Secondary Publication of Japanese Dermatological Association Guidelines: Clinical Questions of Guidelines for Cutaneous Angiosarcoma 2025

Cutaneous angiosarcoma is a rare aggressive malignancy with poor prognosis. Due to its rarity, high-level evidence from randomized controlled trials is limited, and treatment strategies have historically been adapted from other sarcomas. These guidelines aim to provide updated recommendations based on newly available evidence to standardize clinical practice in Japan. The 2024 revision was conducted under the Japanese Dermatological Association's commission, incorporating expert reviews and public comments. Given the lack of an established staging system, recommendations were formulated through systematic literature reviews and a structured consensus process. Five clinical questions were addressed, covering first-line chemoradiotherapy (CRT), management of residual lesions post-CRT, second-line treatment options, the role of pembrolizumab in tumor mutational burden-high cases, and treatment strategies for nonhead-and-neck angiosarcomas. Key recommendations include weakly recommending CRT for large (≥ 5 cm) nonmetastatic tumors, preferring drug modification over excision for residual lesions after CRT, and equally considering docetaxel, pazopanib, or eribulin for paclitaxel-resistant cases. Pembrolizumab was weakly recommended for tumor mutational burden-high cases. For radiation-associated angiosarcoma, surgical treatment was favored over CRT, while Stewart-Treves syndrome cases were treated similarly to head-and-neck angiosarcoma. Future directions emphasize the need for multicenter registry studies and prospective trials to refine treatment strategies. As advances in genomic medicine and immunotherapy evolve, guideline updates will be essential to ensure optimal patient care.

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Publication Details

Journal
The Journal of Dermatology
Published
2025-07-19
DOI
https://doi.org/10.1111/1346-8138.17856
Citations
1
Primary Topic
Vascular Tumors and Angiosarcomas
Type
article
Field-Weighted Citation Impact
1.05
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article

Secondary Publication of Japanese Dermatological Association Guidelines: Clinical Questions of Guidelines for Cutaneous Angiosarcoma 2025

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1 citations
The Journal of Dermatology
Vascular Tumors and Angiosarcomas
1.05
article

Secondary Publication of Japanese Dermatological Association Guidelines: Clinical Questions of Guidelines for Cutaneous Angiosarcoma 2025

Hiroshi Uchi, Yasuhiro Fujisawa, Kohei Oashi, Taku Fujimura, Yusuke Muto, Tomomitsu Miyagaki, Mamiko Masuzawa, Eiji Nakano, Hiroshi Kato, Hiroshi Koga, Yoichi Naito, Yasuo Yoshioka, Yasuhiro Nakamura, Koji Yoshino, Kenji Asagoe
article en
1 citations

Abstract

Cutaneous angiosarcoma is a rare aggressive malignancy with poor prognosis. Due to its rarity, high-level evidence from randomized controlled trials is limited, and treatment strategies have historically been adapted from other sarcomas. These guidelines aim to provide updated recommendations based on newly available evidence to standardize clinical practice in Japan. The 2024 revision was conducted under the Japanese Dermatological Association's commission, incorporating expert reviews and public comments. Given the lack of an established staging system, recommendations were formulated through systematic literature reviews and a structured consensus process. Five clinical questions were addressed, covering first-line chemoradiotherapy (CRT), management of residual lesions post-CRT, second-line treatment options, the role of pembrolizumab in tumor mutational burden-high cases, and treatment strategies for nonhead-and-neck angiosarcomas. Key recommendations include weakly recommending CRT for large (≥ 5 cm) nonmetastatic tumors, preferring drug modification over excision for residual lesions after CRT, and equally considering docetaxel, pazopanib, or eribulin for paclitaxel-resistant cases. Pembrolizumab was weakly recommended for tumor mutational burden-high cases. For radiation-associated angiosarcoma, surgical treatment was favored over CRT, while Stewart-Treves syndrome cases were treated similarly to head-and-neck angiosarcoma. Future directions emphasize the need for multicenter registry studies and prospective trials to refine treatment strategies. As advances in genomic medicine and immunotherapy evolve, guideline updates will be essential to ensure optimal patient care.

The Journal of DermatologyVol. 52(10)
St. Marianna University School of Medicine (JP), Tohoku University (JP), Nagoya City University (JP), National Cancer Centre Japan (JP), National Cancer Center (US), National Hospital Organization Kyushu Cancer Center (JP), Saitama Cancer Center (JP), Saitama International Medical Center (JP), National Cancer Center Hospital East (JP), Okayama Medical Center (JP), Tochigi Medical Center (JP), Japanese Foundation For Cancer Research (JP), Ehime University (JP), Nagoya University (JP), Kitasato University (JP), Alps Electric (Japan) (JP), Saitama Medical University (JP)
Good health and well-being
Openalex Percentile: Top 20%
Vascular Tumors and Angiosarcomas
1.05
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