariately associated and remained significantly associated with postdiagnosis special diet use in the multivariate model. All age groups except patients 60 to 69 years old (YO) were significantly more likely to initiate CAM postdiagnosis than those more than 70 YO (odds ratios [ORs], 2.95-6.68). For education level, only those with some college or a bachelor's degree were more likely to use a special diet postdiagnosis than participants with a graduate degree (OR = 1.84; P = .041). Participants with breast (OR = 4.07; P = .004), colorectal (OR = 5.21; P = .006), and prostate (OR = 6.71; P = .001) cancers were all significantly more likely to initiate a special diet postdiagnosis than participants with melanoma.

Table 3.
Predictors of CAM Initiation After Diagnosis, by CAM Type

Four variables were bivariately associated with postdiagnosis psychotherapy use and remained significant in the multivariate model: sex, age, income level, and cancer type. Women were 1.86 times more likely to use psychotherapy than men (P = .029). All age groups except the youngest (18-29 YO) and the 60- to 69-YO group were significantly more likely to use psychotherapy postdiagnosis than participants in the oldest age group (ORs, 2.72-3.77). For income, participants in the $60,000-$99,000 per year bracket were 1.89 times more likely (P = .041) to use psychotherapy than individuals in the lowest income bracket. Except for those with lung cancer, participants with all cancer types were significantly more likely than those with melanoma to initiate psychotherapy postdiagnosis (ORs ranging from 3.13 for participants with “other” types of cancer to 7.79 for participants with prostate cancer).

Movement-PT had the largest number of variables bivariately associated with postdiagnosis CAM use: sex, age, cancer type, race, marital status, and education. However, after adjusting for other covariates, only cancer type remained statistically significant. Participants with breast (OR = 2.46; P = .28), prostate (OR = 3.39; P = .033) and hematologic (OR = 2.83; P = .019) cancers were more than two times more likely to initiate movement-PT CAM than participants with melanoma.

Only age and cancer type had statistically significant bivariate associations with spirituality. In the adjusted model, participants in all but the youngest age categories (18-29 YO) were significantly more likely to initiate spiritual practices after diagnosis than participants in the oldest age group (ORs, 2.98-3.45). Only participants with colorectal (OR = 3.11; P = .019) or lung (OR = 4.45; P = .003) cancers were more likely than patients with melanoma to initiate spirituality CAM after diagnosis.

Mind-body modalities were bivariately associated with sex, age, and cancer type. Only sex and age remained significant in the multivariate model. Women were 3.98 times more likely than men to initiate mind-body modalities after diagnosis (P < .001). Participants in all age groups were significantly more likely than participants in the oldest age group to initiate mind-body CAM (ORs, 2.63-6.75). There were no differences across cancer type in initiation of mind-body CAM after diagnosis.

Finally, for dietary supplements, sex, age, and cancer type were significantly bivariately associated. However, in the multivariate model, only age and cancer type remained significantly associated. Participants 30 to 39 YO (OR = 2.40; P = .005) and 40 to 49 YO (OR = 1.99; P = .005) were significantly more likely to begin using dietary supplements after diagnosis compared with those more than 70 YO. Participants with breast (OR = 2.37; P = .005), lung (OR = 4.74; P < .001), hematologic (OR = 2.01; P = .039), and gynecologic (OR = 3.19; P = .002) cancers were significantly more likely to begin using dietary supplements after diagnosis compared with participants with melanoma.

Discussion

Better understanding of the prevalence and usage patterns of CAM is integral to optimally managing treatment of patients with cancer. To our knowledge, we report for the first time two significant findings regarding CAM use in a CCC. First, 57.6% of patients reporting CAM use initiated use after diagnosis, suggesting the impact of their changed health status on decision making. Second, in contrast to previous studies, when CAM use was analyzed by specific modality and controlled for covariates, we found important differences in patterns of use compared with findings that grouped and analyzed CAM modalities as a single variable. In aggregate, more women than men use CAM, and “any CAM use” decreases with increasing age after 60 years.7,9,10,12,17 However, when examining CAM modalities independently, men were no less likely than women to initiate use of special diets, movement-PT, spirituality, or dietary supplements after diagnosis. Similarly, younger age was not associated with initiation of movement-PT or mind-body modalities after diagnosis. Further, in multivariate analyses, cancer type was significantly associated with postdiagnosis initiation of all CAM modalities except for mind-body therapies. These data suggest there is not a “typology” of CAM user, but rather, use depends on the characteristics of the person with cancer and the specific CAM modality. Our findings have important implications for clinical oncology practice and institutional policies regarding integration of CAM into conventional cancer care.

