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Combining nanoparticle albumin-bound paclitaxel with camrelizumab in advanced soft tissue sarcoma: activity, safety,
Zhichao Tian1, Yushen Feng2, Yang Yang3
1Department of Bone and Soft Tissue, The Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital, Zhengzhou, China.
Abstract:
Background: It is still uncertain whether Nanoparticle albumin-bound paclitaxel (nab-paclitaxel) and programmed cell death protein 1 (PD-1) inhibitor have synergistic effects on metastatic soft tissue sarcomas (STSs). The purpose of this study was to evaluate the safety and activity of nab-paclitaxel plus camrelizumab (a PD-1 inhibitor) in patients with advanced STS who had previously failed chemotherapy. Methods: In this single-center, open-label, single-arm phase II clinical trial, patients with advanced (unresectable or metastatic) STS who had previously failed chemotherapy received up to six cycles of nab-paclitaxel plus camrelizumab, whereas camrelizumab treatment was continued for up to 1 year. The median progression-free survival (PFS), objective response rate (ORR) and safety were collected and evaluated. Results: This trial included 40 patients (28 men and 12 women). The overall ORR was 22.5%, and the median PFS was 1.65 months (95% confidence interval [CI], 1.3-2.0 months). Patients with epithelioid sarcoma demonstrated a longer PFS compared with those with other histological subtypes (2.3 months vs. 1.5 months, respectively); however, this difference was not significant. Patients who had received only one line of previous chemotherapy had a significantly longer PFS compared with those who had undergone two or more lines of previous chemotherapy (2.8 months vs. 1.3 months, respectively, p = 0.046). In terms of safety, the toxicity of this combination therapy is mild and no serious adverse events have occurred. Conclusion: Nab-paclitaxel plus camrelizumab exhibited modest activity and mild toxicity in treating epithelioid sarcoma, angiosarcoma, and fibrosarcoma. The overall effectiveness of this treatment regimen for advanced STS is relatively low. Further research on combining nab-paclitaxel with effective drugs, including chemotherapy and targeted agents, for these specific STS subtypes is needed.
Insights
This study investigated nanoparticle albumin-bound paclitaxel (nab-paclitaxel) with a PD-1 inhibitor in advanced soft tissue sarcomas (STSs). The combination showed modest activity and mild toxicity, with better outcomes in patients receiving fewer prior chemotherapy lines.
Area of Science:
- Oncology
- Medical Research
- Clinical Trials
Background:
- Metastatic soft tissue sarcomas (STSs) present treatment challenges.
- The efficacy of combining nanoparticle albumin-bound paclitaxel (nab-paclitaxel) with PD-1 inhibitors in advanced STSs remains uncertain.
- Previous chemotherapy failure necessitates exploring novel therapeutic strategies.
Purpose of the Study:
- To evaluate the safety and efficacy of nab-paclitaxel plus camrelizumab (a PD-1 inhibitor) in patients with advanced STS.
- To assess the objective response rate (ORR) and progression-free survival (PFS) of this combination therapy.
- To identify patient subgroups who may benefit more from this treatment regimen.
Main Methods:
- A single-center, open-label, single-arm Phase II clinical trial was conducted.
- 40 patients with advanced STS who failed prior chemotherapy received nab-paclitaxel and camrelizumab.
- Treatment involved up to six cycles of combination therapy, with camrelizumab continued for up to one year. PFS, ORR, and safety were assessed.
Main Results:
- The overall objective response rate (ORR) was 22.5%, with a median progression-free survival (PFS) of 1.65 months.
- Patients with epithelioid sarcoma showed a trend towards longer PFS, though not statistically significant.
- Significantly longer PFS was observed in patients who received only one line of prior chemotherapy (2.8 months) compared to those with two or more lines (1.3 months, p=0.046).
Conclusions:
- Nab-paclitaxel plus camrelizumab demonstrated modest clinical activity and mild toxicity in advanced STS, particularly in epithelioid sarcoma, angiosarcoma, and fibrosarcoma.
- The overall effectiveness for advanced STS was relatively low, suggesting a need for further investigation.
- Future research should explore combining nab-paclitaxel with other agents, including chemotherapy and targeted therapies, for specific STS subtypes.
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