- Research article
- Open Access
An assessment of the impact of herb-drug combinations used by cancer patients
BMC Complementary and Alternative Medicine volume 16, Article number: 393 (2016)
Herb/Dietary Supplements (HDS) are the most popular Complementary and Alternative Medicine (CAM) modality used by cancer patients and the only type which involves the ingestion of substances which may interfere with the efficacy and safety of conventional medicines. This study aimed to assess the level of use of HDS in cancer patients undergoing treatment in the UK, and their perceptions of their effects, using 127 case histories of patients who were taking HDS. Previous studies have evaluated the risks of interactions between HDS and conventional drugs on the basis on numbers of patient using HDSs, so our study aimed to further this exploration by examining the actual drug combinations taken by individual patients and their potential safety.
Three hundred seventy-five cancer patients attending oncology departments and centres of palliative care at the Oxford University Hospitals Trust (OUH), Duchess of Kent House, Sobell House, and Nettlebed Hospice participated in a self-administered questionnaire survey about their HDS use with their prescribed medicines. The classification system of Stockley’s Herbal Medicine’s Interactions was adopted to assess the potential risk of herb-drug interactions for these patients.
127/375 (34 %; 95 % CI 29, 39) consumed HDS, amounting to 101 different products. Most combinations were assessed as ‘no interaction’, 22 combinations were categorised as ‘doubt about outcomes of use’, 6 combinations as ‘Potentially hazardous outcome’, one combination as an interaction with ‘Significant hazard’, and one combination as an interaction of “Life-threatening outcome”. Most patients did not report any adverse events.
Most of the patients sampled were not exposed to any significant risk of harm from interactions with conventional medicines, but it is not possible as yet to conclude that risks in general are over-estimated. The incidence of HDS use was also less than anticipated, and significantly less than reported in other areas, illustrating the problems when extrapolating results from one region (the UK), in one setting (NHS oncology) in where patterns of supplement use may be very different to those elsewhere.
Many studies have recorded a high use of Herbal/Dietary Supplements (HDS) by cancer patients. The MD Anderson Cancer Centre, in USA, reported that 52 % of their cancer patients had used at least one form of Complementary and Alternative Medicine (CAM), and 77 % of those were using herbs and vitamins . Between 25 and 47 % of ethnic Chinese cancer patients living in North America relied on herbal preparations as part of their cancer treatment . In the US, a survey showed that about 63 % of outpatient cancer patients used HDS . In the UK, a systematic review of 11 papers investigating the use of herbal medicines by cancer patients found the prevalence of herbal medicines use varied from 3.1 to 21.8 % among adults and from 4.1 to 20 % in paediatric patients .
In the absence of good efficacy data for most HDS, and given their popularity with patients, the most urgent current concern is assuring their safety (WHO ). Some herbal medicines have been extensively studied and there is clinical evidence for both potential benefits and risks (e.g. Hermann and von Richter ). Many pre-clinical studies which have been carried out to evaluate the safety of HDS in combination with licensed or prescribed drugs are not supported by the clinical evidence when carefully assessed (e.g. ).
Very few studies have been conducted to evaluate the safety of herbal medicines and their combinations used as self-medication, or as recommended by herbal medicine practitioners (Heinrich et al. ). The potential for interactions between herbs and other medicines may be higher due to the large number of components in the herb, compared to the single active substance of conventional medicines . In addition, a single herb or product may be used to treat several conditions, and different herbs may be used to treat the same illness, making interactions difficult to interpret accurately. There is another obstacle, which is the lack of detail in many reports: in one study, about 2000 combinations from 4 electronic databases were screened to assess the probability of interaction, and of 108 cases identified as potential interactions, 70 % did not provide adequate data for this to be achieved. Only 13 % of cases were identified as ‘well-documented’, but warfarin was the conventional medicine most commonly involved, and St John’s wort was the herb cited in most interactions .
Assessing the safety and efficacy of HDS use is further complicated because many studies have reported that cancer patients often do not tell their healthcare providers about their CAM use [2, 34]. Ernst  reported that only 25 % of cancer patients using HDS received advice from their doctors and that communication about HDS was virtually non-existent. Side effects and drug interactions were the most common concerns expressed by the researchers [14, 21, 23, 29] but to date, many documented potential interactions have been extrapolated from in vitro or animal studies, or have not been described in an appropriate context [24, 34].
