FOLFIRINOX for Unresectable Locally Advanced and Borderline Resectable Pancreatic Cancer

• Sponsor: UNC Lineberger Comprehensive Cancer Center (Other)
• Overall Status: Terminated
• CT.gov ID: NCT01688336
• Collaborator: (none)
• Enrollment: 9
• Location: 1
• Arm: 1
• Duration (Months): 58.7
• Patients Per Site Per Month: 0.2

Study Details

Study Description

Brief Summary

This single arm, multi-center phase II clinical trial will assess the safety and efficacy of FOLFIRINOX in the first-line setting in patients with unresectable locally advanced (ULA) and borderline resectable (BR) pancreatic cancer.

Condition or Disease	Intervention/Treatment	Phase
Pancreatic Cancer	Drug: FOLFIRINOX	Phase 2

Detailed Description

FOLFIRINOX regimen was recently presented at an international oncology meeting and represents a new standard in the treatment of metastatic pancreatic cancer for selected patients. With improved overall survival (OS) and response rates (RR) in the metastatic setting, we hypothesize that in patients with less tumor burden, this regimen will be safe and well tolerated, improve OS, progression free survival (PFS), and RR, and improve resectability rates, as compared to historical data from standard single agent gemcitabine therapy for unresectable locally advanced (ULA) patients and standard radiation with concurrent 5 fluorouracil (5FU) chemotherapy for borderline resectable (BR) patients. While both ULA and BR patients will be eligible for the present study, our primary objective concerns ULA patients, and we plan to enroll 45 patients in this group.

Patients meeting eligibility criteria will be consented and treated with FOLFIRINOX every 2 weeks (1 cycle = 4 weeks = 2 treatments). Patients will undergo repeat imaging (CT or MRI) every 2 cycles and reassessed for resectability of the tumor. All patients that are not able to undergo surgical resection, due to insufficient down-staging or patient preference, will continue on protocol-based therapy until disease progression, unacceptable toxicity, study withdrawal, or death.

Study Design

• Study Type: Interventional
• Actual Enrollment: 9 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Phase II Single Arm Clinical Trial of FOLFIRINOX for Unresectable Locally Advanced and Borderline Resectable Pancreatic Cancer
• Study Start Date: Jan 1, 2012
• Actual Primary Completion Date: Aug 22, 2016
• Actual Study Completion Date: Nov 22, 2016

Arms and Interventions

Arm

Intervention/Treatment

Experimental: FOLFIRINOX FOLFIRINOX given to all subjects

Drug: FOLFIRINOX; FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours; Other Names: FOLFIRINOX is a chemotherapy regimen comprised of the following drugs, given in combination -Oxaliplatin -Leucovorin -Irinotecan -5FU

Outcome Measures

Primary Outcome Measures

1. Median Overall Survival (OS) of FOLFIRINOX in Patients With Unresectable Locally Advanced (ULA) Pancreatic Cancer [Up to 3 years]

   All patients who receive at least Day 1 of FOLFIRINOX treatment will be evaluable and followed up for up to 3 years for the primary outcome of overall survival (OS).

Secondary Outcome Measures

1. Overall Survival for Borderline Resectable Patients [Up to 3 years]

   All patients who receive at least Day 1 of FOLFIRINOX treatment will be evaluable and followed up for up to 3 years for the outcome of overall survival (OS)

2. Progression Free Survival (PFS) [the date of first documented progression or date of death from any cause, whichever came first, assessed up to 3 years]

   Progression free survival will be measured from D1 of treatment until evidence of tumor progression (including clinical deterioration related to the underlying pancreatic cancer, as assessed by the investigator) or death from any cause. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Patients that are lost to follow-up will be censored

3. Objective Response Rate [Up to 3 years]

   All patients who have received at least one cycle of treatment will be evaluated. Disease will be evaluated per Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1) for target lesions and assessed by CT and/or MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions. Patients who drop out of the study prior to disease evaluation will not be evaluable for response unless the patient undergoes radiologic evaluation or their disease progresses clinically.

4. Disease Control Rate (DCR) [Up to 3 years]

   Disease control rate will be measured by the percentage of patients with responses (CR) and partial responses (PR) and stable disease (SD), per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI and/or CT: Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Stable Disease (SD), neither sufficient shrinkage to qualify for a Partial Response nor sufficient increase to qualify for Progression of Disease (POD); Complete Response (CR), Disappearance of all target lesions.

