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Property:Inclusion criteria

From CAMIH

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Patients with a primary histologically proven superficial BCC of 4 to 20 mm in greatest diameter  +
Postmenopausal women with stage I–III hormone receptor positive breast cancer scheduled to start treatment with an adjuvant aromatase inhibitors and with a 25(OH)D level B40 ng/ml  +
Patients with locally advanced (neo-adjuvant) and metastatic breast cancer refereed to a medical oncology clinic in Shohada-e-Tajrish hospital in Tehran, Iran, from July 2017 to October 2018; proven malignant biopsy; chemotherapy for at least 3 months  +
Primary brain tumor/brain metastases, Radiotherapy of whole or part of the brain (>60% of brain irradiated) with a dose of 30-60 Gray in a fractionation of 5 " 1.8-3.0 Gray/week, No former radiotherapy in the brain  +
Above 18 year-old and newly diagnosis with histology of solid tumors with Eastern Cooperative Oncology Group (ECOG) performance status B2. All patients must complete surgical resection of primary tumor and planned for at least 3 consecutive cycles of moderately to highly emetogenic adjuvant chemotherapy for curative intent  +
Patients who had all gross cancer removed (microscopic residual disease or residual margin involvement was allowed), scheduled to undergo curative-intent chemotherapy with either taxanes or platinum compounds, have a good performance status (ECOG 0-2), life expectancy ≥6 months, and not have preexisting peripheral neuropathy from any cause  +
Histologically proven, advanced and irresectable adenocarcinoma of the pancreas (UICC Stage IV), had a Karnofsky performance status of >60  +
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Patients with head and neck cancer, who were due to receive radiation on at least two-thirds of the oral cavity; aged 18-85 years with a normal renal function (creatinine clearence > 60ml/min) and an acceptable performance status (Karnofsky performance status > 70%) without any history of radiotherapy were eligible for this study  +
Age of at least 18 years; a diagnosis of lung cancer; patients receiving cisplatin-based regimens; patients receiving standard antiemetic therapy (5-HT3 RAs); the ability to swallow capsules; nonuse of self-prescribed therapies or complementary products  +
Advanced cancer; ≥18 years of age; clinical diagnosis of cancer-related pain that was unalleviated by an optimized maintenance dose of Step 3 opioid therapy (opioid therapy considered optimized if: 1) a dose increase was clinically inappropriate due to opioid-related side effects or 2) further efficacy benefit was not expected at higher doses (for the second definition, patients had to be receiving ≥90 mg morphine equivalents/day, inclusive of maintenance, and breakthrough opioids); each of three consecutive days during the screening period: ≥four opioid breakthrough analgesic episodes per day (averaged over the three days); a stable maintenance opioid therapy dose; average pain ≥four and ≤eight on a 0-10 Numerical Rating Scale (NRS); average pain scores on the NRS that did not change by more than two points (i.e., no more than a two-point difference between the highest and lowest scores, with all scores remaining between four and eight)  +
Histologically proven advanced lung cancer, gastrointestinal tract tumor, breast cancer or brain glioblastoma; measurable neoplastic lesions; progression on classical chemotherapy, radiotherapy or endocrine therapy or poor clinical conditions precluding chemotherapy; patients were eligible after at least 1 month from the last chemotherapy course; life expectancy <6 months  +
Histologically proven metastatic cancer; histological diagnosis of lung cancer or gastrointestinal tumour; measurable lesions  +
18 y old, case of recently diagnosed differentiated papillary or follicular thyroid cancer, undergone total thyroidectomy, referred to the Department of Nuclear Medicine, West China Hospital, for ablation of remnant thyroid tissue, stage pT1–T3, N0–N1, M0. For women of childbearing potential: a negative result on serum human chorionic gonadotropin pregnancy testing required  +
Women with a normal sense of smell; who were diagnosed with breast cancer; who were receiving chemotherapy and experienced nausea and/or vomiting of any severity; had at least two remaining chemotherapy courses using similar chemotherapeutic agents  +