New Molecular Insights, and the Role of Systemic Therapies and Collaboration for Treatment of Epithelioid Hemangioendothelioma (EHE)

Author:

Stacchiotti Silvia,Tap William,Leonard Hugh,Zaffaroni Nadia,Baldi Giacomo G

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Oncology

Reference40 articles.

1. Stacchiotti S, Frezza AM, Blay JY, Baldini EH, Bonvalot S, Bovée JVMG, et al. Ultra-rare sarcomas: a consensus paper from the Connective Tissue Oncology Society community of experts on the incidence threshold and the list of entities. Cancer. 2021;127(16):2934–42. First consensus of expert on the list of entities and incidence threshold in the definition of ultra-rare sarcoma.

2. Stacchiotti S, Miah AB, Frezza AM, Messiou C, Morosi C, Caraceni A, et al. Epithelioid hemangioendothelioma, an ultra-rare cancer: a consensus paper from the community of experts. ESMO Open. 2021;6(3):100170. A consensus paper from the community of experts that has tried to define what should currently be the optimal care of EHE.

3. Rubin BP, Deyrup AT, Doyle LA. Epithelioid haemangioendothelioma, in World Health Organization Classification of Tumours. Soft Tissue and Bone Pathology and Genetics. 5th edition. Lyon, International Agency for Research on Cancer, 2020; 172–175.

4. Errani C, Zhang L, Sung YS, Hajdu M, Singer S, Maki RG, et al. A novel WWTR1-CAMTA1 gene fusion is a consistent abnormality in epithelioid hemangioendothelioma of different anatomic sites. Genes Chromosom Cancer. 2011;50(8):644–53. First report of the fusion gene that characterized EHE.

5. Antonescu CR, Le Loarer F, Mosquera JM, Sboner A, Zhang L, Chen CL, et al. Novel YAP1-TFE3 fusion defines a distinct subset of epithelioid hemangioendothelioma. Genes Chromosom Cancer. 2013;52(8):775–84.

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