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SCar-biopsies After Malignant Colorectal Polypectomy of Uncertain RAdicality (SCAPURA)

Primary Purpose

Colorectal Cancer

Status
Terminated
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Flexible sigmoidoscopy or colonoscopy
Sponsored by
Dr. Frank ter Borg MD PhD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colorectal Cancer focused on measuring Endoscopic resection, Pathology, Rescue surgery

Eligibility Criteria

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

Inclusion Criteria:

  • Aged 18 or above.
  • Endoscopically removed colorectal lesion with the following pathological characteristics:

    • A moderately-to-well differentiated adenocarcinoma.
    • If possible to judge: distance between adenocarcinoma and vertical or lateral resection margin is less than 1 mm.
    • In case of piecemeal resection: unjudgeable radicality (mostly due to loss of orientation and multiple fragments).
    • Absence of / unjudgeable lymphatic / vascular invasion.
    • No or only grade I tumor budding.
  • No suspicion of dissemination on the following investigations: serum carcino-embryonic antigen, a computer tomographic (CT) scan of the abdomen and a chest X-ray; in case of a rectal tumor (less than 15 cm from the anal verge): an additional magnetic resonance imaging of the rectum.
  • Operation is advised in agreement with the Dutch Guideline on Colorectal cancer, planned and agreed on by the patient.
  • Written informed consent is obtained.

Exclusion Criteria:

  • Pathology shows one or more of the following characteristics:

    • A radical en-bloc resection with a free vertical and lateral margin of ≧ 1 mm.
    • A poorly differentiated or signet-cell containing adenocarcinoma.
    • Lymphatic or vascular invasion (if this feature is unjudgeable due to piecemeal resection, no exclusion is done).
    • Tumor budding grade II-III.
  • Suspicion of dissemination on investigations as mentioned in the inclusion criteria.
  • Patients already receiving anti-tumor treatment for another tumor or a synchronic colorectal cancer.
  • Patients in whom a second-look endoscopy would require major and unacceptable effort and / or resources, for instance clinical admission for bowel preparation, long travel, general anesthesia, extremely difficult to reach polypectomy site. Such at the decision of the patient and / or treating physician.
  • Patient is planned for trans-anal surgery.
  • Patient is not planned for surgery.
  • Patient is pregnant.
  • Patient does not provide written informed consent or is unable to provide such.

Sites / Locations

  • Nij Smellinghe Hospital
  • Antonius Hospital Sneek-Emmeloord
  • Medical Center de Veluwe
  • Gelre Hospitals
  • Hospital Gelderse Vallei
  • Radboud University Medical Center
  • Canisius Wilhelmina Hospital
  • Maastricht University Medical Center
  • Maasstad Hospital Pantein
  • Amphia Hospital
  • Catharina Hospital
  • Bernhoven
  • The Netherlands Cancer Institute Antoni van Leeuwenhoekhuis
  • Medical Center Slotervaart
  • Onze Lieve Vrouwe Gasthuis (Oost & West)
  • Academical Medical Center, Gastroenterology department
  • Spaarne Gasthuis
  • Deventer Hospital
  • Ziekenhuis Groep Twente
  • Isala Clinics
  • Meander Medical Center
  • Sint Antonius Hospital
  • IJsselland Hospital
  • Haga Hospital
  • Albert Schweitzer Hospital
  • Rivas Zorggroep
  • Groene Hart Hospital
  • Alrijne Hospital
  • Erasmus Medical Center, Gastroenterology department
  • Franciscus Gasthuis
  • Maasstad Hospital
  • Ikazia Hospital
  • Vlietland Hospital
  • University Medical Center Groningen
  • Martini Hospital
  • University Medical Center Utrecht, Gastroenterology department

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Flexible sigmoidoscopy or colonoscopy

Arm Description

Subjects will undergo these investigation to take biopsies from the polypectomy scar.

Outcomes

Primary Outcome Measures

Sensitivity of biopsies for residual cancer
The number of patients with endoscopic biopsies containing adenocarcinoma divided by the number of patients with adenocarcinoma in the resected specimen.

