A Retrospective Observational Study of Anlotinib in Patients with Platinum-Resistant or Platinum-Refractory

Qingli Cui1, Yanhui Hu1, Dongyang Ma1

  • 1Department of Integrated Traditional and Western Medicine, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou City, Henan Province, People's Republic of China.

Abstract

Insights

Anlotinib, an oral tyrosine kinase inhibitor, showed moderate improvements in progression-free and overall survival for patients with platinum-resistant ovarian cancer. This suggests anlotinib may be a viable new treatment option for this patient group.

Area of Science:

  • Oncology
  • Pharmacology
  • Clinical Trials

Background:

  • Anlotinib is an oral small-molecule tyrosine kinase inhibitor (TKI) targeting tumor angiogenesis and growth, with inhibitory effects on VEGFR2/3.
  • Platinum-resistant or platinum-refractory ovarian cancer presents a significant challenge in treatment, necessitating novel therapeutic strategies.

Purpose of the Study:

  • To evaluate the efficacy and safety of anlotinib in patients with platinum-resistant or platinum-refractory ovarian cancer.
  • To assess anlotinib's impact on objective response, survival outcomes, and adverse events in this patient population.

Main Methods:

  • A retrospective review of medical records for 38 patients treated with anlotinib at the Affiliated Cancer Hospital of Zhengzhou University (May 2018 - March 2020).
  • Analysis included objective response, progression-free survival (PFS), overall survival (OS), and safety profiles.
  • Patients received anlotinib as monotherapy, or in combination with chemotherapy or pembrolizumab.

Main Results:

  • The median PFS was 7.7 months and the median OS was 16.5 months.
  • Anlotinib monotherapy yielded a median PFS of 7.7 months; combination with chemotherapy resulted in a median PFS of 8.0 months.
  • The objective response rate was 42.1%, and the disease control rate was 86.8%. Common adverse effects included hypertension, fatigue, anorexia, and hand-foot syndrome. No treatment-related deaths occurred.

Conclusions:

  • Anlotinib demonstrated moderate improvements in PFS and OS for patients with platinum-resistant or platinum-refractory ovarian cancer.
  • Anlotinib represents a potential new treatment option for this challenging patient group.
  • Further investigation into anlotinib's role in ovarian cancer treatment is warranted.