Actively Recruiting

Phase 2
Age: 18Years - 80Years
All Genders
NCT06249321

mFOLFIRINOX Plus Radiotherapy to Patients With CA19-9-normal Advanced Pancreatic Cancer Refractory to Chemotherapy

Led by Fudan University · Updated on 2025-08-07

30

Participants Needed

1

Research Sites

204 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the efficacy of mFOLFIRINOX plus radiotherapy to Patients with CA19-9-normal Advanced Pancreatic Cancer refractory to chemotherapy.

CONDITIONS

Official Title

mFOLFIRINOX Plus Radiotherapy to Patients With CA19-9-normal Advanced Pancreatic Cancer Refractory to Chemotherapy

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to understand and willing to sign informed consent
  • Age 18 to 80 years
  • ECOG performance status between 0 and 2
  • Confirmed advanced pancreatic adenocarcinoma by tissue or cell analysis
  • Refractory to at least one chemotherapy treatment and no prior radiotherapy
  • Locally advanced or metastatic pancreatic cancer
  • Baseline serum CA19-9 ≤ 37 U/mL, CEA ≤ 5.2 ng/mL, and CA125 ≤ 35 U/mL
  • At least one measurable tumor lesion per RECIST criteria
  • Expected survival of 3 months or longer
  • Adequate organ function based on blood tests
  • Women of childbearing potential and men agree to use contraception during study
Not Eligible

You will not qualify if you...

  • Pregnant or nursing women
  • Primary pancreatic cancer
  • Baseline serum CA19-9 > 37 U/mL, CEA > 5.2 ng/mL, or CA125 > 35 U/mL
  • Non-adenocarcinoma pancreatic cancer confirmed by pathology
  • Digestive tract inflammation such as pancreatitis, cholecystitis, or cholangitis
  • Severe uncontrollable diseases affecting study compliance or results
  • Renal insufficiency or dialysis
  • Serious illnesses that could affect treatment safety
  • Allergy to oxaliplatin or other chemotherapy drugs
  • Unwillingness or inability to follow study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Cancer Center

Shanghai, Shanghai Municipality, China, 200032

Actively Recruiting

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Research Team

Y

Ying Yang, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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