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PANCREATIC CANCER: DYNAMIC ASSESSMENT AT ALL STAGES OF TREATMENT

I

Institut Paoli-Calmettes

Status

Not yet enrolling

Conditions

Pancreatic Cancer Non-resectable

Treatments

Other: collection of blood and tumor samples

Study type

Interventional

Funder types

Other

Identifiers

NCT05802485
PANDORE-PANC-IPC 2021-082

Details and patient eligibility

About

The study consists of a 25 ml blood sample collection:

  • Before the start of treatment
  • Approximately 2 months after the start of induction chemotherapy
  • At the end of induction chemotherapy
  • Prior to local treatment (radiotherapy, surgery)
  • At the time of tumor progression

Collection of tumor material:

  • During the initial diagnostic biopsy
  • On the operating room in case of surgery
  • At tumor biopsy in case of recurrence or progression (optional) As well as the completion of a questionnaire at inclusion.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Non-metastatic pancreatic adenocarcinoma that is not immediately resectable (borderline and locally advanced tumors according to the NCCN 2020 classification)
  • No previous treatment with surgery or chemotherapy
  • Age > 18 years
  • General condition WHO 0-2 (patient whose general condition can allow medical treatment or surgery)
  • Therapeutic management at the Paoli-Calmettes Institute
  • Signature of the informed consent specific to the PANDORE-PANC study
  • Patient affiliated to a social security system or benefiting from such a system

Exclusion criteria

  • Metastatic disease
  • Pancreatic tumor of a histological type other than adenocarcinoma
  • Other tumor under treatment or for which treatments have been completed for < 1 year
  • Pregnant or breastfeeding women
  • Person in an emergency situation
  • Person of legal age under legal protection (guardianship, curatorship or safeguard of justice) or unable to give consent.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

300 participants in 1 patient group

collection of blood and tumor samples
Other group
Treatment:
Other: collection of blood and tumor samples

Trial contacts and locations

0

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Central trial contact

Dominique GENRE, MD

Data sourced from clinicaltrials.gov

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