Clinical Oncological Practice

CAM usage is likely to increase as cancer survival rates and access to CAM therapies continue to improve.34,38 We documented that 75.2% of participants diagnosed with cancer were currently using at least one modality, which is consistent with previous studies.9,10,12,39 Research shows that the majority of patients who use CAM do not discuss their usage with their physicians,10,39 and this can pose safety risks.4,13,17,27-30,32,40 Given the high rates of CAM usage among patients with cancer, and given that the majority of patients in our study initiated use after diagnosis, providers need to communicate early in treatment about potential risks and benefits with the goal of finding the optimal combination of CAM therapies and conventional care. This open communication can demonstrate respect for patients' health-related beliefs and behaviors, foster mutual trust, and possibly encourage better compliance with conventional treatment.41,42

Our findings are clinically relevant, because they demonstrate that there is not one typical CAM user, but rather, CAM usage differs by patient factors and CAM modality. Thus, providers cannot make generalizations about who may or may not be using CAM in the context of cancer care. For providers to initiate and tailor their discussions of CAM use in a meaningful way, it will be important to understand trends in the use of specific CAM modalities as presented herein. For example, dietary supplements, which pose some of the greatest risks for adverse events, are equally likely to be used by men and women. This contradicts previous studies, which reported women as the more prevalent general users of CAM,7,9,10,12,17 a finding that might prevent some providers from querying male patients about CAM use. Similarly, increasing age was not associated with a decreased use of mind-body and movement-PT therapies. Older adults may be at increased risk for adverse events associated with some of these modalities, such as movement (eg, yoga, exercise) and massage therapy, due to frailer skeletal structures. Thus, it would be important for a provider to discuss these options with their older patients. Finally, patients with breast, lung, hematologic, and gynecologic cancers are more likely to use dietary supplements. Providers caring for these patients will benefit from evidence-based information about the potential for supplements to interact with chemotherapeutic agents commonly used in these cancers. Future research should attend to gaining a more thorough understanding of the broad range of predictors of individual types of CAM therapies, as well as disclosure of such use, including clinical-oncologic, psychologic, behavioral, and sociologic factors.

Integration of CAM Into Conventional Care

Our findings support previous studies that show CAM use among patients with cancer is less about whether patients will incorporate CAM therapies and more about which therapies they will choose. Given the high prevalence of use—especially after diagnosis—the knowledgeable integration of CAM into conventional care is becoming necessary to safely and effectively treat patients during and after cancer therapy. There is a growing trend in community-based hospitals offering CAM therapies, as well as establishing integrative medicine clinics and centers. Independent physicians also are providing CAM services or coordinating referral to CAM providers.43 Furthermore, health maintenance organizations and insurance companies are increasingly covering CAM services.44 Although these strategies increase patients' access to CAM therapies, they do not facilitate holistic care in which CAM and conventional providers work collaboratively to employ the best empirically based treatments. Effective integration of CAM and conventional oncology care will require institutions to develop and implement policies, practices, and educational programs that support integrative oncology services. Such an approach will help patients and providers to make informed decisions that maximize benefit and minimize harm.

Limitations

This study has several limitations. First, it was conducted at a single institution, so the sample may not represent all persons with a cancer diagnosis, but rather, the population of cancer patients in the center's catchment area. Individuals more inclined to use CAM therapies might have been more likely to participate, and geographic area mighty affect the variation in CAM modalities as a result of differences in access to providers and knowledge of CAM. However, rates of CAM use were consistent with those from previously published studies.9,10,12,39 The frequencies of cancer diagnoses in our sample differed from national statistics (eg, prostate was the most frequent cancer nationally, but breast was most frequent in our sample). The sample also was restricted to English-literate patients, although a study of acculturation showed that CAM use in the United States is associated with English language proficiency, even after accounting for socioeconomic status, health insurance coverage, self-reported health status, and other demographic variables.45 The sample also predominately included white participants and likely is not representative of the general population of patients with cancer. Finally, a proportion of the eligible patients declined to participate in the study, and the reasons for nonparticipation are unknown.

