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Therapeutic strategy for angiosarcoma in the National Cancer Center Hospital
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- YAMAZAKI Naoya
- <i>Dermatology Division, National Cancer Center Hospital</i>
Bibliographic Information
- Other Title
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- 血管肉腫に対する国立がんセンターの治療戦略
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Description
Angiosarcoma is a rare, highly aggressive tumor. It is a malignant vascular tumor that compromises only approximately 1% of all skin malignancies in Japan. The overall prognosis is poor, with reported 5-year survival rates of approximately 10%. Given the rarity of the tumor, relatively little is known concerning its features, natural history, or optimal treatment. Although surgical resection remains the cornerstone of therapy, because of the pattern of diffuse, clinically undetectable spread, the disease is sometimes difficult to resect completely. Adjuvant radiation therapy has resulted in a significant benefit in local control. Effective systemic treatment options are limited for patients with angiosarcoma. Two taxanes (paclitaxel and docetaxel) demonstrated good efficacy in patients with advanced angiosarcoma. We also reviewed the efficacy of MAID (Mesna/Ifosfamide/Doxorubicin/Dacarbazine) combination chemotherapy in them. Future clinical research should be explored by therapeutic centers for establishing a treatment policy for this rare tumor with a very poor prognosis.[Skin Cancer (Japan) 2009 ; 24 : 385-391]
Journal
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- Skin Cancer
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Skin Cancer 24 (3), 385-391, 2009
The Japanese Skin Cancer Society
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Details 詳細情報について
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- CRID
- 1390001204336314752
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- NII Article ID
- 10027902410
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- NII Book ID
- AN10087647
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- ISSN
- 18843549
- 09153535
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- Text Lang
- ja
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed