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 Display session

178P - Germline testing in non-small cell lung cancer (NSCLC): Real-world impact of the discovery of germline pathogenic variants (PGV) in the INHERITY LC (ILC) study

Date

22 Mar 2024

Session

Poster Display session

Topics

Population Risk Factor

Tumour Site

Presenters

Juan Carlos Laguna Montes

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-6. 10.1016/esmoop/esmoop102576

Authors

J.C. Laguna Montes1, R. Lastra2, O. Higuera Gomez3, M. Zurera Berjaga4, A. Moratiel Pellitero2, S. Menao-Guillen2, M. Arruebo2, M. Potrony1, X. Sole1, A. Arcocha5, L. Moreno1, L. Gutiérrez Sainz6, C. Teixido7, N. Vinolas Segarra1, J. De-Castro6, M.D. Isla Casado2, L. Mezquita1

Author affiliations

  • 1 Hospital Clinic y Provincial de Barcelona, Barcelona/ES
  • 2 Hospital Clinico Universitario Lozano Blesa, Zaragoza/ES
  • 3 Hospital Universitario La Paz, 28046 - Madrid/ES
  • 4 Instituto de Investigación Sanitaria Hospital 12 de Octubre (i+12), Madrid/ES
  • 5 Hospital Clinic of Barcelona, Barcelona/ES
  • 6 Hospital Universitario La Paz, Madrid/ES
  • 7 Hospital Clinic y Provincial de Barcelona, 8036 - Barcelona/ES

Resources

Login to get immediate access to this content.

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

Abstract 178P

Background

It is estimated that around 8% of NSCLC are linked to genetic predisposition. However, there is no criteria for study on Genetic Counseling Units (GCU). In the ILC study we identified 11% of PGVs in patients (pts) with NSCLC. Here, we report the real-world impact of the discovery of PGVs in pts with NSCLC and their families.

Methods

The ILC study is a multicentric prospective study of 148 pts with NSCLC with germline testing performed by NGS (Spain). This is a substudy of 16 pts harboring PGVs in cancer predisposition genes. Clinical and molecular data of the tumors, GCUs study, genetic counseling recommendations for pts/families and their results were collected from medical reports.

Results

Out of 148 pts enrolled, we identified PGVs in 16 (11%) involving CHEK2 (3/19%), NBN (3), ATM (2/13%), BARD1 (1/6%), BRCA2 (1), FAN1 (1), MLH1 (1), MRE11 (1), PALB2 (1), TP53 (1), XRCC2 (1). In PGV-carriers, median age was 60 years (31-79), 63% were female and 69% smokers; 69% had advanced disease, mainly adenocarcinoma histology (69%) and 56% with a somatic driver alteration. Of the 16 PGV-carriers, 14 cases (88%) did not met criteria for genetic testing. After the ILC results, 13 were derived to a GCU. In 7 pts (44%) cancer screening for solid tumors has been initiated while in 6 (37%) was not initiated because of death for cancer progression. In 1 patient with an EGFR mutated lung adenocarcinoma harboring a PGV in MLH1, a prophylactic hysterectomy was performed. We identified 6 pts with PGV with potential therapeutic implications in genes involved in DNA (4/25%) and mismatch repair (1/6%). Regarding the family impact, in 10 families (63%) cascade study was recommended performing germline testing in 27 healthy relatives. Of them, in 12 individuals a PGV was detected in BRCA2, CHEK2, FAN1, MLH1, MRE11, NBN, TP53 and XRCC2. All of them are current under follow-up by GCU for preventive measures.

Conclusions

In this real-world cohort, most of the carriers identified did not met criteria for genetic testing according to the current guidelines. However, the discovery of PGVs in NSCLC led to assessment and follow-up by GCU for both pts and their relatives for cancer screening. Specific criteria for genetic testing in NSCLC are needed.

Legal entity responsible for the study

Hospital Clinic y Provincial de Barcelona.

Funding

ICAPEM: Asociación Para La Investigación Del Cáncer De Pulmón En Mujeres.

Disclosure

J.C. Laguna Montes: Other, Personal, Invited Speaker: Kyowa Kirin; Other, Personal, Other, Travel, Accommodations, Expenses: Rovi, Pierre Fabre. M. Potrony: Other, Personal, Officer, Educational activities: ISDIN. L. Mezquita: Financial Interests, Personal, Invited Speaker: Bristol Myers Squibb, AstraZeneca, Roche, Takeda, Janssen, Pfizer, MSD; Financial Interests, Personal, Advisory Role: Roche, Takeda, Janssen; Non-Financial Interests, Personal, Research Grant: Bristol Myers Squibb, Boehringer Ingelheim, Amgen, Stilla, Inivata; Financial Interests, Personal, Research Grant: AstraZeneca; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Bristol Myers Squibb, Roche, Takeda, AstraZeneca, Janssen. All other 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.