Images in Immunotherapy and Precision Oncology: Angiosarcoma of the Spleen and Liver

Author:

Deshpande Anagha1,Munoz Javier2,Kelemen Katalin3,Dabak Vrushali4,Hanbali Amr5,Kurzrock Razelle678

Affiliation:

1. 1 Mayo Clinic Alix School of Medicine, Scottsdale, AZ, USA

2. 2 Department of Hematology, Mayo Clinic Arizona, Phoenix, AZ, USA

3. 3 Division of Hematopathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Arizona, Phoenix, AZ, USA

4. 4 Department of Hematology and Oncology, Henry Ford Health System, Detroit, MI, USA

5. 5 King Faisal Specialist Hospital, Riyadh, Saudi Arabia

6. 6 Medical College of Wisconsin, Milwaukee, WI, USA

7. 7 Worldwide Innovative Networking in Personalized Cancer Medicine (WIN) Consortium, Paris, France

8. 8 University of Nebraska, Omaha, NE, USA

Abstract

ABSTRACT Primary splenic or hepatic angiosarcomas are ultra-rare and aggressive malignancies associated with poor prognosis. The mainstay treatments are surgical resection and chemotherapy. We report a case of angiosarcoma in a 50-year-old woman who presented with bruising, fatigue, ecchymosis, and hepatosplenomegaly. She was treated with the multi-kinase inhibitor sunitinib for 4 weeks before developing a splenic hemorrhage and succumbing. Recent studies have demonstrated the clinical benefit of immunotherapies in angiosarcomas. Additionally, sequencing techniques have showcased the diverse molecular aberrations involved in angiosarcomas, which offer opportunities for precision-matched targeted therapies such as inhibitors of the VEGF/VEGFR axis and PI3K/Akt/mTor pathway.

Publisher

Innovative Healthcare Institute

Subject

Cancer Research,Oncology,Immunology,Immunology and Allergy

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