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Ex Vivo Intraarterial Methylene Blue Injection Improve Nodal Staging Accuracy in Colorectal Cancer (MB)

Primary Purpose

Lymph Node Metastases, Colorectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Hungary
Study Type
Interventional
Intervention
Methylene blue injection
Sponsored by
St. Borbala Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lymph Node Metastases focused on measuring colorectal, cancer, lymph, node, metastasis, methylene-blue

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Elective operation.
  • Colon or rectum resection performed.
  • Malignant colorectal condition.
  • Curative intent.

Exclusion Criteria:

  • Acute surgery performed
  • Final histology: benign
  • No other pathologic method (apart form Methylene Blue injection) used to improve lymph node yield

Sites / Locations

  • St. Borbala Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Methylene blue

Control

Arm Description

Methylene blue solution (50 mg in 30 ml of saline solution) was injected in the cannulated main supplying artery of the freshly removed specimen, ex vivo. Colorectal specimen was then processed in the routine pathological work-up way.

Colorectal specimens were processed in the routine pathological work-up way.

Outcomes

Primary Outcome Measures

Total number of lymph nodes
Total number of lymph nodes examined by pathologist
Positive lymph nodes
Number of positive lymph nodes found by pathologist
Nodal staging accuracy
Minimum Nr of 12 lymph nodes examined if reported N stage is N0, or positive lymph node=s) found
At least 12 lymph nodes harvested
Minimum Nr of 12 lymph nodes examined by pathologist

Secondary Outcome Measures

Overall survival
Overall survival after operation (in months)

Full Information

First Posted
April 5, 2021
Last Updated
April 11, 2021
Sponsor
St. Borbala Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04842968
Brief Title
Ex Vivo Intraarterial Methylene Blue Injection Improve Nodal Staging Accuracy in Colorectal Cancer
Acronym
MB
Official Title
The Impact of ex Vivo Intra-arterial Methylene Blue Injection on Nodal Staging Accuracy and Survival in Colorectal Cancer.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 15, 2021 (Anticipated)
Primary Completion Date
July 15, 2021 (Anticipated)
Study Completion Date
September 15, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Borbala Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Nodal staging holds both important prognostic and predictive value at colorectal cancer. Regional lymph nodes are located close to the primary tumor in the mesocolon / mesorectum. Current pathology and oncology standards require a separate examination of at least 12 lymph nodes each case to fulfill staging "accuracy" criteria. In order to reach this number of lymph nodes, a precise surgical technique (total mesorectal excision or complete mesocolic excision), as well as a thorough pathological specimen work-up is needed. The aim of the study is to investigate, if ex vivo intra-arterial methylene blue injection by the surgeon can help improving nodal harvesting effectivity of the pathologist, hence leading to a better staging and hopefully even to a better outcome in the long run. In 2014-2015 two surgical centers randomised resected colorectal specimens in 1:1 ratio to methylene-blue injection arm and control (no injection) arm in a total of 200 consecutive cases. Both pathologic and oncologic treatment were led regardless of the injection, reports were just routinely saved in the routine medical documentation. This retrospective study is designed to recall patient-related, surgery-related factors, as well as pathology reports including nodal staging from the medical databases. The investigators aim to find correlation between methylene blue "staining" and lymph node yield. In addition, the investigators plan to crossmatch methylene blue injection, as a process, with long term survival of the patients.
Detailed Description
Background: Colorectal Cancer is the second most common cause of death in Hungary. The most important prognostic and predictive factor of colorectal cancer is the stage of disease at the time of diagnosis. Precise staging, especially nodal staging is highly important for correct planning of oncotherapy, i.e. adjuvant chemotherapy. Nodal staging relies on the proper surgical removal of mesocolon/mesorectum belonging to the the affected colorectal segment, as well as on the thorough pathology work-up of the specimen. Current quality standards require examination of a minimum of 12 lymph nodes in order to reliably report N0 stage. Methylene-blue injection into the main supplying artery of the removed specimen is one of the simplest and most effective techniques described to aid pathologist in lymph node harvesting. Technique of methylene blue injection: First of all, surgeon need to en block remove the affected colorectal segment with its mesecolon/mesorectum. Then the surgeon isolates the main supplying artery and cannulated it with an appropriate-size canula. Methylene blue solution (50 mg methylene blue diluted in in 30 ml saline) is prepared and injected into the freshly removed specimen via the canula until the blue solution appears on the cut edges of the specimen. The specimen can be processed in a routine way (placed in 4% formaldehyde). Aim of the study: The aim is to investigate if the well described and in Western-European healthcare systems well tested technique (Methylene blue injection) can be effectively adapted in an overwhelmed, busy Eastern-European healthcare environment. (Other techniques, including pathology assistant are not affordable in this area.) Apart form testing diagnostic accuracy of the pathologist on specimens with and without methylene blue injection, the investigators would like to assess a potential survival benefit of the suspected improvement of staging effectivity. Timing of the study: Over a 20-month period of 2014 and 2015 two surgical centers in Hungary randomised their elective colorectal resection cases into interventional and control arms. Randomisation was performed with a 1:1 ratio at each site on 100-100 consecutive cases. Further pathology work-up and reporting has been routinely performed without any specific effect on oncology follow-up or treatment. No specific data collection has been performed after the intervention. This study aims to retrospectively select the 100-100 (total of 200) consecutive colorectal resection cases of the given time frame from the official hospital medical recording systems. Pathology reports and other relevant patient clinical records will be collected and statistically assessed. Ethical approval was requested and gained from the Medical Research Council, Hungary, for the retrospective analysis of patient data. Statistical analysis: Power analysis was performed to get the sufficient number of cases (200 cases in total). Case Report Form The retrospectively included cases will be listed in a specific database on a safe medical server. Anthropometric, disease-specific, operation-specific and pathology report details will be extracted out of the official patient documentation system. Patients will be included according to the known interventional interval and the operation type (elective colorectal resection). Cases in the database will be anonymized. No patient-identifying data will be recorded or given to the assessor of the study (statistician).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymph Node Metastases, Colorectal Cancer
Keywords
colorectal, cancer, lymph, node, metastasis, methylene-blue

