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Long-term Observational Study to Evaluate the DFS and OS of Adjuvant FOLFIRINOX Regimen in Pancreatic Cancer Patients

Long-term Observational Study to Evaluate the DFS and OS of Adjuvant FOLFIRINOX Regimen in Pancreatic Cancer Patients

Recruiting
19 years and older
All
Phase N/A

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Overview

This study is designed to evaluate the safety and efficacy of adjuvant FOLFIRINOX regimen in pancreatic cancer patients after curative surgery.

Description

This study is multi-center, prospective, long-term follow-up observational study.

Eligibility

Inclusion Criteria:

  • Age over 19 at the time of obtaining the informed consent form
  • Planning to FOLFIRINOX as adjuvant therapy after pancreatic cancer surgery
  • ECOG 0 or 1
  • Scheduled to RO or R1 resection
  • Organ function capable of chemotherapy

Exclusion Criteria:

  • FOLFIRINOX contraindications among the drug approval requirements
  • Palliative Therapy
  • Experienced toxic reactions or Hypersensitivity reactions of FOLFIRINOX

Study details
    Adjuvant Chemotherapy

NCT06389552

HK inno.N Corporation

16 May 2024

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