There are certainly herb-drug combinations which may result in serious consequences in cancer patients. For example, the concurrent use of enzyme inducers such as St. John’s wort (Hypericum perforatum) can affect many drugs: St John’s wort has been shown to cause a 44 % reduction in the time of imatinib (an anti-cancer drug) remains at therapeutic blood levels . The aim of this study was to therefore investigate real-life HDS use by cancer patients and their experiences of benefit or harm. An individual assessment for each patient was used to assess the risk posed by the drug regime and HDS consumption.
Self-administered questionnaire surveys comprising open-ended and closed-ended questions (see supplementary information) were posted to eligible participants being treated for cancer at the Oxford University Hospitals Trust (OUH) and centres of palliative care at the Sobell House, Duchess of Kent House, and Nettlebed Hospice, located in the Thames Valley Area, UK. Cancer patients were identified by oncology and palliative care consultants at each study centre based on the following inclusion criteria: aged above 18 years, able to speak English, currently receiving treatment for their diagnosed cancer, and able to understand and fill out the questionnaire. Patients were excluded from the study if consultants felt they were unable to participate on medical grounds. All responses were anonymous unless the patients chose to provide contact details in order to receive feedback.
The questionnaire asked patients to record all of the conventional medicines prescribed by their GP, oncologist or palliative care specialist and, if they also took HDS, we asked them to list all products they had taken at the same time as their usual drug regime. Patients were not asked to select from a prepared list in order to explore the variety of products used and to see which substances they actually considered to be HDS. We also asked about their perceived experiences from these HDS use in order to retrospectively identify any experiences of benefit or harm. data such as sources of HDS and advice, and if they had taken HDS before being diagnosed, were gathered for separate analysis.
Questionnaires were posted to eligible participants and completed questionnaires returned to the study team in reply-paid pre-addressed envelopes over the study period (August 2013 – January 2014). Response rates were maximised by encouraging patients to complete and return the questionnaire even if they took no HDS; and patients who were taking HDS were offered the opportunity to receive feedback on the safety of their use. Due to financial constraints a single mailing was used. Where patients indicated that they would like feedback on their use of HDS, they supplied contact details, and a review letter providing information about the safety of the combination they were using was sent. If any risks were identified patients would be advised to contact their oncology or palliative care team to discuss in more detail, in accordance with the Ethical approval protocol.
Assessing potential interactions between HDS and conventional medicines
Combinations of HDS and conventional medicines reported by participants were assessed using the system of classification or the potential for interaction and severity as described in Stockley’s Herbal Medicine’s Interactions (SHMI) (2013). A literature search was also carried out in case very recent data had been published or if a supplement was not included. SHMI is a comprehensive, evidence-based reference for interactions between herbal medicines/dietary supplements and conventional medicines which is regularly updated on-line. It rates interactions in three different categories:
Action: whether or not any action needs to be taken to address the interaction.
Severity: the likely effect on a patient of an unmanaged interaction.
Evidence: the weight of the available evidence.
On the basis of these, one of five symbols is used to describe the combination, ranging from; ‘no interaction’, ‘doubt about outcomes of use’, ‘potentially hazardous outcomes’, ‘significant hazard’ and to ‘life-threatening outcomes’. These symbols are defined as follows:
No interaction: the interaction has not been conclusively demonstrated or is not considered to be clinically significant.
Doubt about outcomes of use: there is doubt about the existence or severity of a suspected interaction, but patients may need some guidance about possible adverse effects, and/or monitoring should be considered.
Potentially hazardous outcome: there may be a potentially hazardous interaction, but the data is poor or sparse and conclusions are difficult to draw.
Significant hazard: current use may result in significant hazard to patients and so careful monitoring or dosage adjustment is needed.
Life-threatening outcome: the interaction is life-threatening, and concurrent use should be avoided.
If SHMI and a literature review raised no concerns, in that no reports of interactions between the drugs, and in the case of the herb, a related herb containing similar constituents, were cited, the combination was assessed as ‘no interaction’. If the combination showed evidence of similar pharmacological activity, for example if the drug and the supplement were known to both possess anti-hypertensive activity, then the combination was categorised as ‘doubt about outcomes of use’. Assessments of interactions between HDS were made, as well as between supplements and conventional medicines, as these had not previously been carried out.
