Colorectal Cancer Clinical Trial
Official title:
Role of Natural Fluorescence of Human Blood Plasma in Patients With Colorectal Cancer.
The aim of the present prospective study was to investigate the fluorescence emission of
human blood plasma of patients with colorectal cancer.
For years, serum tumor markers have been studied for the diagnosis and follow-up of
colorectal cancer, among which carcinoembryonic antigen (CEA) has achieved promising
results. However, the sensitivity of CEA for colorectal cancer is less than 25% and elevated
CEA levels also occur in patients with benign disease, as well as in patients with other
carcinomas. Nevertheless, surveillance programs are often based on the CEA test and
combination with other markers is at present a matter of research. Alternative methods based
on optical fluoroscopy have been introduced in experimental stages for clinical diagnosis of
cancer. Few studies have been reported on the application of native fluorescence
spectroscopy of biofluids in the diagnosis of tumoral diseases. The above reported findings
prompted us to investigate the fluorescence emission of human blood plasma of patients with
colorectal cancer. For this purpose, the blood of patients was collected and the
fluorescence Preliminary measurements on plasma of patients bearing colon cancer showed that
the fluorescence spectra were mainly characterized by the presence of an emission peaking at
620-630 nm, whose excitation spectrum peaked at 405 nm. Hence, an excitation wavelength of
405 nm was selected for the study. The fluorescence emission spectra were recorded in the
range of 430-700 nm.
Eligibility criteria: Gastrointestinal disease or clinical symptoms related to colorectal
cancer risk submitted to endoscopy. Exclusion criteria consisted of age younger than 18
years, history of psychiatric illness, and preoperative radiotherapy.
Outcome: investigated the possible role of the native fluorescence of blood plasma in the
management of colorectal cancer (CRC) and its feasibility as a new tumor marker. Sample of
blood was collected from asymptomatic blood donors and from CRC patients. The native
fluorescence of blood plasma was measured using a conventional spectrofluorimeter.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Screening
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