A Phase 2 Trial of Neoadjuvant Modified FOLFIRINOX Chemotherapy for Resectable Pancreatic Adenocarcinoma

NCT ID: NCT05066802

Last Updated: 2021-10-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-05-11
• Study Completion Date: 2023-05-31

Brief Summary

Within the next decade, pancreatic ductal adenocarcinoma (PDAC) is expected to rise to the second leading cause of cancer-related mortality. To increase the survival, various peri-operative treatments have been tested, and adjuvant FOLFIRINOX or gemcitabine plus capecitabine is now standard of care after surgical resection for localized PDAC. Even with superior survival among various disease extent of PDAC, resectable PDAC still shows poor outcomes with surgery followed by adjuvant chemotherapy. This phase II study is investigating the role of modified-FOLFIRINOX as neoadjuvant treatment for resectable PDAC.

Detailed Description

This phase II study is designed to evaluate the efficacy and safety of modified FOLFIRINOX as neoadjuvant treatment for resectable pancreatic cancer.

Conditions

Resectable Pancreatic Adenocarcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

modified FOLFIRINOX

oxaliplatin 85 mg/m2 D1 + leucovorin 400mg/m2 D1 + irinotecan 150 mg/m2 D1 + 5-FU 2,000 mg/m2 42\~46h continuous infusion, every other week for 6 cycles (12 weeks).

Group Type: EXPERIMENTAL

neoadjuvant modified FOLFIRINOX

Intervention Type: DRUG

oxaliplatin 85 mg/m2 D1 + leucovorin 400mg/m2 D1 + irinotecan 150 mg/m2 D1 + 5-FU 2,000 mg/m2 42\~46h continuous infusion, every other week for 6 cycles (12 weeks) before surgery.

Interventions

neoadjuvant modified FOLFIRINOX

oxaliplatin 85 mg/m2 D1 + leucovorin 400mg/m2 D1 + irinotecan 150 mg/m2 D1 + 5-FU 2,000 mg/m2 42\~46h continuous infusion, every other week for 6 cycles (12 weeks) before surgery.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients with pancreatic ductal adenocarcinoma confirmed by histological or cytopathological examination

2. Pancreatic adenocarcinoma patients evaluated as resectable according to the following criteria in imaging tests including CT or MRI (NCCN guideline criteria, if all of the following criteria are satisfied) A. No tumor contact with the major arterial structures of the Celiac axis [CA], superior mesenteric artery [SMA], and common hepatic artery [CHA].

B. When there is no contact between the tumor and the major vein of the superior mesenteric vein (SMV) or portal vein (PV), or within 180° even if there is contact, and there is no venous atypicality.

3. Patients who have not undergone surgical resection and systemic chemotherapy for pancreatic cancer.

4. Patients whose ECOG activity ability index is 0 to 1

5. Patients who are willing and able to provide written informed consent for this study.

6. Patients over the age of 19 at the time of signing the subject consent form.

7. Patients with evaluable lesions according to RECIST 1.1.

8. Patients with adequate organ function.

Exclusion Criteria

1. Histologic diagnosis other than pancreatic ductal adenocarcinoma (eg, neuroendocrine tumor, etc.)

2. Patients with distant metastases including central nervous system (CNS) metastases or peritoneal metastases

3. Patients with moderate acute or chronic medical conditions or abnormal findings on examination, which are judged to affect the results of this study

4. Patients who have participated in a study in which investigational drugs are used and are currently receiving investigational drugs or used investigational drugs or medical devices within 4 weeks prior to the first administration of this investigational drug.

5. Those who received chemotherapy, targeted small molecule agents, or radiotherapy within 2 weeks prior to Day 1 of the study, or who have not yet recovered (Grade 1 or lower or baseline level) from adverse reactions due to previously administered drugs patient.

6. Patients with known aggravation within the past 3 years or other malignant tumors requiring active treatment.

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Yonsei University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Choong-kun Lee

Role: PRINCIPAL_INVESTIGATOR

Division of Medical Oncology, Yonsei Cancer Center, Yonsei Univ. College of Medicine, Korea

Locations

Division of Medical Oncology, Yonsei Cancer Center, Yonsei Univ. College of Medicine, Korea

Seoul, , South Korea

Site Status: RECRUITING

Countries

South Korea

Central Contacts

Choong-kun Lee

Role: CONTACT

cklee512@yuhs.ac

+82-2-2228-8133

Facility Contacts

Choong-kun Lee

Role: primary

cklee512@yuhs.ac

+82-2-2228-8133

Other Identifiers

4-2019-0485

Identifier Type: -

Identifier Source: org_study_id