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Perioperative Chemotherapy With Bevacizumab for Colorectal Carcinomatosis

Primary Purpose

Colorectal Neoplasms

Status
Active
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
perioperative chemotherapy plus bevacizumab
cytoreductive surgery
Intraperitoneal Oxaliplatin
Sponsored by
University Hospital, Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Neoplasms focused on measuring cytoreductive surgery, hipec, perioperative chemotherapy, peritoneal carcinomatosis, bevacizumab, colorectal surgery

Eligibility Criteria

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

Inclusion Criteria:

  • biopsy proven adenocarcinoma of the colon or rectum and synchronous or metachronous peritoneal carcinomatosis.
  • absence of systemic disease, with the exception of small, superficial liver metastases, requiring only minor surgery.
  • resectable disease at staging, during laparoscopic evaluation and during exploration for cytoreductive surgery and intraperitoneal chemotherapy.
  • complete macroscopic cytoreduction at the time of surgery (CC-0/1)
  • good general health status (Karnofsky index > 70%)
  • expected life expectancy more than 6 months
  • no other malignancy than disease under study
  • serum creatinine < 1.5 mg/dl or a calculated GFR ≥ 60 mL/min/1.73 m
  • serum total bilirubin < 1.5 mg/dl
  • platelet count > 100,000/ml
  • hemoglobin > 9g/dl
  • neutrophil granulocytes > 1,500/ml
  • International Normalized Ration (INR) 2 or < 2
  • Absence of alcohol and/or drug abuse
  • No inclusion in other clinical trials interfering with the study protocol
  • No concurrent chronic systemic immune therapy, chemotherapy, or hormone therapy not indicated in the study protocol
  • Absence of heart failure (NYHA 2 or > 2) or significant coronary artery disease
  • No pregnancy or breast feeding
  • Adequate contraception in fertile patients

Exclusion Criteria:

  • No written informed consent
  • tumour in the presence of obstruction
  • evidence of extra-abdominal disease or extensive liver metastasis
  • peritoneal cancer index > 25
  • active bacterial, viral or fungal infection
  • active gastro-duodenal ulcer
  • parenchymal liver disease (any stage cirrhosis)
  • uncontrolled diabetes mellitus
  • severe obstructive or restrictive respiratory insufficiency
  • psychiatric pathology capable of affecting comprehension and judgment faculty
  • Known allergy to oxaliplatin

Sites / Locations

  • Ghent University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

bevacizumab and CRS with oxaliplatin

Arm Description

Perioperative chemotherapy plus bevacizumab and CRS with oxaliplatin

Outcomes

Primary Outcome Measures

surgical morbidity and mortality
This will be estimated with the Dindo-Clavien classification

Secondary Outcome Measures

progression free survival
time interval between date of surgery and disease progression or death
overall survival
calculated from date of surgery until death
treatment completion rate
percentage of patients receiving all planned courses
chemotherapy-related toxicity
percentage of patients experiencing chemotherapy-related toxicity will be assessed using the Common Terminology Criteria for Adverse Events (NCI-CTCAE) scoring system
pathological gross response of peritoneal tumour deposits to neoadjuvant combination chemotherapy with bevacizumab
will be scored with a 3 level regression scale

Full Information

First Posted
March 9, 2015
Last Updated
December 12, 2022
Sponsor
University Hospital, Ghent
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1. Study Identification

