- Research article
- Open Access
- Open Peer Review
Health services research of integrative oncology in palliative care of patients with advanced pancreatic cancer
© The Author(s). 2016
- Received: 2 April 2016
- Accepted: 21 July 2016
- Published: 2 August 2016
Pancreatic cancer has a dire prognosis and is associated with a high mortality. Palliative patients have special needs and often seek help in integrative oncological concepts (IO) that combine conventional and complementary therapies. Nevertheless there are few recommendations regarding IO in current cancer guidelines. The aims of this study were to report on implementation of IO in everyday palliative care and to analyze patient survival in advanced pancreatic cancer.
This multicenter observational study investigates the implementation of IO and length of survival of patients suffering from advanced pancreatic cancer (stage IV). We analyzed patient’s survival by employing multivariable proportional hazard models using different parametric distribution functions and compared patients receiving chemotherapy only, a combination of chemotherapy and Viscum album (VA) treatment, and VA treatment only.
Records of 240 patients were analyzed. Complementary therapy showed high acceptance (93 %). Most frequent therapy was VA treatment (74 %) that was often administered concomitantly to chemotherapy (64 %). Both therapies had positive effects on patient survival as they had significant negative effects on the hazard in our log-normal model. A second analysis showed that patients with combined chemotherapy and VA therapy performed significantly better than patients receiving only chemotherapy (12.1 to 7.3 month). Patients receiving only VA therapy showed longer survival than those receiving neither chemotherapy nor VA therapy (5.4 to 2.5 months). Our data demonstrates that IO can be implemented in the everyday care of patients without disregarding conventional treatment. Patients combining VA with chemotherapy showed longest survival.
Our data demonstrate the importance and potential of health services research showing that IO treatment can be successfully implemented in the every-day care of patients suffering from advanced pancreatic cancer. Patients combining VA with chemotherapy showed longest survival. To address patients’ needs adequately, future cancer guidelines might increasingly include comments on complementary treatment options in addition to conventional therapies. Further studies should investigate the effect of complementary treatments on survival and quality of life in more detail.
- Pancreatic carcinoma
- Palliative care
- Integrative oncology
- Viscum album
We examined the implementation of integrative oncology in everyday care for palliative pancreatic cancer patients.
We used parametric models to analyze the hazard on patient survival.
Complementary therapies are chosen by a high number of patients.
Chemotherapy and complementary therapy with VA extracts were associated with lower hazards.
Pancreatic cancer is associated with a high mortality rate and thus remains a dire diagnosis for the patient. It is the eighth most frequent cancer diagnosis in Germany and is the fourth most common cause of death from cancer . The nonspecific symptoms often lead to a delayed diagnosis of advanced cancer, resulting in a poor 5-year survival of six to nine percent . Radical resection of the pancreas with adjuvant chemotherapy is the only curable approach , but only about 20 % of cases are resectable at diagnosis . For palliative treatment chemotherapy has proven to be superior to best supportive care only . Since the work of Burris et al. in 1997 , gemcitabine monotherapy has been the standard first line treatment [3, 7]. The combination of gemcitabine with the epidermal growth factor receptor inhibitor erlotinib; a chemotherapy of oxaliplatin, irinotecan, fluorouracil, and leucovorin (FOLFIRINOX) for patients with good performance status; and recently published albumin-bound paclitaxel followed by gemcitabine are alternative options that have shown promising results [8–10] and have found their way into current guidelines [3, 7, 11]. Nevertheless, with 6.24 months for gemcitabine/erlotinib and 11.1 months for FOLFIRINOX, the median survival remains poor. The shock of a cancer diagnosis and facing mortality usually results in a search for social support from family, friends or faith communities . Patients have needs related to dealing with symptoms associated with disease or therapy, which strongly affect their well-being . The major need that conventional medicine primarily focuses on is the need to cure, or at least to prolong survival . Cancer guidelines mostly focus only on this outcome. Patients with advanced cancers often seek fulfillment of their other needs through complementary and alternative medicines (CAM) [13–15]. Patient’s expectations and motivations for using CAM are often not to cure, but to strengthen their immune system and to manage pain or other treatment-related side-effects . The feeling of being active in their own treatment, with an associated level of self-control, is an important motivation for using CAM . This seems to be of increased importance to patients with lengthy disease and treatment durations . Additionally, sometimes patients see CAM as a last resort, providing hope in a situation of extreme distress [16, 17].
The Concerted Action for Complementary and Alternative Medicine Assessment in the Cancer field classifies such therapies as i) herbal products, ii) dietary approaches, iii) mind-body interventions, iv) manipulative and body-based practices or v) other CAM. The number of CAM-users has increased in recent years and is estimated to make up ~40 % of all cancer patients . Simultaneous administration of CAM and conventional therapies without the knowledge of the physician always bears the risk of interference with the standard treatment . In the concept of integrative oncology (IO) this is addressed and a comprehensive, patient centered treatment approach is planned and administered by a team of experts from different fields to avoid treatment interactions and to achieve the best possible outcomes . IO attempts to combine the best of complementary and conventional therapies and to address patients’ needs beyond the alleviation of symptoms . Although many patients evidently use CAM, it is almost not present in German guidelines  and is not documented in German official cancer registries . In the following article we present data on patients with advanced pancreatic cancer documented by the Network Oncology, a conjoint clinical register of hospitals, practitioners and out-patient centers focusing on an IO concept . We report on the amount and types of received complementary and conventional therapies and analyze patient’s survival.
The Network Oncology (NO) has received a positive vote from the ethical committee of the Medical Association Berlin and has been described recently . Using the NO clinical database, all consenting patients treated between August 2005 and November 2014 were thoroughly assessed and analyzed. Records of 459 patients with pancreatic carcinoma (ICD10 C25.*) were reviewed . TNM stages or documented metastases were translated into UICC stages. Only palliative patients of stage IV at initial diagnosis (earliest recorded stage within a month of diagnosis) were included. Surgical interventions were coded according to the German procedure classification 2013 (OPS), the German modification of the international classification of procedures in medicine (ICPM) by the World Health Organization (WHO). Systemic therapies such as chemotherapy, targeted therapies or application of extracts of European mistletoe (Viscum album, VA) in the context of an integrative oncological setting were documented with start and end dates. According to the summary of medicinal product characteristics (SmPCs) VA is indicated in cancer therapy. The rationale is to improve health related quality of life (HRQL) by reducing therapy related symptoms and improving cancer related symptoms  with positive effects on coping, fatigue, sleep, exhaustion, nausea, vomiting and anxiety . Non-pharmaceutical interventions (NPI) such as art therapies, nursing interventions or psychological therapies were documented as dummy variables. Some therapy types were grouped like nursing interventions (embrocation, compress and oil dispersion bath), movement therapies (physiotherapy, eurythmy therapy, ergo therapy), creative therapies (art therapy, music therapy, modeling and crafts therapy) and massage or lymph drainage. Censored patient survival was calculated from diagnosis date until recorded death or until last documented contact. Patients with no death date and no last contact date were excluded from the survival analyses. Kaplan Meier survival was calculated for all patients. To analyze how different factors influence the hazard on patient’s survival we employed proportional hazard models using different parametric distribution functions (log-normal, log-logistic, Weibull, Gompertz and extreme values). Tested parametric hazard models showed evident problems in dealing with long-term survivors. Therefore we excluded extreme values and censored our data to a maximum of 2 years of survival (730.5 days). We included the factors age, gender, chemotherapy and VA as variables as well as the individual number of NPIs and chose the model with the highest maximum likelihood.
To assess the effect of combined chemotherapy and VA therapy, we classified the data based on whether or not a patient received chemotherapy, and if they received VA therapy or not. VA therapy was defined as lasting more than 4 weeks, while the non-intensive group had VA therapy for less than 1 week or not at all. To avoid bias, patients that lived less than 4 weeks were excluded from these analyses. All analyses were conducted using R 3.1.2 [R Foundation for Statistical Computing, Vienna, Austria. http://www.r-project.org/]. Time event analyses used the R-packages ‘eha: Event History Analysis’ version 2.4-2 by Göran Broström and ‘survival: a Package for Survival Analysis in S’ version 2.37-7 by Terry M. Therneau.
