| Literature DB >> 29845888 |
Carolin C Hack1, Janina Hackl1, Nina B M Hüttner1, Hanna Langemann1, Judith Schwitulla1, Svenja Dietzel-Drentwett2, Peter A Fasching1, Matthias W Beckmann1, Anna-Katharin Theuser1.
Abstract
PURPOSE: Although the demand from patients for integrative medicine is increasing, complementary medicine services are still quite heterogeneous and have not been incorporated into clinical routine. The aim of this study was to systematically evaluate improvements in side effects and quality of life associated with a hospital-based integrative medicine program in the modern breast cancer patient care setting.Entities:
Keywords: breast cancer; complementary and alternative medicine; integrative medicine; oncology; patient care; quality of life; side effect management
Mesh:
Year: 2018 PMID: 29845888 PMCID: PMC6142097 DOI: 10.1177/1534735418777883
Source DB: PubMed Journal: Integr Cancer Ther ISSN: 1534-7354 Impact factor: 3.279
Characteristics of the Patients (n = 75), Showing Absolute Numbers, Percentages, and Means.[a]
| Characteristics | n | Percentage | Mean (SD) |
|---|---|---|---|
| Age at baseline (years) | 52.5 (12.1) | ||
| ≥40 | 13 | 17.3 | |
| 41-60 | 43 | 57.3 | |
| >60 | 19 | 25.3 | |
| Disease state at baseline | |||
| Neoadjuvant | 24 | 32.0 | |
| Adjuvant | 36 | 48.0 | |
| Palliative | 15 | 20.0 | |
| Cancer treatment at baseline | |||
| Chemotherapy | 38 | 50.7 | |
| EC + Paclitaxel | 19 | 25.3 | |
| Carboplatin + Paclitaxel | 8 | 10.7 | |
| Eribulin | 5 | 6.7 | |
| Other | 6 | 8.0 | |
| Endocrine therapy | 18 | 24.0 | |
| Letrozole | 8 | 10.7 | |
| Exemestane | 4 | 5.3 | |
| Tamoxifen | 4 | 5.3 | |
| Other | 2 | 2.7 | |
| Targeted therapy | 13 | 17.3 | |
| Trastuzumab | 3 | 4.0 | |
| Pertuzumab + Trastuzumab | 4 | 5.3 | |
| Other | 6 | 8.0 | |
| Bisphosphonates | 11 | 14.7 | |
| No systemic therapy | 17 | 22.7 | |
| Disease state at follow-up | |||
| Palliative, progression of tumor disease | 7 | 9.3 | |
| Palliative, stable disease | 8 | 10.7 | |
| Curative, current chemotherapy or targeted therapy (neoadjuvant/adjuvant) | 19 | 25.3 | |
| Curative, aftercare, endocrine therapy, or bisphosphonates | 40 | 53.3 | |
| Disease state unknown | 1 | 1.3 | |
Abbreviation: EC, epirubicin and cyclophosphamide.
Multiple responses regarding cancer treatments were allowed.
Integrative Medicine Recommendations in the Consultations at Baseline, and Adherence to Individual Treatment Recommendations for at Least 4 Weeks, Evaluated in the Follow-up Interview.[a]
| Treatment Recommendation | Patients Who Received
Recommendation (n = 75) | Patients Stating at Least 4 Weeks’ Adherence | ||
|---|---|---|---|---|
| n | Percentage | n | Percentage | |
| General healthy nutritional therapy | 72 | 96.0 | 65 | 90.3 |
| Well-structured daily routine | 72 | 96.0 | 61 | 84.7 |
| Relaxation techniques | 71 | 94.7 | 53 | 74.6 |
| Regular walking | 69 | 92.0 | 58 | 84.1 |
| Enzyme therapy | 66 | 88.0 | 50 | 75.8 |
| Cold facial affusions | 61 | 81.3 | 35 | 57.4 |
| Mild endurance training | 54 | 72.0 | 35 | 64.8 |
| Oil swishing | 51 | 68.0 | 20 | 39.2 |
| Mild outdoor activities | 48 | 64.0 | 43 | 89.6 |
| IMed infusions[ | 33 | 44.0 | 14 | 42.4 |
| 31 | 41.3 | 15 | 48.4 | |
| Vitamin D | 31 | 41.3 | 30 | 96.8 |
| Vitamin B complex | 29 | 38.7 | 26 | 89.7 |
| Applying stimuli to hands and feet | 28 | 37.3 | 24 | 85.7 |
| Moist, hot hay flower sachet | 27 | 36.0 | 5 | 18.5 |
| Peeling with olive oil and sugar | 26 | 34.7 | 12 | 46.2 |
| Psychological support | 26 | 34.7 | 14 | 53.8 |
| Relaxing baths | 22 | 29.3 | 13 | 59.1 |
| Iberogast (herbal mixture) | 21 | 28.0 | 13 | 61.9 |
| Iceland moss ( | 20 | 26.7 | 16 | 80.0 |
Abbreviation: IMed, integrative medicine.
