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Property:Inclusion criteria

From CAMIH

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B
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).  +
Patients with squamous cell carcinoma of the head and neck region; atom absorption spectrometry showed a deficiency in selenium and the radiation field included 75% of the major salivary glands  +
C
Completely functional erections before surgery (corroborated by the partner and documented in the patient file), bilateral nerve-sparing radical retropubic prostatectomy (indicated on the surgical report) performed for pathologically proven organ-confined disease at least 6 months before screening, no adjuvant or neoadjuvant therapy for prostate cancer, no other treatment for ED before or after surgery, an undetectable postoperative prostate-specific antigen level, and involvement in a stable heterosexual relationship for at least 6 months before surgery  +
Low-burden prostate cancer; choosing active surveillance for disease management; histologically documented prostate adenocarcinoma; extended pattern biopsy within 2 years of enrollment with a Gleason sum six or lower with no pattern four or five; no more than 33% of biopsy cores positive for cancer; no more than 50% of the length of a tumor core involved by carcinoma; three serum prostate-specific antige (PSA) levels done at least 2 weeks apart over the year prior to randomization; all PSA levels <10 ng/ml; life expectancy >3 months; ECOG (Eastern Cooperative Oncology Group) performance score <2  +
Diagnosed with biopsy-proven Head-Neck-Cancer, treated with >4000-cGy intensity-modulated radiotherapy  +
Women diagnosed with ovarian or endometrial cancer; BMI ≥ 18.5 kg/m2; age ≥ 19 years; no medical condition affecting body weight (other than cancer and its associated treatment); not attempting diet modification; women with type 2 diabetes eligible to participate with additional medical supervision from the study physician  +
Women; 21-65 years; history of histologically confirmed resected stage I–III ER negative and progesterone receptor (PR)-negative (defined as <10% ER and PR expression) breast carcinoma; without evidence of disease at trial entry; minimum of 6 months since completion of breast surgery, adjuvant chemotherapy (including trastuzumab), and radiation therapy; Eastern Cooperative Group performance status of 0 to 1; at least one intact breast (no radiation therapy, mastectomy, or breast implant); normal organ and marrow function, including total bilirubin and transaminases within normal institutional limits; Pre- and postmenopausal women: postmenopausal = absence of menses for more than 12 months, history of bilateral oophorectomy, or serum follicle-stimulating hormone (FSH) more than 20 mIU/mL  +
Moderate to severe fatigue, a Karnofsky Performance Status (KPS) score 14 of 50 or more, and carnitine deficiency; carnitine deficiency was defined as free carnitine less than 35 µmol/L for males or less than 25 µmol/L for females (normal range 35-67 and 25-55, respectively), or an acyl-carnitine ratio of more than 0.4 (acylcarnitine ratio 0.4 total acyl-carnitine - free acyl-carnitine/free acyl-carnitine)  +
Histological diagnosis of squamous cell carcinoma of the oral cavity, the oropharynx, the hypopharynx, and/or the larynx; treated by radiotherapy alone, postoperative radiotherapy, radiochemotherapy alone, or postoperative radiochemotherapy; aged 18 to 80 years; no other cancer diagnosis in the past 5 years, except for basal cell and squamous cell carcinoma of the skin  +
D
Patients with a histological diagnosis of early stage breast cancer in an early stage (I or II) for whom adjuvant radiation therapy was indicated  +
Women between 24-85 years; locally advanced, biopsy-confirmed carcinomas of the uterine cervix at stages Ib, IIb or IIIb  +
Had undergone near-total thyroidectomy for DTC (differentiated thyroid cancer), at enrollment considered to be free of cancer metastases (serum thyroglubin level < 10ng/ml, negative anti-TG antibody titer and negative ultrasound neck examination  +
Women who had had radiotherapy for breast cancer and exhibited clinically measurable radiation induced fibrosis that had occurred more than 6 months after radiotherapy completion, without evidence of recurrent or evolutionary cancer or skin pathology  +
Patients with localized or locally advanced head and neck cancer (stage I - IV) with indications for chemoradiotherapy, with or without surgical treatment or prior induction chemotherapy.  +
Patients over 18 years old, with a diagnosis of cancer, attending the hospital as NHS out- patients, wishing to access complementary therapy treatment and able to attend the hospital for four, one-hour sessions.  +