Two hundred and forty (53.7 %) patients showed advanced cancer of UICC stage IV at first diagnosis. Median age was 68 (range 68–89 years). 124 patients were female (51.7 %). There was no significant difference in age between male and female patients. For nine patients a second, independent carcinoma was documented in the patient records. In seven cases this diagnosis occurred more than 1 year before the diagnosis of pancreatic cancer. Four of these cases were breast cancer diagnoses (ICD10 C50.*), the other localities that occurred only once were lung (ICD10 C34.*), prostate gland (ICD10 C61.*), and uterus (ICD10 C55.*). In two cases (ICD10 C34.* and C50.*) secondary diagnosis occurred 1 month and 4 months after the pancreatic diagnosis, respectively.
Number of patients receiving VA therapy
VA therapy in general
Surgical and endoscopic interventions
Pancreatic interventions total
Inner drainage of the pancreas
Partial resection of the pancreas
Endoscopic intervention at the pancreatic duct
Anastomosis of the pancreatic duct
Stomach interventions total
Intestine interventions total
Resections of small or large intestine
By-pass anastomosis of the intestine
Liver interventions total
Resections of the liver
Gall bladder or bile duct interventions total
Endoscopic interventions at the biliary tree
Other abdominal interventions total
Other surgical or endoscopic interventions total
Proportional hazard models on patient survival
Number of NPI
Patients characteristics of the subgroups Gr1 – Gr4
Number of NPI
Massages & lymph drainage
X 2 test
Kruskal Wallis test
Kruskal Wallis test
X 2 test
X 2 test
X 2 test
X 2 test
X 2 test
X 2 = 29.56
X 2 = 18.72
X 2 = 9.93
X 2 = 68.68
X 2 = 1.24
X 2 = 8.33
X 2 = 14.14
X 2 = 4.09
p < 0.001
p = 0.0003
p = 0.0191
p < 0.0001
p = 0.7426
p = 0.0396
p = 0.0027
p = 0.2523
The present health services research data demonstrate the use and acceptance of IO for palliative pancreatic cancer patients. Complementary therapies in IO are adjuncts to conventional cancer treatment, used primarily for symptom control, to enhance physical and emotional strength of patients during and after conventional care. Thus, IO aims to better address patients’ needs by combining the best of conventional medicine and CAM in a comprehensive way . Claiming that only therapies used that were shown to be safe and effective, IO intends to prevent patients from harm by uncontrolled self-medication . However, a common criticism is that many CAM methods are implemented in IO without sufficient risk-benefit analyses according to scientific standards . Recent studies within the NO have addressed this issue and demonstrated safety profiles for key therapies used in IO settings [24, 25]. Patients included in this study tended to be younger compared to the German average of pancreatic cancer patients (men 70 year, women 76 years) . This is in line with many studies reporting that younger age is often associated with CAM use . However, demographic factors seem not to influence survival in pancreatic cancer patients in Germany . A high percentage of our patients used CAM, especially NPI that intend to alleviate symptom burden and side effects, activate patient’s resources and improve patient’s quality of life by intensified care and attention. The latter might play a major role in our patient population, as three of the five most frequent NPIs were therapeutic nursing interventions. According to our analysis nursing interventions were significantly more preferred by women reflecting our previous results . The importance of increased attention that focuses on patient’s needs has been demonstrated by Temel et al. , who showed significant improvements in HRQL, mood and survival in advanced lung cancer patients receiving an early palliative care in comparison to patients receiving standard care. Based on the individual needs of the patient, the early palliative care focused on an early psycho-oncological support and end of life care planning, including anticipation, prevention, and treatment of suffering. It was adapted from the National Consensus Project for Quality Palliative Care. Surprisingly, our data revealed that less than 30 % of patients chose psychosocial support (offered at the time of diagnosis) despite the vast burden associated with the diagnosis. This rather low rate may relate to heterogeneity in offer and acceptance of psychosocial support within the various participating centers and to incomplete documentation of complementary therapies in the early years of the study period.
