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Complementary and Alternative Treatment Use in Breast Cancer Patients in the Eastern Black Sea Region—A Cross-Sectional Study

CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2022; 43(03): 270-277

DOI: DOI: 10.1055/s-0042-1749400

Abstract

Introduction Complementary and alternative therapies (CAMs) are being increasingly and frequently used in the treatment of cancer patients in the last two decades.

Objectives It was aimed to examine the frequency of the use of CAMs in patients with breast cancer who applied to the outpatient clinic.

Materials and Methods Patients who were admitted to our clinic between January 2020 and 2021 and diagnosed with breast cancer for at least 3 months were included in the study. A questionnaire consisting of 37 questions was asked to the patients by the interviewer. Sociodemographic characteristics and CAM methods of the patients were questioned in the questionnaire.

Results This is a cross-sectional study that includes 338 patients. After the questionnaire was completed, the answers were evaluated, and it was detected that 147 (43.4%) patients were using CAM. Herbal treatment methods were preferred most frequently. The most frequently used herbs were turmeric, nettle, ginger, and linden. The second method used was treatments based on religious belief. The use of CAM increased as the income level of the patients increased and the duration of diagnosis increased.

Conclusion It was determined that our patients frequently used CAM methods and mostly preferred herbal methods. Since the use of CAMs during or after treatment may create undesirable results in the treatment of patients, it is necessary to be careful about this issue and inform as well as question the patients about the same.

Ethics

The research was conducted out in line with the principles of the Declaration of Helsinki and was approved by the local ethical committee (No. 2020/31), dated 11.06.2020. The patients were included in the study after the written consent form was read and their signed consent was obtained. After oral explanation was given to illiterate patients and their consent was obtained, a questionnaire was administered in the presence of their attendants.

Publication History

Article published online:
02 July 2022

© 2022. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

Abstract

Introduction Complementary and alternative therapies (CAMs) are being increasingly and frequently used in the treatment of cancer patients in the last two decades.

Objectives It was aimed to examine the frequency of the use of CAMs in patients with breast cancer who applied to the outpatient clinic.

Materials and Methods Patients who were admitted to our clinic between January 2020 and 2021 and diagnosed with breast cancer for at least 3 months were included in the study. A questionnaire consisting of 37 questions was asked to the patients by the interviewer. Sociodemographic characteristics and CAM methods of the patients were questioned in the questionnaire.

Results This is a cross-sectional study that includes 338 patients. After the questionnaire was completed, the answers were evaluated, and it was detected that 147 (43.4%) patients were using CAM. Herbal treatment methods were preferred most frequently. The most frequently used herbs were turmeric, nettle, ginger, and linden. The second method used was treatments based on religious belief. The use of CAM increased as the income level of the patients increased and the duration of diagnosis increased.

Conclusio It was determined that our patients frequently used CAM methods and mostly preferred herbal methods. Since the use of CAMs during or after treatment may create undesirable results in the treatment of patients, it is necessary to be careful about this issue and inform as well as question the patients about the same.

Introduction

Breast cancer is the most frequently diagnosed cancer worldwide, after lung cancer, with more than 2 million cases diagnosed each year.[1] In women, it is the most common cancer that is diagnosed and the second most common cause of cancer-related deaths.[2] There are treatment methods in breast cancer such as surgery, radiotherapy, chemotherapy, hormone therapy, and immunotherapy. Depending on the stage of the disease and the patient's clinic, one or more of these treatment methods can be used. Many side effects such as nausea, vomiting, weakness, suppression of immunity, and impaired blood count may develop during treatment or depending on the disease itself. These side effects and factors such as the long duration of the treatments may lead patients to use complementary and alternative treatments (CAMs) to improve their quality of life.

Complementary therapies like vitamin supplements, massage, yoga, acupuncture, and herbal remedies are supportive treatments used to control symptoms, reduce drug side effects, contribute to the general care of the patient, and improve quality of life. Alternative treatments, on the other hand, are treatments that are used instead of the prescribed patient's medical treatment and whose effectiveness has not been proven yet.[3] CAMs are frequently used in cancer patients. Various studies are reporting that this rate is between 10 and 60% in cancer patients.[4] Across Europe, ∼40% of all cancer patients refer to CAM during their oncological treatment.[5] [6] There has been an increase in the rate of using these treatments in the last two decades.[7] A guideline on CAMs used in breast cancer patients reported that meditation, yoga, and relaxation are routinely recommended for the treatment of problems such as anxiety and mood disorders.[8] This study was aimed to reveal the rates of CAM use in patients with breast cancer after diagnosis, whether receiving chemotherapy or not, the factors affecting this situation, the side effects or benefits observed under these treatments, and the reasons that lead people to try these treatments.

