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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

2358 - Localablative treatment for synchronous oligometastatic lung cancer – a propensity score analysis of 180 patients

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Presenters

Nikolaj Frost

Citation

Annals of Oncology (2018) 29 (suppl_8): viii493-viii547. 10.1093/annonc/mdy292

Authors

N. Frost1, A. Tessmer2, A. Schmittel3, V. van Laak4, S. Ochsenreither5, B. Temmesfeld-Wollbrück1, B. Schmidt4, N. Suttorp1, M. Witzenrath1, C. Grohe2

Author affiliations

  • 1 Department Of Infectious Diseases And Pulmonary Medicine, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 - Berlin/DE
  • 2 Department Of Pulmonary Medicine, Evangelische Lungenklinik Berlin-Buch, Berlin/DE
  • 3 Onkologie Seestrasse, Schwerpunkt Hamatologie und Onkologie, Berlin/DE
  • 4 Department Of Pulmonary Medicine, DRK-Klinikum Berlin-Mitte, Berlin/DE
  • 5 Charité Comprehensive Cancer Center, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 - Berlin/DE

Resources

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Abstract 2358

Background

Localablative treatment (LAT) improves outcome in lung cancer with oligometastatic disease (OMD) and potentially leads to long term survival. The aim of this retrospective study was to evaluate and quantify the additional benefit of LAT in synchronous OMD and to further identify prognostic factors for outcome and survival.

Methods

A propensity score matched pairs analysis was performed on a set of patient and disease variables in 180 patients, treated for synchronous OMD (including non-small cell and neuroendocrine lung cancer) with ≤4 metastatic lesions between 2000 and 2016 in 3 specified lung cancer centers in Berlin, Germany. Patients had either received LAT for all sites of disease (intervention group) by surgery or stereotactic ablative body radiation, or standard chemotherapy, if necessary combined with a palliative-intended local treatment (control group).

Results

Median follow-up time was 32.2 and 18.8 months for the intervention and control group, respectively. Substantial benefits in median progression free survival (PFS, 25.1 vs. 8.2 months; HR, 0.30; 95% CI, 0.21-0.43; p < 0.001) and overall survival (OS, 60.4 vs. 22.5 months; HR, 0.42; 95% CI, 0.28-0.62; p < 0.001) were associated to LAT. Histology of adenocarcinoma (PFS: HR, 0.58; 95% CI, 0.37-0.91; p = 0.02; OS: HR, 0.53; 95% CI,0.33-0.86; p = 0.01) and small primaries (T1a; PFS: HR, 0.36; 95% CI, 0.18-0.70, p = 0.003; OS: HR, 0.39; 95% CI, 0.18-0.84; p = 0.02) also predicted a favorable prognosis concerning PFS and OS. Nodal stage (N0-2 vs. 3; HR, 0.49; 95% CI, 0.25-0.97; p = 0.04) and number of metastases (1 vs. 2-4; HR, 0.63; 95% CI, 0.41-0.96; p = 0.03) were associated with an extended PFS, whereas initial ECOG-PS (0-1 vs. 2; HR, 0.42; 95% CI, 0.20-0.91; p = 0.03) predicted OS.

Conclusions

LAT was the strongest predictor for PFS and OS in patients with OMD and ≤4 metastases. Survival observed in the control group identifies OMD as a subset of lung cancer with a generally more favorable prognosis.

Clinical trial identification

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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