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Resection in Pancreatic Cancer With Minimal Metastatic Disease or Venous Infiltration Trial at Technische Universität München (PaMeViTUM)

Primary Purpose

Pancreatic Cancer

Status
Terminated
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Resection of metastases
Resection of infiltrated veins
Sponsored by
Technical University of Munich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring Pancreatic cancer, metastasis, venous infiltration, Pancreatic cancer with minimal metastatic disease or venous infiltration

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • suspicion of cancer of the pancreas and an intraoperative histologically proven diagnosis of pancreatic adenocarcinoma.
  • intraoperative assessment of tumor as potentially locally resectable
  • COHORT 1: Minimal metastatic disease
  • COHORT 2: Venous infiltration
  • ability to sign the informed consent.
  • Karnofsky performance status > 70.
  • Life-expectancy of more than 3 months.
  • able to attend follow-up.
  • no previous or concurrent malignancy diagnoses, except non-melanoma skin cancer and in situ carcinoma of the cervix.
  • no serious medical, psychological, familial, sociological or geographical conditions potentially hampering compliance with the study protocol and follow-up.
  • patients older than 18 years.
  • no pregnant or lactating women.
  • preoperative evaluation by thin-sliced CT scans with:
  • No evidence of substantial extra-pancreatic disease, i.e. no evidence of malignant ascites, extended liver metastasis (>5 metastatic lesions), spread to other distant abdominal organs, peritoneal metastasis, spread to extra-abdominal organs.
  • No evidence of extension of the tumor into the celiac axis or superior mesenteric artery (T4 disease).
  • intraoperative findings with:
  • tumor assessed as potentially locally resectable.
  • no signs of peritoneal metastasis or tumor manifestations outside of the pancreas and the liver.
  • frozen section: adenocarcinoma

Exclusion Criteria:

  • extrapancreatic disease (except minimal metastatic disease of the liver, see above)
  • concomitant venous infiltration and minimal metastatic disease
  • extension of the tumor into the celiac axis or superior mesenteric artery
  • life expectancy of less than 3 months
  • previous or concurrent malignancy diagnosis, except non-melanoma skin cancer and in situ carcinoma of the cervix
  • conditions potentially hampering compliance (also inclusion criteria)

Sites / Locations

  • Department of Surgery and Institute of Statistics Klinikum rechts der Isar der Technischen Universität München Ismaningerstrasse 22 81675 München, Germany

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

COHORT 1 (minimal metastatic disease): Arm 1 (intervention): resection of the primary tumor, followed by resection of the liver metastasis/metastases Arm 2 (control): exploration and/or gastroenterostomy and/or hepaticojejunostomy/choledochojejunostomy

COHORT 2 (venous infiltration): Arm 1 (intervention): resection of the primary tumor with resection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) Arm 2 (control): resection of the primary tumor with dissection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) plus tumor masses adjacent to these veins; no venous resection

Outcomes

Primary Outcome Measures

Overall survival

Secondary Outcome Measures

Quality of life Perioperative morbidity and mortality 1-year survival and 2-year survival

Full Information

First Posted
March 3, 2009
Last Updated
September 5, 2012
Sponsor
Technical University of Munich
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1. Study Identification

Unique Protocol Identification Number
NCT00855634
Brief Title
Resection in Pancreatic Cancer With Minimal Metastatic Disease or Venous Infiltration Trial at Technische Universität München
Acronym
PaMeViTUM
Official Title
Extended Versus Standard Resection in Two Cohorts of Patients With Adenocarcinoma of the Pancreas: Minimal Metastatic Disease or Venous Infiltration - a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Terminated
Why Stopped
Protocol planned interim analysis after two years showed very low recruitment in cohort 1 and low recruitment in cohort 2.
Study Start Date
August 2009 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Technical University of Munich

