Το Personalis παρουσιάζει δεδομένα από νέα χαρακτηριστικά πλατφόρμας στην 37η ετήσια συνάντηση PlatoBlockchain Data Intelligence της Εταιρείας Ανοσοθεραπείας του Καρκίνου (SITC). Κάθετη αναζήτηση. Ολα συμπεριλαμβάνονται.

Το Personalis παρουσιάζει δεδομένα από χαρακτηριστικά νέας πλατφόρμας στην 37η ετήσια συνάντηση της Εταιρείας Ανοσοθεραπείας του Καρκίνου (SITC)

MENLO PARK, Calif.–(BUSINESS WIRE)–Personalis, Inc. (Nasdaq: PSNL) today announced that the company will share data resulting from expanded features of its NeXT Platform® at the Society for Immunotherapy of Cancer (SITC) Annual Meeting, November 8-12 in Boston, with three abstracts that highlight advanced R&D applications of next-generation sequencing (NGS) in immuno-oncology.

“To understand the complex dynamics of cancer and ultimately better predict response to therapy, we need to advance the tools we’re using to characterize the tumor microenvironment. We continue to build upon the suite of technologies in our ImmunoID NeXT Platform® to enable the high-resolution study of immuno-oncology targets in an array of contexts, including improved neoantigen prediction, immune-composition profiling, and composite biomarker signatures,” said Sean Boyle, PhD, Executive Director of Bioinformatics Science at Personalis.

The company will present the following posters at SITC2022, as well as with customers including the Parker Institute for Cancer Immunotherapy (Abstracts 559 and 587) and Geneos Therapeutics (Abstracts 691 and 692).

Τίτλος: A combination of antigen presentation and T-cell recognition features improves neoantigen immunogenicity predictions (Abstract 51)

Επισκόπηση: Tumor neoantigen burden outperformed tumor mutational burden in prediction of patient response to checkpoint inhibitor immunotherapy by better capturing the biological mechanism underlying response. However, immune recognition of neoantigens by T-cells requires more than antigen presentation, which has been the focus of tumor neoantigen burden thus far. To address this need, we extend the existing SHERPA® MHC-presentation framework to predict neoantigen immunogenicity. By combining antigen presentation and T-cell recognition features in a two-tiered model, we can better predict immunogenic neoantigens and make progress towards using neoantigens as biomarkers to assess checkpoint inhibitor efficacy.

Τίτλος: Sensitive prediction of immunotherapy response by integrating immune infiltration and neoantigen presentation score in late-stage melanoma (Abstract 119)

Επισκόπηση: Single-modality biomarkers such as tumor mutational burden (TMB) often fail to reliably predict response to immune checkpoint blockade (ICB), likely due to incomplete characterization of the complex tumor-immune interactions that influence treatment efficacy. We previously developed the composite biomarker, neoantigen presentation score (NEOPS™), which integrates neoantigen processing and presentation potency, and showed it outperformed TMB and other single-modality biomarkers in predicting ICB response in melanoma. Here, we combined NEOPS with the assessment of tumor immune infiltration and demonstrated more accurate patient stratification for ICB response.

Τίτλος: Transcriptome augmentation provides accurate and sensitive quantification of genes associated with the tumor microenvironment (Abstract 146)

Επισκόπηση: While malignant cells dictate much of the tumor biology, there is evidence that the tumor microenvironment (TME) also plays a significant role in disease progression and response to therapy. The role of the immune cells is particularly relevant in immunotherapy, and multiple transcriptome-based biomarkers have shown utility in predicting the efficacy of immune checkpoint blockade. However, little is known about the benefits of enhancing the depth and uniformity of transcriptome sequencing coverage for quantifying the TME cell type composition. Using the ImmunoID NeXT Platform®, which combines high-quality exome and transcriptome sequencing with advanced informatics to comprehensively characterize the tumor and TME from a single FFPE tumor sample, applying augmented transcriptome coverage to the assessment of TME benefited the identification of marker genes for cell type enrichment analysis without introducing bias.

Σχετικά με το Personalis

Η Personalis, Inc. κατέχει ηγετική θέση στην προηγμένη γονιδιωματική του καρκίνου, επιτρέποντας την επόμενη γενιά θεραπειών και διαγνωστικών ακριβείας για τον καρκίνο. ο Πλατφόρμα Personalis NeXTΤο ® έχει σχεδιαστεί για να προσαρμόζεται στην περίπλοκη και εξελισσόμενη κατανόηση του καρκίνου, παρέχοντας στους βιοφαρμακευτικούς πελάτες και κλινικούς ιατρούς πληροφορίες για όλα τα περίπου 20,000 ανθρώπινα γονίδια, μαζί με το ανοσοποιητικό σύστημα, από ένα μόνο δείγμα. Για να ενεργοποιηθεί η αλληλουχία του καρκίνου, το Personalis' Κλινικό Εργαστήριο κατασκευάστηκε με έμφαση στην κλινική ακρίβεια, την ποιότητα, τα μεγάλα δεδομένα, την κλίμακα και την αποτελεσματικότητα. Το εργαστήριο είναι ευθυγραμμισμένο με το GxP, καθώς και οι τροποποιήσεις βελτίωσης του κλινικού εργαστηρίου του 1988 και διαπιστευμένο από το Κολλέγιο Αμερικανών Παθολόγων. Για περισσότερες πληροφορίες, επισκεφθείτε το Ιστοσελίδα Personalis και Κέντρο ειδήσεων και ακολουθήστε το Personalis στο LinkedIn και Twitter.

Προσωρινές δηλώσεις

All statements in this press release that are not historical are “forward-looking statements” within the meaning of U.S. securities laws, including statements relating to attributes or advantages of the NeXT Platform, Personalis’ business opportunities, leadership, plans or expectations, or other future events. Such forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from any anticipated results or expectations expressed or implied by such statements. Factors that could materially affect actual results can be found in Personalis’ filings with the U.S. Securities and Exchange Commission, including Personalis’ most recent reports on Forms 8-K, 10-K and 10-Q, and include those listed under the caption “Risk Factors.” Personalis disclaims any obligation to update such forward-looking statements.

Επικοινωνία

Investor Relations Contact for Personalis:
Caroline Corner

investors@personalis.com
415-202-5678

Media Contact for Personalis:
Ο ναός της Τζένιφερ

pr@personalis.com
650-752-1300

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