Secondary Outcome Measures

90-day mortality after rescue surgery
The number of patients that died within 91 day after the operation for presumed residual adenocarcinoma.
The sensitivity of biopsies for residual cancer in the bowel wall
The number of patients with endoscopic biopsies containing adenocarcinoma divided by the number of patients with adenocarcinoma in the resected bowel wall (regardless of regional lymph nodes)
The number of complications (defined according to GCP) after biopsies from the polypectomy scar
The number of patients with bleeding or perforation after taking biopsies from the polypectomy scar, requiring at least prolongation of treatment, or admission to hospital, or delay or speeding up of surgery.
The sensitivity of global endoscopic assessment of polypectomy site for residual cancer at initial and follow-up endoscopy (to take scar biopsies)
The number of patients in whom the endoscopic resection initially and/or at follow-up endoscopic was assessed as incomplete and who also have residual cancer in the surgically resected specimen divided by the total number of patients in whom the endoscopic resection was judged to be incomplete.
The proportion of patients with residual cancer in the resected specimen if malignancy was unsuspected during the endoscopic polypectomy
The number of patients in whom the malignancy was initially unsuspected during endoscopic polypectomy and who also have residual cancer in the surgical specimen divided by the total number of patients in whom the malignancy was initially unsuspected during endoscopic polypectomy.

Full Information

First Posted
December 15, 2014
Last Updated
December 13, 2019
Sponsor
Dr. Frank ter Borg MD PhD
Collaborators
Erasmus Medical Center, The Netherlands Cancer Institute, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), UMC Utrecht
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1. Study Identification

Unique Protocol Identification Number
NCT02328664
Brief Title
SCar-biopsies After Malignant Colorectal Polypectomy of Uncertain RAdicality
Acronym
SCAPURA
Official Title
The Sensitivity of Scar-biopsies for Residual Colorectal Adenocarcinoma After Endoscopic Resection With Uncertain Radicality
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Terminated
Why Stopped
Interim analysis showed no added value of second look endoscopy
Study Start Date
August 2015 (Actual)
Primary Completion Date
May 2019 (Actual)
Study Completion Date
May 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dr. Frank ter Borg MD PhD
Collaborators
Erasmus Medical Center, The Netherlands Cancer Institute, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), UMC Utrecht

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
After endoscopic removal of a colorectal polyp that harbors (unexpected) adenocarcinoma, pathology usually can not guarantee a radical resection from an oncological point of view. In such case, additional surgical resection is advised. However, only in 15% of patients, residual adenocarcinoma is found. This study investigates the sensitivity of biopsies from the polypectomy scar for residual adenocarcinoma.
Detailed Description
Rationale: colorectal polyps may harbor adenocarcinoma. Numbers are increasing due to the nationwide colorectal screening program. After endoscopic removal, rescue surgery is often performed because radicality can not be guaranteed by the pathologist. However, in 85% of surgical specimen no residual malignancy is found. Given morbidity and mortality associated with surgery a method to diagnose residual cancer is needed. Biopsies from the polypectomy site are variably used to reduce the likelihood of residual tumor at the polypectomy site under these circumstances. However, the sensitivity of such biopsies is unknown. Objective: to evaluate the sensitivity of second-look endoscopic biopsies from the polypectomy site for residual tumor. Study design: prospective cross-sectional design using a multi-center approach. Study population: patients planned for rescue surgery for the sole reason of (potentially) irradical endoscopic resection of a colorectal adenocarcinoma without poor differentiation, lymphovascular invasion or tumor budding and without other signs of dissemination. Intervention: endoscopic biopsies from the polypectomy site before operation. Main study parameters/endpoints: sensitivity of second-look biopsies from the polypectomy site for residual tumor in the resected bowel and postoperative mortality. Various other factors will be assessed that might be associated with residual cancer. Nature and extent of the burden and risks associated with participation and benefit: Depending on the situation: a): In case a tattoo needs to be done of the polypectomy site, a second endoscopy is done anyway and taking biopsies (painless) will be of no extra burden; b): In case no tattoo needs to be done a sigmoidoscopy (lesion distal to the splenic flexure) or colonoscopy (proximal to the splenic flexure) needs to be arranged for the purpose of this study. A sigmoidoscopy takes 10-20 minutes. Preparation consists of two enemas. A colonoscopy takes 20-30 minutes. Preparation consists of drinking 3 litre of MoviPrep®, both usually doe at home. Notice that the patient has recent experience with colonoscopy. If necessary, both investigations can be arranged under conscious sedation (the rule in colonoscopy), which also implies day-care admission. The risk of complications of a second endoscopy is estimated < 1:5000. The benefit of a 2nd colonoscopy is the discovery of new polyps in 10-25% of cases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Endoscopic resection, Pathology, Rescue surgery

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
246 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Flexible sigmoidoscopy or colonoscopy
Arm Type
Other
Arm Description
Subjects will undergo these investigation to take biopsies from the polypectomy scar.
Intervention Type
Procedure
Intervention Name(s)
Flexible sigmoidoscopy or colonoscopy
Intervention Description
Depending on the localization of the scar of the malignant polyp, either a flexible sigmoidoscopy or colonoscopy will be done to take biopsies from the polypectomy scar.
Primary Outcome Measure Information:
Title
Sensitivity of biopsies for residual cancer
Description
The number of patients with endoscopic biopsies containing adenocarcinoma divided by the number of patients with adenocarcinoma in the resected specimen.
Time Frame
up to 1 year
Secondary Outcome Measure Information:
Title
90-day mortality after rescue surgery
Description
The number of patients that died within 91 day after the operation for presumed residual adenocarcinoma.
Time Frame
91 days from surgery
Title
The sensitivity of biopsies for residual cancer in the bowel wall
Description
The number of patients with endoscopic biopsies containing adenocarcinoma divided by the number of patients with adenocarcinoma in the resected bowel wall (regardless of regional lymph nodes)
Time Frame
up to 1 year
Title
The number of complications (defined according to GCP) after biopsies from the polypectomy scar
Description
The number of patients with bleeding or perforation after taking biopsies from the polypectomy scar, requiring at least prolongation of treatment, or admission to hospital, or delay or speeding up of surgery.
Time Frame
up to 30 days
Title
The sensitivity of global endoscopic assessment of polypectomy site for residual cancer at initial and follow-up endoscopy (to take scar biopsies)
Description
The number of patients in whom the endoscopic resection initially and/or at follow-up endoscopic was assessed as incomplete and who also have residual cancer in the surgically resected specimen divided by the total number of patients in whom the endoscopic resection was judged to be incomplete.
Time Frame
up to 1 year
Title
The proportion of patients with residual cancer in the resected specimen if malignancy was unsuspected during the endoscopic polypectomy
Description
The number of patients in whom the malignancy was initially unsuspected during endoscopic polypectomy and who also have residual cancer in the surgical specimen divided by the total number of patients in whom the malignancy was initially unsuspected during endoscopic polypectomy.
Time Frame
up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 or above. Endoscopically removed colorectal lesion with the following pathological characteristics: A moderately-to-well differentiated adenocarcinoma. If possible to judge: distance between adenocarcinoma and vertical or lateral resection margin is less than 1 mm. In case of piecemeal resection: unjudgeable radicality (mostly due to loss of orientation and multiple fragments). Absence of / unjudgeable lymphatic / vascular invasion. No or only grade I tumor budding. No suspicion of dissemination on the following investigations: serum carcino-embryonic antigen, a computer tomographic (CT) scan of the abdomen and a chest X-ray; in case of a rectal tumor (less than 15 cm from the anal verge): an additional magnetic resonance imaging of the rectum. Operation is advised in agreement with the Dutch Guideline on Colorectal cancer, planned and agreed on by the patient. Written informed consent is obtained. Exclusion Criteria: Pathology shows one or more of the following characteristics: A radical en-bloc resection with a free vertical and lateral margin of ≧ 1 mm. A poorly differentiated or signet-cell containing adenocarcinoma. Lymphatic or vascular invasion (if this feature is unjudgeable due to piecemeal resection, no exclusion is done). Tumor budding grade II-III. Suspicion of dissemination on investigations as mentioned in the inclusion criteria. Patients already receiving anti-tumor treatment for another tumor or a synchronic colorectal cancer. Patients in whom a second-look endoscopy would require major and unacceptable effort and / or resources, for instance clinical admission for bowel preparation, long travel, general anesthesia, extremely difficult to reach polypectomy site. Such at the decision of the patient and / or treating physician. Patient is planned for trans-anal surgery. Patient is not planned for surgery. Patient is pregnant. Patient does not provide written informed consent or is unable to provide such.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank ter Borg, MD PhD
