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E-Poster Display

1331P - Correlation between development and grade of immune-related toxicities and outcomes during treatment with immune checkpoint inhibitors in non-small cell lung cancer patients

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Pablo Ayala de Miguel

Citation

Annals of Oncology (2020) 31 (suppl_4): S754-S840. 10.1016/annonc/annonc283

Authors

P. Ayala de Miguel1, J. López Gallego1, I. Gorospe García2, P.R. Rivera Vargas1, A. Posada Restrepo1, A. Acero Caballero3, J. Aires Machado4, R. Alonso Calderón1, J.M. Rodríguez García1, P. Borrega García1

Author affiliations

  • 1 Medical Oncology Department, Hospital San Pedro De Alcantara, 10003 - Caceres/ES
  • 2 Medical Oncology, San Pedro de Alcántara University Hospital, 10002 - Cáceres/ES
  • 3 Medical Oncology Department, Hospital Don Benito-Villanueva, 6400 - Don Benito (Badajoz)/ES
  • 4 Medical Oncology Department, Hospital Ciudad de Coria, 10800 - Coria (Cáceres)/ES

Resources

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Abstract 1331P

Background

The use of immune-checkpoint inhibitors (ICI) is associated with the development of new immune-related adverse effects (irAEs) in some patients. Our aim was to study if there is any correlation between the development and grade of irAEs and the efficacy of ICI.

Methods

We collected data of 138 patients (83% male) diagnosed of advanced NSCLC and treated with ICI between December 2015 and March 2020 in our institutions. The median age was 66 years (range 48-85). Fifty-nine percent had adenocarcinoma histology, 40% squamous. Six percent had stage III-B at the start of immunotherapy, 35.5% stage IVa, 26.8% IVb and 31.2% IVc. Fifty percent of the patients had unknown or negative PDL1, 16.7% had expression in 1-49% of tumor cells and 32.6% expression of more than 50%. Twenty-three percent received immunotherapy at 1st line and 76.8% in 2nd or later. Several variables as clinical, tumour-related and therapeutical were included and univariate and multivariate Cox regression analysis were performed.

Results

irAEs occured in 49% of patients; 12% developed grade 3 to 4 toxicities. More frequent irAEs were fatigue (24%), rash (16%) and arthralgias (15%). The appearance of any grade of toxicity was associated with improved progression-free survival (PFS) (median 18.07 months vs 4.97 months; HR 12.81; p < 0.001). Patients who developed grade 3 or worse irAEs had longer PFS than those who develop grade 1 or 2 irAEs and those who did not suffered any irAEs (27.23 vs. 16.60 vs. 4.87 months; HR 7.02; p < 0.001). The use of corticosteroids during treatment with ICI was not related to PFS.

Conclusions

Development of serious irAEs during treatment with ICI was associated with better outcomes in our population. The use of corticosteroids during immunotherapy did not affect the efficacy of treatment.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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