The use of advanced organ imaging in radiotherapy of the upper-abdomen for kidney response assessment and treatment optimisatio
- Conditions
- Pancreatic cancerStomach cancerCancer - PancreaticCancer - Stomach
- Registration Number
- ACTRN12609000322235
- Lead Sponsor
- Sir Charles Gairdner Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 35
Patient has histologically/cytologically proven adenocarcinoma of the pancreas or upper-gastrointestinal (GI) tract. Metastatic disease status excluded on whole body computed tomography (CT) series.
Locoregional staging of primary disease has been undertaken with dual phase (arterial and portal) spiral CT.
Adequate bone marrow function: Haemoglobin (Hb)>10, White Blood Cells (WBC)>3.5 (Neutrophilis>1.5), Platelets >100
Serum creatinine <150
Patient has given written informed consent.
Performance status is East Coast Oncology Group (ECOG) grade 0, 1 or 2
Major co-morbid illnesses that, in the opinion of the investigator, would jeopardise the likely completion of the treatment program.
Patients with significant loss of bodyweight (>15% weight loss since diagnosis).
Treatment with any previous cytotoxic chemotherapy for the malignancy.
Previous abdominal radiotherapy.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Observed change in regional kidney function as indicated by SPECT signal[Baseline, 4 weeks, 12 weeks, 26 weeks, 52 weeks, 78 weeks];Change in glomerular filtration rate (GFR) measured via serum creatinine in blood analysis[Baseline, 4 weeks, 12 weeks, 26 weeks, 52 weeks, 78 weeks]
- Secondary Outcome Measures
Name Time Method rea and electrolyte levels assessed via blood analysis[Baseline, 4 weeks, 12 weeks, 26 weeks, 52 weeks, 78 weeks]
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