Efficacy and Safety of Treating Refractory Bone and Soft Tissue Sarcoma with Anlotinib in Different Treatment

Meng Cai1,2,3, Jie Zhu1, Guangxin Zhou1,2

  • 1Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing, Jiangsu, China.

Abstract

Insights

Anlotinib demonstrates efficacy in refractory bone and soft tissue sarcoma. Combination therapy with chemotherapy did not significantly improve outcomes compared to anlotinib alone, suggesting anlotinib is effective as a first-line treatment.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Refractory bone and soft tissue sarcoma present significant treatment challenges.
  • Identifying effective therapeutic strategies is crucial for improving patient outcomes.

Purpose of the Study:

  • To evaluate the efficacy and safety of anlotinib in patients with refractory bone and soft tissue sarcoma.
  • To compare anlotinib monotherapy with anlotinib plus chemotherapy.

Main Methods:

  • Retrospective analysis of 47 patients with refractory bone and soft tissue sarcoma treated with anlotinib.
  • Evaluation of overall response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS).
  • Assessment of adverse reactions.

Main Results:

  • Among 13 osteosarcoma patients, 54% achieved stable disease (SD), with median PFS of 4.4 months and median OS of 15.7 months.
  • In 31 soft tissue sarcoma patients, ORR was 19%, DCR was 71%, median PFS was 5.4 months, and median OS was 17.9 months.
  • Anlotinib plus chemotherapy showed a higher ORR (38%) than monotherapy (6%), but this was not statistically significant in all analyses. Common grade 3/4 adverse events included pneumothorax and pleural effusion.

Conclusions:

  • Anlotinib monotherapy exhibits encouraging efficacy and favorable tolerability in refractory bone and soft tissue sarcoma.
  • Anlotinib plus chemotherapy did not demonstrate a significant clinical benefit over anlotinib alone.
  • Anlotinib may be more effective as a first-line treatment for refractory bone and soft tissue sarcoma.

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