5. Rate of Resectability (RR) [Up to 3 years]

   Rate of resectability will be evaluated by determining the percentage of patients who were initially deemed to have ULA or borderline resectable (BR) disease and, following any period of treatment, were subsequently deemed to have resectable disease and undergo surgical resection. The denominator will reflect all patients with ULA or BR disease.

Other Outcome Measures

1. Correlation of Tumor Markers (Ca19-9, CEA) With Outcomes (RR, DCR, PFS, and OS). [Up to 3 years]

   Tumor markers (Ca19-9, CEA) will be measured at baseline, every eight weeks and at end of treatment, and will be correlated with outcomes resectability response (RR),disease control rate (DCR), progression free survival (PFS) and overall survival (OS).

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Biopsy confirmed adenocarcinoma of the pancreas.

• Measurable or non-measurable but evaluable (as determined by Response Evaluation Criteria in Solid Tumors version 1.1 [RECIST 1.1]) unresectable locally advanced (ULA) or borderline resectable (BR) disease that is not amenable to curative intent therapy. Baseline CT abdomen and chest (or MRI abdomen) within 28 days prior to initiation of FOLFIRINOX is required.

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

• No prior chemotherapy or chemoradiotherapy for pancreatic cancer.

• Age ≥ 18 years of age.

• Laboratory requirements at study entry:

• Hemoglobin ≥ 10 g/dL (transfusions are acceptable)

• absolute neutrophil count (ANC) ≥ 1.5 x 109/L

• Platelets ≥ 100 x 109/L

• Creatinine ≤ 1.5 x upper limit of normal (ULN), or creatinine clearance ≥ 50 mL/min (estimated by Cockcroft-Gault or measured)

• Total bilirubin ≤ 1.5 x ULN

• aspartate aminotransferase/Alanine Aminotransferase (AST/ALT) ≤ 3 x ULN

• Gamma-Glutamyl Transferase (GGT) ≤ 5 x ULN

• Life expectancy of at least 6 months.

• Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test performed within 14 days prior to initiation of FOLFIRINOX.

• WOCBP and men must agree to use adequate contraception prior to study entry, for the duration of study participation, and 8 weeks after the end of treatment.

• Before patient registration, written informed consent must be given.

Exclusion Criteria:

• Local recurrence or resectable recurrence of pancreatic cancer.

• Other malignancies within the past 3 years except for adequately treated cervical or vulvar carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis & T1). Any cancer curatively treated >3 years prior to entry is permitted.

• Hypersensitivity to 5FU, oxaliplatin or other platinum agent, or irinotecan or to their excipients. Known dihydropyrimidine dehydrogenase (DPD) enzyme deficiency.

• Participation in any investigational drug study within 4 weeks preceding the start of study treatment. Patients are not permitted to participate in another investigational drug study while being treated on this protocol.

• Cardiac disease: Congestive heart failure symptoms > class II New York Heart Association (NYHA). Unstable angina (anginal symptoms at rest) or new onset angina beginning within the last 3 months. Myocardial infarction within the past 6 months. Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.

• History of or suspected Gilbert's Disease (baseline testing not required).

• Baseline peripheral neuropathy/paresthesia grade ≥ 1.

• Active hepatitis B, unless patient has been on stable meds for at least 2 months (baseline testing not required).

• Active clinically serious infections (> grade 2).

• Any other hemorrhage/bleeding event > CTCAE Grade 3 within the 12 weeks prior to the first dose FOLFIRINOX.

• Evidence or history of bleeding diathesis or coagulopathy. Note: If therapeutic anticoagulation required, the investigator is encouraged to switch patient to (or maintain on) low molecular weight heparin during the trial.

• Major surgery, open biopsy or significant traumatic injury within 8 weeks of first study drug. A core pancreatic or liver biopsy does not preclude the patient from the study.

• Unable or unwilling to discontinue use of ketoconazole or St John's wort. Use of CYP3A4 enzyme-inducing drugs and strong CYP3A4 inhibitors is discouraged, but not contraindicated.

• Active drug or alcohol abuse.

• Pregnant or lactating women.

• Psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Lineberger Comprehensive Cancer Center	Chapel Hill	North Carolina	United States	27599

Sponsors and Collaborators

• UNC Lineberger Comprehensive Cancer Center

Investigators

• Principal Investigator: Autumn J McRee, MD, University of North Carolina

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• UNC Lineberger Comprehensive Cancer Center homepage
• National Cancer Institute (NCI) homepage

Publications

None provided.

• Responsible Party: UNC Lineberger Comprehensive Cancer Center
• ClinicalTrials.gov Identifier: NCT01688336
• Other Study ID Numbers: LCCC 1105
• First Posted: Sep 19, 2012
• Last Update Posted: Oct 6, 2017
• Last Verified: Sep 1, 2017

• Keywords provided by UNC Lineberger Comprehensive Cancer Center: Pancreatic; Phase II; FOLFIRINOX; Unresectable; Regimen; First-line; Resectable; Borderline; Oxaliplatin; Leucovorin; Irinotecan; 5FU; Lineberger; University of North Carolina
• Additional relevant MeSH terms: Pancreatic Neoplasms; Leucovorin; Oxaliplatin; Irinotecan; Folfirinox

Study Results

Participant Flow

Recruitment Details	11 patients were consented. One patient was consented but not treated due to metastatic disease and one patient was consented and not treated due to disease progression prior to protocol therapy. 9 patients went on study.

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) Fluorouracil (5FU) (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Period Title: Overall Study
STARTED	9
COMPLETED	9
NOT COMPLETED	0

Baseline Characteristics

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Overall Participants	9
Age (years) [Mean (Full Range) ]
Mean (Full Range) [years]	63.2
Sex: Female, Male (Count of Participants)
Female	6 66.7%
Male	3 33.3%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino	1 11.1%
Not Hispanic or Latino	7 77.8%
Unknown or Not Reported	1 11.1%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native	0 0%
Asian	0 0%
Native Hawaiian or Other Pacific Islander	0 0%
Black or African American	4 44.4%
White	5 55.6%
More than one race	0 0%
Unknown or Not Reported	0 0%
Region of Enrollment (Count of Participants)
United States	9 100%

Outcome Measures

1. Primary Outcome

Title	Median Overall Survival (OS) of FOLFIRINOX in Patients With Unresectable Locally Advanced (ULA) Pancreatic Cancer
Description	All patients who receive at least Day 1 of FOLFIRINOX treatment will be evaluable and followed up for up to 3 years for the primary outcome of overall survival (OS).
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

Patients with unresectable locally advanced pancreatic cancer.

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	5
Median (95% Confidence Interval) [months]	28.5

2. Secondary Outcome

Title	Overall Survival for Borderline Resectable Patients
Description	All patients who receive at least Day 1 of FOLFIRINOX treatment will be evaluable and followed up for up to 3 years for the outcome of overall survival (OS)
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	4
Median (95% Confidence Interval) [Months]	9.0

3. Secondary Outcome

Title	Progression Free Survival (PFS)
Description	Progression free survival will be measured from D1 of treatment until evidence of tumor progression (including clinical deterioration related to the underlying pancreatic cancer, as assessed by the investigator) or death from any cause. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Patients that are lost to follow-up will be censored
Time Frame	the date of first documented progression or date of death from any cause, whichever came first, assessed up to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	9
Median (95% Confidence Interval) [Months]	10.7

4. Secondary Outcome

Title	Objective Response Rate
Description	All patients who have received at least one cycle of treatment will be evaluated. Disease will be evaluated per Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1) for target lesions and assessed by CT and/or MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions. Patients who drop out of the study prior to disease evaluation will not be evaluable for response unless the patient undergoes radiologic evaluation or their disease progresses clinically.
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	9
Number (95% Confidence Interval) [percentage of patients]	11

5. Secondary Outcome

Title	Disease Control Rate (DCR)
Description	Disease control rate will be measured by the percentage of patients with responses (CR) and partial responses (PR) and stable disease (SD), per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI and/or CT: Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Stable Disease (SD), neither sufficient shrinkage to qualify for a Partial Response nor sufficient increase to qualify for Progression of Disease (POD); Complete Response (CR), Disappearance of all target lesions.
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	9
Number (95% Confidence Interval) [percentage of patients]	89