Movement therapies were also common in our population and might contribute to patient improvement by giving the patient a feeling of still being able to lead an active life. Although positive emotional states are able to boost patients’ immune systems and have other benefits, it is likely that no amount of well-being can overcome such serious diseases like pancreatic cancer . Other frequently used mind-body interventions were creative therapies that also address physical and emotional needs. Evidence suggests that such interventions might also have a positive impact on HRQL but more research is needed to draw a conclusion on their effectiveness [30, 31].
Generally, pancreatic cancer patients have a short survival time with an overall 5-year survival rate of between six to nine percent in Germany [1, 2]. Review of international literature and the SEER database, still indicates a 5-year survival of less than five percent [4, 32, 33]. In our data restricted to palliative patients, we documented a 2-year survival for 3.3 % of the patients. Our proportional hazard model demonstrated that older people and males faced a slightly higher risk of dying, whereas both chemotherapy and VA were associated with a relevant decrease of the hazard.
For patients diagnosed with already advanced cancer that received only best supportive care, a survival of 2.3 to 2.7 months is reported [33, 34], matching with our results of the stratified survival analysis. In our data this patient population lived significantly shorter compared to patients that received no chemotherapy but received VA for at least 4 weeks. Anticancer therapy with VA extracts is common in German speaking countries . It has been reported to increase HRQL and attenuate adverse drug reactions to conventional therapies [36–38]. Whether VA can contribute to survival is the issue of a controversial debate . A comprehensive overview on the mode of action of VA extracts is given by the following reviews [36, 39]. Results of our group on assessment of safety of intravenous and subcutaneous VA therapy in cancer patients revealed that it was safe with common dose-related expected effects and mild local (<5 cm) or temperature-related (<38 °C) adverse drug reactions and no serious adverse reactions [24, 25]. From our data we cannot conclude on the causality of VA and survival prolongation, but our result matches the result of Tröger et al.  in direction and magnitude. In their prospective randomized controlled study on VA treatment in patients with advanced pancreatic cancer they found a median survival of 4.8 months compared to 2.7 months in the best supportive care group. Our data also shows that VA alone seems not to be an equivalent to chemotherapy; but it might be a beneficial add-on to conventional chemotherapy as these patients showed longest survival. To evaluate the impact of VA as an add-on to standard chemotherapy on survival further confirmative randomized controlled trials are highly warranted. VA is well tolerated with gemcitabine  and recent studies have indicated a possible influence of VA on survival in patients with pancreatic carcinomas [42, 43]. This is in line with a systematic literature review on VA and cancer treatment . A limitation of our study is that survival is likely to be underestimated. Whenever there was no exact death date documented we used the last documented date related to the patient as last contact date to calculate survival. The amount of censored data to the number of documented deaths is almost constant throughout the observed period. Nevertheless, missing death dates affect the calculation of survival. Additionally, as an observational study it suffers from potential missing or erroneous data and a heterogeneous patient population. Another limitation of this study it that the impact of the NPI in combination with conventional and/or VA treatment cannot be assessed within our data, since we are lacking systematic HRQL data. NPI are not well described in terms of prognostic relevance. However, there are positive effects of exercise on cancer-related fatigue  and overall survival in patients with breast-, and colon cancer [46, 47] and cognitive behavioral treatments and mindfulness orientated therapies in cancer-related fatigue. Whereas multimodal concepts are already established in chronic pain treatment [48, 49], their evaluation in cancer therapy is relatively new. In an exploratory analysis in breast cancer survivors with chronic cancer-related fatigue, psycho- and sleep education and eurythmy therapy where superior to aerobic training . Patient-reported outcome measures (PROMS) have been developed for many years  and have been successfully applied in oncology [52–54]. While palliative chemotherapy in patients with end-stage cancer has been questioned to improve quality of life , in the future HRQL data and PROMS might contribute to the evaluation of the influence of single NPI-interventions and multimodal therapeutic approaches in cancer treatment.
Despite these limitations, our study provides an accurate picture of the current clinical use and the potential importance of IO in caring for pancreatic cancer patients.
Our data demonstrates the importance and potential of health services research showing that IO treatment can be implemented in the every-day care of patients suffering from advanced pancreatic cancer. It also shows that IO treatment does not disregard conventional treatment. Our results suggest that IO therapies might have a beneficial effect on patient’s survival. However, there are few recommendations regarding IO in the current cancer guidelines . As patients often use CAM, even without discussion with their practitioner , more attention should be given to this issue to help practitioners to address patients’ needs adequately and to prevent patients from harm by unqualified self-medication. These data demonstrate how health services research can reflect real life conditions and thus might contribute to ongoing discussion of treatment guidelines and direction of future research in this field.
CAM, complementary and alternative medicine; FOLFIRINOX, chemotherapy regimen with oxaliplatin, irinotecan, fluorouracil and leucovorin; HRQL, health related quality of life; ICPM, international classification of procedures in medicine; IO, integrative oncology; NPI, non-pharmacological intervention; PROMS, patient-reported outcome measures; SEER, Surveillance, Epidemiology, and End Results Program of the National Cancer Institute; TNM, Classification of Malignant Tumours of the Union for International Cancer Control; UICC, Union for International Cancer Control; VA, extracts of European mistletoe Viscum album; WHO, World Health Organization
The authors would like to thank all medical documentation officers, all Network Oncology partners, and participating institutions. The authors would like to thank Dr. Anja Thronicke, Forschungsinstitut Havelhöhe, Germany for her valuable support as well as Dr. Katja Adie, Royal Cornwall Hospitals NHS Trust, UK for proof reading and language correction of the manuscript.
The Network Oncology project was funded by the Software AG Stiftung Darmstadt -Germany, Weleda AG Arlesheim -Switzerland, Abnoba GmbH Pforzheim -Germany, and Helixor GmbH Rosenfels -Germany. By contract, researchers were independent from the funder.
Availability of data and materials
The datasets analyzed during the current study are available from the corresponding author on reasonable request.
JA performed data acquisition, analysis and interpretation as well as drafting the manuscript. MS, MK, GS, FS and HM helped to draft the manuscript. FS was responsible for the overall study design, supervised the study. All authors read and approved the final manuscript.
HM has been a member of Weleda AG directory board since March 2012. FS reports personal fees from Weleda AG, MK reports personal fees from Helixor GmbH outside the submitted work. The other authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The Network Oncology database was designed to be compliant with the European Directive on Data Protection, which has implications for record linkage studies, databases, and registers, and the Network Oncology project has received a positive vote from the ethical committee of the Medical Association Berlin.
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- Kaatsch P, Spix C, Hentschel S, Katalinic A, Luttmann S, Stegmaier C, et al. Krebs in Deutschland 2007/2008, in Robert Koch-Institut. 8th ed. Berlin:Robert Koch-Institut: 2012.Google Scholar
- Hiripi E, Gondos A, Emrich K, Holleczek B, Katalinic A, Luttmann S, et al. Survival from common and rare cancers in Germany in the early 21st century. Ann Oncol. 2012;23:472–9.View ArticlePubMedGoogle Scholar
- Seufferlein T, Bachet JB, Van Cutsem E, Rougier P, ESMO Guidelines Working Group. Pancreatic adenocarcinoma: ESMO-ESDO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2012;23 Suppl 7:vii33–40.View ArticlePubMedGoogle Scholar
