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

2694 - Impact of early steroids use on clinical outcomes of patients with advanced NSCLC treated with immune checkpoint inhibitors

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

Topics

Supportive Care and Symptom Management;  Immunotherapy

Tumour Site

Presenters

Giovanni Fucà

Citation

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

Authors

G. Fucà1, M. Poggi2, G. Galli2, M. Imbimbo2, G. Lo Russo2, D. Signorelli2, M. Vitali2, M. Ganzinelli2, N. Zilembo2, F. de Braud2, M.C. Garassino2, C. Proto2

Author affiliations

  • 1 Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 - Milan/IT
  • 2 Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan/IT

Resources

Login to access the resources on OncologyPRO.

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

Abstract 2694

Background

In advanced non-small cell lung cancer (NSCLC), immune checkpoint inhibitors (ICIs) significantly improved patients (pts) prognosis, even if many factors could impair their efficacy. The impact of steroids (well below the immunosuppressant dose) on ICIs outcomes is debatable, although a quite number of pts starts immunotherapy while on, or early recurs to steroids as supportive care medications or for mild AEs. Here, we aimed at assessing the impact of early steroids use on clinical outcomes of ICIs treatment in a series of pts with advanced NSCLC.

Methods

All consecutive pts with advanced NSCLC who started ICIs at our institution from Apr 2013 to Dec 2017 were retrospectively reviewed. Pts with at least one instrumental response assessment were included. Early use of steroids was defined as the use of a daily prednisone-equivalent dose ≥ 10 mg for at least 1 day within 28 days from ICIs initiation. Chi-square test or Fisher's exact test were used to analyze the association of early use of steroids with pts’ characteristics. The Kaplan-Meier method and the Cox proportional-hazards model were used for survival analyses.

Results

Out of 151 pts included, 35 (23 %) made early use of steroids. Most of the pts (96%) received single agent anti PD-1/PD-L1, while 6 pts (4%) received combinatorial PD-L1+CTLA-4 blockade. Early use of steroids was negatively associated with disease control (OR 0,32; 95% CI 0.14-0.71, P = .006) and positively associated with ≥2 metastatic sites (OR 3,08, 95% CI 1.33-7.89; P = .01) and ECOG PS ³ 2 (OR 4.57; 95% CI 1.10-20.37; P = .03). With a median follow-up of 32.7 months, early use of steroids conferred a worse median progression-free survival (PFS) (1.98 vs 3.94 months; HR 1.80; 95% CI 1.20-2.80; P = .003). In the multivariable model including other covariates significantly associated with PFS (i.e. ECOG PS and PD-L1 status), the early use of steroids was confirmed to be independently associated with poorer PFS (HR 1.88; 95% CI 1.08-3.28; P = .03).

Conclusions

We found that the early use of steroids independently affects clinical outcomes in patients with advanced NSCLC treated with ICIs. If these findings will be further validated, such use in this setting should be carefully evaluated and avoided when not strictly needed.

Clinical trial identification

Legal entity responsible for the study

Giovanni Fucà.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

D. Signorelli: Consultancies: AstraZeneca, Boehringer Ingelheim, BMS. M.C. Garassino: Consultancies: MSD, BMS, AstraZeneca, Eli Lilly. C. Proto: Consultancies: MSD, BMS. 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.