Unique Protocol Identification Number
NCT02399410
Brief Title
Perioperative Chemotherapy With Bevacizumab for Colorectal Carcinomatosis
Official Title
BEV-IP: Perioperative Chemotherapy With Bevacizumab in Patients Undergoing Cytoreduction and Intraperitoneal Chemoperfusion for Colorectal Carcinomatosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 2015 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Bev-IP trial is designed to assess the feasibility and efficacy of a combined treatment consisting of perioperative combination chemotherapy with the vascular endothelial growth factor A inhibitor bevacizumab and cytoreductive surgery with intraperitoneal oxaliplatin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms
Keywords
cytoreductive surgery, hipec, perioperative chemotherapy, peritoneal carcinomatosis, bevacizumab, colorectal surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
bevacizumab and CRS with oxaliplatin
Arm Type
Experimental
Arm Description
Perioperative chemotherapy plus bevacizumab and CRS with oxaliplatin
Intervention Type
Drug
Intervention Name(s)
perioperative chemotherapy plus bevacizumab
Intervention Description
preoperative and postoperative combination chemotherapy with bevacizumab
Intervention Type
Procedure
Intervention Name(s)
cytoreductive surgery
Intervention Description
complete or nearly complete removal of synchronous or metachronous peritoneal carcinomatosis from CRC.
Intervention Type
Drug
Intervention Name(s)
Intraperitoneal Oxaliplatin
Intervention Description
Pump-driven intraperitoneal administration of oxaliplatin
Primary Outcome Measure Information:
Title
surgical morbidity and mortality
Description
This will be estimated with the Dindo-Clavien classification
Time Frame
until 3 months after surgery and intraperitoneal chemotherapy
Secondary Outcome Measure Information:
Title
progression free survival
Description
time interval between date of surgery and disease progression or death
Time Frame
24 months after finishing the adjuvant chemotherapy
Title
overall survival
Description
calculated from date of surgery until death
Time Frame
24 months after finishing the adjuvant chemotherapy
Title
treatment completion rate
Description
percentage of patients receiving all planned courses
Time Frame
day 1 after termination of adjuvant chemotherapy
Title
chemotherapy-related toxicity
Description
percentage of patients experiencing chemotherapy-related toxicity will be assessed using the Common Terminology Criteria for Adverse Events (NCI-CTCAE) scoring system
Time Frame
1 month after termination of the adjuvant chemotherapy
Title
pathological gross response of peritoneal tumour deposits to neoadjuvant combination chemotherapy with bevacizumab
Description
will be scored with a 3 level regression scale
Time Frame
day 1 after termination of the cytoreductive surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: biopsy proven adenocarcinoma of the colon or rectum and synchronous or metachronous peritoneal carcinomatosis. absence of systemic disease, with the exception of small, superficial liver metastases, requiring only minor surgery. resectable disease at staging, during laparoscopic evaluation and during exploration for cytoreductive surgery and intraperitoneal chemotherapy. complete macroscopic cytoreduction at the time of surgery (CC-0/1) good general health status (Karnofsky index > 70%) expected life expectancy more than 6 months no other malignancy than disease under study serum creatinine < 1.5 mg/dl or a calculated GFR ≥ 60 mL/min/1.73 m serum total bilirubin < 1.5 mg/dl platelet count > 100,000/ml hemoglobin > 9g/dl neutrophil granulocytes > 1,500/ml International Normalized Ration (INR) 2 or < 2 Absence of alcohol and/or drug abuse No inclusion in other clinical trials interfering with the study protocol No concurrent chronic systemic immune therapy, chemotherapy, or hormone therapy not indicated in the study protocol Absence of heart failure (NYHA 2 or > 2) or significant coronary artery disease No pregnancy or breast feeding Adequate contraception in fertile patients Exclusion Criteria: No written informed consent tumour in the presence of obstruction evidence of extra-abdominal disease or extensive liver metastasis peritoneal cancer index > 25 active bacterial, viral or fungal infection active gastro-duodenal ulcer parenchymal liver disease (any stage cirrhosis) uncontrolled diabetes mellitus severe obstructive or restrictive respiratory insufficiency psychiatric pathology capable of affecting comprehension and judgment faculty Known allergy to oxaliplatin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wim P Ceelen, MD,PhD
Organizational Affiliation
University Hospital, Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ghent University Hospital
City
Gent
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

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Perioperative Chemotherapy With Bevacizumab for Colorectal Carcinomatosis

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