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

ePoster Display

1659P - Immune checkpoint inhibitors plus VEGF tyrosine kinase inhibitors as second-line or later therapy for patients with extensive stage small cell lung cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Immunotherapy

Tumour Site

Small Cell Lung Cancer

Presenters

Ning Yan

Citation

Annals of Oncology (2021) 32 (suppl_5): S1164-S1174. 10.1016/annonc/annonc680

Authors

N. Yan1, S.X. Guo1, M.J. Li1, S.Y. Huang1, Q.Q. Guo1, D. Geng1, H.X. zhang1, X. Li2

Author affiliations

  • 1 Oncology Department, The First Affiliate Hospital of Zhengzhouy School of Medicine, 450002 - zhengzhou/CN
  • 2 Medical Oncology, The First Affiliated Hospital of Zhengzhou University, 450052 - Zhengzhou/CN

Resources

Login to get immediate access to this content.

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

Abstract 1659P

Background

Immune checkpoint inhibitors (ICIs) have greatly changed the current treatment status of extensive-stage small-cell lung cancer (ES-SCLC) and are approved to be used in the first-line setting of ES-SCLC. However. treatment choices in second line or above in ES-SCLC setting remains limited. Hence, the present retrospective study aimed to evaluate the efficacy of ICIs plus anti-VEGF/VEGFR agents in ES-SCLC patients in the second line or later setting, and preliminarily explore the predictive value of neutrophil-to-lymphocyte ratio (NLR) in ES-SCLC.

Methods

Patients with ES-SCLC who have received anti-PD-1/PD-L1-based therapy between 2019 and 2020 in the First Affiliated Hospital of Zhengzhou University were retrospectively screened. The progression-free survival (PFS), overall survival (OS), objective response rate (ORR) and disease control rate (DCR) were estimated. The correlation between NLR and the response of the combined regimen was evaluated.

Results

35 patients were ultimately included in the present study. All of them were administered with ICIs plus anti-angiogenesis agents in the second line or later setting. confirmed ORR was 17.6.0% (95%CI: 4.1%-31.1%), the DCR reached 47.1% (95%CI:29.4%-64.7%) the median PFS reached 8 months (95% CI: 3.5-12.5). At the time of data cutoff, the median OS was not reached. In univariable logistic regression analysis, patients with NLR greater than or equal to 5 were associated with poorer PFS compared with less than 5 (the median PFS 4 months vs 20.4 months, p=0.0174, HR=2.642, 95% CI: 0.94-7.4). In addition, median OS in NLR≥5 group were also significantly shorter than that in NLR < 5 group (p=0.0198, HR=8.579, 95% CI: 1.31-56.4). Additionally, the ORR was numerically higher in the NLR<5 group than that in the NLR≥5 group (21.7% [95% CI: 3.5-40] vs 8.3% [95% CI: -10-26.7], p=0.39).

Conclusions

ICIs plus anti-angiogenesis inhibitors show potential antitumor activity in second line or later settings in ED-SCLC patients. And the current work indicated NLR could be a promising predictive marker for the response of the combined regimen. The data warrant confirmation by randomized clinical studies.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

The Joint Construction Project of Henan Province and Ministry (No. LHGJ20190013).

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.