Despite its limitations, this study provides important information about the types of CAM therapies used by patients with specific cancers, and more important, the initiation of use after diagnosis. In addition, we report independent patient characteristics associated with incident CAM use after diagnosis. These results might be used to facilitate patient-provider communication about CAM use, especially during treatment planning immediately after a cancer diagnosis, and to lay the groundwork for developing educational and clinical models integrating CAM and traditional medicine for comprehensive cancer treatment, palliation, and survivorship care. Future studies should confirm our findings in a more representative sample that includes patients undergoing treatment in community settings as well as CCCs.

Acknowledgment

Funding for this study was provided by the Cancer Institute of New Jersey (A.I.P.).

Appendix

Table A1.

CAM Therapies: General Types and Specific Therapies

Type of CAM TherapySpecific Therapies
Special dietLacto-ovo vegetarian (no meat)
Vegan (no meat, dairy, eggs)
Macrobiotic
Gerson's diet treatment
Other (list)
PsychotherapySocial worker
Psychologist
Psychiatrist
Support group
Other (list)
Movement/PTExercise
Yoga
Tai chi
Chi gong
Chiropractic/osteopathic
Massage
Other (list)
Mind/bodyImagery/visualization
Hypnosis
Meditation
Biofeedback
Massage therapy
Reiki
Energy healing/therapeutic touch
Journaling
Music therapy
Other (list)
Spiritual practicesPrayer
Prayer/spiritual healing (by others)
Other (list)
Dietary supplementsMultivitamins/minerals
Vitamin E
Vitamin C
Soy supplement (isoflavones, pills)
Echinacea
Garlic (pill form)
Selenium
Saw palmetto
Green tea (EGCG, pills)
Coenzyme Q10
St. John's wort
Melatonin
Essiac
Mistletoe (Iscador)
Milk thistle
PC SPES
Laetrile
Shark cartilage
Bovine cartilage (Catrix)
Other (list)
Additional therapiesHomeopathy
Ayurvedic remedies
Bioelectro-magnetic therapies
Acupuncture
Folk remedies
Other (list)

Abbreviations: CAM, complementary and alternative medicine; EGCG, epigallocatechin gallate; PC SPES, herbal supplement promoted for prostate health, containing the herbs crysanthemum morifolium, ganoderma lucidum, glycyrrhiza glabra, isatis indigotica, panax pseudoginseng, rabdosia rubescens, scutelleria baicalensis, and serenoa repens; recalled in 2012 after prescription medications found in product; PT, physical therapy.

Authors' Disclosures of Potential Conflicts of Interest

The author(s) indicated no potential conflicts of interest.

Author Contributions

Conception and design: All authors

Provision of study materials or patients: Oliver Lontok, Maureen Huhmann, Linda Patrick-Miller

Collection and assembly of data: Adam I. Perlman, Oliver Lontok, Maureen Huhmann, Linda Patrick-Miller

Data analysis and interpretation: Adam I. Perlman, J. Scott Parrott, Leigh Ann Simmons, Linda Patrick-Miller

