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Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
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.
Methods:
The medical data of 47 patients with refractory bone and soft tissue sarcoma, who received anlotinib from January 2019 to December 2020, were retrospectively collected. The overall response rate (ORR) and disease control rate (DCR) were evaluated according to the solid tumor response evaluation version 1.1 standard. The progression-free survival (PFS), overall survival (OS), and adverse reactions were recorded.
Results:
A total of 44 patients, including 13 with osteosarcoma and 31 with soft tissue sarcoma, were enrolled in this study. Among patients with osteosarcoma, no patients achieved complete response (CR) or partial response (PR), while seven patients (54%) had stable disease (SD). Besides, the median PFS (m-PFS) was 4.4 months, and the median OS (m-OS) was 15.7 months. Among patients with soft tissue sarcoma, the ORR and DCR were 19% and 71%, respectively. The median m-PFS was 5.4 months, and m-OS was 17.9 months. Anlotinib plus chemotherapy had a higher ORR compared with anlotinib monotherapy (6% vs. 38%, P = 0.047). The most common grade 3/4 adverse reactions were pneumothorax (5%) and pleural effusion (5%), and no treatment-related deaths occurred.
Conclusions:
Anlotinib alone showed encouraging efficacy and favorable tolerability in refractory bone and soft tissue sarcoma. Anlotinib plus chemotherapy did not show a significant clinical benefit compared with anlotinib alone. Anlotinib showed better tumor control when used as first-line drug treatment in refractory bone and soft tissue sarcoma.
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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