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PREOPANC-4 Implementation Program for Locally Advanced Pancreatic Cancer

Nationwide Implementation Program for Optimal Multidisciplinary Management and Resection of Locally Advanced Pancreatic Cancer (PREOPANC-4)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05524090
Acronym
PREOPANC-4
Enrollment
223
Registered
2022-09-01
Start date
2021-07-01
Completion date
2030-12-31
Last updated
2022-09-01

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

Conditions

Chemotherapy Effect, Locally Advanced Pancreatic Adenocarcinoma, Pancreatic Adenocarcinoma Non-resectable, Pancreatic Cancer

Keywords

Nationwide implementation International Best-Practice, The Netherlands, International Best-Practice, Patient Selection, Patient-centered

Brief summary

A prospective, nationwide, implementation program of the international standard of excellence for locally advanced pancreatic cancer (LAPC) care in the Netherlands (2021\[7\]-2030\[6\]), including a multidisciplinary training program by the four leading international expert centers. The PREOPANC-4 project aims a safe and patient-centered implementation of the international standards of excellence for LAPC (surgery) in the Netherlands.

Detailed description

Rationale: Non-metastasized locally advanced pancreatic cancer (LAPC) is diagnosed in 35% of all pancreatic cancer patients and is traditionally treated with palliative care. Recently, the multidisciplinary management of LAPC has evolved by the introduction of modern multi-agent induction chemotherapies, leading to an increased resection rate and improved outlook for five-year survival. In contrast, five-year survival after chemotherapy without surgery is virtually non-existent. In the Netherlands, the LAPC resection rate after induction chemotherapy remains low with 8% versus 25% in international centers of excellence, leading to missed opportunities for five-year survival in a selected subgroup of LAPC patients. Explanations for this large difference include the spectrum of chemotherapy use, interpretation of diagnostics, patient selection, and surgical techniques. Objective: A safe and patient-centered implementation of the international standards of excellence for LAPC (surgery) in the Netherlands. Study design: A prospective, nationwide, implementation program of the international standard of excellence for LAPC care in the Netherlands (2021\[7\]-2030\[6\]), including a multidisciplinary training program by the four leading international expert centers (i.e. University of Heidelberg, University of Colorado, NYU Langone, and MD Anderson Cancer Center). Subsequently, the three Dutch centers with the highest surgical volume and documented experience in LAPC surgery will implement this highly complex LAPC surgery in close collaboration with the other Dutch Pancreatic Cancer Group (DPCG) centers. Patients who meet the inclusion criteria will be discussed within an online (inter)national expert panel to properly select patient for surgery. In addition, the other DPCG centers can present their LAPC patients to this panel for advice about (surgical) treatment options and if these patients should be referred to the three high-volume DPCG centers for surgery. Outcomes will be compared with a historical Dutch LAPC cohort, using propensity score matching. Study population: Adult patients with pathology confirmed non-metastasized LAPC and non-progressive disease after at least four months of (modified) FOLFIRINOX or gemcitabine-nab-paclitaxel induction chemotherapy and fit for major surgery. Study aim: The primary study aim is to double the LAPC resection rate in the Netherlands from 8% to 16% with adequate survival and morbidity targets. Primary targets: 1. Survival: After resection, mOS of 25 months, 1-year survival \>90%, and 5-year survival \>20%. These outcomes will be compared to the Dutch cohort of patients (2015-2020) with RECIST non-progressive LAPC after induction chemotherapy who did not undergo surgical exploration; 2. In-hospital morbidity and mortality: in-hospital/30-day mortality ≤5% and in-hospital major morbidity of \<50% after resection, which will be compared with a recent Dutch cohort (2015-2020) of resected patients with borderline resectable and locally advanced pancreatic cancer after induction/neoadjuvant therapy. Secondary targets: 1. Non-inferior radical resection (R0) rate as compared to a recent Dutch cohort (2015-2020) of resected patients with borderline resectable and locally advanced pancreatic cancer after induction/neoadjuvant therapy; 2. Non-inferior quality of life, mental and physical health status, and potential side effects on the long-term follow-up, compared to a control cohort of Dutch LAPC patients; 3. Non-inferior patients' healthcare satisfaction, compared to the Dutch historical cohort of pancreatic cancer patients.