Organizational Affiliation
Department of Gastroenterology & Hematology, Deventer Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Nij Smellinghe Hospital
City
Drachten
State/Province
Friesland
ZIP/Postal Code
9202NN
Country
Netherlands
Facility Name
Antonius Hospital Sneek-Emmeloord
City
Sneek
State/Province
Friesland
ZIP/Postal Code
8601ZK
Country
Netherlands
Facility Name
Medical Center de Veluwe
City
Apeldoorn
State/Province
Gelderland
ZIP/Postal Code
7332BP
Country
Netherlands
Facility Name
Gelre Hospitals
City
Apeldoorn
State/Province
Gelderland
ZIP/Postal Code
7334
Country
Netherlands
Facility Name
Hospital Gelderse Vallei
City
Ede
State/Province
Gelderland
ZIP/Postal Code
6716RP
Country
Netherlands
Facility Name
Radboud University Medical Center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands
Facility Name
Canisius Wilhelmina Hospital
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6532SZ
Country
Netherlands
Facility Name
Maastricht University Medical Center
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6229
Country
Netherlands
Facility Name
Maasstad Hospital Pantein
City
Beugen
State/Province
Noord-Brabant
ZIP/Postal Code
5835DV
Country
Netherlands
Facility Name
Amphia Hospital
City
Breda
State/Province
Noord-Brabant
ZIP/Postal Code
4819EV
Country
Netherlands
Facility Name
Catharina Hospital
City
Eindhoven
State/Province
Noord-Brabant
ZIP/Postal Code
5623EJ
Country
Netherlands
Facility Name
Bernhoven
City
Uden
State/Province
Noord-Brabant
ZIP/Postal Code
5406PT
Country
Netherlands
Facility Name
The Netherlands Cancer Institute Antoni van Leeuwenhoekhuis
City
Amsterdam
State/Province
Noord-Holland
ZIP/Postal Code
1066 CX
Country
Netherlands
Facility Name
Medical Center Slotervaart
City
Amsterdam
State/Province
Noord-Holland
ZIP/Postal Code
1066EC
Country
Netherlands
Facility Name
Onze Lieve Vrouwe Gasthuis (Oost & West)
City
Amsterdam
State/Province
Noord-Holland
ZIP/Postal Code
1091AC
Country
Netherlands
Facility Name
Academical Medical Center, Gastroenterology department
City
Amsterdam
State/Province
Noord-Holland
ZIP/Postal Code
1105 AZ
Country
Netherlands
Facility Name
Spaarne Gasthuis
City
Haarlem
State/Province
Noord-Holland
ZIP/Postal Code
2035RC
Country
Netherlands
Facility Name
Deventer Hospital
City
Deventer
State/Province
Overijssel
ZIP/Postal Code
7416 SE
Country
Netherlands
Facility Name
Ziekenhuis Groep Twente
City
Hengelo
State/Province
Overijssel
ZIP/Postal Code
7555DL
Country
Netherlands
Facility Name
Isala Clinics
City
Zwolle
State/Province
Overijssel
ZIP/Postal Code
8025AB
Country
Netherlands
Facility Name
Meander Medical Center
City
Amersfoort
State/Province
Utrecht
ZIP/Postal Code
3813TZ
Country
Netherlands
Facility Name
Sint Antonius Hospital
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3435CM
Country
Netherlands
Facility Name
IJsselland Hospital
City
Capelle Aan Den IJssel
State/Province
Zuid-Holland
ZIP/Postal Code
2906ZC
Country
Netherlands
Facility Name
Haga Hospital
City
Den Haag
State/Province
Zuid-Holland
ZIP/Postal Code
2545AA
Country
Netherlands
Facility Name
Albert Schweitzer Hospital
City
Dordrecht
State/Province
Zuid-Holland
ZIP/Postal Code
3318AT
Country
Netherlands
Facility Name
Rivas Zorggroep
City
Gorinchem
State/Province
Zuid-Holland
ZIP/Postal Code
4206CC
Country
Netherlands
Facility Name
Groene Hart Hospital
City
Gouda
State/Province
Zuid-Holland
ZIP/Postal Code
2803HH
Country
Netherlands
Facility Name
Alrijne Hospital
City
Leiden
State/Province
Zuid-Holland
ZIP/Postal Code
2334CK
Country
Netherlands
Facility Name
Erasmus Medical Center, Gastroenterology department
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3015 CE
Country
Netherlands
Facility Name
Franciscus Gasthuis
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3045PM
Country
Netherlands
Facility Name
Maasstad Hospital
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3079DZ
Country
Netherlands
Facility Name
Ikazia Hospital
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3083AN
Country
Netherlands
Facility Name
Vlietland Hospital
City
Schiedam
State/Province
Zuid-Holland
ZIP/Postal Code
3118JH
Country
Netherlands
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Facility Name
Martini Hospital
City
Groningen
ZIP/Postal Code
9728NT
Country
Netherlands
Facility Name
University Medical Center Utrecht, Gastroenterology department
City
Utrecht
ZIP/Postal Code
3508 GA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data collection is within current OpenClinica standard and not shared
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SCar-biopsies After Malignant Colorectal Polypectomy of Uncertain RAdicality

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