日本皮肤病协会指南的二次出版:皮肤血管肉瘤指南的临床问题2025。

IF 2.7 3区 医学 Q2 DERMATOLOGY
Yasuhiro Fujisawa, Yasuo Yoshioka, Koji Yoshino, Taku Fujimura, Yoichi Naito, Mamiko Masuzawa, Kohei Oashi, Eiji Nakano, Hiroshi Kato, Yusuke Muto, Hiroshi Koga, Tomomitsu Miyagaki, Hiroshi Uchi, Yasuhiro Nakamura, Kenji Asagoe
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引用次数: 0

摘要

摘要皮肤血管肉瘤是一种罕见且预后不良的恶性肿瘤。由于其罕见性,来自随机对照试验的高水平证据有限,并且治疗策略历来适用于其他肉瘤。这些指南旨在根据新获得的证据提供更新的建议,以使日本的临床实践标准化。2024年的修订是在日本皮肤病协会委员会下进行的,纳入了专家评审和公众意见。由于缺乏既定的分期系统,建议是通过系统的文献综述和结构化的共识过程制定的。讨论了五个临床问题,包括一线放化疗(CRT)、CRT后残余病变的处理、二线治疗选择、派姆单抗在肿瘤突变负担高病例中的作用以及非头颈部血管肉瘤的治疗策略。关键的建议包括:对于较大(≥5cm)的非转移性肿瘤,弱推荐CRT;对于CRT后的残余病变,更倾向于药物改良而不是切除;对于紫杉醇耐药病例,同样考虑多西他赛、帕唑帕尼或伊瑞布林。Pembrolizumab被弱推荐用于肿瘤突变负担高的病例。对于放射相关血管肉瘤,手术治疗优于CRT,而Stewart-Treves综合征病例的治疗与头颈部血管肉瘤相似。未来的方向强调需要多中心注册研究和前瞻性试验来完善治疗策略。随着基因组医学和免疫疗法的发展,指南的更新对于确保最佳的患者护理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
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