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

3302 - Prior or Concurrent Radiotherapy and Nivolumab Immunotherapy in Non-Small Cell Lung Cancer

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

Gishan Ratnayake

Citation

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

Authors

G. Ratnayake1, M. Shankar2, K. Roberts3, R. Mason4, B.G.M. Hughes1, Z. Lwin1, V. Jain3, K.J. O'Byrne5, B. Chua1

Author affiliations

  • 1 Cancer Care Services, Royal Brisbane and Women's Hospital, 4029 - Brisbane/AU
  • 2 Department Of Radiation oncology, Townsville Hospital, 4814 - Townsville/AU
  • 3 Department Of Medical Oncology, Mater Adults Hospital, 4101 - Brisbane/AU
  • 4 Department Of Medical Oncology, Princess Alexandra Hospital, 4102 - Brisbane/AU
  • 5 Cancer Services, Princess Alexandra Hospital, 4102 - Woolloongabba/AU

Resources

Login to access the resources on OncologyPRO.

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

Abstract 3302

Background

Preclinical and retrospective clinical studies suggest that combining radiotherapy (RT) with programmed cell death protein 1 (PD-1) blockade may elicit a synergistic anti-tumour response. We aimed to assess whether prior or concurrent RT was associated with improved disease control in patients with metastatic non-small cell lung cancer (NSCLC) treated with nivolumab.

Methods

We conducted a retrospective study of patients receiving nivolumab as second or subsequent line therapy for metastatic NSCLC across four tertiary oncology centers. All patients received nivolumab at a dose of 3mg/kg every 2 weeks intravenously. Survival and toxicity data were collected prospectively. Patients were categorized into those who received any RT for NSCLC (with curative or palliative intent, thoracic or otherwise) prior to or during nivolumab therapy, and those with no history of RT for NSCLC. Kaplan-Meier survival analysis was performed for progression-free survival (PFS) and overall survival (OS) following commencement of nivolumab.

Results

85 patients (32 female, 53 male) received nivolumab between July 2015 and December 2016. Patients had a median age of 67 years (range 42-84) at commencement of nivolumab and were followed up for a median of 15 months. 65 patients (76.4%) received RT prior to or during nivolumab and 20 patients (23.6%) received nivolumab alone. Baseline characteristics of age, performance status, histology, smoking status, sites of metastatic disease and previous therapy were similar between the two groups. Prior or concurrent RT was associated with prolongation of PFS, median 2.8 months with RT versus 1.3 months without RT (P = 0.02, HR = 0.494, 95% CI 0.279-0.873). The median OS of the group receiving RT was 6.4 months vs 4.2 months for the no RT group but the difference did not reach statistical significance (p = 0.20). RT was not associated with an increase in toxicity and Grade 2 or greater pneumonitis rates were low in both groups (RT 4.6% vs no RT 5%).

Conclusions

RT prior to or concurrent with nivolumab for metastatic NSCLC was associated with superior PFS over nivolumab alone with no evidence of increase in adverse effects. RT may potentiate the effect of anti-PD-1 immunotherapy in NSCLC.

Clinical trial identification

Legal entity responsible for the study

Royal Brisbane and Womens’ Hospital, Herston, Queensland.

Funding

Has not received any funding.

Editorial Acknowledgement

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.