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Poster session 20

1368P - LUMINATE 102: A real-world study on biomarker testing rates among patients with non-small cell lung cancer (NSCLC) across lines of therapy

Date

21 Oct 2023

Session

Poster session 20

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Charu Aggarwal

Citation

Annals of Oncology (2023) 34 (suppl_2): S755-S851. 10.1016/S0923-7534(23)01943-9

Authors

C. Aggarwal1, Q. Xu2, S. Ng3, R. Kamalakar4, S.A. Crawford2, S. Beruti2, A. Myftiu2, M.B. Beasley5

Author affiliations

  • 1 Medicine - Hematology/oncology Department, University Of Pennsylvania, 19104 - Philadelphia/US
  • 2 Global Health Economics Outcomes And Research, Abbvie Inc. - Headquarters, 60064 - North Chicago/US
  • 3 Global Health Economics Outcomes And Research, Abbvie Inc., North Chicago/US
  • 4 Rwe Analytics, Abbvie Inc., North Chicago/US
  • 5 Pathology, Mount Sinai Hospital, 10029 - New York/US

Resources

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Abstract 1368P

Background

Molecular testing for biomarkers in patients (pts) with advanced/metastatic NSCLC (a/mNSCLC) is essential for diagnostic testing and use of targeted therapy. Testing patterns across lines of therapy (LOT) for pts with a/mNSCLC remain unclear.

Methods

This retrospective real-world study used ConcertAI Patient360™ database to assess biomarker testing patterns among adults with nonsquamous a/mNSCLC (2017–2022). Eligible pts received ≥1 LOT with ≥90-day follow-up. Biopsy and biomarker testing assessed actionable genetic alterations (ALK, BRAF, EGFR, KRAS, NTRK, RET, ROS1) and PD-L1 by LOT (first-, second-, third-line [1L, 2L, 3L]), test modality (IHC, FISH, CISH, NGS, PCR), and sample type (tissue/liquid).

Results

4528 pts were included; median age 67 years and from a community setting (76%). NGS rate at 1L was 57% overall (2017–2022) and increased to 80% during 2020–2022. Testing for ≥1 biomarker was 85% (1L), 31% (2L), 26% (3L) (overall, 2017–2022); and 89% (1L), 37% (2L), 28% (3L) (2020–2022). EGFR, BRAF, KRAS, RET, and ROS1 (Table) were mostly tested using NGS (56% at 1L vs 51% IHC, 21% FISH, and 10% PCR). Testing was most often conducted with tissue at 1L (64%) and liquid in 2L+ (41% each of tested 2L pts and 3L pts). At 2L, only 6% of pts had tissue re-biopsy, which dropped to 4% in 3L. Pts with 1L targeted therapy had higher re-testing (41% vs 25%, P<0.001) rates regardless of sample type in 2L than those who did not. Table: 1368P

N Any biomarker (%) PD-L1 (%) ALK (%) BRAF (%) EGFR (%) KRAS (%) METexon14 (%) NTRK (%) RET (%) ROS1 (%)
1L 4528 85 71 73 65 78 64 46 40 55 71
2L 1394 31 19 24 23 26 22 19 15 21 24
3L 473 26 14 20 20 22 19 16 11 18 21

Conclusions

Tissue was most frequently used in 1L for biomarker testing by NGS for genetic alterations or IHC for PD-L1; however, tissue was not regularly re-biopsied in 2L+ settings. Biomarker testing rates drop as pts navigate through LOT. Re-testing rate is higher among pts with an actionable mutation in 1L. Standardization of biomarker testing post-1L is needed to facilitate optimal later-line treatment decisions and individualized care for pts with a/mNSCLC.

Clinical trial identification

Editorial acknowledgement

Medical writing support was provided by Hayley Ellis, PhD, of Fishawack Facilitate Ltd, part of Fishawack Health, funded by AbbVie.

Legal entity responsible for the study

AbbVie.

Funding

AbbVie funded this real-world study and participated in the study design, research, analysis, interpretation of data, and the review and approval of the publication. All authors had access to relevant data and participated in the drafting, review, and approval of this publication. No honoraria or payments were made for authorship.

Disclosure

C. Aggarwal: Financial Interests, Institutional, Research Funding: AstraZeneca, Genentech, Incyte, Macrogenics, Merck Sharp & Dohme, MedImmune; Financial Interests, Institutional, Funding, Consultation fees: Genentech, Lilly, Celgene Merck, AstraZeneca, Blueprint Genetics, Shionogi, Daiichi Sankyo/AstraZeneca, Regeneron/Sanofi, Eisai, BeiGene, Turning Point, Pfizer, Janssen, Boehringer Ingelheim. Q. Xu, S. Ng, R. Kamalakar, S.A. Crawford, S. Beruti, A. Myftiu: Financial Interests, Personal, Full or part-time Employment: AbbVie; Financial Interests, Personal and Institutional, Stocks/Shares: AbbVie. M.B. Beasley: Financial Interests, Institutional, Advisory Board: AbbVie, AstraZeneca, Daiichi Sankyo.

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