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

Prognostic and Predictive Markers of Treatment Response in Patients With Pancreatic Adenocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05776342
Acronym
CANOPE
Enrollment
4050
Registered
2023-03-20
Start date
2003-01-01
Completion date
2031-12-31
Last updated
2025-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Adenocarcinoma

Brief 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.

Interventions

None listed

Sponsors

GERCOR - Multidisciplinary Oncology Cooperative Group
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Overall Survival (OS) rateUp to 7 years from the date of initial cancer diagnosis (or until death if it occurs before 17 years)Defined as the time interval between the start date of treatment (surgery, first cycle of L1 chemotherapy, or first radiotherapy session) and the date of death regardless of the cause. Living or lost to follow-up patients will be censored at the date of the last news

Secondary

MeasureTime frameDescription
Number of patient with objective response rateUp to 7 yearsEvaluation according to RECIST v1.1, Choi or iRECIST criteria. Study the population followed for pancreatic adenocarcinoma according to tumor stages (localized, borderline, locally advanced, metastatic or recurrent after surgery) and according to treatments.
Number of patient with stability rateUp to 7 yearsEvaluation according to RECIST v1.1, Choi or iRECIST criteria. Study the population followed for pancreatic adenocarcinoma according to tumor stages (localized, borderline, locally advanced, metastatic or recurrent after surgery) and according to treatments.
Number of patient with tumor progressionUp to 7 yearsEvaluation according to RECIST v1.1, Choi or iRECIST criteria. Study the population followed for pancreatic adenocarcinoma according to tumor stages (localized, borderline, locally advanced, metastatic or recurrent after surgery) and according to treatments.
Progression-free survival (PFS) rateUp to 7 yearsDefined as the time interval between the start date of treatment (surgery, first cycle of L1 chemotherapy, or first radiotherapy session) and the date of first progression or date of death regardless of the cause. Living patients without progression or lost to follow-up will be censored at the date of the last news
Number of patients who received maintenance treatment in the first-lineUp to 7 yearsStudy the profiles of patients receiving maintenance treatment in 1st-line chemotherapy
Number of patients who received second and third-line treatmentsUp to 7 yearsStudy the profiles of patients receiving 2nd and 3rd lines of chemotherapy
Number of patient with grade 3/4 treatment-related toxicitiesUp to 7 yearsToxicity rates according to CTCAE v5.0 classification. Study the population followed for pancreatic adenocarcinoma according to tumor stages (localized, borderline, locally advanced, metastatic or recurrent after surgery) and according to treatments.

Countries

France

Contacts

Primary ContactAngelique VIENOT, MD
regulatory.Affairs@gercor.com.fr01402985 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026