Genomic Sequencing Augments Diagnosis of Lymphoid Cancer

Next-generation sequencing technologies have been instrumental in accelerating discovery in cancer genomics via whole-genome sequencing (WGS), whole-transcriptome sequencing (RNA sequencing), and deep-targeted sequencing. Two methods are commonly used for such targeted approaches: capture hybridization–based sequencing and amplicon-based sequencing, each having its own advantages and disadvantages.

Scientists at the University of British Columbia (Vancouver, BC, Canada) and their colleagues established that hybrid-capture sequencing is the method of choice for sequencing “actionable” gene mutations across the most common forms of lymphoid cancer. Due to its applicability in routinely acquired formalin-fixed, paraffin-embedded tissues, this assay can be implemented by clinical laboratories into routine diagnostic workflows. A cohort of matched tumor and normal DNA specimens was assembled from 229 patients, including 30 CLL, 80 DLBCL, and 119 FL cases. Formalin-fixed paraffin-embedded (FFPE) tissue blocks and peripheral blood DNA samples for all FL and DLBCL cases were acquired from the BC Cancer Agency (Vancouver, BC, Canada) lymphoma tumor bank.

The team used various techniques to analyze the blood and tissue samples. These included for WGS, specimens for 66 of 229 patients from the original cohort were frozen and embedded in OCT compound for DNA and RNA extractions, as well as frozen sections for histological correlation; capture sequencing with the Illumina MiSeq; Amplicon and Sanger Sequencing; Whole-Genome Library Construction and Sequencing performed on an Illumina HiSeq2500 or HiSeqX instruments.

Samples were sequenced using a panel of 20 lymphoma-specific genes via capture hybridization using Sure Select and amplicon sequencing using Illumina TruSeq Custom Amplicon. The study focused on the development of a sequencing pipeline to personalize lymphoma management establishes feasibility of capture sequencing of routinely acquired FFPE tissue (DLBCL) and fresh cell preparations (CLL) in a single assay. The team demonstrated the superiority of hybrid-capture sequencing over amplicon-based method with respect to assay sensitivity in an approach intended to cover a large capture space across the coding region of 32 genes.

Christian Steidl, MD, an Associate Professor and senior investigator of the study, said, “Our developed assay harnesses the power of modern sequencing for clinical diagnostics purposes and potentially better deployment of novel treatments in lymphoid cancers. We believe our study will help establish evidence-based approaches to decision making in lymphoid cancer care.” The study was published on February 8, 2018, in The Journal of Molecular Diagnostics.

Related Links:
University of British Columbia
BC Cancer Agency