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

5983 - Immune-Related Adverse Events (irAEs) and Survival (OS) in Metastatic Non-small Cell Lung Cancer (mNSCLC) Patients (pts) Treated With Immunotherapy

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

Management of Systemic Therapy Toxicities;  Immunotherapy;  Supportive Care and Symptom Management

Tumour Site

Presenters

Marcos Meliàn Sosa

Citation

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

Authors

M. Meliàn Sosa, C. Puchades, J.A. Mendez, A. Torres, C. Rodrigo, G. Gimeno, E. Rama, A. Martínez-Castillo, J. Caballero Daroqui, J. Gomez Codina, O. Juan-Vidal, D. Lorente

Author affiliations

  • Medical Oncology, Hospital Universitari i Politècnic La Fe, 46026 - Valencia/ES

Resources

Login to access the resources on OncologyPRO.

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

Abstract 5983

Background

Immunotherapy represents a new standard of care in first and second line treatment of advanced NSCLC. Immune related adverse events (irAEs) have been proposed as an indicator of treatment efficacy.

Methods

Retrospective analysis of mNSCLC patients treated with anti-PD/anti-PDL1 with or without anti-CTLA4 therapy. Electronic patient records were reviewed; irAEs were identified and graded according to CTC AE v4.03 criteria. The association with survival was evaluated in uni- (UV) and multivariable (MV) Cox-regression models.

Results

64 pts were identified; 41 (64.1%) were adenocarcinomas and 27 (42.2%) received immunotherapy in first-line. 44 pts (68.8%) received antiPD1/PDL1 monotherapy, and 20 pts (31.2%) received antiPDL1 + antiCTLA4. 15 pts (25%) developed irAEs: gastrointestinal (17.6%), endocrine (11.8%), cutaneous (17.6%), other (33.3%). Treatment was interrupted in 8 (53.3%) and suspended in 5 (33.3%) pts. 7 (50%) pts received high dose corticosteroids. No toxic deaths occurred. iRAEs were not significantly increased in pts receiving combination therapy (30% vs 20%, p = 0.377). Median OS was 6.5 m (95%CI: 0.24-12.7). Pts experiencing irAEs had a significantly higher OS (HR: 0.2; 95%CI: 0.07-0.58; p = 0.003) in UV analysis, and was independent of other prognostic factors in MV analysis (Table).Table: 1391P MV Cox-regression survival model

FactorHR (95%CI)p-value
irAE (yes vs no)0.18 (0.06 – 0.53)0.002
Histology1.11 (0.99 – 1.24)0.061
ECOG PS0.82 (0.42 – 1.59)0.551
Treatment line (first line vs second or further)1.06 (0.52 – 2.18)0.868
Treatment type (monotherapy vs combination)2.25 (1.02 – 4.99)0.045

Conclusions

The development of irAEs may identify pts with a higher likelihood of benefitting from immunotherapy in NSCLC. These findings will require prospective validation in well-designed clinical trials.

Clinical trial identification

Legal entity responsible for the study

Instituto Investigación Sanitaria La Fe.

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.