A phase II study of anlotinib in the first-line treatment of locally advanced or metastatic soft tissue sarcoma.

Authors

null

Xin Huang

The Second Affiliated Hospital Zhejiang University School of Medicine, Hangzhou, China

Xin Huang , Zhaoming Ye , Tao Li , Yongzhong Wei , Shoufeng Wang , Yunxia Liu , Jia Chen

Organizations

The Second Affiliated Hospital Zhejiang University School of Medicine, Hangzhou, China, Cancer Hospital of the University of Chinese Academy of Sciences, Hangzhou, China, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China, Drum Tower Hospital Affiliated to Nanjing University School of Medicine, Nanjing, China, Hangzhou Third Hospital, Hangzhou, China, Cancer Hospital of Nanjing Medical University, Nanjing, China

Research Funding

No funding received
None

Background: Standard treatment for patients with unresectable locally advanced or metastatic soft-tissue sarcoma is chemotherapy based on anthracyclines, while the tolerance of chemotherapy is limited. We assessed if anlotinib, a multitarget tyrosine kinase inhibitor, is efficacy and safety for the first-line treatment of these patients. Methods: This is an open-label, single-arm, multicenter, phase II clinical trial (NCT03792542) including 44 planned subjects. Eligible patients were aged 18-70 years old, diagnosed with locally advanced or metastatic soft-tissue sarcoma and had at least one measurable lesion according to RECIST 1.1. Other inclusion criteria included ECOG PS 0̃2, chemotherapy and anti-angiogenesis treatment naïve. Patients were administrated 12mg anlotinib once daily for 14 days every 3 weeks until disease progression or unacceptable toxicity. The primary endpoint was progression-free survival (PFS). Safety assessment was done in patients who received at least one dose of anlotinib. Here we report the results of a planned interim analysis. Results: From April 2019 to December 2020, 29 patients (16 males and 13 females) were enrolled from 7 hospitals in China. The median age is 57 (range 23-69). Pathological types included liposarcoma (n = 8), undifferentiated pleomorphic sarcoma (n = 5), fibrosarcoma (n = 5), synovial sarcoma (n = 4), and others (n = 7). At the data cutoff date on December 31, 2020, the median duration of treatment was 5.3 months, and the median PFS was not reached. 26 patients were eligible for the evaluation of tumor response.1 achieved partial response (PR) and the objective response rate (ORR) was 3.85% (1/26). 24 had stale disease (SD) and the disease control rate (DCR) was 96.2% (25/26). The clinical benefit rate (CBR), defined as the proportion of patients who achieved durable disease control (CR/PR/SD) more than 4 and 6 months, were 65.4% (17/26) and 38.5% (10/26) respectively. Most adverse events (AE) were grade 1 or 2. The most common grade 3 AE was hypertension (17.2%). No grade 4 AEs or treatment related death occurred in this study through the last follow-up. Conclusions: This interim analysis showed anlotinib of promising efficacy and favorable tolerance in the first-line treatment of locally advanced or metastatic soft- tissue sarcoma. Clinical trial information: NCT03792542

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Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Sarcoma

Track

Sarcoma

Sub Track

Soft Tissue Tumors

Clinical Trial Registration Number

NCT03792542

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr e23531)

DOI

10.1200/JCO.2021.39.15_suppl.e23531

Abstract #

e23531

Abstract Disclosures