Biomarker testing of lung cancer in North America versus globally.

M Matthew Paul Smeltzer (University of Memphis, School of Public Health, Memphis, TN) J Jennifer C. King (International Association for the Study of Lung Cancer, Denver, CO) C Casey Connolly (International Association for the Study of Lung Cancer, Denver, CO) K Kristen Brunson (Genentech Inc, South San Francisco, CA) M Maiyan Chau (AstraZeneca, Gaithersburg, MD) S Shuyan Chen A Anna Kerpel-Fronius (National Korányi Institute for Pulmonology, Budapest, Hungary) S Sylvie Lantuejoul (Department of Biopathology, Léon Bérard Centre, Lyon, France) A Anant Mohan A Allison Plaxco (University of Memphis, Memphis, TN) J Jessica Rice U Upal Kunal Basu Roy (LUNGevity Foundation, Bethesda, MD) R Ricardo S. Santos (Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein, São Paulo, Brazil) G Gavitt Alida Woodard (Yale School of Medicine, New Haven, CT) M Murry Wynes (International Association for the Study of Lung Cancer, Aurora, CO) A Amanda Young (5University of Memphis, Memphis, United States) Y Yasushi Yatabe R Ross A. Soo (Department of Hematology–Oncology, National University Cancer Institute, Singapore) K Karen Kelly (International Association for the Study of Lung Cancer, Denver, CO)

Abstract

8541 Background: Biomarker testing is essential to optimize lung cancer (LC) care, yet uptake of testing is suboptimal due to lack of access, cost, and long turnaround times (TAT). Recent advances now require biomarker testing in early-stage LC. In 2024, the International Association for the Study of Lung Cancer (IASLC) launched a 2 nd global survey to measure improvements and barriers to implementation of testing. We compared results from North America (NA) with global results by high income (HIC) and low or middle income countries (LMIC). Methods: A multi-disciplinary committee of oncologists, pathologists, pulmonologists, epidemiologists, and advocacy partners created the survey. We used mixed methods, with focus groups and in-depth interviews informing the quantitative survey with IRB oversite. Chi-square tests were utilized to compare frequencies between NA v Other HIC (OHIC) and HIC v LMIC. Results: Of the 1677 responses globally, 1501 were from HIC and 176 from LMIC. HIC included 337 responses from NA (287 United States and 50 Canada). Nearly all NA respondents (99%) believe biomarker testing significantly impacts patient outcomes and 94% report a clear understanding of who should be tested (v 91% OHIC, p=0.09). In NA, 66% and 40% ranked biomarker testing as highly important in late- and early- stage LC, respectively (64% and 28% OHIC, p=0.68 and p<0.01). Only 45% of NA respondents were satisfied with biomarker testing conditions (v 52% OHIC, p=0.03), and 69% estimate at least half of LC patients receive biomarker testing (71% OHIC), an increase from 45% in the 2018 survey (p<0.01). We found 40% of respondents from NA sometimes or often began treatment prior to obtaining biomarker results (41% OHIC). Key barriers identified were cost (23%), time (22%), and sample quality (20%), consistent with global and OHIC trends. Mean TAT in NA was 17.1 days (SD 7.8) v 16.1 days (SD 9.0) in HIC. Insufficient tumor was the primary cause for re-biopsy in late and early-stage patients for NA (58%) and HIC (48%). Lastly, 14% of NA reported no additional training in next-generation sequencing beyond medical education (16% OHIC). Globally, conditions were worse in LMIC v HIC including those who sometimes or often begin treatment prior to obtaining biomarker results (73% v 41%, p<0.01) and those who are confident or extremely confident in the adequacy of testing at their institution (48% v 68%, p<0.01). Conclusions: Respondents from NA believe they understand the value of biomarker testing for LC and who should be tested. Testing practices have reportedly improved since 2018, yet less than half of NA respondents are satisfied with biomarker testing practices and many patients are still treated without biomarker information. Responses from NA were similar to OHIC, with some exceptions, but significant disparities were evident in LMIC. We identified key barriers that should be addressed to optimize testing practices and patient outcomes.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 8541-8541
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (19)

M

Matthew Paul Smeltzer

University of Memphis, School of Public Health, Memphis, TN

J

Jennifer C. King

International Association for the Study of Lung Cancer, Denver, CO

C

Casey Connolly

International Association for the Study of Lung Cancer, Denver, CO

K

Kristen Brunson

Genentech Inc, South San Francisco, CA

M

Maiyan Chau

AstraZeneca, Gaithersburg, MD

S

Shuyan Chen

A

Anna Kerpel-Fronius

National Korányi Institute for Pulmonology, Budapest, Hungary

S

Sylvie Lantuejoul

Department of Biopathology, Léon Bérard Centre, Lyon, France

A

Anant Mohan

A

Allison Plaxco

University of Memphis, Memphis, TN

J

Jessica Rice

U

Upal Kunal Basu Roy

LUNGevity Foundation, Bethesda, MD

R

Ricardo S. Santos

Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein, São Paulo, Brazil

G

Gavitt Alida Woodard

Yale School of Medicine, New Haven, CT

M

Murry Wynes

International Association for the Study of Lung Cancer, Aurora, CO

A

Amanda Young

5University of Memphis, Memphis, United States

Y

Yasushi Yatabe

R

Ross A. Soo

Department of Hematology–Oncology, National University Cancer Institute, Singapore

K

Karen Kelly

International Association for the Study of Lung Cancer, Denver, CO