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Property:Inclusion criteria

From CAMIH

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D
Both sexes, age ≥ 18 years; tumors of oropharynx or oral cavity; no prior radiotherapy; primary or secondary radiotherapy; written informed consent; expected compliance  +
E
- Completed external beam radiation or seed implantation for a pelvic malignancy, including cancer of the prostate, cervix, or uterus at least six months before enrollment - At least two symptoms (diarrhea, rectal urgency, rectal pain, tenesmus, rectal bleeding, and fecal incontinence) with a severity score of 3 (moderate problem-cannot be ignored; no effect on daily activities) on at least a weekly basis  +
Patients receiving standardized abdomen and pelvic irradiation 5000 cGy (1000 cGy weekly) for prostate, uterus, cervix, bladder, rectum and colon  +
Histologically proven cancer of the head and neck (Karnofsky’s performance status ≥70) who were to receive curative radiotherapy or chemoradiotherapy  +
F
Diagnosis of cancer and receiving cisplatin-based regimens at least for two cycles of the chemotherapy, receiveing one of the standard antiemetic regimens [5-HT3 antagonist (granisetrone) and corticostreoid (hydrocortisone)], being able to swallow capsules  +
Aged less than 55 years, who were referred to our institute for 131I therapy to ablate the remnant thyroid tissue or to treat metastatic tumor, were enrolled in this study; all patients were in a hypothyroid state with serum thyroid stimulating hormone levels higher than 25 mIU/l  +
Advanced incurable stage of cancer; ≥ 18 years of age; clinical diagnosis of cancer-related pain unalleviated by an optimized maintenance dose of Step 3 opioid therapy; ≤ 4 opioid breakthrough analgesic episodes per day (averaged over the 3 days); stable maintenance opioid therapy dose; average pain ≥ 4 and ≤ 8 on a 0–10 NRS; average pain scores on the NRS that did not change by more than 2 points from the beginning to end of screening (i.e. no more than a 2-point difference between the highest and lowest scores, with all scores remaining between 4 and 8  +
Advanced incurable stage of cancer; ≥18years of age; clinical diagnosis of cancer-related pain unalleviated by an optimized maintenance dose of Step 3 opioid therapy; ≤4 opioid breakthrough analgesic episodes per day (averaged over the 3 days); stable maintenance opioid therapy dose; average pain ≥ 4 and ≤8 on a 0–10 NRS; average pain scores on the NRS that did not change by more than 2 points from the beginning to end of screening (i.e. no more than a 2-point difference between the highest and lowest scores, with all scores remaining between 4 and 8  +
Patients with a confirmed histologic diagnosis of cancer of the oral cavity and oropharynx referred to Radiotherapy; Admission requirements consisted of: (1) a minimal irradiated buccal mucosal area 12.2 cm2 or greater; the limits of this area, measured on verification films, were the hard palate (superior), the floor of the mouth (inferior), the anterior border of the vertical portion of the mandible (posterior), and the distal border of the irradiation field (anterior); (2) age at least 21 years; (3) Zubrod performance status grade 2 or lower; (4) tolerance of solid food at study entry  +
≥18 years old, had advanced and/or metastatic cancer in palliative phase (any type of cancer), a life expectancy of at least three months as assessed by one of the three study physician and 25-OHD ≤50 nmol/L  +
Primary treatment for prostate cancer (radical prostatectomy or definitive local radiation including external beam radiation, brachytherapy or both); prostate specific antigen (PSA) within the past two months of between 3 and 20ng/ml if prior local radiation or between 0.4 and 20 ng/ml if prior radical prostatectomy; prostate specific antigen doubling time (PSADT) >3 and <36 months; BMI ≥24 kg/m2  +
G
Underwent a transurethral resection (TUR) for a histologically confirmed low-grade or high-grade non-invasive urothelial carcinoma (transitional cell carcinoma of the bladder), stage Ta, T1, or carcinoma in situ (Tis)  +
Aged ≥18 years; any malignancy of any stage; receiving intravenous chemotherapy of moderate or high emetogenic risk; receive at least two more consecutive cycles; refractory CINV (defined as emesis, and/or nausea of moderate severity on a 5-point rating scale, and/or requiring use of rescue medications) in earlier chemotherapy cycles despite guideline-consistent antiemetic prophylaxis consisting of corticosteroids, a 5-HT3 antagonist, and an NK-1 antagonist with or without olanzapine where indicated  +
Biopsy-proven squamous cell carcinoma of the head and neck: oral cavity or oropharynx staged T1-T3 at subsites, alveolo-buccal, oral tongue, base of tongue, epiglottis/vallecula, tonsil and pharyngeal wall (lateral or posterior); previous chemotherapy was allowed  +
H
At least 18 years of age with newly diagnosed brain tumor with serum level of 25 (OH) vitamin D ≤20 ng/dL  +
Head and neck cancer patients scheduled to receive ≥2,000 cGy of external beam radiotherapy to ≥30% of the oral cavity; ≥18 years of age; life expectancy of ≥3 months (as determined by the physician’s judgment); Eastern Cooperative performance score of 0, 1, or 2; be able to take oral medications reliably and be alert and competent; receiving amifostine and/or concomitant chemotherapy was allowed  +
Women >18 years; indication for radiotherapy for breast cancer after lumpectomy or partial mastectomy; chemotherapy as part of the treatment regimen was acceptable  +
Patients referred to local curative radiotherapy with external beam radiotherapy (EBRT), in combination with hormone ablation; Adenocarcinoma of the prostate must be histologically confirmed on biopsy; life expectancy greater than 5 years; no metastatic disease detected during physical examination, standard radiography, bone scan, and magnetic resonance spectroscopy (MRS); no prior hormone therapy, radiotherapy or systemic treatment for prostate cancer and no other malignancy  +