Abstract 144P
Background
Immune checkpoint blockers (ICB) are in the forefront of contemporary clinical oncology and have become an integral part of treatment of many malignancies, including metastatic head and neck cancers (HNC). Nevertheless, tumor response to ICB varies widely, with known predictive biomarkers, such as combined PDL score (CPS) showing limited predictive value. We present results of a blind retrospective analysis of a novel predictive digital pathology biomarker of ICB in HNC.
Methods
We obtained high resolution Hematoxylin and Eosin (H&E) slides from tumor-tissue samples of 26 cases of metastatic HNC patients treated with first-line PD-1 inhibitors, all with CPS>1%. We applied our ENLIGHT-DP pipeline to generate, in a blinded manner, individual response scores to PD-1 inhibition for each slide. ENLIGHT-DP has two main steps: (i) prediction of mRNA expression directly from an H&E slide using DeepPT, our digital-pathology based algorithm; (ii) use of these values as input to ENLIGHT, our transcriptome-based precision oncology platform, which generates a score that predicts response to targeted therapies and ICB (based on a 10-gene signature in this case, composed of the key genetically interacting genes of PD-1). We then unblinded the clinical response (RECIST1.1), and evaluated ENLIGHT-DP’s performance.
Results
ENLIGHT-DP’s score is predictive of response in this cohort, which had an overall response rate of 54% (14/26), with ROC AUC = 0.65. Using a predefined threshold for binary classification of response derived from independent data, 6 of 8 patients that were predicted to respond by ENLIGHT-DP indeed responded (75% PPV, 43% sensitivity, Odds Ratio of 3.75). In comparison, stratification by CPS exhibits no predictive power (PPV of 50% and 58%, respectively, for CPS > 20% and CPS 1-19%, and AUC of 0.46 for CPS as a continuous score).
Conclusions
ENLIGHT-DP demonstrates high predictive power for response to ICB in first-line HNC, outperforming the commonly used CPS marker. Importantly, our approach does not require training on prior treatment outcomes, and can therefore be generalized to drugs for which such data is unavailable or scarce.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
O. Tirosh, L. Gugel, G. Dinstag, Y. Kinar, T. Gottlieb, R. Aharonov: Financial Interests, Personal, Full or part-time Employment: Pangea Biomed. All other authors have declared no conflicts of interest.
Resources from the same session
142P - Exploring tumor mutational burden and frameshift mutations as predictors of immune checkpoint inhibitor efficacy
Presenter: Mai Hoshino
Session: Poster session 08
143P - Efficacy of immunotherapy in gastro-intestinal (GI) tumors with mismatch repair deficient (MMRd) unusual phenotype
Presenter: Emily Alouani
Session: Poster session 08
145P - Predicting the efficacy of immunotherapy in non-small cell lung cancer using machine learning based on simple clinical characteristics and biochemical indexes
Presenter: Lei Cheng
Session: Poster session 08
146P - Biomarkers and intrinsic/acquired resistance mechanisms for atezolizumab plus chemoradiotherapy in MSS locally advanced rectal cancer: An exploratory analysis of a single center, phase II study
Presenter: Wentao Tang
Session: Poster session 08
147P - Comparison of immune-checkpoint inhibitor therapy predictive marker tests microsatellite instability (MSI) and mismatch-repair deficiency (dMMR)
Presenter: Maja Nádorvári
Session: Poster session 08
148P - Clinical significance of CD4+ T cell subsets in peripheral blood for anti-PD-1/PD-L1 therapy
Presenter: Yoshimichi Haruna
Session: Poster session 08
149P - Evaluation of HLA genotype as predictive biomarker for immunological and clinical responses upon vaccination with PolyPEPI1018 cancer vaccine against colorectal cancer
Presenter: Joleen Hubbard
Session: Poster session 08
150P - Phase I/IIa trial of CD200R1 inhibitor 23ME-00610: Exploratory analyses of tissue-based and genetic biomarkers
Presenter: Albiruni Ryan Abdul Razak
Session: Poster session 08
151P - Enhanced pharmacodynamic effects upon combination of cibisatamab and FAP-4-1BBL in 3L+ mMSS CRC patients
Presenter: Ignacio Melero
Session: Poster session 08
152P - Exploratory biomarker analysis of phase III ASTRUM-004 study: Serplulimab plus chemotherapy as first-line treatment for advanced squamous non-small-cell lung cancer
Presenter: Caicun Zhou
Session: Poster session 08