A respondent was defined as a user of HDS if they reported that they had used herbal medicines or dietary supplements. Responses were categorised according to patient sociodemographic, cancer diagnosis, previous use of HDS, specific HDS being taken, prescribed medicines taken concurrently, and the individual HDI assessments. The data obtained from the questionnaires were entered into the (SPSS V.21) to calculate summary statistics, for the proportions of participants in each category, with 95 % confidence intervals. All data entry was double checked. HDS use, conventional medicine use, and HDS-conventional combinations presented as median and the interquartile range (IQR), for each of these measures.
Three hundred seventy-five out of 1457 (26 %; 95 % CI 24, 28) cancer patients who were approached, having been identified by oncology and palliative care consultants at each study centre, participated in the study. Of these responders, 127 out of 375 (33.9 %; 95 % CI: 29, 38) reported using HDS, before or after their diagnosis with cancer. The other 235 responders did not use HDS, but gave details of their demographics, including their diagnoses. In our sample, females (74; 58.3 %) used HDS slightly more than males (53; 41.7 %); however, the responders were also predominantly female. Patients aged 60 years and above (74; 58.3 %) used HDS more than other age groups. Breast, prostate, and melanoma cancer patients were the most commonly HDS users (40; 31.5 %), (26; 20.5 %), and (22; 17.3 %) respectively. The demographic characteristics of participants, both HDS users and non-users, are shown in Table 1.
HDS users reported 1255 herb-drug combinations, for a median rate of 11.5 (IQR, 2.5–14) per user. Overall, 101 different HDS were used concurrently with other medicines, for a median 1.5 (IQR, 1–4) per user, with 167 different conventional drugs, for a median of 1 (IQR: 1–6) per user. Glucosamine, cod liver oil, vitamins, omega 3 fatty acids, green tea, garlic, selenium, and fish oil were the most common HDS taken; the numbers of patients reporting these and others are shown in Table 2. Cod liver oil, omega-3 fatty acids and fish oil are related products but there are some differences in their composition and the way they are marketed, and patients cited them by product name.
We also examined the HDS taken by patients with specific cancer types, to see if any group showed a preference for a specific HDS, and as such might be at particular risk. Breast cancer patients reported taking the widest range of DHS, citing over 24 different types of product, as shown in Table 3, and the most popular HDS were similar to those for the overall cohort of responders, i.e. cod liver oil, vitamins, glucosamine, omega 3 fatty acids and green tea. Prostate cancer patients reported using 15 different HDS; the most popular again being cod liver oil, glucosamine, vitamins, green tea and omega 3 fatty acids, as shown in Table 4. Melanoma patients reported using 9 different HDS products, again conforming to the general pattern of the responders overall, shown in Table 5. Renal, brain, gastro-oesophageal, pancreatic and bowel cancer patients also reported using a variety of different HDS but there were insufficient numbers of each diagnosis to analyse separately.
Interactions between HDS and conventional medicines
Most of the herb-drug combinations (1225; 97.6 %) were categorised as ‘no interaction’, 22 combinations were categorised as interactions with “doubt about outcomes of use”, 5 combinations as interactions with “Potentially hazardous outcome”, one combination as an interaction with “Significant hazard”, and one combination as an interaction with “Life-threatening outcome”, as shown in Table 6.
Eighty-seven (75.7 %) HDS users reported that they had experienced benefits, with 82 attributing these to HDS. Only 4 (3.4 %) patients experienced problems, 2 believing they were caused by HDS; however, no adverse drug events (ADE) were recorded. 28 (24.7 %) patients responded that they had not experienced either benefit or harm during their HDS usage. 8 (6.3 %) patients had reported that they used HDS but did not report their experiences about HDS usage.
