Literature DB >> 31550814

[Efficacy and safety of Anlotinib as a third-line chemotherapy for metastatic colorectal cancer].

N Li1, Q Huang, M J Zhang, Z D Chen.   

Abstract

Objective: To evaluate the efficacy and safety of Anlotinib as a third-line therapy in patients with metastatic colorectal cancer.
Methods: Anlotinib was administered to patients with advanced colorectal cancer who had received ≥ second-line standardized treatment, with 12 mg daily lasting for 2 weeks and withdrawal of drugs for a week. The relevant clinical information and treatment protocols were recorded.The efficacy and safety of anlotinib were followed up.
Results: A total of 26 patients were enrolled in the study group, and 24 patients could be evaluated, including 2 cases of partial response (PR) and 16 cases of stable disease (SD).The object response rate (ORR) and disease control rate (DCR) were 8.3% and 75%, respectively. The median progression-free survival (PFS) and overall survival (OS) was 4.3 months (95% CI: 2.9-5.7 months) and 14.7 months (95% CI: 10.0-19.4 months), respectively. The most common adverse reactions were fatigue in 17 cases (17/26) and hand-foot skin reactions in 16 cases (16/26). Analysis of Kaplan-Meier revealed that without liver metastasis (95% CI: 11.7-32.3, P=0.011) and left-sided colonic cancer (95% CI: 11.7-46.1, P=0.014) were related to longer OS.
Conclusion: Anlotinib as a third-line therapy for advanced colorectal cancer is feasible with high disease control rate and minor side effects.

Entities:  

Keywords:  Anlotinib; Clinical effects; Metastatic colorectal cancer; Targeted therapy

Mesh:

Substances:

Year:  2019        PMID: 31550814     DOI: 10.3760/cma.j.issn.0376-2491.2019.36.010

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Za Zhi        ISSN: 0376-2491


  1 in total

1.  Anlotinib as a promising inhibitor on tumor growth of oral squamous cell carcinoma through cell apoptosis and mitotic catastrophe.

Authors:  Zhaoming Deng; Wei Liao; Wei Wei; Guihua Zhong; Chao He; Hongbo Zhang; Qiaodan Liu; Xiwei Xu; Jun Liang; Zhigang Liu
Journal:  Cancer Cell Int       Date:  2021-01-09       Impact factor: 5.722

  1 in total

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