A Retrospective Validations Microsatellite Instability (MSI) Testing v Mismatch Repair (MMR) in Gastric Adenocarcinoma

Sponsor
Royal Cornwall Hospitals Trust (Other)
Overall Status
Completed
CT.gov ID
NCT04232020
Collaborator
(none)
50
1
5.9
8.5

Study Details

Study Description

Brief Summary

To compare the Idylla microsatellite instability test versus mismatch repair immunohistochemistry (IHC) in gastric adenocarcinoma.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Mismatch repair

Detailed Description

Gastric adenocarcinoma is a common form of cancer which is associated with a poor prognosis. Up to 22% of gastric adenocarcinomas arise via the microsatellite instability (MSI) / mismatch repair (MMR) pathway. These cases can be detected either by mismatch repair immunohistochemistry (IHC) or microsatellite instability testing. Detection of mismatch repair deficiency or microsatellite instability is important because patients with this type of gastric adenocarcinoma are shown to benefit from a different therapeutic approach. High concordance between mismatch repair immunohistochemistry and microsatellite instability testing has already been demonstrated. The implementation of either method is largely based on local availability. The Idylla MSI test presents a novel method of establishing MSI status in comparison to pre-existing MSI testing platforms. The Idylla MSI tests uses a fully automated, ultra-rapid system that can work on formalin-fixed, paraffin embedded tissue with no need for preceding DNA extraction. Implementation of the Idylla MSI test could reduce reporting turnaround times and requires less technical expertise to perform in comparison to other platforms.

The investigators department does not currently have the facilities to perform MSI testing on any platform, so the advantages of introducing the Idylla MSI test would also include the generic advantages of MSI testing. These advantages include: the ability to quickly check cases shown to have possible MMR loss on IHC (i.e. equivocal cases) with MSI testing; and providing an alternative to MMR IHC for screening of Lynch syndrome, reducing the burden on reporting pathologists and reduce the inter-observer variability associated with IHC interpretation.

The Idylla MSI test already demonstrates high concordance with other MSI testing platforms but has yet to be compared to the department's accepted standard of MMR IHC. This project aims to compare the Idylla MSI test to in-house MMR IHC to establish whether the two methods are concordant in reporting MMR / MSI status in gastric adenocarcinoma.

Study Design

Study Type:
Observational
Actual Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Retrospective Validation of Idylla Microsatellite Instability Testing Versus Mismatch Repair Immunohistochemistry in Gastric Adenocarcinoma Biopsies
Actual Study Start Date :
Feb 7, 2020
Actual Primary Completion Date :
Jul 31, 2020
Actual Study Completion Date :
Aug 5, 2020

Outcome Measures

Primary Outcome Measures

  1. Idylla MSI test using Idylla MSI Cartridges to assess suitability [6 months]

    MMR IHC panels will be passed to the histopathology team for interpretation. Cases will be interpreted and results will be determined by either a) loss of staining or b) no loss of staining of any individual antibody

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient consent

  • Adequate tissue including adequate tumour burden

  • Diagnosis of adenocarcinoma in this biopsy

Exclusion Criteria:
  • No patient consent

  • Inadequate tissue or block not present in archive

  • No adenocarcinoma in biopsy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Royal Cornwall Hospital Truro Cornwall United Kingdom TR1 3LQ

Sponsors and Collaborators

  • Royal Cornwall Hospitals Trust

Investigators

  • Principal Investigator: Mary Jones, Senior Biomedical Scientist

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Royal Cornwall Hospitals Trust
ClinicalTrials.gov Identifier:
NCT04232020
Other Study ID Numbers:
  • 2019.RCHT.107
First Posted:
Jan 18, 2020
Last Update Posted:
Oct 8, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 8, 2020