Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology

Author:

Schott Inna1,Liffers Sven-Thorsten23,Farzaliyev Farhad4ORCID,Falkenhorst Johanna15ORCID,Steinau Hans-Ulrich6,Treckmann Jürgen-Walter6ORCID,Podleska Lars Erik4ORCID,Pöttgen Christoph7ORCID,Schildhaus Hans-Ulrich8ORCID,Ahrens Marit9ORCID,Dirksen Uta105ORCID,Murat Fatma-Zehra1ORCID,Siveke Jens T.123ORCID,Bauer Sebastian15ORCID,Hamacher Rainer15ORCID

Affiliation:

1. Department of Medical Oncology, Sarcoma Center, West German Cancer Center, University Hospital Essen, Essen, Germany

2. Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Essen, Germany

3. Division of Solid Tumor Translational Oncology, German Cancer Consortium (DKTK,Partner Site Essen) and German Cancer Research Center, DKFZ, Heidelberg, Germany

4. Department of Orthopedic Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany

5. German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany

6. Department of General, Visceral and Transplantion Surgery, Sarcoma Center, West German Cancer Center, University Hospital Essen, Essen, Germany

7. Department of Radiotherapy, West German Cancer Center, University Hospital Essen, Essen, Germany

8. Institute of Pathology, West German Cancer Center, University Hospital Essen, Essen, Germany

9. Medical Clinic II, University Hospital Frankfurt, Frankfurt am Main, Germany

10. Pediatrics III Pediatric Hematology, Oncology, Immunology, Cardiology, Pulmonology, West German Cancer Center, University Hospital Essen, Essen, Germany

Abstract

Background. Angiosarcomas are rare and heterogeneous tumors with poor prognosis. The clinical subtypes are classified depending on the primary site and etiology. Methods. We conducted a retrospective, monocentric study of 136 patients with localized AS between May 1985 and November 2018. Overall survival (OS), local recurrence-free survival (LRFS), and metastasis-free survival (MFS) were estimated using the Kaplan–Meier method. To identify prognostic factors, univariate and multivariate analyses were performed based on Cox regressions. Results. The median age was 67 years (19–72.8 years). Primary sites were cutaneous (27.2%), breast (38.2%), and deep soft tissue (34.6%). The majority was primary angiosarcomas (55.9%) followed by postradiation (40.4%) and chronic lymphedema angiosarcomas (2.9%). Prognosis significantly differed depending on the primary site and etiology. Shortest median OS and MFS were observed in deep soft tissue angiosarcomas, whereas cutaneous angiosarcomas, angiosarcomas of the breast, and radiation-associated angiosarcomas displayed worse median LRFS. Univariate analyses showed better OS for tumor size <10 cm ( p  = 0.009), negative surgical margins ( p  = 0.021), and negative lymph node status ( p  = 0.007). LRFS and MFS were longer for tumor size <10 cm ( p  = 0.012 and p  = 0.013). In multivariate analyses, age <70 years was the only independent positive prognostic factor for OS in all subgroups. For LRFS, secondary AS of the breast was a negative prognostic factor (HR: 2.35; p  = 0.035). Conclusions. Different behaviors and prognoses depending on the primary site and etiology should be considered for the treatment of this heterogeneous disease. In cutaneous angiosarcomas of the head/neck and postradiation angiosarcomas of the breast, local recurrence seems to have a crucial impact on OS. Therefore, improved local therapies and local tumor staging may have to be implemented. However, in deep soft tissue angiosarcomas, distant recurrence seems to have a major influence on prognosis, which indicates a benefit of additional perioperative chemotherapy.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Hindawi Limited

Subject

Radiology, Nuclear Medicine and imaging,Oncology

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