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.

Frontiers in Pharmacology
|February 16, 2024
PubMed

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.