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Property:Inclusion criteria

From CAMIH

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M
N
Head and neck cancers who were on schedule for radiotherapy with at least 2000 Gy ot >30% of oral cavity, with or without chemotherapy  +
Women aged 18 to 75 years with a confirmed histological diagnosis of localized breast cancer, after breast lumpectomy, and scheduled to receive adjuvant radiotherapy  +
Patients with histologically proven Ta/T1, NO or NX, MO transitional cell carcinoma ofthe bladder completely removed by transurethral resection or fulguration before the start of oral therapy; no previous therapy other than transurethral resection or fulguration; estimated survival of more than 3 years  +
Pathologically confirmed, unresectable locally advanced or metastatic adenocarcinoma of the colon or rectum with measurable disease per version 1.1 of the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines; patients were eligible if they received prior neoadjuvant or adjuvant chemotherapy or chemoradiation as long as the last dose of treatment was more than 12 months prior to cancer recurrence; Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, normal baseline organ function, and no evidence of hypercalcemia or conditions predisposing to hypercalcemia (ie, hyperparathyroidism).  +
Biopsy-proved prostate cancer; received no other therapy for their prostate cancer; current PSA less than 50 ng/mL; older than 18 years; no history of chemotherapy and/or radiation for any malignancy in the previous 5 years; good performance status; normal renal function (creatinine ≤ institutional upper limits of normal); normal hepatic function (total bilirubin, aspartate aminotransferase (AST; SGOT)/alanine aminotransferase (ALT; SGPT) ≤ institutional upper limits of normal)  +
≥ 21 years old, with stage I-III hormone receptor-positive breast cancer, who were beginning adjuvant aromatase inhibitor therapy; post-menopausal, defined as any of the following: age ≥ 60 years old; history of bilateral oophorectomy; or serum estradiol and FSH concentrations in the post-menopausal range, along with either amenorrhea for 12 months or previous hysterectomy; if the patient was < 60 years old at the time of study enrollment and had completed chemo- therapy, post-menopausal status had to have been confirmed prior to chemotherapy  +
O
Preoperative contrast-enhanced computed tomography was available within 30 days of the scheduled surgery. Criteria for hepatectomy included: * Absence or controllability of ascites. * Serum total bilirubin level ≤2 mg/dL (no patients required diuretics for ascites)  +
Histologically confirmed colorectal cancer (adenocarcinoma); histological stage III colon cancer or rectosigmoid cancer resected with D2 or more lymph node dissection; age 20-80 years old; Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1; no prior chemotherapy or radiotherapy for target disease; oral intake is possible; preservation of primary organ function (white blood cell count ≥3,000 /mm3 and >12,000 /mm3, neutrophil count ≥1,500 /mm3, haemoglobin ≥9.0 g/dL, platelet count ≥100,000 /mm3; serum creatinine <1.5 mg/dL, serum total bilirubin <1.5 mg/dL, aspartate aminotransferase (ALT) <100 IU/L); able to start protocol treatment within 8 weeks of surgical procedure  +
P
Patients with solid malignancies and a Karnofsky Performance Status between 70 to 100  +
Patients with solid malignancies and Karnofsky Performance Status 70–100  +
Women who had cancer (mainly new cases of advanced breast cancer diagnosed by the oncologist and thus undergoing their first experience of chemotherapy) who were initially assigned to the components of TEC regimen, including docetaxel, epirubicin, and cyclophosphamide  +
Patients diagnosed with non-metastatic prostate cancer (N0 and M0 as confirmed by negative chest X-ray, bone scintigraphy and pelvic MRI or CT); scheduled for either radical prostatectomy or high-dose radiotherapy consisting of a combination of high-dose rate brachytherapy and pelvic external beam radiotherapy  +
Adult patients with active cancer and chronic pain (moderate or severe despite a stable opioid regimen that could not be made more effective by further opioid dose titration); stable, average pain: NRS: ≥4≤ 8 (no change in 3 days > 2 points)  +
Stage II-IVMO cancer of the head and neck; radiotherapy in adjuvant or definitive setting; Karnofsky performance > 70.  +
Patients with high-grade gliomas (anaplastic astrocytoma or glioblastoma multiforme)  +
R
Age over 18, having the experience of chemotherapy with nausea and vomiting, having at least two chemotherapy episodes. Consists of 50-100 mg Cisplatin, with or without other chemotherapy agents with similar amount and prescription in two chemotherapy cycles without having any plans for radiotherapy among cycles; presence in ward for 24 hours ( in order to investigate the PRN; having no nausea and vomiting experiences for some reasons except for chemotherapy; lack of receiving PRN in 24 past hours; lack of treatment with corticosteroid drugs during considered cycles; lack of afflictions to hepatitis, digestion system blockage, brain malignancy and cerebral metastasis and clotting disorder on the basis of recorded information in files; lack of using the anti-clot drug  +
From 18 to 68 years, in complete remission of the disease and bone marrow (NCCN guidelines), with optimal kidney and liver functions  +