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Management of Cutaneous Angiosarcoma: an Update Review
Siwei Bi1, Ai Zhong1, Xiya Yin2
1Department of Burn and Plastic Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Cutaneous angiosarcoma (cAS) is a rare cancer. Treatment involves surgery, radiotherapy, and chemotherapy, with paclitaxel as a primary option, and targeted therapies under investigation for resistant cases.
Area of Science:
- Oncology
- Dermatology
- Surgical Oncology
Background:
- Cutaneous angiosarcoma (cAS) is a rare, aggressive vascular malignancy.
- Local invasion is a characteristic feature of cAS, complicating surgical management.
- Current treatment paradigms are evolving, with increasing interest in multimodal approaches.
Purpose of the Study:
- To review and summarize current treatment strategies for cutaneous angiosarcoma.
- To highlight the role of surgery, radiotherapy, and chemotherapy in managing cAS.
- To discuss emerging therapeutic options for advanced or resistant disease.
Main Methods:
- Literature review of studies on cutaneous angiosarcoma treatment.
- Analysis of established and investigational therapeutic regimens.
- Synthesis of evidence regarding surgical, radiotherapeutic, and chemotherapeutic interventions.
Main Results:
- Wide-margin excision is recommended for localized cAS.
- Preoperative and postoperative radiotherapy are suggested due to cAS's invasive nature.
- Neoadjuvant therapies may enable less extensive surgical procedures.
- Radiotherapy or chemoradiotherapy are options for unresectable metastatic cAS.
- Paclitaxel is a recognized first-line chemotherapy.
- Targeted agents and immunotherapy are being investigated for taxane-resistant tumors.
Conclusions:
- Multimodal treatment, including surgery and radiotherapy, is crucial for cAS.
- Neoadjuvant and adjuvant therapies play a significant role in optimizing surgical outcomes and managing local invasion.
- Ongoing research into novel agents offers hope for patients with refractory or metastatic cAS.
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