6. Secondary Outcome

Title	Rate of Resectability (RR)
Description	Rate of resectability will be evaluated by determining the percentage of patients who were initially deemed to have ULA or borderline resectable (BR) disease and, following any period of treatment, were subsequently deemed to have resectable disease and undergo surgical resection. The denominator will reflect all patients with ULA or BR disease.
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	9
Number (95% Confidence Interval) [percentage of patients]	22

7. Other Pre-specified Outcome

Title	Correlation of Tumor Markers (Ca19-9, CEA) With Outcomes (RR, DCR, PFS, and OS).
Description	Tumor markers (Ca19-9, CEA) will be measured at baseline, every eight weeks and at end of treatment, and will be correlated with outcomes resectability response (RR),disease control rate (DCR), progression free survival (PFS) and overall survival (OS).
Time Frame	Up to 3 years

Outcome Measure Data

Analysis Population Description

Data were not collected

Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) Fluorouracil (5FU) (400mg/m2)bolus then 2400 mg/m2 over 46 hours
Measure Participants	0

Adverse Events

Time Frame	24 weeks
Arm/Group Title	FOLFIRINOX
Arm/Group Description	FOLFIRINOX given to all subjects FOLFIRINOX: FOLFIRINOX will be given intravenously on Days 1, 15, and 28 of each 28 day cycle. Drugs are given in combination in this order: Oxaliplatin (85 mg/m2) Leucovorin (400mg/ m2) Irinotecan (180 mg/m2) 5FU (400mg/m2)bolus then 2400 mg/m2 over 46 hours
All Cause Mortality
	FOLFIRINOX
	Affected / at Risk (%)	# Events
Total	7/9 (77.8%)
Serious Adverse Events
	FOLFIRINOX
	Affected / at Risk (%)	# Events
Total	2/9 (22.2%)
General disorders
Death	1/9 (11.1%)
Infections and infestations
Urinary Tract Infection	1/9 (11.1%)
Renal and urinary disorders
Renal Calculi	1/9 (11.1%)
Other (Not Including Serious) Adverse Events
	FOLFIRINOX
	Affected / at Risk (%)	# Events
Total	9/9 (100%)
Blood and lymphatic system disorders
Anemia	7/9 (77.8%)
Gastrointestinal disorders
Abdominal Pain	3/9 (33.3%)
Anorexia	1/9 (11.1%)
Diarrhea	4/9 (44.4%)
Mucositis Oral	2/9 (22.2%)
Nausea	4/9 (44.4%)
Vomiting	1/9 (11.1%)
General disorders
Chills	1/9 (11.1%)
Edema Limbs	1/9 (11.1%)
Fatigue	4/9 (44.4%)
Fever	1/9 (11.1%)
Infections and infestations
Vaginal Infection	1/9 (11.1%)
Investigations
Alanine Aminotransferase Increased	3/9 (33.3%)
Alkaline Phosphatase Increased	6/9 (66.7%)
Aspartate Aminotransferase Increased	3/9 (33.3%)
Blood Bilirubin Increased	1/9 (11.1%)
Creatinine Increased	2/9 (22.2%)
Ggt Increased	5/9 (55.6%)
Lipase Increased	1/9 (11.1%)
Lymphocyte Count Decreased	2/9 (22.2%)
Neutrophil Count Decreased	8/9 (88.9%)
Platelet Count Decreased	6/9 (66.7%)
White Blood Cell Decreased	5/9 (55.6%)
Metabolism and nutrition disorders
Hyperglycemia	1/9 (11.1%)
Hypermagnesemia	1/9 (11.1%)
Hypertriglyceridemia	5/9 (55.6%)
Hyperuricemia	4/9 (44.4%)
Hypoalbuminemia	6/9 (66.7%)
Hypocalcemia	4/9 (44.4%)
Hypokalemia	5/9 (55.6%)
Hypomagnesemia	3/9 (33.3%)
Hypophosphatemia	1/9 (11.1%)
Nervous system disorders
Dysgeusia	1/9 (11.1%)
Peripheral Sensory Neuropathy	4/9 (44.4%)
Syncope	1/9 (11.1%)
Psychiatric disorders
Insomnia	1/9 (11.1%)
Renal and urinary disorders
Proteinuria	1/9 (11.1%)
Respiratory, thoracic and mediastinal disorders
Postnasal Drip	1/9 (11.1%)
Skin and subcutaneous tissue disorders
Rash Maculo-Papular	1/9 (11.1%)
Vascular disorders
Hypertension	2/9 (22.2%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.