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 16

1163P - Impact of brain metastases in synchronous single organ oligometastatic lung cancer (OMD)

Date

10 Sep 2022

Session

Poster session 16

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Hevron Al Sheik

Citation

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

Authors

H. Al Sheik1, J. Roeper2, K. Wedeken2, L.C. Heukamp3, F. Griesinger2

Author affiliations

  • 1 Department Of Internal Medicine-oncology, Carl von Ossietzky University Oldenburg, 26211 - Oldenburg/DE
  • 2 Department Of Internal Medicine-oncology, Pius Hospital, 26211 - Oldenburg/DE
  • 3 Molecular Pathology, Hematopathology Hamburg, 22547 - Hamburg/DE

Resources

Login to get immediate access to this content.

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

Abstract 1163P

Background

Local radical therapy (LRT) improves survival in oligometastatic non-small cell lung cancer (OMD) patients. The scientific evidence on re-treatments and the role of brain involvement during the course of disease is scarce. We therefore performed a retrospective analysis to evaluate follow-up therapies after LRT and to describe predictors of survival.

Methods

106 patients with synchronous, single organ OMD with ≤3 metastases from one certified North-German lung cancer center were included and analyzed. All underwent thorough initial staging with PET scan, brain imaging (CT or MRT) and mediastinal staging.

Results

106 patients were included (median age 67 [37–89], adenocarcinoma 66% (n=70), male 60% (n=64), ECOG 0 and 1 83% (n=88), current or ex heavy smoker 90% (n=95)). 27% had brain (n=29), 8% liver (n=8), 62% other extracranial metastases (n=66) and one patient had no metastases. The OS was 11 months for all patients. Patients who receive LRT (n=67) have a significantly longer OS than patients without (n=39) (13 months vs. 8 months, p<0.006). LRT for every relapse was possible for 48% of all patients (n=15/31) and more likely in patients with brain metastases (60 vs. 40%). 92% (n=33/36) of all patients with brain metastases (including relapse) have received a LRT. Repeated LRT (n=9/36) resulted in numerically longer OS (21 months vs. 11. months; p<0.419)

Conclusions

Use of repeated LRT in relapsed synchronous single organ OMD results in a long-term favorable outcome. Brain control is crucial and determines survival. More cases and detailed data will be presented at the meeting.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

J. Roeper: Financial Interests, Personal, Invited Speaker: Boehringer Ingelheim, AstraZeneca, Roche. L.C. Heukamp: Financial Interests, Personal, Invited Speaker, Advisory Board: Boehringer Ingelheim, AstraZeneca, Roche, Pfizer, MSD, BMS, Novartis, Siemens. F. Griesinger: Financial Interests, Personal, Invited Speaker, Advisory Board and Research Grant: Boehringer Ingelheim, AstraZeneca, BMS, MSD, Roche, Siemens, Takeda, Pfizer, Lilly, Novartis, Celgene, Ariad, AbbVie, Amgen, Tesaro/GSK. 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.