Multiple recommendations and responses were possible. Only patients who had received each recommendation were included in the analysis of compliance.
IMed infusions: intravenous vitamin infusions containing various vitamins (vitamin C, vitamin B1, vitamin B6, vitamin B12) and some minerals (magnesium and calcium) that were produced by the pharmacy of the University Hospital Erlangen on application day in a standardized way and applied in the Department of Gynecology and Obstetrics within the scope of the integrative treatment.
Achievement of Individual Treatment Goals, as Evaluated by Patients at the Follow-up Interview, Showing the Numbers of Patients Who Stated Each Therapy Goal: Percentages and Median.[a]
| Treatment Goal | Patients Stating Goal at Baseline, n (%) | Extremely Satisfied, n (%) | Very Satisfied, n (%) | Satisfied, n (%) | Adequate, n (%) | Dissatisfied, n (%) | Very Dissatisfied, n (%) | Don’t Know, n (%) | Median |
|---|---|---|---|---|---|---|---|---|---|
| Relief of cancer symptoms | 33 (44.0) | 1 (3.0) | 13 (39.4) | 9 (27.3) | 1 (3.0) | 0 (0.0) | 1 (3.0) | 8 (24.2) | 2 |
| Reduction of side effects of conventional therapy | 60 (80.0) | 2 (3.3) | 24 (40.0) | 19 (31.7) | 1 (1.7) | 0 (0.0) | 2 (3.3) | 12 (20.0) | 2 |
| Improvement in disease-related quality of life | 56 (74.7) | 7 (12.5) | 19 (33.9) | 18 (32.1) | 2 (3.6) | 1 (1.8) | 1 (1.8) | 8 (14.3) | 2 |
| Improvement in coping with disease | 42 (56.0) | 2 (4.7) | 17 (40.5) | 12 (28.6) | 2 (4.7) | 1 (2.4) | 2 (4.7) | 6 (14.3) | 2 |
| Stabilization of body, mind, and spirit | 59 (73.3) | 3 (5.1) | 21 (35.6) | 23 (39.0) | 6 (10.2) | 1 (1.7) | 2 (3.4) | 3 (5.1) | 3 |
| Active participation in treatment of the disease | 56 (74.7) | 17 (30.4) | 24 (42.9) | 9 (16.1) | 1 (1.8) | 0 (0.0) | 1 (1.8) | 4 (7.1) | 2 |
| Slowing of tumor progression | 64 (85.3) | 8 (12.5) | 6 (9.4) | 2 (3.1) | 0 (0.0) | 0 (0.0) | 2 (3.1) | 46 (71.9) | 2 |
| Prolonging survival time | 51 (68.0) | 4 (7.8) | 1 (2.0) | 4 (7.8) | 0 (0.0) | 0 (0.0) | 2 (3.9) | 40 (78.4) | 3 |
At the follow-up interview, the patients were asked how satisfied they were with the extent to which their treatment goals had been achieved (1, extremely satisfied; 2, very satisfied; 3, satisfied; 4, adequate; 5, dissatisfied; 6, very dissatisfied; don’t know). Of the 75 patients enrolled, only the patients who stated each treatment goal at the baseline were included in the analysis of the achievement of individual therapy goals.
Reduction in the Side Effects of Conventional Therapy.[a]
| Reduction in Side Effects of Conventional Therapies | ||||
|---|---|---|---|---|
| Achieved, n (%) | Partly Achieved, n (%) | Not Achieved, n (%) |
| |
| Age (years) | .586[ | |||
| ≥40 | 4 (44%) | 4 (44%) | 1 (11%) | |
| 41-60 | 17 (59%) | 11 (38%) | 1 (3%) | |
| ≥60 | 5 (50%) | 5 (50%) | 0 (0%) | |
| Treatment state at initial presentation | .022[ | |||
| Neoadjuvant | 12 (67%) | 5 (28%) | 1 (6%) | |
| Adjuvant | 6 (30%) | 13 (65%) | 1 (5%) | |
| Palliative | 8 (80%) | 2 (20%) | 0 (0%) | |
| Course of disease | .102[ | |||
| Palliative, progression | 2 (40%) | 2 (40%) | 1 (1%) | |
| Palliative, stable disease | 5 (100%) | 0 (0%) | 0 (0%) | |
| Curative, current chemotherapy, or targeted therapy | 7 (58%) | 5 (42%) | 0 (0%) | |
| Curative, aftercare, endocrine therapy, or bisphosphonates | 12 (46%) | 13 (50%) | 1 (4%) | |
Only patients who stated this goal at baseline were included in the analysis (achieved = rated at 1 + 2; partly achieved = rated at 3 + 4; not achieved = rated at 5 + 6).