Materials and Methods

This is a single-center, cross-sectional study conducted between January 2020 and January 2021. A total of 338 volunteers from patients over the age of 18, who applied to Karadeniz Technical University outpatient clinics and chemotherapy units, who were followed up with a breast cancer diagnosis, were included in the study. Patients with poor performance, communication problems, and those who did not want to participate in the survey were not included in the study.

After reviewing the literature, a total of 37 questions were asked by a single interviewer (medical oncologist) to explore the use of CAM.[9] [10] [11] The primary outcome of our study was to detect the frequency of the use of CAM in breast cancer patients. The secondary outcome was to detect the most common CAM that is used by the patients. In the survey, the sociodemographic status of the patients such as age, place of birth, education level, place of residence, occupation, number of children, income level, and medical characteristics such as diagnosis time, family history, disease stage, and other accompanying diseases were questioned. Questions based on whether they use CAM, if they do, what they use, how long they use it, why and with what expectation they use it, in which periods of the disease they use it, whether they experience any side effects while using it, what kind of side effects develop in those who do, whether they benefit or not were asked to the patients. Additionally, q u e s t i o n s like how the beneficiaries benefited, where they heard about these treatments, how much they paid monthly for these treatments, whether they informed their follow-up doctors, why those who did not inform, why the informants did, and whether they continued the CAMs were asked.

Statistical Analysis

Data analysis was done in IBM SPSS Statistics 25.0 (IBM Corporation, Armonk, New York, United States) package program. Whether the distribution of discrete numerical variables was close to normal was examined using the Kolmogorov–Smirnov test. For discrete numerical variables, they were expressed as mean ± standard deviation or median (minimum- maximum), while categorical variables were expressed as several cases and in percent (%). The significance of the difference between the groups in terms of mean values was evaluated with the Student's t-test, and the significance of the difference in terms of discrete numerical variables with a far-normal distribution was evaluated with the Mann–Whitney U test. Pearson's χ2 test was used in the analysis of categorical data unless otherwise stated. On the other hand, if the expected frequency is below 5 in at least ¼ of the cells in the 2 × 2 cross tables, the categorical data in question were evaluated with Fisher's exact probability test, in cases where the expected frequency was between 5 and 25, evaluation was made with continuity corrected χ2 test. Multivariate logistic regression analysis was used to determine the most determinant factor in differentiating the group that did not use CAM before versus the group that used CAM. All variables found to be p < 0.25 as a result of univariate statistical analyzes were included in the regression model as candidate factors. In addition, odds ratio, 95% confidence interval (CI), and Wald statistics for each variable were calculated. For p < 0.05, the results were considered statistically significant.

Results

The mean age of the patients included was 52.8 ± 11.6 years. When the clinical and demographic characteristics of the patients using and not using CAM were compared, there was no statistically significant difference found between the groups in terms of mean age, marital status, number of children, education level, place of residence, occupation, active employment, family history, and disease stage (p > 0.05). On the other hand, the income level of the group using alternative treatment was statistically significantly higher (p < 0.001) and the duration of diagnosis was statistically significantly longer (p = 0.030) compared with the group that did not use alternative treatment ([Table 1]). The percentage of coexisting disease was 42.9%. Hypertension is the most frequent coexisting disease and there was no statistically significant difference between the group not using CAM and the group using CAM in terms of comorbidities (p > 0.05).


Table 1

Demographic and clinical characteristics of the cases according to the groups using and not using CAM

Of the 39 patients who had never tried these alternative treatments, 43.6% considered trying them. [Table 2] shows 147 (43.4%) patients using CAM, the reasons for taking these treatments, their expectations while taking them, when and for how long they started using CAM, whether they continued these treatments, whether they had side effects, and whether they benefit from these treatments. [Table 3] shows where the patients using CAM have heard about these treatments, the monthly cost of these treatments, whether they have informed their follow-up doctor about it, whether they found these treatments to be effective from their medical treatments, and whether there was anyone who had applied them before. The distribution of treatment types used by patients who have tried CAMs is shown in [Table 4].


