TY - JOUR
T1 - Prognostic Factors for Long-Term Survival after Surgical Resection of Primary Cardiac Sarcoma
AU - Aboud, Anas
AU - Farha, Kassar
AU - Hsieh, Wan Chin
AU - Brasch, Frank
AU - Ensminger, Stephan
AU - Gummert, Jan
AU - Renner, André
N1 - Publisher Copyright:
© 2019 Georg Thieme Verlag. All rights reserved.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/6/27
Y1 - 2019/6/27
N2 - Background âPrimary cardiac sarcoma (CS) is an extremely rare disease. This study aims to identify possible prognostic factors for long-term survival. Methods âA total of 17 consecutive patients who were treated for primary CS between 2003 und 2018 at two cardiac centers were investigated. Clinical data and histological characteristics of the tumors were analyzed. Long-term follow-up of all patients were performed. Results âThe median age was 54 years (range: 23-74). The tumors originated from the left side of the heart in nine patients. Histologically, there were four angiosarcomas, three intimal sarcomas, and three synovial sarcomas. One- A nd 7-year survivals were 81.9 and 18.2%, respectively. Low expression levels of K i-67 tended to be associated with increased survival (log-rank p = 0.06). Adjuvant chemotherapy but not radiotherapy regardless of existing metastases was associated with significantly increased survival (log-rank p = 0.001). Conclusion âAngiosarcoma was the most common type of CS. The survival of CS patients is poor but prognostic factors, such as K i-67, may help estimate the course of the disease. Survival could be improved significantly with chemotherapy.
AB - Background âPrimary cardiac sarcoma (CS) is an extremely rare disease. This study aims to identify possible prognostic factors for long-term survival. Methods âA total of 17 consecutive patients who were treated for primary CS between 2003 und 2018 at two cardiac centers were investigated. Clinical data and histological characteristics of the tumors were analyzed. Long-term follow-up of all patients were performed. Results âThe median age was 54 years (range: 23-74). The tumors originated from the left side of the heart in nine patients. Histologically, there were four angiosarcomas, three intimal sarcomas, and three synovial sarcomas. One- A nd 7-year survivals were 81.9 and 18.2%, respectively. Low expression levels of K i-67 tended to be associated with increased survival (log-rank p = 0.06). Adjuvant chemotherapy but not radiotherapy regardless of existing metastases was associated with significantly increased survival (log-rank p = 0.001). Conclusion âAngiosarcoma was the most common type of CS. The survival of CS patients is poor but prognostic factors, such as K i-67, may help estimate the course of the disease. Survival could be improved significantly with chemotherapy.
UR - http://www.scopus.com/inward/record.url?scp=85077017220&partnerID=8YFLogxK
U2 - 10.1055/s-0039-1692409
DO - 10.1055/s-0039-1692409
M3 - Journal articles
C2 - 31250414
AN - SCOPUS:85077017220
SN - 0171-6425
VL - 67
SP - 665
EP - 671
JO - Thoracic and Cardiovascular Surgeon
JF - Thoracic and Cardiovascular Surgeon
IS - 8
ER -