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Property:Specifications on cancer therapies

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Irradiation of the entire brain or at least 60 % with a dose of 30-60 Gray fractionated over 5 x 1.8-3.0 Gray/week  +
Moderately to highly emetogenic chemotherapy: 93% highly emetogenic, of which 68% anthracycline-based and 21% platinum-based  +
Open or Laparoscopic surgery for gastric or colorectal cancer + Peripheral postoperative parenteral nutrition (PPN): glucose, amino acid, lipid emulsion  +
At entry 88% of patients in the placebo and 92% of patients in the L-Carnitine group received chemotherapy.  +
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* Radiation therapy: 5 fractions per week at 60-70 Gy cumulative doses over 6 weeks to 7 weeks * Chemotherapy: 18 (48.6%) patients from the selenium and 16 (47.1%) from the placebo arm with cisplatin (30-50mg/m2 weekly, during radiation) * Grade of neutropenia and renal failure was evaluated based on the NCI CTCAE * Creatinine level increase of > 0.3 mg/dL or 1.5–2.0 mg/dL above baselinewas considered as renal failure and a neutrophil count decrease to 1000–500 mm3 was considered as grade 3 of this toxicity * After 7 weeks no differencences in the incidence of other adverse effects related to chemoradiation such as neutropenia and renal failure in the selenium arm and the placebo arm   +
The location of the fungating malignant wounds were: breast (n=24), neck (n=2), groin (n=2), spine (n=1); anus (n=1)  +
Intervention arm: Dose of radiotherapy (cGy): 6,824 (463.5), Placebo arm: Dose of radiotherapy (cGy): 6,651 (1,056.3); Intervention arm: Duration of radiotherapy: 56 (8.7), Placebo arm: Duration of radiotherapy: 54 (11.8); Intervention arm: concurrent chemotherapy: 20 (41) Placebo arm: concurrent chemotherapy: 20 (42)  +
Intervention arm: Dose of radiotherapy (cGy): 6,824 (463.5), Placebo arm: Dose of radiotherapy (cGy): 6,651 (1,056.3); Intervention arm: Duration of radiotherapy: 56 (8.7), Placebo arm: Duration of radiotherapy: 54 (11.8); Intervention arm: concurrent chemotherapy: 20 (41), Placebo arm: concurrent chemotherapy: 20 (42)  +
Daily fraction was 180 cGy to 200 cGy in five weekly fractions, total dose prescribed was 7,000 cGy; No significant difference in the radiation dose, fraction, and duration was identified between intervention and placebo arm; all patients received concomitant chemotherapy with 5-fluorouracil and cis-platinum  +
Nasopharyngeal Cancer: daily fractionations of 180 cGy to 200 cGy in 5 weekly fractions; total dose: 7000 cGy Oral Cancer: 7000 cGy was given to patients without surgery and 6000 cGy was prescribed as adjuvant treatment if they received an operation, unilateral irradiation was performed for cancers arising from retromolar, unilateral gum, lip, or single focus of buccal mucosa; whereas bilateral irradiation was done for tumors arising from mouth floor or multiple foci of buccal mucosa  +
Patients, for whom no other effective standard therapy was available, because of lack of response to previous chemotherapies or a poor clinical status precluding chemotherapy. Previous chemotherapy (patients were eligible after at least 1 month from the last chemotherapy course): Aloe arm: 20/24 Control arm: 21/26  +
Chemotherapy: Non-small cell lung cancer: Chemotherapy consisted of cisplatin (CDDP) plus etoposide (VP16) or weekly vinorelbine (VNR) Small cell lung cancer: Chemotherapy consisted of cisplatin (CDDP) plus etoposide (VP16) Colorectal cancer: low-dose oxaliplatin (OXA) plus 5-fluorouracil (5-FU) Gastric cancer: weekly 5-fluorouracil Pancreatic adenocarcinoma: weekly gemcitabine (GEM)  +
In all patients: High (>90%) emetic risk * 5-Flouracil + epirubicin + cyclophosphamide (FEC): 45% (SD 75.0) * Docetaxel + doxorubicin and cyclophosphamide (TAC): 7% (SD 11.7) Low (10—30%) emetic risk * Docetaxel: 8% (SD 13.3)  +