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Surgical Resection of Synchronous Pulmonary or Hepatic Oligometastatic Pancreatic Ductal Adenocarcinoma (PHOLIPANC) Following Pre-operative Liposomal Irinotecan Combined With Oxaliplatin and 5-Fluoracil/Folinic Acid (NALIRIFOX): A Phase II Open-Label Single Arm Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a clinical trial that tests a surgical treatment. Everyone in the study will get the same treatment, and there is no comparison or placebo group. Patients can join the study if they have pancreatic cancer that has spread to only a few spots in the liver or lungs. They must be receiving a type of chemotherapy called NALIRIFOX before surgery (this is called neoadjuvant chemotherapy). If the cancer gets worse during or after the first 4 cycles of chemotherapy, the patient will be removed from the study. If the cancer stays the same or gets smaller after the first 4 cycles, doctors will check if the main tumor can be removed with surgery. If the tumor cannot be removed, the patient will get 4 more cycles of chemotherapy as standard of care. If the main tumor can be removed, the patient will have surgery 2-6 weeks after finishing chemotherapy. During surgery, doctors will try to remove both the main tumor and the small tumors in the liver or lungs. If, during surgery, the doctor finds that the main tumor actually cannot be removed, the patient may receive 4 more cycles of chemotherapy starting 2-4 weeks after surgery.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Histologically confirmed diagnosis of treatment-naïve limited hepatic or pulmonary metastatic adenocarcinoma of the pancreas

• Meet the definition of limited hepatic or pulmonary metastasis according to Computed Tomography/Magnetic Resonance Imaging (CT/MRI) that is done prior to the starting of any anticancer treatment. Either CT scan of chest, abdomen, and pelvis with intravenous contrast or a combination of MRI of abdomen and pelvis and CT scan of chest is acceptable radiographic imaging. CT/MRI can be done at an outside facility but must be reviewed by a local radiologist.

‣ Definition of limited hepatic metastasis: 1 to 5 metastases in CT/MRI, which are potentially resectable or treatable by ablative procedures.

• Note 1: Patients also fulfil this inclusion criterion if a hepatic metastasis was partly or entirely removed as part of the diagnosis and is thus not detectable by CT/MRI scan at screening.

∙ Note 2: If more than 5 metastases are unexpectedly detected during surgery, it is not a violation of this inclusion criterion if the excess metastases had not been detectable by CT/MRI scan at screening.

⁃ Definition of limited pulmonary metastasis: 1 to 4 pulmonary nodules seen on CT/MRI, suspicious for pulmonary metastases as per the multidisciplinary tumor board radiologist and surgeon.

• Eastern Cooperative Oncology Group (ECOG) performance status 0-1

• Patients ≥18 years at the time of signing the informed consent

• Being a candidate for chemotherapy with NALIRIFOX

• Patient's written informed consent prior to any trial-specific procedure

• Patient's legal capacity to consent to participation in the clinical trial.

Locations
United States
Texas
The University of Texas Health Science Center San Antonio
RECRUITING
San Antonio
Contact Information
Primary
Lei Zheng, MD, PhD
zhengl@uthscsa.edu
(210) 450-1406
Time Frame
Start Date: 2026-03-02
Estimated Completion Date: 2028-12
Participants
Target number of participants: 40
Treatments
Active_comparator: Lung Oligometastatic Cohort
Participants who have pulmonary oligometastatic pancreatic tumor
Active_comparator: Liver Oligometastatic Cohort
Participants who have hepatic oligometastatic pancreatic tumor
Sponsors
Collaborators: Ipsen
Leads: The University of Texas Health Science Center at San Antonio

This content was sourced from clinicaltrials.gov

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