Abstract 1362P
Background
In aNSCLC, pretreatment CTs help determine TNM stage, an important prognostic factor in treatment decisions, as well as determination of clinical trial eligibility/stratification. However, CTs contain prognostic features beyond TNM stage that are not easily quantifiable or reproducible. We examine an imaging-based artificial intelligence algorithm to predict overall survival (OS) compared to TNM staging.
Methods
IPRO, a fully automated deep learning system extracting 5,341 features from chest CT (including tumor burden, and body/cardiovascular composition), was trained on an independent dataset to generate mortality risk scores. We retrospectively evaluate IPRO compared to TNM stage to predict OS from 2,894 subjects diagnosed with aNSCLC at 17 cancer centers in Alberta from 2008 - 2017. Kaplan-Meier and Cox regression methods are used to estimate covariate effects on OS including a model stratified by stage. We evaluate Harrell’s c-index and AIC as measures of goodness of fit comparing models with IPRO, TNM stage, and IPRO + stage (full model). Smaller values for AIC and larger values of the c-index indicate better models.
Results
Median OS was 4.3 months, 80.3% of patients were stage IV at diagnosis, and 52.6% were male. Hazard ratios for OS by IPRO within stage were 1.39 (IIIB) and 1.34 (IV), suggesting IPRO associations were similar by stage group. The c-index for IPRO was larger than for TNM staging. Removing IPRO from the full model resulted in a larger deterioration in AIC than removal of TNM staging.
Conclusions
IPRO provides better discrimination of OS compared to TNM stage based on the c-index. The addition of stage in the full model negligibly improves goodness of fit. This suggests IPRO is a better predictor of OS than stage in this population and may provide greater utility as a prognostic factor in clinical research. Future analyses will include biomarker status and incorporation of other anatomic regions into the model. Table: 1362P
Summary of goodness of fit statistics
Model | C-index | AIC |
Stage (IIIB vs IV) | 0.54 | 39461.40 |
IPRO | 0.60 | 39299.62 |
Full model (IPRO + stage) | 0.61 | 39226.61 |
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Altis Labs, Inc.
Funding
Digital Supercluster, Altis Labs, Inc.
Disclosure
O.F. Khan: Financial Interests, Personal, Invited Speaker: Merck, Gilead, Novartis; Financial Interests, Personal, Advisory Board: Pfizer, Knight Therapeutics, AstraZeneca. J. Riskas:Financial Interests, Personal, Financially compensated role: Altis Labs, Inc.; Financial Interests, Personal, Stocks/Shares: Altis Labs, Inc. S.A. Haider, O. Samorodova, J. Hennessy, V. Sivan, D. Shah: Financial Interests, Personal, Full or part-time Employment: Altis Labs, Inc.; Financial Interests, Personal, Stocks/Shares: Altis Labs, Inc. A. Mitchell: Financial Interests, Personal, Full or part-time Employment: Altis Labs, Inc.; Financial Interests, Personal, Stocks or ownership: Altis Labs, Inc. F. Baldauf-Lenschen: Financial Interests, Personal, Ownership Interest: Altis Labs, Inc.; Financial Interests, Personal, Full or part-time Employment: Altis Labs, Inc. S. Raman: Financial Interests, Institutional, Research Grant: AstraZeneca, Knight Therapeutics; Financial Interests, Personal, Speaker, Consultant, Advisor: Bayer, AstraZeneca, Tersera, Sanofi, Verity Pharma. N.B. Leighl: Financial Interests, Personal, Other, CME/independent lectures: MSD, BMS; Financial Interests, Personal, Invited Speaker, independent lectures: Novartis, Takeda; Financial Interests, Personal, Invited Speaker, independent CME lecture: BeiGene; Financial Interests, Personal, Invited Speaker, Independent CME lectures: Janssen; Financial Interests, Institutional, Research Grant: AstraZeneca, Lilly, MSD, Pfizer, Janssen, Inivata/NeoGenomics, Novartis; Other, Travel funding to deliver independent CME lectures: AstraZeneca; Other, Travel funding to deliver independent CME lecture: Janssen, MSD, Sanofi, Guardant Health. All other authors have declared no conflicts of interest.
Resources from the same session
1393TiP - A phase II/III study to evaluate the optimal dose, safety, and efficacy of livmoniplimab (Livmo) in combination with budigalimab (Budi) plus chemotherapy (CT) vs pembrolizumab (Pembro) plus CT in untreated metastatic non-small cell lung cancer (mNSCLC)
Presenter: Nicolas Girard
Session: Poster session 06
1394TiP - KRYSTAL-7: A phase III study of first-line adagrasib plus pembrolizumab versus pembrolizumab alone in patients with advanced NSCLC with KRASG12C mutation
Presenter: Marina Garassino
Session: Poster session 06
1395TiP - A randomized phase III trial evaluating oral BAY 2927088, compared with standard of care, as first-line treatment of locally advanced or metastatic NSCLC harboring HER2-activating mutations (SOHO-02)
Presenter: Antonio Passaro
Session: Poster session 06
1397TiP - Phase III trial of the therapeutic cancer vaccine OSE2101 versus docetaxel in patients with metastatic non-small cell lung cancer and secondary resistance to immunotherapy
Presenter: Stephen Liu
Session: Poster session 06
Resources:
Abstract
1398TiP - Be6A Lung-01, a phase III study of sigvotatug vedotin (SV), an investigational antibody-drug conjugate (ADC) versus docetaxel in patients (pts) with previously treated non-small cell lung cancer (NSCLC)
Presenter: Solange Peters
Session: Poster session 06
1399TiP - Phase III, double-blind study of cannabis sativa extract in pain management and quality of life in patients with metastatic lung cancer: Protocol of a study (IPElife trial)
Presenter: Danielli Matias
Session: Poster session 06
1728P - Results of TNT: A phase II study using talimogene laherparepvec, nivolumab and trabectedin for advanced leiomyosarcoma and liposarcoma [NCT# 03886311]
Presenter: Sant Chawla
Session: Poster session 06
1729P - Update on SAINT: A phase II study using trabectedin (T) in combination with ipilimumab (I) and nivolumab (N) in previously treated soft tissue sarcoma
Presenter: Anmol Dia Agarwal
Session: Poster session 06
1730P - Preliminary results of phase II study on preoperative intensity-modulated radiotherapy with concurrent PARP inhibitor for patients with non-metastatic inoperable or borderline operable extremity and trunk soft tissue sarcoma
Presenter: NingNing Lu
Session: Poster session 06
Resources:
Abstract