To hear about similar clinical trials, please enter your email below

Trial Title: Prognostic and Predictive Markers of Treatment Response in Patients With PAC.

NCT ID: NCT05776342

Condition: Pancreatic Adenocarcinoma

Conditions: Official terms:
Adenocarcinoma

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Other

Summary: The objective of this study is to identify prognosis and predictive markers of response to treatments (surgery, chemotherapy,...) in patients with pancreatic adenocarcinoma. The effectiveness and tolerance of these treatments in current practice is also evaluated.

Detailed description: The modest efficacy of current therapies for pancreatic cancer calls for the development of prognostic factors to guide patient selection and clinical decision-making based on tumor aggressiveness and risk of death. The aim of this study is to identify prognostic and predictive factors of response to treatments administered in pancreatic adenocarcinoma, based on a multicenter cohort established on a population derived from current clinical practice. By accurately stratifying patients according to their estimated survival, prognostic tools could aid therapeutic decisions and optimize patient selection in future clinical trials.

Criteria for eligibility:

Study pop:
Retro-prospective (diagnosis between 2003 and 2022) and prospective (diagnosis between 2023 and 2030) cohorts of patients with pancreatic adenocarcinoma

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Patient with histologically confirmed pancreatic adenocarcinoma. - Disease at a resectable, borderline, locally advanced, initially metastatic, or recurrent stage after surgery - Diagnosis between January 1, 2003, and December 31, 2030. - First-line treatment with chemotherapy and/or radiotherapy and/or clinical trials. - Age ≥ 18 years. - Written informed consent Exclusion Criteria: - Patient under guardianship, curatorship, or judicial protection. - Pregnant or breastfeeding women. - Any medical, psychological, or social situation that could prevent compliance with the protocol as assessed by the investigator. - Refusal to participate in the study

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: CHU Jean Minjoz

Address:
City: Besançon
Country: France

Status: Recruiting

Contact:
Last name: Angélique VIENOT, MD

Investigator:
Last name: Angélique VIENOT, MD
Email: Principal Investigator

Facility:
Name: Hôpital Beaujon

Address:
City: Clichy
Country: France

Status: Recruiting

Contact:
Last name: Louis DE MESTIER, MD

Facility:
Name: CHU - Henri Mondor

Address:
City: Créteil
Country: France

Status: Not yet recruiting

Contact:
Last name: Christophe TOURNIGAND, MD

Facility:
Name: CHU Lille

Address:
City: Lille
Country: France

Status: Recruiting

Contact:
Last name: Anthony TURPIN, MD

Facility:
Name: Centre Léon Bérard

Address:
City: Lyon
Country: France

Status: Not yet recruiting

Contact:
Last name: Pauline ROCHEFORT, MD

Facility:
Name: HRU Nancy Site Brabois

Address:
City: Nancy
Country: France

Status: Recruiting

Contact:
Last name: Marie MULLER, MD

Facility:
Name: Hôpital Georges Pompidou

Address:
City: Paris
Country: France

Status: Recruiting

Contact:
Last name: Jeanne NETTER, MD

Facility:
Name: Hôpital Saint Antoine

Address:
City: Paris
Country: France

Status: Recruiting

Contact:
Last name: Antoine DARDENNE

Facility:
Name: Institut Mutualiste Montsouris

Address:
City: Paris
Country: France

Status: Not yet recruiting

Contact:
Last name: David MALKA, MD

Facility:
Name: CHU Poitiers

Address:
City: Poitiers
Country: France

Status: Not yet recruiting

Contact:
Last name: David TOUGERON, MD

Investigator:
Last name: David TOUGERON, MD
Email: Principal Investigator

Facility:
Name: CHU Reims

Address:
City: Reims
Country: France

Status: Not yet recruiting

Contact:
Last name: Olivier BOUCHE, MD

Facility:
Name: CHU Pontchaillou

Address:
City: Rennes
Country: France

Status: Not yet recruiting

Contact:
Last name: Astrid LIEVRE, MD

Investigator:
Last name: Astrid LIEVRE, MD
Email: Principal Investigator

Facility:
Name: Institut Curie

Address:
City: Saint-Cloud
Country: France

Status: Not yet recruiting

Contact:
Last name: Cindy NEUZILLET, MD

Facility:
Name: IHU - Institut de chirurgie guidée par l'imagerie

Address:
City: Strasbourg
Country: France

Status: Not yet recruiting

Contact:
Last name: Julieta MONTANELLI, MD

Facility:
Name: Hôpital Paul Brousse

Address:
City: Villejuif
Country: France

Status: Recruiting

Contact:
Last name: Pascal HAMMEL, MD

Start date: January 1, 2003

Completion date: December 31, 2031

Lead sponsor:
Agency: GERCOR - Multidisciplinary Oncology Cooperative Group
Agency class: Other

Source: GERCOR - Multidisciplinary Oncology Cooperative Group

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05776342

Login to your account

Did you forget your password?