- Vincent A, Herman J, Schulick R, Hruban RH, Goggins M. Pancreatic cancer. Lancet. 2011;378:607–20.View ArticlePubMedPubMed CentralGoogle Scholar
- Yip D, Karapetis C, Strickland A, Steer CB, Goldstein D. Chemotherapy and radiotherapy for inoperable advanced pancreatic cancer. Cochrane Database Syst Rev. 2006;19:CD002093.Google Scholar
- Burris H, Moore MJ, Andersen J, Green MR, Rothenberg ML, Modiano MR, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol. 1997;15:2403–13.PubMedGoogle Scholar
- Al-Haddad M, Eloubeidi MA. Interventional EUS for the diagnosis and treatment of locally advanced pancreatic cancer. JOP. 2010;11:1–7.PubMedGoogle Scholar
- Conroy T, Desseigne F, Ychou M, Bouché O, Guimbaud R, Bécouarn Y, et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. New Eng J Med. 2011;364:1817–25.View ArticlePubMedGoogle Scholar
- Moore MJ, Goldstein D, Hamm J, Figer A, Hecht JR, Gallinger S, et al. Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol. 2007;25:1960–66.View ArticlePubMedGoogle Scholar
- Von Hoff DD, Ervin T, Arena FP, Chiorean EG, Infante J, Moore M, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. New Eng J Med. 2013;369:1691–703.View ArticleGoogle Scholar
- Seufferlein T, Porzner M, Heinemann V, Tannapfel A, Stuschke M, Uhl W. Ductal pancreatic adenocarcinoma: Surgery, pathology work-up, and neoadjuvant, adjuvant, and palliative treatments. Dtsch Arztebl Int. 2014;111:396.PubMedPubMed CentralGoogle Scholar
- Baum M, Cassileth BR, Daniel R, Ernst E, Filshie J, Nagel GA, et al. The role of complementary and alternative medicine in the management of early breast cancer: recommendations of the European Society of Mastology (EUSOMA). Eur J Cancer. 2006;42:1711–14.View ArticlePubMedGoogle Scholar
- Paul M, Davey B, Senf B, Stoll C, Muenstedt K, Muecke R, et al. Patients with advanced cancer and their usage of complementary and alternative medicine. J Cancer Res Clin Oncol. 2013;139:1515–22.View ArticlePubMedGoogle Scholar
- Cramer H, Cohen L, Dobos G, Witt CM. Integrative Oncology: Best of Both Worlds Theoretical, Practical, and Research Issues. Evid Based Complement Alternat Med. 2013. doi:10.1155/2013/383142.Google Scholar
- Pirri C. Integrating complementary and conventional medicine. CancerForum 2011;35.Google Scholar
- Verhoef MJ, Balneaves LG, Boon HS, Vroegindewey A. Reasons for and characteristics associated with complementary and alternative medicine use among adult cancer patients: a systematic review. Integr Cancer Ther. 2005;4:274–86.View ArticlePubMedGoogle Scholar
- Schildmann J, Ritter P, Salloch S, Uhl W, Vollmann J. ‘One also needs a bit of trust in the doctor…’: a qualitative interview study with pancreatic cancer patients about their perceptions and views on information and treatment decision-making. Ann Oncol. 2013;24:2444–9.View ArticlePubMedGoogle Scholar
- 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. 2011;11:187–203.View ArticlePubMedGoogle Scholar
- Huebner J, Follmann M. Complementary medicine in guidelines of the German guideline program in oncology: comparison of the evidence base between complementary and conventional therapy. J Cancer Res Clin Oncol. 2013;139:1481–8.View ArticlePubMedGoogle Scholar
- Schad F, Axtner J, Happe A, Breitkreuz T, Paxino C, Gutsch J, et al. Network Oncology (NO)-a clinical cancer register for health services research and the evaluation of integrative therapeutic interventions in anthroposophic medicine. Forsch Komplementmed. 2013;20:353–60.View ArticlePubMedGoogle Scholar
- Zaenker KS, Matthes H, Bock PR, Hanisch J. A specific mistletoe preparation (Iscador-Qu®) in Colorectal Cancer (CRC) patients: more than just supportive care? J Cancer Sci Ther. 2012;4:264–70.View ArticleGoogle Scholar