Interventions

OTHERImplementation - International best-practice care

The PREOPANC-4 project aims to safely implement the international standard of excellence for LAPC management and surgery using a multidisciplinary best-practice training program, based on the experiences of four leading international expert centers (i.e. NYU Langone Health, University of Colorado, Heidelberg University, and MD Anderson Cancer Center). We hypothesize that the PREOPANC-4 implementation project will result in the improvement in multidisciplinary patient management and selection in line with current international best-practice.

Sponsors

UMC Utrecht
CollaboratorOTHER
Erasmus Medical Center
CollaboratorOTHER
Leiden University Medical Center
CollaboratorOTHER
University Medical Center Groningen
CollaboratorOTHER
Radboud University Medical Center
CollaboratorOTHER
Maastricht University Medical Center
CollaboratorOTHER
Medisch Spectrum Twente
CollaboratorOTHER
Isala
CollaboratorOTHER
Frisius Medisch Centrum
CollaboratorOTHER
Onze Lieve Vrouwe Gasthuis
CollaboratorOTHER
Amphia ziekenhuis
CollaboratorUNKNOWN
Jeroen Bosch Ziekenhuis
CollaboratorOTHER
Catharina Ziekenhuis Eindhoven
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
Heidelberg University
CollaboratorOTHER
M.D. Anderson Cancer Center
CollaboratorOTHER
NYU Langone Health
CollaboratorOTHER
Dutch Cancer Society
CollaboratorOTHER
Maag Lever Darm Stichting
CollaboratorOTHER
Deltaplan Alvleesklierkanker
CollaboratorUNKNOWN
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age 18 years or older * Pathology-confirmed (LAPC)\* * CT-based non-progressive disease (RECIST criteria) after at least 4 months of systemic chemotherapy (\[m\]FOLFIRINOX / gemcitabine-nab-paclitaxel).

Exclusion criteria

* Metastatic pancreatic cancer prior to induction chemotherapy. * According to the Dutch Pancreatic Cancer Group (DPCG) definition: \>90 degrees arterial tumor involvement (i.e. superior mesenteric artery, celiac axis, and/or hepatic artery) and/or portovenous involvement of either \>270 degrees or occlusion.

Design outcomes

Primary

MeasureTime frameDescription
Resection rateImmediately after completing the inclusion period (December 31, 2024).Resection rate of the pancreatic tumor
Overall survival (OS)After completing the follow-up period (December 31, 2029)OS from time of resection (mOS, 1-year OS & 5-year OS)
In-hospital mortalityYearly assessment throughout the inclusion periodMortality after resection (during primary hospitalization)
In-hospital major morbidityYearly assessment throughout the inclusion periodClavien-Dindo grade IIIa or higher major morbidity after resection (during primary hospitalization)

Secondary

MeasureTime frameDescription
Quality of lifeMeasured at 3, 6, 9, 12, 18, and 24 months from diagnosis, followed by yearly measurements.EORTC QLQ-C30: global health status Outcome measures will be calculated, according to the validated questionnaire manuals.
Shared decision-making: patients' healthcare satisfactionMeasured at 3, 6, 9, 12, 18, and 24 months from diagnosis, followed by yearly measurements.APECC decision-making self-efficacy scale. Outcome measures will be calculated, according to the validated questionnaire manuals.
R0 resection rateImmediately after completing the inclusion period (December 31, 2024).R0 (microscopic radical resection \>1mm) versus R1 (microscopic residual tumor ≤1mm). NB. For the anterior margin, only direct ingrowth is considered as R1.

Countries

Netherlands

Contacts

Primary ContactThomas F Stoop, MD
t.f.stoop@amsterdamUMC.nl+316 547 555 11
Backup ContactMarc G Besselink, MD, MSc, PhD
m.g.besselink@amsterdamUMC.nl+316 16 15 83 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026