FOLFOX vs Gemcitabine in Patients With Metastatic Pancreatic Cancer Non-fit to FOLFIRINOX

Pancreatic Adenocarcinoma Clinical Trial

— GEMFOX  

Official title:

Randomized Phase 3 Trial Comparing FOLFOX to Gemcitabine in Metastatic First-line in Patients With Pancreatic Adenocarcinoma and Non-fit for FOLFIRINOX

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04167007
• Other study ID #: D20180177
• Secondary ID: 2019-001364-30
• Status: Recruiting
• Phase: Phase 3
• Start date: July 20, 2020
• Est. completion date: July 2025

Study information

• Verified date: August 2020
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Jean-Baptiste BACHET, MD, PhD
• Phone: 0142161041 / 0142161045
• Email: jean-basptiste.bachet[@]aphp.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Pancreatic adenocarcinoma (PAC) incidence increases regularly in Western countries and it is expected to become the second leading cause of cancer-related mortality in 2020. The prognosis of this disease remains very poor with an overall 5-year survival rate less than 5%.

The FOLFIRINOX regimen (5-fluorouracil [5-FU], folinic acid, irinotecan, and oxaliplatin) and the combination of nab-paclitaxel with gemcitabine demonstrated to be more effective than gemcitabine alone, and are both validated as standard first-line treatment options for metastatic PAC. However, the use of FOLFIRINOX is limited to patients with ECOG performance status (PS) 0-1 and aged less than 75 years. Nab-paclitaxel is currently not reimbursed in France.

Description:

This trial is an open label, multicenter, randomized phase III trial comparing gemcitabine vs FOLFOX in patients with metastatic pancreatic adenocarcinoma and non-fit for FOLFIRINOX. Adults fulfilling inclusion criteria and non-inclusion criteria will be randomized between a FOLFOX arm and a gemcitabine arm. The primary endpoint is the overall survival (OS) at 24 months. The secondary objectives are : objective response rate and disease control rate (RECIST v1.1, in case of evaluable lesion), duration of response, duration of disease control, progression free survival (PFS), the evolution of biomarkers Ca 19-9 and CEA under treatment, the toxicities according to International Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, the safety of both arms, the quality of life, the dose intensity (DI) of each protocol, the Quality-Adjusted Survival, and the rate and type of second-line / third-line regimens chemotherapy. With an expected median survival time in the control group of 5 months, an accrual period of 3 years and a minimum follow-up period of 2 years, a total of 199 patients per group are required to detect a hazard ratio of 0.75 based on a 5% two-sided type I error rate and a power of 80%, leading to a total number of 400 patients to include.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 400
• Est. completion date: July 2025
• Est. primary completion date: July 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Signed and dated informed consent, and willing and able to comply with protocol requirements,

2. Histologically or cytologically proven adenocarcinoma of the pancreas,

3. In absence of histologically or cytologically proven adenocarcinoma, a cluster of clinical, biological and radiological arguments consistent with the diagnosis: among these, a hypodense pancreatic tumor at CT and a Ca 19-9 greater than 500 UI/ml are essential prerequisites,

4. Metastatic disease confirmed (stage IV),

5. No prior therapy for metastatic disease (in case of previous adjuvant therapy, interval from end of chemotherapy and relapse must be >12 months),

6. Age =18 years ,

7. Patient non-fit for FOLFIRINOX,

8. For patients with ECOG performance status (PS ) =2, an albuminemia level >25 g/l is required,

9. Haematological status: neutrophils (ANC) >2x109/L; platelets >100x109/L; haemoglobin =9g/dL,

10. Adequate renal function: serum creatinine level <150µM, and estimated creatinine clearance >30ml/min,

11. Adequate liver function: AST (SGOT) and ALT (SGPT) =2.5xULN (=5xULN in case of liver metastases),

12. Total bilirubin =3 x ULN,

13. QT / QTc interval at baseline ECG (performed within 1 month before randomization) < than 450 msec for men and < than 470 msec for women,

14. Baseline evaluations performed before randomization: clinical and blood evaluations no more than 2 weeks (14 days) prior to randomization, tumor assessment (CT-scan or MRI, evaluation of non-measurable lesions) no more than 3 weeks (21 days) prior to randomization,

15. Female patients must be surgically sterile, or be postmenopausal, or must commit to using reliable and appropriate methods of contraception during the study and during at least six months after the end of study treatment (when applicable). All female patients with reproductive potential must have a negative pregnancy test (ß HCG) within 7 days prior to starting protocol treatment. Breastfeeding is not allowed.

16. Male patients must agree to use effective contraception in addition to having their partner use a contraceptive method as well during the trial and during at least six months after the end of the study treatment

17. Affiliation to a French social security system (recipient or assign).

Exclusion Criteria:

1. History or evidence upon physical examination of CNS metastasis unless adequately treated (e.g. non irradiated CNS metastasis, seizure not controlled with standard medical therapy),

2. Local or locally advanced disease (stage I to III),

3. Patient uses warfarin,

4. Patient receiving concomitant radiotherapy,

5. Electrolytic report uncontrolled: hypercalcemia and/or hypokalemia and/or hypomagnesemia,

6. Pre-existing permanent neuropathy (NCI grade =2 ),

7. Poor nutritional status

8. Known dihydropyrimidine dehydrogenase (DPD) total or partial deficiency (DPD activity dosage at inclusion visit),

9. Concomitant unplanned antitumor therapy (e.g. chemotherapy, molecular targeted therapy, immunotherapy),

10. Treatment with any other investigational medicinal product within 28 days prior to study entry,

11. Other serious and uncontrolled non-malignant disease (eg. active infection requiring systemic therapy, coronary stenting or myocardial infarction or stroke in the past 6 months),

12. Known or historical active infection with HIV, or known active infection untreated with hepatitis B or hepatitis C ,

13. Known uncontrolled bacterial infection

14. History or active interstitial lung disease (ILD),

15. Other concomitant or previous malignancy, except: i/ adequately treated in-situ carcinoma of the uterine cervix, ii/ basal or squamous cell carcinoma of the skin, iii/ cancer in complete remission for >5 years,

16. Patients with known allergy to active substance or any excipient of study drugs,

17. Allergy to iodinated contrast product

18. Concomitant administration of live, attenuated virus vaccine and concomitant administration of prophylactic phenytoin.