The HDI assessments showed that 11 HDS were involved in some risk of interaction: cod liver oil, St John’s wort, omega-3 oils, glucosamine, senna, green tea, EPA (eicosapentaenoic acid), fish oil, garlic, ginkgo, and evening primrose oil. Of the conventional medicines, 20 drugs were involved: aspirin, dipyridamole, clopidogrel, warfarin, dalteparin, heparin, insulin, omeprazole, sertraline, amitriptyline, risperidone, epirubicin, doxorubicin, paracetamol, co-codamol, amlodipine, lisinopril, atorvastatin, simvastatin, and pravastatin.
Interactions between different HDSs
All combinations of HDS were deemed safe overall in the circumstances in which they were used, and the few cases which may have given cause for serious concern had already been resolved (see Table 7), usually because the patient had stopped taking the particular supplement before completing the questionnaire. Some herbal medicines have intrinsic properties which may case HDIs in large doses: for example, stimulant laxatives such as senna alter intestinal transit and in large doses or over a period of time may affect the absorption of any herb or drug taken at the same time, but these are predictable effects and can be avoided. The other issue is that supplements containing similar constituents may be taken together, for example evening primrose oil and star flower oil, which are both sources of gamolenic acid; however, as this compound is relatively safe the combination is unlikely to be harmful.
In a recent systematic review, Alsanad et al.  sought to determine the proportion of cancer patients deemed to be at risk from HDIs from the actual combinations they were taking, but only 5 studies were found which explored this issue specifically [8, 18, 20, 31, 37]. HDS are the most popular form of CAM used by cancer patients and have the greatest potential to cause harm, not only by causing adverse effects or by inappropriate use, but also by interacting with conventional medicines. There is thus a need to identify individual cancer patients taking HDS who might be at risk from HDIs, rather than making a global risk assessment based on population studies.
Our HDS safety assessments examined the actual combinations taken by each patient. Several combinations which would have been assessed as harmful on theoretical grounds did not actually produced an adverse effect in practice. It should be emphasised that our HDI assessments were not an estimation of risk, as originally intended, since they were done after the patient had taken the combination, and no patient reported any ADE. Instead it is an exploration of the levels of use of specific HDS with prescribed and/or licensed medicines and the patients’ experiences of taking these combinations.
Certain combinations were retrospectively judged as not clinically significant, despite having been previously categorised in other resources as carrying some risk, for example ‘Doubt about outcomes of use’, ‘Potentially hazardous outcomes’, or ‘Significant hazard’ as detailed in the Table 2. Our assessments also recorded the incidence of patients taking combinations which have been previously been judged to be inadvisable, but which did not result in a harmful outcome. In these cases, categorised as ‘Potentially hazardous outcomes’, ‘Significant hazard’ and ‘Life-threatening outcomes’, the patient would have been advised NOT to take the combination if they had enquired beforehand. No ill effects were reported, but whether this is because the risk is indeed theoretical or because the patient was simply fortunate, cannot be determined in a study of this type.
Cod liver oil, St John’s wort, omega 3 oils, glucosamine, senna, green tea, EPA (eicosapentaenoic acid), fish oil, garlic, ginkgo, and evening primrose were the HDSs involved in the risk of interaction with the conventional medicines: aspirin, dipyridamole, clopidogrel, warfarin, dalteparin sodium, heparin, insulin, omeprazole, sertraline, amitriptyline, risperidone, epirubicin, doxorubicin, paracetamol, co-codamol, amlodipine, lisinopril, atorvastatin, simvastatin, and pravastatin. Many anti-cancer drugs are metabolised by cytochrome P450 (CYP) enzymes, and especially CYP3A4, . The interaction occurs if the HDS induces or inhibits the metabolizing enzymes or affects the drug transporter of the drug , but these should return to normal levels once the HDS use ceases .
A number of HDSs, such as ginkgo biloba, dan shen, liquorice, ma huang, have been implicated in reports of interaction with conventional medicines, and the drugs involved (warfarin, protease inhibitors and some anti-cancer drugs) have well-documented interaction profiles with other drugs [9, 15, 33]. St John’s wort has been involved in many HDI reports with other drugs  including anticancer agents, and for example, its interaction with imatinib occurs due to both induction of the metabolic enzymes CYP3A4 and CYP2C19 and the transporter of imatinib, leading to a lowering of plasma levels . Therefore, it should certainly be avoided in cancer patients as a precaution [15, 25]. On the other hand, cancer patients often use garlic as a supplement, and although it has been suggested that garlic may alter metabolism of anti-cancer drugs such as docetaxel, a recent study found no in vitro interaction . A risk of gastrointestinal bleeding has also been associated with garlic use [1, 28]: again, garlic is consumed by many people as food, and no ADEs reports have been published to date, so is unlikely to cause harm.
