| Literature DB >> 31816062 |
Kirsty Wienand1,2, Bjoern Chapuy1,2,3, Chip Stewart4, Andrew J Dunford4, David Wu5, Jaegil Kim4, Atanas Kamburov4, Timothy R Wood4, Fathima Zumla Cader1,2, Matthew D Ducar6,7, Aaron R Thorner1,7, Anwesha Nag1,7, Alexander T Heubeck8, Michael J Buonopane8, Robert A Redd9, Kamil Bojarczuk1,2, Lee N Lawton1, Philippe Armand1,2, Scott J Rodig10, Jonathan R Fromm5, Gad Getz2,4,11,12, Margaret A Shipp1,2.
Abstract
Classical Hodgkin lymphoma (cHL) is composed of rare malignant Hodgkin Reed-Sternberg (HRS) cells within an extensive, but ineffective, inflammatory/immune cell infiltrate. HRS cells exhibit near-universal somatic copy gains of chromosome 9p/9p24.1, which increase expression of the programmed cell death protein 1 (PD-1) ligands. To define genetic mechanisms of response and resistance to PD-1 blockade and identify complementary treatment targets, we performed whole-exome sequencing of flow cytometry-sorted HRS cells from 23 excisional biopsies of newly diagnosed cHLs, including 8 Epstein-Barr virus-positive (EBV+) tumors. We identified significantly mutated cancer candidate genes (CCGs) as well as somatic copy number alterations and structural variations and characterized their contribution to disease-defining immune evasion mechanisms and nuclear factor κB (NF-κB), JAK/STAT, and PI3K signaling pathways. EBV- cHLs had a higher prevalence of genetic alterations in the NF-κB and major histocompatibility complex class I antigen presentation pathways. In this young cHL cohort (median age, 26 years), we identified a predominant mutational signature of spontaneous deamination of cytosine- phosphate-guanines ("Aging"), in addition to apolipoprotein B mRNA editing catalytic polypeptide-like, activation-induced cytidine deaminase, and microsatellite instability (MSI)-associated hypermutation. In particular, the mutational burden in EBV- cHLs was among the highest reported, similar to that of carcinogen-induced tumors. Together, the overall high mutational burden, MSI-associated hypermutation, and newly identified genetic alterations represent additional potential bases for the efficacy of PD-1 blockade in cHL. Of note, recurrent cHL alterations, including B2M, TNFAIP3, STAT6, GNA13, and XPO1 mutations and 2p/2p15, 6p21.32, 6q23.3, and 9p/9p24.1 copy number alterations, were also identified in >20% of primary mediastinal B-cell lymphomas, highlighting shared pathogenetic mechanisms in these diseases.Entities:
Year: 2019 PMID: 31816062 PMCID: PMC6963251 DOI: 10.1182/bloodadvances.2019001012
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529