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

172P - Real-world data of anolotinib for lung cancers with liver metastases in China

Date

22 Mar 2024

Session

Poster Display session

Topics

Tumour Site

Thoracic Malignancies

Presenters

Minglei Zhuo

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-4. 10.1016/esmoop/esmoop102575

Authors

M. Zhuo1, Z. Wang2, Y. Qin3

Author affiliations

  • 1 Peking University Cancer Hospital & Institute, Beijing/CN
  • 2 Shandong Cancer Hospital and Institute, Jinan/CN
  • 3 The First Affiliated Hospital of Zhengzhou University, 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 172P

Background

Despite the high incidence rate and poor prognosis of lung cancers with liver metastases, effective treatment for this population remains an unmet need. Anlotinib (a novel anti-angiogenesis agent) could reprogramme the tumor microenvironment and normalize tumor vessel, improving the liver immunosuppressive microenvironment and liver metastases. However, the real-world evidence with anlotinib for this population is limited. Here we report the real-world data of efficacy and safety of anlotinib for non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) with liver metastases in China.

Methods

We reviewed the real-world records of patients treated with anlotinib in any line of treatment for solid tumors with liver metastases through 5 large hospitals in China from Jan, 2016 to Feb, 2023. Patients with hepatocellular carcinoma and those who had received locoregional therapy during anlotinib treatment were excluded. In this abstract, we present data from patients with NSCLC and SCLC. Progression-free survival (PFS) and hepatic PFS (hPFS) were estimated using the Kaplan-Meier method and compared using the log-rank test.

Results

475 patients were enrolled and 141 patients with lung cancers were analyzed, including 98 (69.5%) NSCLC and 43 (30.5%) SCLC. At data cut-off (Feb 28, 2023), the median follow-up was 7.27 months (95% CI, 6.97-7.63). The median PFS of NSCLC and SCLC were 5.80 months (95% CI, 5.00-7.20), 5.43 months (95% CI, 4.30-NE). The median hPFS of NSCLC and SCLC were 6.43 months (95% CI, 5.00-NE), 7.27 months (95% CI, 4.53-NE). The median OS of NSCLC and SCLC were 7.63 months (95% CI, 7.20-NE), NR (95% CI, 7.37-NE). There was not statistically significant between NSCLC and SCLC in PFS (p=0.63), hPFS (p=0.74) and OS (p=0.55). 27 (19.2%) patients had treatment-emergent adverse events (TEAEs) and 3 patients (2.1%) had ≥3 TEAEs. Most frequent TEAEs were hematological (19.2%) and gastrointestinal (5.0%) toxicities.

Conclusions

This study provides the largest real-world experience of anlotinib in solid tumors with liver metastases to date. For NSCLC and SCLC with liver metastases, anlotinib could be an effective and safe treatment option.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

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.