Abstract

Practices in somatic variant interpretation and classification vary between Canadian clinical molecular diagnostic laboratories, and understanding of current practices and perspectives is limited. To define gaps and future directions, including consensus guideline development, the Somatic Curation and Interpretation Across Laboratories (social) project examined the present state of somatic variant interpretation in Canadian molecular laboratories, including testing volumes and methods, data sources and evidence criteria, and application of published classification guidelines. Individuals who perform somatic variant interpretation in Canadian centres were invited to participate in an online survey. Invitees included laboratory directors (certified as Fellows of the Canadian College of Medical Geneticists or the American College of Medical Geneticists), md or md and phd molecular pathologists, and other phd experts, including phd specialists in variant annotation or bioinformatics. Current testing methods, volumes, and platforms in next-generation sequencing, use of variant annotation resources and evidence criteria, and preference for variant classification schemes were evaluated. Responses were received from 37 participants in 8 provinces. A somatic variant classification scheme jointly supported by the Association for Molecular Pathology (amp), the American Society of Clinical Oncology (asco), and the College of American Pathologists (cap) was used by 47% of respondents; an alternative guideline or a combination of published guidelines was used by 35% of respondents. The remaining 18% did not use a published scheme. Only 41% of respondents used a published scheme without alteration. Although all respondents indicated that there is a need for Canadian laboratories to adopt a somatic variant classification guideline, only 38% of respondents felt that it should be mandatory to adopt the amp/asco/cap-endorsed guideline. Data from the social project identified high variability in current practice, yet strong support for standardization of solid-tumour somatic variant interpretation across Canadian institutions. Aligning classification methods will reduce variation in cross-institutional classification and reporting practices, aiding in consistent practice nationwide.

Highlights

  • Molecular profiling to inform drug treatment choice or patient management by identifying somatic variants in tumour tissue is an important tool in current clinical care for Canadian patients with solid tumours

  • A somatic variant classification scheme jointly supported by the Association for Molecular Pathology, the American Society of Clinical Oncology, and the College of American Pathologists was used by 47% of respondents; an alternative guideline or a combination of published guidelines was used by 35% of respondents

  • Of the available somatic interpretation guidelines, the most broadly recognized scheme is the guideline endorsed by the Association for Molecular Pathology, the American Society of Clinical Oncology, and the College of American Pathologists, which was developed based on a survey, a literature review, and committee member expertise[1]

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Summary

Introduction

Molecular profiling to inform drug treatment choice or patient management by identifying somatic variants in tumour tissue is an important tool in current clinical care for Canadian patients with solid tumours. The extent of its clinical applicability within the context of the Canadian health care system is unclear, because of differences in test and drug funding, legislation, and laboratory accreditation requirements. Practices in somatic variant interpretation and classification vary between Canadian clinical molecular diagnostic laboratories, and understanding of current practices and perspectives is limited. To define gaps and future directions, including consensus guideline development, the Somatic Curation and Interpretation Across Laboratories (social) project examined the present state of somatic variant interpretation in Canadian molecular laboratories, including testing volumes and methods, data sources and evidence criteria, and application of published classification guidelines

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