Total (n = 338)

Nonuser (n = 191)

User (n = 147)

p-Value

Age (years)

52.8 ± 11.6

53.7 ± 10.8

51.6 ± 12.5

0.096[a]

Marital status

0.977[b]

Never married

24 (7.1%)

13 (6.8%)

11 (7.5%)

Married

283 (83.7%)

161 (84.3%)

122 (83.0%)

Divorced

12 (3.6%)

7 (3.7%)

5 (3.4%)

Widow

19 (5.6%)

10 (5.2%)

9 (6.1%)

Number of children

2 (0–5)

2 (0–5)

3 (0–5)

0.357[c]

Education status

0.502[b]

Illiterate

51 (15.1%)

32 (16.8%)

19 (12.9%)

Primary school

171 (50.6%)

94 (49.2%)

77 (52.4%)

Middle school

21 (6.2%)

14 (7.3%)

7 (4.8%)

High school

51 (15.1%)

30 (15.7%)

21 (14.3%)

University

44 (13.0%)

21 (11.0%)

23 (15.6%)

Abode

0.678[b]

Village, town

44 (13.0%)

27 (14.1%)

17 (11.6%)

District

125 (37.0%)

72 (37.7%)

53 (36.0%)

Province

169 (50.0%)

92 (48.2%)

77 (52.4%)

Job

0.495[b]

Housewife

263 (77.8%)

152 (79.6%)

111 (75.5%)

Health employee

10 (3.0%)

4 (2.1%)

6 (4.1%)

Teacher

20 (5.9%)

9 (4.7%)

11 (7.5%)

Other

45 (13.3%)

26 (13.6%)

19 (12.9%)

Working status

0.709[d]

Working

31 (9.2%)

19 (9.9%)

12 (8.2%)

Not working

307 (90.8%)

172 (90.1%)

135 (91.8%)

Income level

<0 href="#FN214080607-3">b]

≤1,000 TL

195 (57.7%)

128 (67.0%)

67 (45.6%)

1,001–3,000 TL

84 (24.8%)

37 (19.4%)

47 (32.0%)

>3,000 TL

59 (17.5%)

26 (13.6%)

33 (22.4%)

Diagnosis time

0.030[b]

<1>

184 (54.4%)

116 (60.7%)

68 (46.2%)

1–5 years

84 (24.9%)

41 (21.5%)

43 (29.3%)

>5 years

70 (20.7%)

34 (17.8%)

36 (24.5%)

Family history

71 (21.0%)

42 (22.0%)

29 (19.7%)

0.613[b]

Stage

0.055[b]

Early

83 (24.6%)

44 (23.0%)

39 (26.5%)

Locally advanced

144 (42.6%)

92 (48.2%)

52 (35.4%)

Metastatic

111 (32.8%)

55 (28.8%)

56 (38.1%)

Table 2

Findings related to the experiences of cases who have tried alternative treatment before (n = 147)

Number of cases

%

Reason for seeking alternative treatment

Failure to respond to medical treatment

10

6.8

Disbelief in medical treatment

1

0.7

Environmental effects

60

40.8

Hopelessness, despair

21

14.3

Believing that alternative therapy can be helpful

95

64.6

Other

1

0.7

The expectation in the use of alternative therapy

Supporting and assisting the treatment given by the doctor

74

50.3

Decreasing complaints

61

41.5

Recovering from illness

86

58.5

Other

4

2.7

At what stage of the disease did the patient start using it?

From the moment of diagnosis

110

74.8

As the disease progresses

37

25.2

How long did the patient use it?

 < 1 year

117

79.6

1–3 years

23

15.6

 > 3 years

7

4.8

Currently using an alternative therapy

82

55.8

Continuing medical treatment with alternative therapy

137

93.2

Side effects associated with alternative therapy

8

5.4

How did the patient find alternative therapy?

Useful

55

37.4

Little useful

10

6.8

Indecisive

59

40.1

Useless

11

7.5

Harmful

3

2.0

Didn't use enough

20

13.6

How was the alternative treatment helpful? ( n  = 68)

İncreased resistance

20

29.4

Felt better

18

26.5

Blood values are improved

9

13.2

Complaints are decreased

24

35.3

Not used enough

2

2.9

Table 3

Findings related to the experiences of subjects who had previously tried CAM (n = 147)

Number of cases

%

Where did the patient hear about alternative therapy?