Cancer patients may sometimes feel the need for a mild sedative or tranquilliser, and the herb valerian is a very popular ingredient in herbal sleeping and relaxation products. Valerian has been said to “interfere in an unwanted way with oncological cancer therapy” or “can diminish the efficacy of cancer therapeutics” (e.g. Sloan Kettering Center 2012, cited by ). Kelber et al. examined the pre-clinical studies and concluded that ‘available animal and human pharmacodynamic studies did not verify any interaction potential’ and ‘there is no specific evidence questioning their safety, also in cancer patients’ . In our study, the incidence of HDS use was less than anticipated, and significantly less than reported in other areas, again illustrating further problems when extrapolating results from one region (the UK), and in one setting (NHS oncology), where patterns of supplement use may be very different to those elsewhere.
Cancer patients regard HDS highly, as shown by many studies, and also the volume of sales of these products (Chrystal et al. ). The HDS identified in our study were used by patients with a broad range of diagnoses, and none was used only by a those in a particular group. Certain HDS were more popular in certain groups, as shown in Tables 3, 4 and 5, but the sample size was insufficient to draw any firm conclusions on these. Thus it is necessary to deal with the issue of HDIs in a realistic and pragmatic manner, because over-reaction to potential dangers and inaccuracies in reporting may cause patients to ignore even good advice on this subject. Another important issue is how the lack of evidence of HDS safety and efficacy should be addressed, as well as how the current evidence should be interpreted. In other words, there is a strong demand for an appropriate and robust framework for evaluating HDS safety and efficacy at different levels of patients’ needs, which includes social, epidemiological, and clinical studies .
It is crucial to alert and educate patients about the possibility of HDIs but it would be counter-productive to scare them with unfounded negative speculation at a time when they are particularly vulnerable. Clinicians should feel able to discuss any treatments that might be helpful, as well as warning of possible dangers, since there is a lack of awareness of these , and given the wide use of HDS, they need to be better informed. ADEs and HDIs related to HDS can be reported in the same way as adverse reactions to conventional medicines, in the UK via the Yellow Card Scheme, but happens infrequently. Whether this is because ADEs involving HDS are unusual or because of under-reporting is not clear, but if improved, would go some way to increasing the accuracy of the risk assessment of these combinations .
Our study revealed that more than 100 different HDS were being used to manage cancer and other health issues, and our assessment of the numerous combinations of these with conventional medicines and other HDS showed that the majority of patients were not at great risk of HDIs. Most previous studies have assessed the safety of HDS use theoretically and without exploring the actual products used by cancer patients. Much of the available drug interaction evidence is based on pre-clinical studies, which do not always translate well into clinical experience, and in many case reports, data regarding the identity, composition, purity and even the dose of the herb is incomplete . This may give an overestimate of risk based on speculation. Our survey was retrospective and most of the patients surveyed had been taking the combination for some time without experiencing any adverse events, but the sample size was not sufficient to conclude that the risk fir some supplements has been inflated on this evidence. As it would be unethical to deliberately give patients any combinations of drugs (including herbs) which may cause harm, the only feasible method of assessing risk at present is to collect evidence retrospectively from patients who are using or have used HDSs. This will provide documented evidence upon which healthcare professionals and cancer patients can based their judgement as to whether taking a particular HDS is advisable or not.
Adverse drug event
Complementary and alternative medicine
Oxford University Hospital
Research Governance Group
Stockley’s herbal medicine’s interactions
World Health Organisation
Abebe W. Herbal medication: potential for adverse interactions with analgesic drugs. J Clin Pharm Ther. 2002;27:391–401.
Afifi FU, Wazaify M, Jabr M, Treish E. The use of herbal preparations as complementary and alternative medicine (CAM) in a sample of patients with cancer in Jordan. Complement Ther Clin Pract. 2010;16:208–12.
