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Poster session 07

79P - Comprehensive genomic profiling provides patients access to novel matched therapies in a diverse real-world cohort of advanced lung cancer patients

Date

14 Sep 2024

Session

Poster session 07

Topics

Targeted Therapy;  Molecular Oncology;  Cancer Diagnostics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Jyoti Patel

Citation

Annals of Oncology (2024) 35 (suppl_2): S238-S308. 10.1016/annonc/annonc1576

Authors

J.D. Patel1, K. Nadhamuni2, A. Mitra3, M. CARTY2, H. Nimeiri4, I. Klein5, R. Pelossof6

Author affiliations

  • 1 Medicine Dept., Northwestern University Feinberg School of Medicine, 60611 - Chicago/US
  • 2 Data Science, Tempus Labs, 93012 - Camarillo/US
  • 3 Clinical Development, Tempus AI, 60654 - Chicago/US
  • 4 Oncology Clinical Development, Tempus Labs, Inc., 60654 - Chicago/US
  • 5 Medical Affairs, Tempus Labs, Inc., 60654 - Chicago/US
  • 6 600 West Chicago, Tempus Labs, Inc., 60654 - Chicago/US

Resources

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Abstract 79P

Background

ESMO and NCCN have recommended Comprehensive Genomic Profiling (CGP) to identify patients eligible for matched targeted treatment. Here, we assess adherence with guideline-recommended targeted therapy recommendations and assess the time from genomic sequencing to the initiation of targeted medication in a diverse, real-world dataset of advanced NSCLC patients.

Methods

We retrospectively analyzed de-identified metastatic NSCLC records from the Tempus multimodal database, which encompasses molecular and clinical data from diverse clinics across the United States sequenced with the Tempus xT assay from 2018-2022. The following guideline recommended actionable genomic variants were assessed: EGFR mutations, ALK fusions, ROS1 fusions, KRAS G12C mutations, BRAF V600E, RET fusions, MET ex14 skipping mutations, and NTRK1/2/3 fusions. Patients were defined as adherent if they received matched targeted therapy recommended in guidelines within 24 months of sequencing; genomic sequencing may have occurred prior to matched therapy recommendation.

Results

Among 1,407 evaluable patients, 16.5% (N= 232) had a targeted actionable variant detected by CGP. The overall adherence rate of matched targeted therapy was 87% (N=201). The adherence rate varied by actionable variant, with the highest adherence rate of 100% for EGFR exon 19 deletions (n=57), and the lowest rate 47% for BRAF V600E (n=17). Notably, a minority of adherent patients (13.4%, n=27) were sequenced prior to the FDA approval of these targeted agents and inclusion in guidelines. For these patients the median time from CGP to initiation of matched therapy was 10 months. For the remaining patients, this time was 0.6 months.

Conclusions

In a real-world, retrospective analysis of a cohort of advanced NSCLC patients, most oncologists utilized CGP to identify and treat patients with guideline-recommended variant matched targeted therapy, with adherence rates varying by variant. Importantly, even patients that received CGP results prior to FDA approval of novel therapies, received matched therapy once they were included in guidelines.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Tempus AI.

Disclosure

J.D. Patel: Financial Interests, Personal, Advisory Board: Takeda, AstraZeneca, AbbVie, AnHeart, BMS, Gilead, Sanofi, Takeda, Guardant; Financial Interests, Personal, Advisory Board, also travel support: Daiichi Sankyo; Financial Interests, Personal, Other, travel: Tempus. K. Nadhamuni: Financial Interests, Institutional, Full or part-time Employment: Tempus Labs; Financial Interests, Institutional, Stocks/Shares: Tempus Labs; Financial Interests, Institutional, Other, Full time employee: Tempus Labs. A. Mitra: Financial Interests, Personal, Full or part-time Employment: Tempus AI; Financial Interests, Personal, Stocks/Shares: Tempus Ai, Guardant Health. M. Carty: Financial Interests, Institutional, Full or part-time Employment: Tempus Labs; Financial Interests, Institutional, Stocks/Shares: Tempus Labs; Financial Interests, Institutional, Advisory Board: Tempus Labs. H. Nimeiri: Financial Interests, Personal, Full or part-time Employment: Tempus; Financial Interests, Personal, Stocks/Shares: Tempus, AbbVie. I. Klein: Financial Interests, Institutional, Full or part-time Employment, Full time employee, also granted shares in the company with potential future value.: Tempus Labs, Inc.; Financial Interests, Institutional, Stocks/Shares, Granted as part of overall compensation, may have future value.: Tempus Labs, Inc.; Non-Financial Interests, Member of Board of Directors, This is a not for profit organization (503c) that advocates for appropriate medication oversight and usage in the US healthcare system, based on literature regarding waste and medical error in today's system: Get the Meds Right. R. Pelossof: Financial Interests, Personal, Full or part-time Employment: Tempus; Financial Interests, Personal, Other, RSUs: Tempus.

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