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4364 Evaluating the Clinical Utility of Real-Time Comprehensive Whole Exome Sequencing and RNA-Seq for Patients with Diffuse Large B-Cell Lymphoma

Program: Oral and Poster Abstracts
Session: 621. Lymphomas: Translational – Molecular and Genetic: Poster III
Hematology Disease Topics & Pathways:
Research, Translational Research, Clinical Practice (Health Services and Quality), Clinical Research, Treatment Considerations, Biological therapies, Technology and Procedures, Study Population, Human, Molecular testing
Monday, December 9, 2024, 6:00 PM-8:00 PM

Dai Chihara, MD, PhD1, Kumudha Balakrishnan, MPhil, MSc, PhD1*, Gita Masand, PhD1*, Robert Andrew Harkins, MD, MS2, Neha Akkad, MD3, Anna Novokreshchenova, MS4*, Alexander Bagaev, PhD5*, Nikita Kotlov, PhD5*, Ekaterina Postovalova, PhD4*, Eduardo Shugaev-Mendosa, MD4*, Yuliya Gracheva, MS4*, Kelley Lauziere4*, Leznath Kaneunyenye4*, Brianna McKenna4*, Amber Berlinski4*, McKenna Walsh4*, Linnea Larson4*, Mariam Kotsinyan4*, Anna Samokhina4*, Sheila T Yong4*, Krystle Nomie, PhD5*, Nathan H. Fowler, MD6*, Christopher R. Flowers, MD, MS1 and Jason R. Westin, MD1

1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX
2Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX
3Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TT
4BostonGene, Corp., Waltham, MA
5BostonGene Corp., Waltham, MA
6BostonGene, Waltham, MA

Introduction: Due to the rapidly evolving landscape of targeted therapies, there is an unmet need for comprehensive molecular profiling to guide treatment decisions for patients with lymphoma. The POLARIX trial showed significant impact of cell-of-origin (COO) in response to polatuzumab-vedotin, demonstrating the unmet need for a reliable real-time assay for molecular profiling to better assign novel treatment to patients with diffuse large B-cell lymphoma (DLBCL) who require treatments within a few weeks from the diagnosis or recurrence. To address this need, we designed a pilot study to assess the feasibility and turnaround time (TAT) of a comprehensive whole exome sequencing (WES) and transcriptome sequencing (RNA-seq) assay in patients with DLBCL for clinical decision-making (NCT05464823).

Methods: Patients aged ≥18 years with DLBCL were eligible. Formalin-fixed paraffin-embedded tissues at diagnosis or recurrent disease underwent WES, RNA-seq, and copy number analysis with concomitant peripheral blood or saliva for germline DNA sequencing. Samples with <20% tumor purity and median coverage of <150x for tumor and/or <100x for normal samples were labeled as quantity not sufficient (QNS). Genomic and transcriptomic data were profiled to define DLBCL COO (Alizadeh et al. Nature 2000), dark zone signature (Dzsig; Ennishi et al. J Clin Oncol. 2019), LymphGen (Wright et al. Cancer Cell 2020), and lymphoma microenvironment (LME; Kotlov et al. Cancer Discov. 2021) classification to uncover clinically relevant biomarkers and match patients with clinical trials on ClinicalTrials.gov.

Results: Among 92 patients analyzed to date, 77 patients (40 with newly diagnosed disease and 37 with relapsed/refractory disease) received WES and RNA-seq, yielding 73 reports with clinical information (treatment options and clinical trial matching) and 4 QNS reports without actionable findings. The remaining 15 samples were rejected as they failed pathology quality control for next-generation sequencing. COO, Dzsig, LymphGen, and LME were classifiable in approximately 90% of patients. The median TAT was 8 days for the result reports (range: 5–22 days), and 73% of custom reports had at TAT ≤10 days.

WES identified frequent TP53 (n=23, 30%) and MYD88 (n=13, 17%) alterations. COOs were designated as activated B-cell type (ABC) in 31 patients (46%) or germinal center B-cell type in 37 patients (54%). The LymphGen classifier showed subtypes MCD (n=8, 12%), EZB MYC- (n=8, 12%), and other (n=18, 26%) as the most common. LME classification revealed most LMEs as mesenchymal (n=49, 70%) and immune-depleted (n=14, 20%), immune-inflamed (n=5, 7%), and germinal center-like (n=2, 3%) were less frequent. Clinically actionable and relevant findings, such as ABC subtype (n=31), TP53 loss (n=23), Dzsig+ (n=10), and CARD11 mutations which are associated with ibrutinib resistance (n=3), were identified in 58 samples. Molecular profiling supported screening for clinical trials, and on average, 8 potential clinical trials were identified from ClinicalTrials.gov per the full report although majority of trials were not lymphoma focused trials.

