Evaluation of GEMCITEST in Patients With Pancreatic Cancer and Treated by Chemotherapy

Pancreatic Cancer Clinical Trial

— GEMCIPANC  

Official title:

Evaluation of GEMCITEST in Patients With Pancreatic Cancer and Treated by Chemotherapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03599154
• Other study ID #: GEMCIPANC
• Status: Completed
• Start date: January 30, 2018
• Est. completion date: November 25, 2020

Study information

• Verified date: May 2021
• Source: Centre Georges Francois Leclerc
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Pancreatic cancer has a 5-year overall survival rate around 5%. It is the 6th most common cancer in France (11 600 new annual cases in 2012) and the 4th leading cause of cancer deaths in France and Europe.

Many translational research has tried to identify biomarkers in pancreatic cancer. Only the expression of hENT1 evaluated on the tumor tissue with the mouse antibody seems really relevant by providing a predictive value of the effectiveness of gemcitabine adjuvant. In a metastatic situation, there is no predictive marker of the effectiveness of chemotherapy treatments.

GemciTest(TM), studied in this study, is developed by the company Acobiom. Test based on the qRT-PCR technology that allows the establishment of a molecular signature of 10 genes that showed its interest as a biomarker in 60 patients with metastatic pancreatic adenocarcinoma treated with gemcitabine. Retrospective analysis differentiated 2 patient populations:

• 22 patients with a "favorable" expression gene with a median survival of 14.9 months

• 35 patients with an "adverse" expression gene with a median survival of 5.1 months

Primary objective: To evaluate in patients with pancreatic cancer, treated with Gemcitabine alone or combined (nab-paclitaxel) or with Folfirinox, the prognostic value of the GemciTest(TM) test on overall survival and response to treatment.

To realize this study, only one 2.5 mL blood sample is taken before starting chemotherapy. The standard practice data is then saved.

100 patients will be included.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: November 25, 2020
• Est. primary completion date: November 25, 2020
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Cytologically or histologically confirmed pancreatic cancer

2. Patient seeking first-line chemotherapy for pancreatic cancer

3. Age> 18 years

4. Presence of at least 1 measurable tumor lesion according to RECIST 1.1 criteria

5. Performance index = 2

6. Patient able and willing to comply with the study procedures according to the protocol

7. Patient able to understand, sign and date informed consent

8. Affiliation to a social security scheme.

Exclusion Criteria:

1. Contraindication to chemotherapy

2. Anti-tumor therapy, experimental or not, recent in the last 4 weeks before the inclusion of the patient

3. Active infection requiring antibiotics within 14 days before inclusion

4. Patients unable to understand, read and / or sign informed consent

5. Persons benefiting from a protection system for adults (including tutorship and guardianship)

6. Pregnant or lactating women

Related Conditions & MeSH terms

• Pancreatic Cancer
• Pancreatic Neoplasms

Locations

Country	Name	City	State
France	Centre Georges François Leclerc	Dijon

Sponsors (1)

Lead Sponsor	Collaborator
Centre Georges Francois Leclerc

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival	Overall survival is defined as survival between Day 1 of the first line of chemotherapy and death	average of 1 year