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Property:Inclusion criteria

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R
Hormone receptor positive invasive nonmetastatic breast cancer (Stage I-IIIB), had completed at least 8 weeks of anastrozole as adjuvant therapy prior to study entry, and were experiencing new or worsening musculoskeletal pain unrelated to any history of trauma; serum 25OHD level between 10 and 29 ng/ml, serum calcium B10.3 mg/dl, and 24 h urine calcium excretion B250 mg/g creatinine  +
Undergone surgical resection of the colon or of rectal adenocarcinoma, and were on adjuvant or palliative treatment  +
Patients in remission after chemotherapy with taxanes, platinumderivatives, or vinca alkaloids and who presented with symptoms of CIPN  +
Diagnosed with cancer, may have received ≥1 chemotherapy cycle, and were scheduled for at least three additional chemotherapy cycles, chemotherapy must have been given without concurrent radiation therapy or interferon and without planned interruption by radiation therapy or surgery, must have experienced nausea of any severity in any chemotherapy cycle before study enrollment, as well as scheduled to receive a 5-HT3 receptor antagonist (e.g., Zofran®, Kytril®, Navoban®, or Anzemet®) plus dexamathasone at all chemotherapy cycles  +
Diagnosed with noninflammatory breast cancer or carcinoma in situ and prescribed radiotherapy without concurrent chemotherapy at the University of Rochester Cancer Center  +
S
Diagnosis of head or neck cancer; age ≥18 years; Karnofsky performance > 70 (i.e. able to carry out normal activity and work)  +
18–75 years, diagnosed with colorectal cancer, scheduled to receive oxaliplatin‑based regimens, more than 6 month life expectancy  +
Women with a normal sense of smell; had a diagnosis of breast cancer; were receiving chemotherapy and experiencing nausea and/or vomiting of any severity (previously described in our earlier article13); were due to receive at least two further chemotherapy courses using similar chemotherapeutic agents  +
Patients between 20 and 60 years; histological diagnosis of breast cancer, history of receiving at least one chemotherapy injection, receiving single-day cycles of chemotherapy (each cycle separated from next by≥2 weeks); experiencing vomiting in previous sessions, and having normal values of hematologic and biomedical laboratory parameters.  +
Older than 18 years, had a histologically docu- mented diagnosis of head and neck cancer, and had a Karnof- sky Performance Status Scale score of at least 70  +
Pathologically or cytologically proven adenocarcinoma of the prostate, metastatic disease (documented by computed tomograpghy, magnetic resonance imaging, or bone scan), disease progression after medical or surgical castration (documented by PSA, radiologic imaging of soft-tissue lesions, and/or bone scan; life expectancy longer than 3 months, normal liver and kidney function, Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2, and testosterone lower than 50 ng/dL  +
Post-menopausal women >18 years of age, with stage I-IIIA breast cancer, being treated with anastrozole, letrozole or exemestane for at least 30 days and experiencing aromatase inhibitor (AI)–associated musculoskeletal symptoms (AIMSS) at enrollment (prior to the run-in period)  +
Female; over 18 years of age; newly diagnosed histologically proven early breast cancer (T1, T2 [<3 cm], N0, N1a, M0); received breast surgery; WHO status 0 or 1; willing to give written, informed consent; and able to complete questionnaires  +
Females with approved ovarian cancer who underwent primary cytoreductive surgery, willingness to participate in the study.  +
Age over 18 years, a dose of radiation received over 4,500 cGy, the radiation received during the period 6 to 7 weeks, minor and major salivary glands involvement, one or two sides of the face in the field of radiation, and over the last three months of receiving radiation.  +