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
PaMeViTUM is a mono-centric prospective randomized controlled trial that compares different operating procedures in patients with pancreatic cancer and minimal metastatic disease or venous infiltration.
Detailed Description
PaMeViTUM is a mono-centric prospective randomized controlled trial comparing different operating procedures in patients with pancreatic cancer and minimal metastatic disease or venous infiltration. Patients will be randomized intraoperatively after fulfilling all inclusion criteria (in particular: suspicion of cancer of the pancreas and an intraoperative histologically proven diagnosis of pancreatic adenocarcinoma; intraoperative assessment of tumor as potentially locally respectable). If no metastases and no infiltration of the portal vein are detected during the operation, the standard resection will be performed (for tumors of the pancreatic head: (pylorus-preserving) pancreaticoduodenectomy; for tumors of the pancreatic body/tail: distal (left) pancreatic resections; for tumors of the head and body/tail: total pancreatectomy). In the case of tumor infiltration of the pyloric region or the distal stomach, a classical pancreaticoduodenectomy will be performed. If the patient has pancreatic cancer with minimal metastatic disease (COHORT 1) and fulfills all inclusion criteria, she/he will be randomized into one of the following arms: Arm 1 (intervention): resection of the primary tumor, followed by resection of the liver metastasis/metastases Arm 2 (control): exploration and/or gastroenterostomy and/or hepaticojejunostomy/choledochojejunostomy If there are no liver metastases, following mobilization (and potentially also the dissection of the pancreas at the pancreatic head), the extension of the tumor towards the superior mesenteric/splenic/portal vein is examined. If there is venous infiltration (COHORT 2) and the patient fulfills the inclusion criteria, she/he will be randomized into one of the following arms: Arm 1 (intervention): resection of the primary tumor with resection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) Arm 2 (control): resection of the primary tumor with dissection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) plus tumor masses adjacent to these veins; no venous resection The aim of this study is to demonstrate that an extension of the resectability criteria in patients with pancreatic cancer and 1) minimal metastatic disease OR 2) venous infiltration improves overall survival. A secondary aim of the study is to prove that resection in these patient cohorts improves quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
Pancreatic cancer, metastasis, venous infiltration, Pancreatic cancer with minimal metastatic disease or venous infiltration

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
355 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
COHORT 1 (minimal metastatic disease): Arm 1 (intervention): resection of the primary tumor, followed by resection of the liver metastasis/metastases Arm 2 (control): exploration and/or gastroenterostomy and/or hepaticojejunostomy/choledochojejunostomy
Arm Title
2
Arm Type
Active Comparator
Arm Description
COHORT 2 (venous infiltration): Arm 1 (intervention): resection of the primary tumor with resection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) Arm 2 (control): resection of the primary tumor with dissection of the portal vein (and/or superior mesenteric vein/splenic vein (SMV/SV) plus tumor masses adjacent to these veins; no venous resection
Intervention Type
Procedure
Intervention Name(s)
Resection of metastases
Intervention Description
resection of the primary tumor, followed by resection of the liver metastasis/metastases
Intervention Type
Procedure
Intervention Name(s)
Resection of infiltrated veins
Intervention Description
resection of the primary tumor with resection of the portal vein (and/or superior mesenteric vein/splenic
Primary Outcome Measure Information:
Title
Overall survival
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Quality of life Perioperative morbidity and mortality 1-year survival and 2-year survival
Time Frame
Additional 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: suspicion of cancer of the pancreas and an intraoperative histologically proven diagnosis of pancreatic adenocarcinoma. intraoperative assessment of tumor as potentially locally resectable COHORT 1: Minimal metastatic disease COHORT 2: Venous infiltration ability to sign the informed consent. Karnofsky performance status > 70. Life-expectancy of more than 3 months. able to attend follow-up. no previous or concurrent malignancy diagnoses, except non-melanoma skin cancer and in situ carcinoma of the cervix. no serious medical, psychological, familial, sociological or geographical conditions potentially hampering compliance with the study protocol and follow-up. patients older than 18 years. no pregnant or lactating women. preoperative evaluation by thin-sliced CT scans with: No evidence of substantial extra-pancreatic disease, i.e. no evidence of malignant ascites, extended liver metastasis (>5 metastatic lesions), spread to other distant abdominal organs, peritoneal metastasis, spread to extra-abdominal organs. No evidence of extension of the tumor into the celiac axis or superior mesenteric artery (T4 disease). intraoperative findings with: tumor assessed as potentially locally resectable. no signs of peritoneal metastasis or tumor manifestations outside of the pancreas and the liver. frozen section: adenocarcinoma Exclusion Criteria: extrapancreatic disease (except minimal metastatic disease of the liver, see above) concomitant venous infiltration and minimal metastatic disease extension of the tumor into the celiac axis or superior mesenteric artery life expectancy of less than 3 months previous or concurrent malignancy diagnosis, except non-melanoma skin cancer and in situ carcinoma of the cervix conditions potentially hampering compliance (also inclusion criteria)
Facility Information:
Facility Name
Department of Surgery and Institute of Statistics Klinikum rechts der Isar der Technischen Universität München Ismaningerstrasse 22 81675 München, Germany
City
München
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
33102398
Citation
Argentiero A, Calabrese A, Sciacovelli AM, Delcuratolo S, Solimando AG, Brunetti O. Complete Response of Synchronous Liver Metastasis in a Pancreatic Ductal Adenocarcinoma, When Surgery Could Represent a Therapeutic Option. Can J Gastroenterol Hepatol. 2020 Oct 9;2020:8679751. doi: 10.1155/2020/8679751. eCollection 2020.
Results Reference
derived

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Resection in Pancreatic Cancer With Minimal Metastatic Disease or Venous Infiltration Trial at Technische Universität München

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