Manuscript writing: All authors

Final approval of manuscript: All authors

References

1. Eisenberg DM, Kessler RC, Foster C, et al. Unconventional medicine in the United States. Prevalence, costs, and patterns of use. N Engl J Med. 1993;328:246–252. [PubMed]
2. Eisenberg DM, Davis RB, Ettner SL, et al. Trends in alternative medicine use in the United States, 1990-1997: Results of a follow-up national survey. JAMA. 1998;280:1569–1575. [PubMed]
3. Eisenberg DM, Kessler RC, Van Rompay MI, et al. Perceptions about complementary therapies relative to conventional therapies among adults who use both: Results from a national survey. Ann Intern Med. 2001;135:344–351. [PubMed]
4. Ernst E. Intangible risks of complementary and alternative medicine. J Clin Oncol. 2001;19:2365–2366. [PubMed]
5. Nahin RL, Straus SE. Research into complementary and alternative medicine: Problems and potential. BMJ. 2001;322:161–164. [PMC free article] [PubMed]
6. Boon H, Westlake K, Stewart M, et al. Use of complementary/alternative medicine by men diagnosed with prostate cancer: Prevalence and characteristics. Urology. 2003;62:849–853. [PubMed]
7. Adams M, Jewell A. The use of complementary and alternative medicine by cancer patients. International Semin Surg Oncol. 2007;4:10. [PMC free article] [PubMed]
8. Fouladbakhsh JM, Stommel M, Given BA, et al. Predictors of use of complementary and alternative therapies among patients with cancer. Oncol Nurs Forum. 2005;32:1115–1122. [PubMed]
9. Yates JS, Mustian KM, Morrow GR, et al. Prevalence of complementary and alternative medicine use in cancer patients during treatment. Support Care Cancer. 2005;13:806–811. [PubMed]
10. Mao JJ, Farrar JT, Xie SX, et al. Use of complementary and alternative medicine and prayer among a national sample of cancer survivors compared to other populations without cancer. Complement Ther Med. 2007;15:21–29. [PubMed]
11. Hann D, Allen S, Ciambrone D, et al. Use of complementary therapies during chemotherapy: Influence of patients' satisfaction with treatment decision making and the treating oncologist. Int Cancer Ther. 2006;5:224–231. [PubMed]
12. Richardson MA, Sanders T, Palmer JL, et al. Complementary/alternative medicine use in a comprehensive cancer center and the implications for oncology. J Clin Oncol. 2000;18:2505. [PubMed]
13. Mansky PJ, Wallerstedt DB. Complementary medicine in palliative care and cancer symptom management. Cancer J. 2006;12:425–431. [PubMed]
14. Barnes P, Bloom B, Nahin R. CDC National Health Statistics Report No. 12. Atlanta, GA: Centers for Disease Control and Prevention; 2008. Complementary and alternative medicine use among adults and children: United States, 2007. [PubMed]
15. Astin JA. Why patients use alternative medicine: Results of a national study. JAMA. 1998;279:1548–1553. [PubMed]
16. Barnes PM, Powell-Griner E, McFann K, et al. Complementary and alternative medicine use among adults: United States, 2002. Sem Integr Med. 2004;2:54–71.
17. Chang KH, Brodie R, Choong MA, et al. Complementary and alternative medicine use in oncology: A questionnaire survey of patients and health care professionals. BMC Cancer. 2011;11:196. [PMC free article] [PubMed]
18. Davies AA, Davey Smith G, Harbord R, et al. Nutritional interventions and outcome in patients with cancer or preinvasive lesions: Systematic review. J Natl Cancer Inst. 2006;98:961–973. [PubMed]
19. Bardia A, Barton DL, Prokop LJ, et al. Efficacy of complementary and alternative medicine therapies in relieving cancer pain: A systematic review. J Clin Oncol. 2006;24:5457–5464. [PubMed]
20. Molassiotis A, Potrata B, Cheng KK. A systematic review of the effectiveness of Chinese herbal medication in symptom management and improvement of quality of life in adult cancer patients. Complement Ther Med. 2009;17:92–120. [PubMed]
21. Ma H, Sullivan-Halley J, Smith A, et al. Estrogenic botanical supplements, health-related quality of life, fatigue, and hormone-related symptoms in breast cancer survivors: A HEAL study report. BMC Complement Altern Med. 2011;11:109. [PMC free article] [PubMed]
22. Finnane A, Liu Y, Battistutta D, et al. Lymphedema after breast or gynecological cancer: Use and effectiveness of mainstream and complementary therapies. J Altern Complement Med. 2011;17:867–869. [PubMed]
