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Circulating Tumor DNA as a Prognostic Marker in Patients With Pancreatic Cancer

J

Ji Kon Ryu

Status

Unknown

Conditions

Pancreatic Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT03214991
1704-108-847

Details and patient eligibility

About

The aim of this study is to determine the usefulness of circulating tumor DNA as a prognostic factor in patients with pancreatic cancer.

Full description

There is currently no strong prognostic factor in pancreatic cancer. K-ras is the most commonly mutated gene in pancreatic cancer, with a mutation rate of 75% to 95%. These high mutation rates are expected to be useful for diagnosis and prognostic factors in future. Currently, K-ras mutation tests are often performed in tissues, and there are various limitations, in particular, limited obtaining of sufficient tissues. In this regard, analyzing the prognosis of pancreatic cancer through non-invasive blood testing has significant advantages. And Prognosis analysis through blood tests can be done through blood circulating tumor DNA. The relationship between prognosis and blood circulating tumor DNA has already been studied in other cancers such as colorectal cancer, and there have been several studies in pancreatic cancer. However, there are not many research results yet, and there are cases in which the results differ from study to study. Therefore, the purpose of this study is to compare the overall survival of patients with pancreatic cancer diagnosed by EUS-FNA according to the presence and amount of blood circulating tumor DNA with K-ras mutation.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with pancreatic cancer through EUS-FNA.

Exclusion criteria

  • Severe mental illness
  • Severe co-morbidity (ESRD, Advanced COPD, severe Heart failure, poorly controlled blood sugar)
  • Pregnancy
  • Patients who have received chemotherapy
  • Coagulopathy

Trial contacts and locations

1

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Central trial contact

Ji Kon Ryu, MD, PhD; Young Hoon Choi, MD

Data sourced from clinicaltrials.gov

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