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Five to six years ago specimens from a total fo 200 consecutive colorectal cancer resection cases were randomized into two groups: 1. main supplying artery was cannulated and injected with methylene blue solution, 2. no intervention, routine specimen handling.
Masking
ParticipantOutcomes Assessor
Masking Description
Outcome assessor was blinded
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Methylene blue
Arm Type
Experimental
Arm Description
Methylene blue solution (50 mg in 30 ml of saline solution) was injected in the cannulated main supplying artery of the freshly removed specimen, ex vivo. Colorectal specimen was then processed in the routine pathological work-up way.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Colorectal specimens were processed in the routine pathological work-up way.
Intervention Type
Other
Intervention Name(s)
Methylene blue injection
Intervention Description
Methylene blue solution is injected ex vivo in the main supplying artery trunk of the freshly removed colorectal specimen. (50 mg in 30 ml saline)
Primary Outcome Measure Information:
Title
Total number of lymph nodes
Description
Total number of lymph nodes examined by pathologist
Time Frame
Within 4 weeks after operation (at pathology work-up)
Title
Positive lymph nodes
Description
Number of positive lymph nodes found by pathologist
Time Frame
Within 4 weeks after operation (at pathology work-up)
Title
Nodal staging accuracy
Description
Minimum Nr of 12 lymph nodes examined if reported N stage is N0, or positive lymph node=s) found
Time Frame
Within 4 weeks after operation (at pathology work-up)
Title
At least 12 lymph nodes harvested
Description
Minimum Nr of 12 lymph nodes examined by pathologist
Time Frame
Within 4 weeks after operation (at pathology work-up)
Secondary Outcome Measure Information:
Title
Overall survival
Description
Overall survival after operation (in months)
Time Frame
5 years (60 months) after operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective operation. Colon or rectum resection performed. Malignant colorectal condition. Curative intent. Exclusion Criteria: Acute surgery performed Final histology: benign No other pathologic method (apart form Methylene Blue injection) used to improve lymph node yield
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Balazs Banky, PhD
Phone
36208231642
Email
bankybalazs@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nora Susztak, MD
Phone
36307283224
Email
n.susztak@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Balazs Banky, PhD
Organizational Affiliation
St. Borbala Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Borbala Hospital
City
Tatabánya
ZIP/Postal Code
2800
Country
Hungary

12. IPD Sharing Statement

Plan to Share IPD
No

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Ex Vivo Intraarterial Methylene Blue Injection Improve Nodal Staging Accuracy in Colorectal Cancer

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