23. Kutner JS, Smith MC, Corbin L, et al. Massage therapy versus simple touch to improve pain and mood in patients with advanced cancer. Ann Intern Med. 2008;149:369–379. [PMC free article] [PubMed]
24. Hervik J, Mjåland O. Acupuncture for the treatment of hot flashes in breast cancer patients, a randomized, controlled trial. Breast Cancer Res Treat. 2009;116:311–316. [PubMed]
25. Beer TM, Benavides M, Emmons SL, et al. Acupuncture for hot flashes in patients with prostate cancer. Urology. 2010;76:1182–1188. [PMC free article] [PubMed]
26. Frisk J, Spetz AC, Hjertberg H, et al. Two modes of acupuncture as a treatment for hot flushes in men with prostate cancer—A prospective multicenter study with long-term follow-up. Eur Urol. 2009;55:156–163. [PubMed]
27. Lundahl A, Hedeland M, Bondesson U, et al. The effect of St. John's wort on the pharmacokinetics, metabolism and biliary excretion of finasteride and its metabolites in healthy men. Eur J Pharm Sci. 2009;36:433–443. [PubMed]
28. Frye RF, Fitzgerald SM, Lagattuta TF, et al. Effect of St John's wort on imatinib mesylate pharmacokinetics. Clin Pharmacol Ther. 2004;76:323–329. [PubMed]
29. Smith P, Bullock JM, Booker BM, et al. The influence of St. John's wort on the pharmacokinetics and protein binding of imatinib mesylate. Pharmacotherapy. 2004;24:1508–1514. [PubMed]
30. Komoroski BJ, Parise RA, Egorin MJ, et al. Effect of the St. John's wort constituent hyperforin on docetaxel metabolism by human hepatocyte cultures. Clin Cancer Res. 2005;11:6972–6979. [PubMed]
31. American Cancer Society. Macrobiotic diet. Find support and treatment Web site. http://www.cancer.org/Treatment/TreatmentsandSideEffects/ComplementaryandAlternativeMedicine/DietandNutrition/macrobiotic-diet.
32. Corbin L. Safety and efficacy of massage therapy for patients with cancer. Cancer Control. 2005;12:158. [PubMed]
33. Tasaki K, Maskarinec G, Shumay DM, et al. Communication between physicians and cancer patients about complementary and alternative medicine: Exploring patients' perspectives. Psycho-oncology. 2002;11:212–220. [PubMed]
34. Hann D, Baker F, Denniston M, et al. Long-term breast cancer survivors' use of complementary therapies: Perceived impact on recovery and prevention of recurrence. Integr Cancer Ther. 2005;4:14. [PubMed]
35. Eisenberg DM, Kessler RC, Van Rompay MI, et al. Perceptions about complementary therapies relative to conventional therapies among adults who use both: Results from a national survey. Ann Intern Med. 2001;135:344–351. [PubMed]
36. Adams JS, Hewison M. Unexpected actions of vitamin D: New perspectives on the regulation of innate and adaptive immunity. Nat Clin Pract Endocrinol Metabol. 2008;4:80–90. [PMC free article] [PubMed]
37. Siegel R, Ward E, Brawley O, et al. Cancer statistics, 2011. CA Cancer J Clin. 2011:212–236. [PubMed]
38. Verhoef MJ, Balneaves LG, Boon HS, et al. Reasons for and characteristics associated with complementary and alternative medicine use among adult cancer patients: A systematic review. Integr Cancer Ther. 2005;4:274–286. [PubMed]
39. Oh B, Butow P, Mullan B, et al. Patient-doctor communication: Use of complementary and alternative medicine by adult patients with cancer. J Soc Integr Oncol. 2010;8:56–64. [PubMed]
40. Kessler DA. Cancer and herbs. N Engl J Med. 2000;342:1742–1743. [PubMed]
41. Leventhal H, Benyamini Y, Brownlee S, et al. Illness representations: Theoretical foundations. In: Petrie KJ, Weinman JA, editors. Perceptions of Health and Illness: Current Research and Applications. Amsterdam, the Netherlands: Harwood Academic Publishers; 1997.
42. Durant JR. Alternative medicine: An attractive nuisance. J Clin Oncol. 1998;16:1–2. [PubMed]
43. Institute of Medicine. Complementary and alternative medicine in the United States. Washington DC: National Academies Press; 2005.
44. Pelletier K, Astin J. Integration and reimbursement of complementary and alternative medicine by managed care and insurance providers: 2000 update and cohort analysis. Altern Ther Health Med. 2002;8:38. [PubMed]
45. Su D, Li L, Pagán JA. Acculturation and the use of complementary and alternative medicine. Soc Sci Med. 2008;66:439–453. [PubMed]

Articles from Journal of Oncology Practice are provided here courtesy of American Society of Clinical Oncology