Alsanad SM, Williamson EM, Howard RL. Cancer patients at risk of herb/food supplement–drug interactions: a systematic review. Phytother Res. 2014;28:1749–55.
Champy P, Melot A, Guérineau Eng V, Gleye C, Fall D, Höglinger GU, Ruberg M, Lannuzel A, Laprévote O, Laurens A, Hocquemiller R. Quantification of acetogenins in Annona muricata linked to atypical parkinsonism in Guadeloupe. Mov Disord. 2005;20:1629–33.
Chrystal K, Allan S, Forgeson G, Isaacs R. The use of complementary/alternative medicine by cancer patients in a New Zealand regional cancer treatment centre. NZ Med J. 2003;116:875–903.
Cui Y, Shu XO, Gao Y, Wen W, Ruan ZX, Jin F, Zheng W. Use of complementary and alternative medicine by Chinese women with breast cancer. Breast Cancer Res Treat. 2004;85:263–70.
Ernst E. The current position of complementary/alternative medicine in cancer. Eur J Cancer. 2003;39:2273–7.
Engdal S, Klepp O, Nilsen OG. Identification and exploration of herb-drug combinations used by cancer patients. Integr Cancer Ther. 2009;8:29–36.
Fugh-Berman A, Ernst E. Herb-drug interactions: review and assessment of report reliability. Br J Clin Pharmacol. 2001;52:587–95.
Goey A, Beijnen J, Schellens J. Herb–Drug Interactions in Oncology. Clin Pharmacol Ther. 2014;95:354–5.
Gratus C, Damery S, Wilson S, Warmington S, Routledge P, Grieve R, Steven N, Jones J, Greenfield S. The use of herbal medicines by people with cancer in the UK: a systematic review of the literature. QJM. 2009;102:831–42.
Heinrich M, Barnes J, Gibbons S, Williamson EM. Fundamentals of Pharmacognosy and Phytotherapy. 2012. Elsevier Health Sciences.
Hermann R, von Richter O. Clinical evidence of herbal drugs as perpetrators of pharmacokinetic drug interactions. Planta Med. 2012;78(13):1458–77.
Hübner J. Complementary and alternative medicine in oncology. Versicherungsmedizin. 2013;65:79–83.
Izzo AA. Interactions between herbs and conventional drugs: overview of the clinical data. Med Princ Pract. 2012;21:404–28.
Izzo AA, Kim SH, Radhakrishnan R, Williamson EM. A critical approach to evaluating clinical efficacy, adverse events and drug interactions of commonly used herbal remedies. Phytother Res. 2016;30:691–700.
Kelber O, Nieber K, Kraft K. Valerian: no evidence for clinically relevant interactions. Evid Based Complement Alternat Med. 2014;2014:879396.
Lee AH, Ingraham SE, Kopp M, Foraida MI, Jazieh AR. The incidence of potential interactions between dietary supplements and prescription medications in cancer patients at a Veterans Administration Hospital. Am J Clin Oncol. 2006;29:178–82.
Mathijssen RH, Verweij J, DE Bruijn P, Loos WJ, Sparreboom A. Effects of St. John’s wort on irinotecan metabolism. J Natl Cancer Inst. 2002;94:1247–9.
McCune JS, Hatfield AJ, Blackburn AA, Leith PO, Livingston RB, Ellis GK. Potential of chemotherapy-herb interactions in adult cancer patients. Support Care Cancer. 2004;12:454–62.
Mclay J, Stewart D, George J, Rore C, Heys S. Complementary and alternative medicines use by Scottish women with breast cancer. What, why and the potential for drug interactions? Eur J Clin Pharmacol. 2012;68:811–9.
Meijerman I, Beijnen JH, Schellens JH. Herb-drug interactions in oncology: focus on mechanisms of induction. Oncologist. 2006;11:742–52.
Molassiotis A, Panteli V, Patiraki E, Ozden G, Platin N, Madsen E, Browall M, Fernandez-Ortega P, Pud D, Margulies A. Complementary and alternative medicine use in lung cancer patients in eight European countries. Complement Ther Clin Pract. 2006;12:34–9.
Rotblatt M, Ziment I. Evidence-based herbal medicine. Philadelphia: Hanley & Belfus; 2002.