19. Patients under legal protection or unable to consent

20. Participation in another interventional research

Related Conditions & MeSH terms

• Adenocarcinoma
• Pancreatic Adenocarcinoma

Intervention

Drug:
• Gemcitabine
Gemcitabine at 1000 mg/m² as intravenous (IV) infusion over 30-40 minutes on days 1, 8, and 15, followed by 1 week of rest, every 28 days
• FOLFOX
Oxaliplatin at 85 mg/m² given as a 2 hours IV infusion on days 1 and 15; Folinic acid 400 mg/m² (racemic form) or 200 mg/m² (L-form) in 250 ml glucose 5% solution given as a 2 hours IV infusion on days 1 and 15; and 5-FU 2400 mg/m² administered as continuous 46-hour IV infusion on days 1-3 and 15-17, every 28 days.

Locations

Country	Name	City	State
France	APHP - Groupe Hospitalier Pitié-Salpêtrière	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival (OS) at 24 months	OS will be defined as the delay between the date of inclusion and the date of death (whatever the cause) or the date of last news if the patient is alive.	At 24 months after inclusion
Secondary	Objective response rate	RECIST criteria 1.1 in case of evaluable lesion	At 24 months after inclusion
Secondary	Disease control rate	RECIST criteria 1.1 in case of evaluable lesion	At 24 months after inclusion
Secondary	Duration of response	The time interval between the first occurrence of partial or complete response according to RECIST criteria and secondary progression (clinic or radiologic)	Tumor assessment will be done every 2 cycles (1cycle = 28 days), assessed up to 24 months after inclusion
Secondary	Duration of disease control	The time interval between the first occurrence of disease control (stabilization or partial response or complete response) according to RECIST criteria and secondary progression (clinic or radiologic)	Tumor assessment will be done every 2 cycles (1 cycle = 28 days), assessed up to 24 months after inclusion
Secondary	Progression Free Survival (PFS)	In most cases, patient will have a radiologic evaluation and radiologic progression will be defined according to RECIST criteria. In absence of radiologic evaluation (decision of investigator), clinic progression would be defined by investigators according to clinical deterioration of PS, increase of symptoms, and/or increase of tumor markers.	From inclusion to the date of first event (progression or death) or date of last news if the patient is alive without progression, assessed up to 60 months
Secondary	Carbohydrate antigen 19-9 (CA-19-9) and carcinoembryonic antigen (CEA) levels		At baseline (at selection or inclusion visit before starting treatment) and then each 2 cycles (every 8 weeks) until end of treatment, up to 24 months
Secondary	Toxicities: Type, frequency and severity of adverse events and serious adverse events	Toxicities will be described and grades according to International Common Terminology Criteria for Adverse Events (CTCAE) version 4.0	From inclusion to end of treatment, up to 24 months
Secondary	Safety: Rate of serious adverse events, grade 3-4 toxicities (hematologic and non-hematologic)	Rate of serious adverse events, grade 3-4 toxicities (hematologic and non-hematologic). Adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4.0.	From inclusion to end of treatment, up to 24 months
Secondary	inLongitudinal changes in Quality of life (EORTC QLQ C-30 questionnaire and a consensual geriatric minimum data set (SOFOG) for patients =75 years)	Quality of life will be studied by means of the EORTC QLQ C-30 questionnaire (30 questions, score from 30 to 126) and a consensual geriatric minimum data set (SOFOG: 7 questions, score from 0 to 24) for patients =75 years at inclusion and at each cycle. A 5-point deterioration in HRQoL scores will be considered as the minimal clinically important difference (MCID). Time until MCID will be analyzed (for each questionnaire) and compared between the two groups. The dynamic change under treatment will be compared at each cycle.	At inclusion, before starting treatment, and then Day 1 of each cycle (every 4 weeks, 1 cycle = 28 days) until end of treatment, up to 24 months
Secondary	Dose intensity of each protocol	The dose intensity (DI) of each protocol will be calculated based on the number of cycles received by each patient. The relative DI will be calculated as the ratio of the DI to the DI indicated in the protocol (obtained as the dose specified per cycle in mg/m²)	During the entire treatment period, up to 24 months
Secondary	Quality-adjust Time Without Symptoms of disease or Toxicities (Q-TWiST)	The Q-TWiST method combines treatment benefits and risks into a single measure by partitioning survival time into three health states and subsequently assigning quality-of life weights to the survival time in each state. The primary Q-TWiST analysis will be performed using the Intention-to-treat analysis(ITT) population, and will be supplemented with analyses in the per-protocol population (i.e., patients who received =80% of the protocol-defined treatment during the first 6 weeks of treatment) and analysed in pre-specified subgroups: age (<75 years, =75 years), baseline PS (0-1, 2), liver metastases (Yes, No), and tumour location (head, other).	During the entire treatment period, up to 24 months
Secondary	Rate of second and third line	For the patients who will stop the treatment of the protocol (for progression, toxicity or other reason...), we will register the date of beginning and of last administration of each new line of chemotherapy administered during the follow-up.	From end of study treatment to patient death, assessed up to 60 months.