Television

28

19.0

Newspaper

2

1.4

Friend

66

44.9

Family members

52

35.4

Internet

22

15.0

Doctor

14

9.5

Own decision

23

15.6

The average cost of alternative therapy

None

14

9.5

≤50 TL

44

29.9

51–100 TL

34

23.1

101–200 TL

8

5.4

201–500 TL

12

8.2

501–1000 TL

14

9.5

 > 1000 TL

21

14.3

Explaining to the doctor whether the patient is using CAM

Yes

57

38.8

Reason for disclosure

Interaction with chemotherapy

10

17.5

Side effect

23

40.4

Due to being asked

9

15.8

Whether it is harmful

5

8.8

Thinking that the doctor should know

14

24.6

Other

3

5.3

No

90

61.2

Reason for nondisclosure

Short time use

15

16.7

Considering not necessary

47

52.2

Thinking that it will hurt

13

14.4

Other

15

16.7

Alternative therapy versus drug therapy

Finding more effective

9

6.1

Finding less effective

65

44.2

Indecisive

73

49.7

If alternative treatment was administered by someone else

The patient was informed in advance

91

63.2

The patient was not informed in advance

53

36.8

Table 4

Frequency distributions of alternative treatment types used/tried by subjects who have tried CAM

All variables found to be p < 0.25 as a result of univariate statistical analyses were included in the regression model as candidate factors. There is no candidate level effect statistically when the characteristics such as education level and place of residence were taken into the regression model as confounding factors. The factors that were the most deciding in differentiating the groups who tried an alternative treatment and those who did not, respectively, income level and duration of diagnosis. Regardless of other factors, those with an income between 1,000 and 3,000 TL were 2.85 (95% CI: 1.617–5.030) times more likely to seek alternative treatment than those with an income below 1,000 TL. This difference was 3.03 (95% CI: 1.431–6.421) times higher for those with an income of more than 3,000 TL (p < 0.001 and p = 0.004). When adjustments were made for other factors, the tendency to choose alternative treatment increased 1.860 times (95% CI: 1.045–3.308) statistically in patients who had been diagnosed for 1 to 5 years compared with those diagnosed less than 1 year ago (p = 0.035). In [Table 5], the combined effects of the factors that are thought to be determinative in differentiating these two groups were analyzed by multivariate logistic regression analysis.

Number of cases

%

Herbal mix

31

21.1

Turmeric

23

15.6

Religious faith-based treatment

22

15.0

Nettle

18

12.2

Ginger

16

10.9

Linden

13

8.8

Honey

11

7.5

Grape molasses

9

6.1

Black seeds

9

6.1

Cerago

9

6.1

Psychotherapy

8

5.4

Exercise

8

5.4

Garlic

6

4.1

Leech

6

4.1

Blueberries

5

3.4

Cinnamon

5

3.4

Carob

5

3.4

St. John's Wort (Tipton weed)

4

2.7

Vitamin

4

2.7

Kefir

3

2.0

Rosehip

3

2.0

Oregano

2

1.4

Celery

1

0.7

Other

58

39.5

Total

147

100.0

Examination of the effects of factors thought to be determinative in differentiating the groups using and not using CAM therapy together with multivariate logistic regression analysis—alternative table

Discussion

Classical treatment methods such as surgery, chemotherapy, radiotherapy, and endocrine therapy can cause many physical and psychological side effects such as fatigue, nausea, vomiting, anxiety, pain, and depression in breast cancer patients.[12] [13] Patients seek to get rid of these side effects and improve their quality of life, so CAMs are among the methods frequently used in breast cancer patients.[14] [15] In this study, which we conducted with 338 patients in our clinic, 147 (43.4%) of the patients were using CAMs. Various studies in the literature show that this rate varies between 20 and 80%.[15] [16] This rate varies similarly in studies conducted in our country.[17] [18]

In our study, no statistically significant difference was found between the use of CAM and the patients' mean age, marital status, number of children, educational status, place of residence, occupation, active employment or not, and family history. However, the income level of the group using CAM was found to be statistically significantly higher than the group that did not use it. Independent of other factors, it was determined that those with an income level of 1,000 to 3,000 TL were 2.8 times more likely to turn to alternative treatment, and those with an income of more than 3,000 TL were found to be 3.03 times more likely. Similar to our study, in the study conducted in China in 2004 on the use of CAM in patients followed up with breast cancer, an increase in the use of CAM was found with an increase in income level.[19] This is because patients cannot allocate additional budgets for these treatments.