- Kienle GS, Kiene H. Influence of Viscum album L (European mistletoe) extracts on quality of life in cancer patients: a systematic review of controlled clinical studies. Integr cancer ther. 2010. doi:10.1177/1534735410369673.PubMedGoogle Scholar
- Gorski DH. Integrative oncology: really the best of both worlds? Nat Rev Cancer. 2014;14:692–700.Google Scholar
- Steele ML, Axtner J, Happe A, Kröz M, Matthes H, Schad F. Adverse drug reactions and expected effects to therapy with subcutaneous mistletoe extracts (Viscum album L.) in cancer patients. J Evid Based Complementary Altern Med. 2014. doi:10.1155/2014/724258.Google Scholar
- Steele ML, Axtner J, Happe A, Kröz M, Matthes H, Schad F. Safety of intravenous application of mistletoe (Viscum album L.) preparations in oncology: an observational study. J Evid Based Complementary Altern Med. 2014. doi:10.1155/2014/236310.Google Scholar
- Truant TL, Porcino AJ, Ross BC, Wong ME, Hilario CT. Complementary and alternative medicine (CAM) use in advanced cancer: a systematic review. J Support Oncol. 2013;11:105–13.View ArticlePubMedGoogle Scholar
- Kuhn Y, Koscielny A, Glowka T, Hirner A, Kalff JC, Standop J. Postresection survival outcomes of pancreatic cancer according to demographic factors and socio-economic status. Eur J Surg Oncol. 2010;36:496–500.View ArticlePubMedGoogle Scholar
- Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, et al. Early palliative care for patients with metastatic non–small-cell lung cancer. New Eng J Med. 2010;363:733–42.View ArticlePubMedGoogle Scholar
- Diener E, Chan MY. Happy people live longer: subjective well-being contributes to health and longevity. Appl Psychol Health Well Being. 2011;3:1–43.View ArticleGoogle Scholar
- Archie P, Bruera E, Cohen L. Music-based interventions in palliative cancer care: a review of quantitative studies and neurobiological literature. Support Care Cancer. 2013;21:2609–24.View ArticlePubMedPubMed CentralGoogle Scholar
- Wood MJM, Molassiotis A, Payne S. What research evidence is there for the use of art therapy in the management of symptoms in adults with cancer? A systematic review. Psychooncology. 2011;20:135–45.View ArticlePubMedGoogle Scholar
- Hidalgo M. Pancreatic cancer. New Eng J Med. 2010;362:1605–17.View ArticlePubMedGoogle Scholar
- Güngör C, Hofmann BT, Wolters‐Eisfeld G, Bockhorn M. Pancreatic cancer. Br J Pharmacol. 2014;171:849–58.View ArticlePubMedPubMed CentralGoogle Scholar
- Pelzer U, Schwaner I, Stieler J, Adler M, Seraphin J, Dörken B, et al. Best supportive care (BSC) versus oxaliplatin, folinic acid and 5-fluorouracil (OFF) plus BSC in patients for second-line advanced pancreatic cancer: a phase III-study from the German CONKO-study group. Eur J Cancer. 2011;47:1676–81.View ArticlePubMedGoogle Scholar
- Horneber M, Bueschel G, Huber R, Linde K, Rostock M. Mistletoe therapy in oncology. Cochrane Database Syst Rev. 2008. doi:10.1002/14651858.CD003297.pub2.PubMedGoogle Scholar
- Kienle GS, Kiene H. Influence of Viscum album L. (European mistletoe) extracts on quality of life in cancer patients: a systematic review of controlled clinical studies. Integr Cancer Ther. 2010;9:142–57.View ArticlePubMedGoogle Scholar
- Kienle GS, Glockmann A, Schink M, Kiene H. Viscum album L. extracts in breast and gynaecological cancers: a systematic review of clinical and preclinical research. J Exp Clin Cancer Res. 2009;28:79.View ArticlePubMedPubMed CentralGoogle Scholar
- Eisenbraun J, Scheer R, Kröz M, Schad F, Huber R. Quality of life in breast cancer patients during chemotherapy and concurrent therapy with a mistletoe extract. Phytomedicine. 2011;18:157.View ArticleGoogle Scholar
- Bar-Sela G. White-Berry Mistletoe (Viscum album L.) as complementary treatment in cancer: Does it help? Eur J Integr Med. 2011;3:e55–62.View ArticleGoogle Scholar