Spearman’s rank correlation.
Kruskal-Wallis Test.
Improvement in Quality of Life.[a]
| Improvement in Quality of Life | ||||
|---|---|---|---|---|
| Achieved, n (%) | Partly Achieved, n (%) | Not Achieved, n (%) |
| |
| Age (years) | .586[ | |||
| ≥40 | 7 (78%) | 1 (11%) | 1 (11%) | |
| 41-60 | 15 (58) | 10 (38%) | 1 (4%) | |
| ≥60 | 4 (31%) | 9 (69%) | 0 (0%) | |
| Treatment state at initial presentation | .746[ | |||
| Neoadjuvant | 10 (59%) | 7 (41%) | 0 (0%) | |
| Adjuvant | 11 (55%) | 7 (35%) | 2 (10%) | |
| Palliative | 5 (45%) | 6 (55%) | 0 (0%) | |
| Course of disease | .026[ | |||
| Palliative, progression | 1 (17%) | 5 (83%) | 0 (0%) | |
| Palliative, stable disease | 5 (100%9 | 0 (0%) | 0 (0%) | |
| Curative, current chemotherapy, or targeted therapy | 8 (62%) | 5 (38%) | 0 (0%) | |
| Curative, aftercare, endocrine therapy, or bisphosphonates | 12 (50%) | 10 (42%) | 2 (8%) | |
Only patients who stated this goal at baseline were included in the analysis (achieved = rated at 1 + 2; partly achieved = rated at 3 + 4; not achieved = rated at 5 + 6).
Spearman’s rank correlation.
Kruskal-Wallis Test.
Self-reported Reduction in Symptoms Associated With Integrative Medicine, as Evaluated in the Follow-up Interview.[a]
| No. | Symptom | Patients (n = 75), n (%) | Yes, Symptom Stopped, n (%) | Yes, Symptom Significantly Improved, n (%) | Yes, Symptom Improved Slightly, n (%) | No, Symptom Unchanged, n (%) | No, Symptom Slightly Worse, n (%) | No, Symptom Significantly Worse, n (%) | Don’t Know, n (%) | No Response, n (%) |
|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Tiredness/fatigue/lack of motivation | 51 (68.0) | 2 (3.9) | 11 (21.6) | 21 (41.2) | 14 (27.5) | 0 (0.0) | 2 (3.9) | 1 (2.0) | 0 (0.0) |
| 2 | Depressive mood | 26 (34.7) | 2 (7.7) | 6 (23.1) | 8 (30.8) | 10 (38.5) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
| 3 | Impaired cognitive function | 22 (29.3) | 1 (4.6) | 6 (27.3) | 6 (27.3) | 9 (40.9) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
| 4 | Climacteric complaints/hot flushes | 20 (26.7) | 4 (20.0) | 6 (30.0) | 4 (20.0) | 1 (5.0) | 0 (0.0) | 1 (5.0) | 3 (15.0) | 1 (5.0) |
| 5 | Polyneuropathy | 18 (24.0) | 2 (11.1) | 5 (27.8) | 4 (22.2) | 3 (16.7) | 1 (5.6) | 2 (11.1) | 1 (5.6) | 0 (0.0) |
| 6 | Bone pain | 17 (22.7) | 1 (5.9) | 3 (17.7) | 3 (17.7) | 5 (29.4) | 0 (0.0) | 1 (5.9) | 1 (5.9) | 3 (17.7) |
| 7 | Sleep disturbances | 16 (21.3) | 1 (6.3) | 3 (18.6) | 6 (37.5) | 4 (25.0) | 1 (6.3) | 0 (0.0) | 1 (6.3) | 0 (0.0) |
| 8 | Back pain | 15 (20.0) | 1 (6.7) | 1 (6.7) | 5 (33.3) | 6 (40.0) | 2 (13.3) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
| 9 | Constipation | 14 (18.7) | 6 (42.9) | 6 (42.9) | 2 (14.3) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
| 10 | Dysgeusia | 14 (18.7) | 4 (28.6) | 1 (7.1) | 2 (14.3) | 4 (28.6) | 1 (7.1) | 0 (0.0) | 0 (0.0) | 2 (14.3) |
The analysis was limited to the top 10 symptoms most frequently stated by the patients. Multiple responses were allowed. Among the 75 patients enrolled, only the patients who stated the relevant symptoms at baseline were included in the analysis of the reduction in particular symptoms.