Russo E, Scicchitano F, Whalley BJ, Mazzitello C, Ciriaco M, Esposito S, Patanè M, Upton R, Pugliese M, Chimirri S. Hypericum perforatum: pharmacokinetic, mechanism of action, tolerability, and clinical drug–drug interactions. Phytother Res. 2014;28:643–55.
Suchard JR, Wallace KL, Gerkin RD. Acute cyanide toxicity caused by apricot kernel ingestion. Ann Emerg Med. 1998;32:742–4.
Tian R, Koyabu N, Morimoto S, Shoyama Y, Ohtani H, Sawada Y. Functional induction and de-induction of P-glycoprotein by St. John’s wort and its ingredients in a human colon adenocarcinoma cell line. Drug Metab Dispos. 2005;33:547–54.
Thomsen M, Schmidt M, Vitetta L, Sali A. Do herbs increase the risk of herb–drug interactions for patients with arthritis? Ann Rheumatic Dis. 2005;64:1527–28.
Tuna S, Dizdar O, Calis M. The prevalence of usage of herbal medicines among cancer patients. System. 2011;83:32.
Vickers KA, Jolly KB, Greenfield SM. Herbal medicine: women’s views, knowledge and interaction with doctors: a qualitative study. BMC Complement Altern Med. 2006;6:40.
Werneke U, Earl J, Seydel C, Horn O, Crichton P, Fannon D. Potential health risks of complementary alternative medicines in cancer patients. Br J Cancer. 2004;90:408–13.
WHO. Traditional medicine strategy: 2014–2023 [Online]. World Health Organization; 2013. Available: http://www.who.int/medicines/publications/traditional/trm_strategy14_23/. Accessed 21 Apr 2016.
Williamson EM. Interactions between herbal and conventional medicines. Expert Opin Drug Saf. 2005;4:355–78.
Williamson EM, Driver SB, Baxter K, Lee CR. Stockley’s Herbal Medicine’s Interactions: a guide to the interactions of herbal medicines. London: Pharmaceutical Press; 2013.
Wold RS, Lopez ST, Yau CL, Butler LM, Pareo-Tubbeh SL, Waters DL, Garry PJ, Baumgartner RN. Increasing trends in elderly persons’ use of non-vitamin, non-mineral dietary supplements and concurrent use of medications. J Am Diet Assoc. 2005;105:54–63.
Zachariae R, Johannessen H. A methodological framework for evaluating the evidence for Complementary and Alternative Medicine (CAM) for cancer. Cancers. 2011;3:773–88.
Zeller T, Muenstedt K, Stoll C, Schweder J, Senf B, Ruckhaeberle E, Becker S, Serve H, Huebner J. Potential interactions of complementary and alternative medicine with cancer therapy in outpatients with gynecological cancer in a comprehensive cancer center. J Cancer Res Clin. 2013;139:357–65.
We would like to thank all staff from Oxford University Hospitals Trust, Duchess of Kent House, Sobell House, and Nettlebed Hospice who assisted in this study, and especially Prof Nicola Stoner at OUH, for her help and support in its preparation.
Availability of data and materials
The datasets supporting the conclusions of this study are included within the article and the additional file.
All authors participated in the design, data collection, analysis, and writing of the article. All authors have read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approvals and consent to participate
Approval for the study was obtained from the NRES Committee South Central/Berkshire (reference 12/SC/0664), University of Reading Research Committee (reference 13/23), NHS Organisational approval for NHS-led units- Oxford University Hospital Research and Development Department OUH R&D (R&D reference: 10394) and the Research Governance Group (RGG) at Sue Ryder Care (reference 2103–03). The study was self-administered questionnaire-based and the act of returning a completed questionnaire was considered as consent to participate in the study. Patients were considered to be capable of giving informed consent based on their doctors’ recommendations.
About this article
Cite this article
Alsanad, S.M., Howard, R.L. & Williamson, E.M. An assessment of the impact of herb-drug combinations used by cancer patients. BMC Complement Altern Med 16, 393 (2016). https://doi.org/10.1186/s12906-016-1372-x
- Complementary medicines
- Alternative medicines
- Herb-drug interactions
- Herbal medicines
- Dietary supplements
- Conventional medicines