There are studies in the literature showing that patients with a life expectancy of less than 1 year apply to these treatments more frequently.[20] In our study, no significant difference was found in terms of the stage of the disease and these treatments. When adjusted for other factors, orientation to alternative treatment was found to be statistically significant 1.8 times more in those who were diagnosed for 1 to 5 years compared with those who were diagnosed less than 1 year ago. It was thought that the reason for this was the prolongation of the treatment period, increase in exposure to drug side effects, and accordingly, personal research and referral from the patient's relatives.

There are many herbs and herbal products that cancer patients frequently use, but the interaction between drugs used in cancer treatment and herbal products can be high.[21] [22] In our study, the majority of our patients who applied to CAM were using herbal treatments. Herbal treatments were most often used in admixture. The single most commonly used methods were turmeric, nettle, ginger, and linden. Similar to our study, there are studies in which herbal treatment options are frequently used.[23] It was thought that the reason for frequent referral to herbal treatments was because patients thought that herbal treatments were safer, cheaper, and easily accessible. Since herbal CAMs may interact with many therapeutic agents, it is important to warn patients about this issue. It was understood that methods such as psychotherapy, aromatherapy, meditation, acupuncture, homeopathy, relaxation exercises, which were determined to be used frequently in studies conducted in Europe, were less tried for cancer treatment. Also, in case of Turkey, since the patients did not have sufficient knowledge on this subject, the same was perceived.[24]

Since the majority of the patients in our study believed that these treatments were beneficial, they resorted to these methods to cure their diseases and to support the treatment given by their doctors. They started CAMs most often with the suggestion of their friends. Again, the majority of patients stated that these treatments were less effective than their original treatment. These findings were also consistent with the literature.[25] About 38.8% of the patients told like how side effects. However, 61.2% of the patients did not report the use of CAM stating that they did not find it necessary. This situation may be because patients believe that these treatments are innocent and do not have enough information about the toxicities that may develop. Only 5% of the patients stated that they developed side effects related to CAM. This rate was thought to be low because the patients did not attribute the side effects they experienced to CAMs.

The most important limitation of this study is that it is single-centered and cross-sectional. For this reason, it may not reflect the CAM usage of the whole country. It is possible to reach more comprehensive results with a study involving a multicenter design.

Conclusion

Our study showed that the use of CAM was quite high in breast cancer patients. Doctors should question this situation in every patient, and patients should be informed about their decisions. Thus, it may be possible to protect patients from possible side effects and interruption of treatment because of them.

Conflict of Interest

There is no conflict of interest.

Ethics

The research was conducted out in line with the principles of the Declaration of Helsinki and was approved by the local ethical committee (No. 2020/31), dated 11.06.2020. The patients were included in the study after the written consent form was read and their signed consent was obtained. After oral explanation was given to illiterate patients and their consent was obtained, a questionnaire was administered in the presence of their attendants.

