Carcinoma, Pancreatic Ductal Clinical Trial
Official title:
A Clinical Validation Study on the Efficacy of MicroRNA-25 Level Detection in Assisting the Diagnosis of Pancreatic Cancer
Pancreatic cancer represents the most lethal of the common malignancies, with a 5-year survival rate of less than 5%. For patients who, when are diagnosed of pancreatic cancer, are eligible for potentially curative resection, the mortality and morbidity rates after surgery can improve significantly, but who accounts for no more than 20% of all pancreatic patients. It is therefore an effective way to improve the treatment efficacy for pancreatic cancer by discovering novel detection methods for pancreatic cancer, especially at early stages. MicroRNAs have been proved in recent years as functional disease markers, and circulating microRNA-25 is reported of high pancreatic cancer specificity and can be used as a novel marker for pancreatic cancer. A detection kit "MicroRNA (microRNA-25) Qualitative Detection Kit (Fluorescent PCR Method)" is produced and proven to be effective in assisting the diagnosis of pancreatic cancer through clinical trials held independently in three state-level hospitals in China. To further validate the efficacy of the kit, the researchers in this study intend to compare the sensibility and specificity of microRNA-25 level detection and other diagnosis methods, including detection of conventional tumor markers (CA19-9, CA125, CA50, CEA) and imaging (CT, MRI, PET/CT), both in separation and combined, in the diagnosis of pancreatic cancer.
Pancreatic cancer (mainly pancreatic ductal adenocarcinoma, PDAC) is a disease with extremely
poor prognosis, and is often fatal. Surgical resection is the only potentially curative
technique for management of PDAC, but only approximately 15% to 20% of patients are
candidates for pancreatectomy at the time of diagnosis. For these patients, however, the
mortality and morbidity rates after surgery can improve significantly. It is therefore an
effective way to improve the treatment efficacy for pancreatic cancer by discovering novel
detection methods for pancreatic cancer, especially at early stages.
MicroRNAs are a type of non-encoding single-stranded small RNAs with a length of ~22nt. They
can regulate the expression of their target mRNAs by inhibiting their translation into
proteins. MicroRNAs participate in all physiological and pathological activities, and their
abnormal expression profiles are proven to be closely related to the occurrence and
development of diseases, including cancer. Recent studies have further proved that not only
tissue/cell-line based microRNAs, but circulating microRNAs can be stably detected, and their
expression profiles can function as novel markers to be used in the diagnosis and prognosis
of diseases.
Pancreatic cancer specific microRNA profiles have also been reported, amongst which
microRNA-25 is found to be significantly upregulated in pancreatic cancer patients. There are
also studies try to improve the efficacy of pancreatic cancer diagnosis by combining
detection of microRNA and CA19-9. Further are there studies proving microRNA-25 as a highly
potential marker for pancreatic cancer. A detection kit "MicroRNA (microRNA-25) Qualitative
Detection Kit (Fluorescent PCR Method)" is produced and proven to be effective in assisting
the diagnosis of pancreatic cancer through clinical trials held independently in three
state-level hospitals in China.
To further validate the efficacy of the kit, the researchers in this study intend to compare
the sensibility and specificity of microRNA-25 level detection and other diagnosis methods,
including detection of conventional tumor markers (CA19-9, CA125, CA50, CEA) and imaging (CT,
MRI, PET/CT), both in separation and combined, with Cohort One in the diagnosis of pancreatic
cancer at early stages, to validate the efficacy of microRNA-25 detection in the
differentiation of pancreatic cancer and other related diseases, to investigate the relation
between microRNA-25 level and pancreatic staging. Patients in Group One will receive a
microRNA-25 level detection at the time of diagnosis, along with conventional tumor marker
detection and imaging tests, and then be confirmed by pathological study. And, to investigate
the efficacy of microRNA-25 level detection in the curative efficacy evaluation and relapse
monitoring, patients of Group Two (selected from Group One) will receive a microRNA-25 level
detection within one month after surgery and before starting adjuvant therapy, followed by a
microRNA-25 level detection every three months along with normal follow-up tests, until
relapse is observed with imaging tests.
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