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JIN Huimin, LIN Lihong, ZHAO Zhen, GONG Xishuang. Efficacy and Safety of Anlotinib Combined with PD-1 Blockades for Patients with Advanced Epithelial Ovarian Cancer[J]. Cancer Research on Prevention and Treatment, 2022, 49(10): 1059-1064. DOI: 10.3971/j.issn.1000-8578.2022.22.0211
Citation: JIN Huimin, LIN Lihong, ZHAO Zhen, GONG Xishuang. Efficacy and Safety of Anlotinib Combined with PD-1 Blockades for Patients with Advanced Epithelial Ovarian Cancer[J]. Cancer Research on Prevention and Treatment, 2022, 49(10): 1059-1064. DOI: 10.3971/j.issn.1000-8578.2022.22.0211

Efficacy and Safety of Anlotinib Combined with PD-1 Blockades for Patients with Advanced Epithelial Ovarian Cancer

More Information
  • Corresponding author:

    GONG Xishuang, E-mail: 15836345777@163.com

  • Received Date: March 06, 2022
  • Revised Date: July 21, 2022
  • Available Online: January 12, 2024
  • Objective 

    To investigate the efficacy and safety of anlotinib combined with PD-1 blockades for patients with advanced epithelial ovarian cancer (EOC).

    Methods 

    A retrospective study was performed, enrolling 33 patients with advanced EOC who failed standard systematic therapy. All patients were administered with anlotinib combined with PD-1 blockades. The efficacy and safety profile were determined during treatment.

    Results 

    The objective response rate of the 33 patients was 36.4% (95%CI: 20.4%-54.9%) and the disease control rate of the patients was 81.8% (95%CI: 64.5%-90.0%). The median PFS and OS of the 33-patient cohort were 7.6 months (95%CI: 3.1-12.1) and 19.6 months (95%CI: 15.1-24.1), respectively. The most common treatment-related adverse reactions were fatigue (66.7%), nausea and vomiting (54.5%), hypertension (48.5%), and diarrhea (39.4%). Furthermore, multivariate Cox regression analysis indicated that ECOG performance status and FIGO stage were independent factors for predicting the PFS of the combination regimen for patients with advanced EOC.

    Conclusion 

    Anlotinib combined with PD-1 blockades preliminarily exhibit satisfactory efficacy and tolerable safety profile for patients with advanced EOC.

  • Competing interests: The authors declare that they have no competing interests.

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