References

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  2. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer Statistics, 2021. CA Cancer J Clin 2021; 71 (01) 7-33
  3. Cassileth BR, Deng G. Complementary and alternative therapies for cancer. Oncologist 2004; 9 (01) 80-89
  4. Weiger WA, Smith M, Boon H, Richardson MA, Kaptchuk TJ, Eisenberg DM. Advising patients who seek complementary and alternative medical therapies for cancer. Ann Intern Med 2002; 137 (11) 889-903
  5. Fremd C, Hack CC, Schneeweiss A. et al. Use of complementary and integrative medicine among German breast cancer patients: predictors and implications for patient care within the PRAEGNANT study network. Arch Gynecol Obstet 2017; 295 (05) 1239-1245
  6. Molassiotis A, Fernández-Ortega P, Pud D. et al. Use of complementary and alternative medicine in cancer patients: a European survey. Ann Oncol 2005; 16 (04) 655-663
  7. Horneber M, Bueschel G, Dennert G, Less D, Ritter E, Zwahlen M. How many cancer patients use complementary and alternative medicine: a systematic review and metaanalysis. Integr Cancer Ther 2012; 11 (03) 187-203
  8. Greenlee H, Balneaves LG, Carlson LE. et al; Society for Integrative Oncology. Clinical practice guidelines on the use of integrative therapies as supportive care in patients treated for breast cancer. J Natl Cancer Inst Monogr 2014; 2014 (50) 346-358
  9. Bebis H, Akpunar D, Coşkun S, Özdemir S. Complementary and alternative treatments in patients with breast cancer: a literature review. J Educ Res Nurs 2014; 11 (02) 6-15
  10. Chang KH, Brodie R, Choong MA, Sweeney KJ, Kerin MJ. Complementary and alternative medicine use in oncology: a questionnaire survey of patients and health care professionals. BMC Cancer 2011; 11: 196
  11. Kristoffersen AE, Quandt SA, Stub T. Use of complementary and alternative medicine in Norway: a cross-sectional survey with a modified Norwegian version of the international questionnaire to measure use of complementary and alternative medicine (I-CAM-QN). BMC Complement Med Ther 2021; 21 (01) 93
  12. Nayeri ND, Bakhshi F, Khosravi A, Najafi Z. The effect of complementary and alternative medicines on quality of life in patients with breast cancer: a systematic review. Indian J Palliat Care 2020; 26 (01) 95-104
  13. Findley PA, Sambamoorthi U. Preventive health services and lifestyle practices in cancer survivors: a population health investigation. J Cancer Surviv 2009; 3 (01) 43-58
  14. Fouladbakhsh JM, Stommel M. Gender, symptom experience, and use of complementary and alternative medicine practices among cancer survivors in the U.S. cancer population. Oncol Nurs Forum 2010; 37 (01) E7-E15
  15. DiGianni LM, Garber JE, Winer EP. Complementary and alternative medicine use among women with breast cancer. J Clin Oncol 2002; 20 (18, Suppl): 34S-38S
  16. Gray RE, Fitch M, Goel V, Franssen E, Labrecque M. Utilization of complementary/alternative services by women with breast cancer. J Health Soc Policy 2003; 16 (04) 75-84
  17. Kurt H, Keşkek Ş, Çil T. et al. Meme kanserli hastalarda tamamlayıcı/alternatif tedavi kullanımı. Türk Onkoloji Dergisi 2013; 28 (01) 10-15
  18. Yeşil H, Kıran B, Alkan H. et al. Afyon Kocatepe Üniversitesi'nde Meme Kanseri Tanisi İle Takip Edilmekte Olan Hastalarda Tamamlayici Ve Alternatif Tedavi Kullanimi. Kocatepe Tıp Dergisi 2018; 19 (02) 42-47
  19. Cui Y, Shu XO, Gao Y. et al. Use of complementary and alternative medicine by Chinese women with breast cancer. Breast Cancer Res Treat 2004; 85 (03) 263-270
  20. Schönekaes K, Micke O, Mücke R. et al. [Use of complementary/alternative therapy methods by patients with breast cancer]. Forsch Komplementarmed Klass Naturheilkd 2003; 10 (06) 304-308
  21. Graham JG, Quinn ML, Fabricant DS, Farnsworth NR. Plants used against cancer - an extension of the work of Jonathan Hartwell. J Ethnopharmacol 2000; 73 (03) 347-377
  22. Ernst E. The role of complementary and alternative medicine. BMJ 2000; 321 (7269): 1133-1135
  23. Paul M, Davey B, Senf B. et al. Patients with advanced cancer and their usage of complementary and alternative medicine. J Cancer Res Clin Oncol 2013; 139 (09) 1515-1522
  24. Molassiotis A, Scott JA, Kearney N. et al. Complementary and alternative medicine use in breast cancer patients in Europe. Support Care Cancer 2006; 14 (03) 260-267
  25. Mohd Mujar NM, Dahlui M, Emran NA. et al. Complementary and alternative medicine (CAM) use and delays in presentation and diagnosis of breast cancer patients in public hospitals in Malaysia. PLoS One 2017; 12 (04) e0176394

Address for correspondence

Evren Fidan, MD
Department of Medical Oncology, Karadeniz Technical University
Trabzon 61200
Turkey   


Publication History

Article published online:
02 July 2022

© 2022. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

Odds ratio

References

  1. Sung H, Ferlay J, Siegel RL. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71 (03) 209-249
  2. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer Statistics, 2021. CA Cancer J Clin 2021; 71 (01) 7-33
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