- Tröger W, Galun D, Reif M, Schumann A, Stankovic N, Milićević M. Viscum album [L.] extract therapy in patients with locally advanced or metastatic pancreatic cancer: a randomised clinical trial on overall survival. Eur J Cancer. 2013;49(18):3788–97.View ArticlePubMedGoogle Scholar
- Mansky PJ, Wallerstedt DB, Sannes TS, Stagl J, Johnson LL, Blackman MR, et al. NCCAM/NCI phase 1 study of mistletoe extract and Gemcitabine in patients with advanced solid tumors. Evid Based Complement Alternat Med. 2013. doi:10.1155/2013/964592.PubMedPubMed CentralGoogle Scholar
- Matthes H, Friedel WE, Bock PR, Zanker KS. Molecular mistletoe therapy: friend or foe in established anti-tumor protocols? A multicenter, controlled, retrospective pharmaco-epidemiological study in pancreas cancer. Curr Mol Med. 2010;10:430–9.View ArticlePubMedGoogle Scholar
- Schad F, Axtner J, Buchwald D, Happe A, Popp S, Kröz M, et al. Intratumoral mistletoe (Viscum album L) therapy in patients with unresectable pancreas carcinoma: a retrospective analysis. Integr Cancer Ther. 2014;13:332–40.View ArticlePubMedGoogle Scholar
- Ostermann T, Raak C, Büssing A. Survival of cancer patients treated with mistletoe extract (Iscador): a systematic literature review. BMC Cancer. 2009;9:451.View ArticlePubMedPubMed CentralGoogle Scholar
- Brown JC, Huedo-Medina TB, Pescatello LS, Pescatello SM, Ferrer RA, Johnson BT. Efficacy of exercise interventions in modulating cancer-related fatigue among adult cancer survivors: a meta-analysis. Cancer Epidemiol Biomarkers Prev. 2011;20:123–33.View ArticlePubMedGoogle Scholar
- Holmes MD, Chen WY, Feskanich D, Kroenke CH, Colditz GA. Physical activity and survival after breast cancer diagnosis. JAMA. 2005;293:2479–86.View ArticlePubMedGoogle Scholar
- Meyerhardt JA, Giovannucci EL, Holmes MD, Chan AT, Chan JA, Colditz GA, et al. Physical activity and survival after colorectal cancer diagnosis. J Clin Oncol. 2006;24:3527–34.View ArticlePubMedGoogle Scholar
- Hechler T, Dobe M, Kosfelder J, Damschen U, Hübner B, Blankenburg M, et al. Effectiveness of a 3-week multimodal inpatient pain treatment for adolescents suffering from chronic pain: statistical and clinical significance. Clin J Pain. 2009;25:156–66.View ArticlePubMedGoogle Scholar
- Pfingsten M, Hildebrandt J, Leibing E, Franz C, Saur P. Effectiveness of a multimodal treatment program for chronic low-back pain. Pain. 1997;73:77–85.View ArticlePubMedGoogle Scholar
- Kröz M, Reif M, Glinz A, Berger B, Nikolaou A, Zerm R, et al. Multimodal and combined multimodal-aerobic therapy in breast cancer survivors with cancer-related fatigue. ASCO Annual Meeting Proceedings. 2015;33(Suppl):e20717.Google Scholar
- Nelson EC, Eftimovska E, Lind C, Hager A, Wasson JH, Lindblad S. Patient reported outcome measures in practice. BMJ. 2015;350:g7818.View ArticlePubMedGoogle Scholar
- Ashley L, Jones H, Thomas J, Forman D, Newsham A, Morris E, et al. Integrating cancer survivors’ experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors). BJC. 2011;105:74–81.View ArticleGoogle Scholar
- Corner J, Wagland R, Glaser A, Richards M. Qualitative analysis of patients’ feedback from a PROMs survey of cancer patients in England. BMJ Open. 2013;3:e002316.View ArticlePubMedPubMed CentralGoogle Scholar
- Downing A, Morris EJ, Richards M, Corner J, Wright P, Sebag-Montefiore D, et al. Health-related quality of life after colorectal cancer in England: a patient-reported outcomes study of individuals 12 to 36 months after diagnosis. J Clin Onc. 2015. doi:10.1200/JCO.2014.56.6539.Google Scholar
- Prigerson HG, Bao Y, Shah MA, Paulk ME, LeBlanc TW, Schneider BJ, et al. Chemotherapy use, performance status, and quality of life at the end of life. JAMA Oncol. 2015;1:778–84.View ArticlePubMedPubMed CentralGoogle Scholar
- Newsom-Davis T, Kenny L, Al-Shakarchi I, George J, Wong E, Waxman J. Voodoo dolls and the cancer patient: patients do trust their doctors. QJM. 2009;102:311–9.View ArticlePubMedGoogle Scholar