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Property:Inclusion criteria

From CAMIH

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S
Malignancy confirmed by histopathology, combination chemotherapy including cyclophosphamide, occurrence of at least 2 episodes of vomiting in previous chemotherapy cycle and age above 18 years. All patients received cyclophosphamide 500-1000 mg I.V. in combination with other chemotherapeutic agents.  +
Women aged 18–80 years at the time of study enrolment; body mass index (BMI) in the range 25–40 kg/m<sup>2</sup> ; received chemotherapy (neo-adjuvant or adjuvant with any medically-prescribed gent/regime) for treatment of invasive breast cancer; reported no current use of tobacco (past 12 months); no chronic illness such as diabetes, cardiovascular disease (or to be taking medications to control blood glucose and/or blood lipids) or cancer other than the previously treated breast cancer; willing to refrain from all weight loss diets and supplements for a study period of 6 month  +
Lung or breast cancer, 21 years or older; Patients who speak english and give informed consent  +
Presence of any type of metastatic cancer and a pain score of 2 or higher on the 0–10 pain scale during the current hospitalization. Additional criteria for the patient-partner dyad were being 21 years of age or older; living together as spouses or domestic partners, family members, or friends; English speaking; living within a 75- to 100-mile radius of the hospital; partner availability for 30 minutes from 2–10 pm; and willingness to participate as evidenced by verbalizing understanding and signing an informed consent form.  +
Advanced, incurable cancer; cancer-related anorexia-cachexia syndrome; weight loss (≥ 5% over 6 months), not explained by other diseases or recent surgery; Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 2: estimated life expectancy of 3 months; Creatinine, bilirubin, and transaminase values no higher than 3x the maximum normal value; Unchanged antineoplastic therapy for 4 weeks and unchanged supportive treatment (analgesics, sedatives, tranquilizers, and anticholinergics) for 1 week before baseline assessments  +
Biopsy-proven localized (nonmetastatic) prostate cancer documented within 48 months before enrolling in the trial, Gleason score of <8, serum PSA level of <50 ng/mL, age <85 years, life expectancy of ≥3 years, elected to forgo front-line therapy and chose to be followed by active surveillance, limited daily selenium supplementation to no more than 50 μg from non-study sources  +
Stage II-IVM0 carcinoma in the head-neck-area; radiotherapy (at least 50 Gy); Karnofsky power > 60; both primary radical radiotherapy and postoperative radiotherapy patients were eligible  +
Aged 18–75 years, Grade ≥3 neuropathy, as determined by NCI-CTC criteria version 3.0, while receiving paclitaxel, cisplatin or vinblastine treatment, and/or grade ≥2 neuropathy persisting for at least one month after the discontinuation of either drug, and neurotoxicity for <6 months; at least one abnormality on electrophysiological examination; Karnofsky physical score (KPS) of ≥60; absolute neutrophil count of ≥1.5×10<sup>9</sup>/l, hemoglobin count of ≥80 g/l, platelet count of ≥75×10<sup>9</sup>/l, total bilirubin counts of 1.5-fold less than normal value, glutamic-pyruvic transaminase (GPT/ALT) and glutamic-oxalacetic transaminease (GOT/AST) no more than 2.5-fold greater than the normal value; normal blood urea nitrogen, serum creatinine and electrocardiogram (ECG) findings. During the study, the use of steroids, analgesic or neuroprotectant drugs was not permitted.  +
T
Diagnosis of hematological tumor; white blood cell count 3–12×10<sup>9</sup>/l, platelet count ≥60×10<sup>9</sup> /l, absolute neutrophil count ≥10<sup>9</sup> /l; average score of the difficulty of mandibular impacted third molar extraction ≥14, patients had difficulties with tooth extraction; informed consent form signed by patients  +
Women aged 18 years or older with documented breast cancer who had received a first cycle of AC chemotherapy and who experienced vomiting or moderate to severe nausea, defined as a nausea score of ≥40 on a visual analog scale of 0 (no nausea) to 100 (unbearable nausea). Their treatment plan included at least two more cycles of AC  +
- Histologically confirmed HNSCC classified as stage I or II baccording to criteria of American Joint Committee on Cancer and radically treated with surgery and/or radiotherapy - Performance status 0-2 - Adequate liver, kidley, cardiac function  +
18 years or older, had major abdominal surgery for mainly hepatocellular cancer and gastric cancer in the 24 hours prior, alert, awake, in a stable medical condition, able to verbally communicate, received general anesthetics, and used PCAs for pain  +
U
Definite pathological diagnosis of differentiated thyroid cancer (DTC), presented to department for <sup>131</sup>I treatment  +
A histopathological diagnosis of epithelial carcinoma of the digestive tract (esophagus, stomach, small intestine, colon, and rectum), clinical stages I to III; aged 30 to 90 years at entry; diagnosis and initial surgery at the International University of Health and Welfare Hospital; not taking vitamin D supplements or active vitamin D; and no history of urinary tract stones  +
Patients with gynecological cancers (ovarian, cervical, endometrial, vulvar carcinoma; stage 1-4, recurrence), ECOG status 0-2, carboplatin-paclitaxel chemotherapy  +
Patients who were older than 18 years; were examined with second and third stage colorectal cancer; received CRT during postoperative and preoperative periods; were able to speak, read, and understand Turkish; and had agreed to participate in the study.  +
V
- Non-small-cell lung cancer (stages pT1–2, N0–1, and T3N0), cancer of the larynx (Tis, T1–3, and N0–1), or cancer of the oral cavity (T1–2 and N0–1) - Performance status 0–2 - Treated with curative intent  +
Patients with solid malignancies and good functional status (Karnofsky Performance Status 70–100) candidates to receive Cisplatin-chemotherapy  +