Conclusion: We demonstrated clinical utility and acceptable TAT using a comprehensive WES and RNA-seq assay in a cohort of patients with DLBCL. The full test reports included findings on significant alterations, COO, Dzsig, LymphGen, and LME subtypes, treatment options, and clinical trial matches. These robust findings, coupled with rapid TAT, demonstrate the real-world feasibility of using integrated WES and RNA-seq to design biology-driven trials and guide clinical decision-making for patients with lymphoma initiating a new line of therapy.

Disclosures: Chihara: Genentech: Research Funding; BMS: Research Funding; SymBio pharmaceutical: Honoraria; BeiGene: Honoraria; Ono pharmaceutical: Research Funding; Genmab: Research Funding. Novokreshchenova: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Bagaev: BostonGene: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company, Patents & Royalties: BostonGene, Corp.. Kotlov: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company, Patents & Royalties: BostonGene, Corp.. Postovalova: BostonGene Corporation: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company, Patents & Royalties: BostonGene. Shugaev-Mendosa: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Gracheva: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Lauziere: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Kaneunyenye: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. McKenna: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Berlinski: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Walsh: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Larson: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Kotsinyan: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Samokhina: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Yong: BostonGene, Corp.: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Nomie: BostonGene: Current Employment, Current equity holder in private company, Current equity holder in publicly-traded company. Fowler: BostonGene: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company; CelGene: Consultancy; Roche/Genentech: Consultancy, Research Funding; TG Therapeutics: Consultancy; Bayer: Consultancy; Novartis: Consultancy; Verastem: Consultancy. Flowers: Morphosys: Research Funding; Kite: Research Funding; Amgen: Research Funding; Denovo Biopharma: Consultancy; TG Therapeutics: Research Funding; Seagen: Consultancy; Celgene: Consultancy, Research Funding; Novartis: Research Funding; AstraZeneca: Consultancy; Pharmacyclics: Research Funding; Janssen Pharmaceuticals: Research Funding; Cellectis: Research Funding; Acerta: Research Funding; Iovance: Research Funding; Nektar: Research Funding; Sanofi: Research Funding; 4D: Research Funding; Cancer Prevention and Research Institute of Texas: CPRIT Scholar in Cancer Research: Research Funding; BostonGene: Research Funding; Pfizer: Research Funding; Bio Ascend: Consultancy; Bristol Myers Squibb: Consultancy; Guardant: Research Funding; Xencor: Research Funding; BeiGene: Consultancy; Adaptimmune: Research Funding; Allogene: Research Funding; Bayer: Consultancy, Research Funding; Burroughs Wellcome Fund: Research Funding; Eastern Cooperative Oncology Group: Research Funding; Takeda: Research Funding; Ziopharm National Cancer Institute: Research Funding; EMD Serono: Research Funding; Spectrum: Consultancy; Pharmacyclics / Janssen: Consultancy; N-Power Medicine: Consultancy, Current holder of stock options in a privately-held company; Karyopharm: Consultancy; Foresight Diagnostics: Consultancy, Current holder of stock options in a privately-held company; Genentech/Roche: Consultancy, Research Funding; Genmab: Consultancy; Gilead: Consultancy, Research Funding; AbbVie: Consultancy, Research Funding. Westin: Nurix: Consultancy, Research Funding; Novartis: Consultancy, Research Funding; Morphosys/Incyte: Consultancy, Research Funding; Janssen: Consultancy, Research Funding; Genentech, Inc.: Consultancy, Research Funding; Bristol Myers Squibb: Consultancy, Research Funding; Regeneron: Consultancy; ADC Therapeutics: Consultancy, Research Funding; Allogene: Consultancy, Research Funding; Kite/Gilead: Consultancy, Research Funding; Pfizer: Consultancy; AstraZeneca: Consultancy, Research Funding; AbbVie/GenMab: Consultancy.

*signifies non-member of ASH