39 Interim analysis of ovarian cancer by the us national cancer moonshot's tri-federal (DOD/NCI/VA) applied proteogenomic organizational learning and outcomes (APOLLO) research network. (18th September 2019)

• Record Type: Journal Article
• Authors: Maxwell, GL; Bateman, NW; Soltis, AR; Wang, G; Dalgard, CL; Petricoin, EF; Tarney, CM; Rojas, C; Havrilesky, L; Cohn, DE; Wells, JM; Hu, H; Hamilton, CA; Shriver, CD; Wilkerson, M; Casablanca, Y; Darcy, K; Conrads, TP
• Is Part Of: International journal of gynecological cancer. Volume 29(2019)Supplement 3
• Page Start: A23
• Page End: A24
• Publication Date: 2019-09-18
• Subjects: Generative organs, Female -- Cancer -- Periodicals; 616.99465
• DOI: 10.1136/ijgc-2019-IGCS.39
• Languages: English
• ISSNs: 1048-891X

Abstract

Abstract : Objectives: Although studies including TCGA have selected for pure tumors to enhance detection of cancer-related biomarkers, many impure tumors are associated with poor prognosis raising concerns over historical selection bias. Enrichment techniques to prep tumor micro-compartments was aligned with comprehensive proteogenomic analysis in an advanced stage high grade serous ovarian cancer (HGSOC) patient cohort to detect novel, clinically-relevant alterations. Methods: 87 fresh-frozen tumor specimens were selected from a cohort of over 630 patients to reflect a continuum of tumor purity balanced by progression and disease distribution. A whole tumor (WT) specimen and one enriched for tumor epithelium was prepared for each case using laser microdissection (LMD). Specimens were analyzed by whole genome sequencing (WGS), mRNA-seq, quantitative global/phosphoproteomics, and reverse phase protein array. Results: LMD enrichment increased median tumor purity estimated by WGS from 56% in WT to 79% ( P< 4e-11, MWW U test) and significantly enhanced identification of somatic single nucleotide variants (SNVs) (27%, P <3e-7) and short indels (16%, P <4e-4). Following LMD, 83% of cases characterized as mesenchymal expression subtype (C4) in WT samples were reclassified to other molecular subtypes ( P <0.001). LMD tumors with an immune expression subtype (C1) had improved progression-free survival (PFS) compared with other molecular subtypes (p=0.009). Differential proteomic analyses focused on signaling alterations correlating with altered PFS, homologous recombination deficiency and immune signaling. Conclusions: These data demonstrate feasibility of cohort-level proteogenomic characterization of the tumor microenvironment and establishes a non-restrictive paradigm for patient inclusion and specimen prep in support of the prospective mission-scale analyses associated with APOLLO.