Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 15

1120P - Medical practice analysis of sex-specific trends in advanced non-small cell lung cancer (NSCLC) in biomarker testing and treatment in Europe and Asia

Date

10 Sep 2022

Session

Poster session 15

Topics

Genetic and Genomic Testing

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Carmen Escorial

Citation

Annals of Oncology (2022) 33 (suppl_7): S448-S554. 10.1016/annonc/annonc1064

Authors

C. Escorial1, L. Mendoza2, L. Schnetter1, F. Tetzlaff3

Author affiliations

  • 1 Real World Solutions, IQVIA Commercial GmbH & Co. OHG/IQVIA RDS GmbH - Zentrale, 60549 - Frankfurt am Main/DE
  • 2 Mss H/o Eu, IQVIA RDS Czech Republic s.r.o., 186 00 - Prague/CZ
  • 3 Global Oncology - Central, East & South Europe, IQVIA, 60549 - Frankfurt am Main/DE

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1120P

Background

Several papers have reported a trend of rising lung cancer incidence among women. In addition, sex has also been reported as a critical factor in lung cancer incidence and survival. To evaluate if there are sex-specific biomarkers and treatment approaches in advanced NSCLC, we studied the prevalence of biomarker testing rates and results for disease relevant mutations (EGFR, ALK, ROS1) and the corresponding treatment landscape.

Methods

Anonymized patient-level data collected through a web-based survey between January and December 2021 from 16,062 NSCLC drug treated patients was analyzed, excluding clinical trials. The survey excluded any data captured in observational or interventional clinical studies, registries and real-world databases. The study collected real-world data in France, Germany, Italy, Spain, UK, China, Japan and South Korea.

Results

The percentage of biomarker tested women (w) and men (m) patients in Europe were as follows (w / m): EGFR (86% / 77%), ALK (83% / 75%) and ROS1 (69% / 61%). In Asia: EGFR (89% / 74%), ALK (70% / 61%) and ROS1 (54% / 46%). Out of the biomarker tested population, 38% of women were EGFR mutant, compared to 18% of men in Europe, while 66% of women were EGFR mutant and 39% of men in Asia. There were not different percentages of ALK and ROS1 mutations between sexes. The treatment approach for the mutated population presented significant differences among women and men. Women patients with EGFR mutant were more frequently treated with Osimertinib in Europe (67% / 59%) while the difference was not as marked in Asia (38% / 36%). Substantial sex differences were also observed in patients treated with Alectinib in Europe, (74% / 56%) and Asia (67% / 46%) for women and men, respectively. Likewise, ROS1 mutated women patients were more treated than men with Crizotinib in Europe (57% / 43%) and Asia (55% / 48%).

Conclusions

Women were tested more frequently for all biomarkers and showed more EGFR mutations. Looking at the treatment approaches, a higher percentage of treatment with Osimertinib was found in Europe compared to Asia. There is sex-specific treatment management for patients with ALK and ROS1 mutations, where women received treatment with Alectinib and Crizotinib (respectively) more often than men.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

IQVIA.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.