TY - JOUR
T1 - Evaluation of the use and efficacy of (neo)adjuvant chemotherapy in angiosarcoma
T2 - A multicentre study
AU - Constantinidou, Anastasia
AU - Sauve, Nicolas
AU - Stacchiotti, Silvia
AU - Blay, Jean Yves
AU - Vincenzi, Bruno
AU - Grignani, Giovanni
AU - Rutkowski, Piotr
AU - Guida, Michele
AU - Hindi, Nadia
AU - Klein, Alexander
AU - Thibaud, Valentin
AU - Sufliarsky, Jozef
AU - Desar, Ingrid
AU - Steeghs, Neeltje
AU - Litiere, Saskia
AU - Gelderblom, Hans
AU - Jones, Robin L.
N1 - Publisher Copyright:
©
PY - 2020/8/26
Y1 - 2020/8/26
N2 - Introduction Angiosarcomas constitute approximately 2% to 3% of all soft tissue sarcomas, are characterised by an aggressive clinical behaviour and poor outcome. Optimal management of localised angiosarcomas consists of complete surgical resection with or without radiation. However, due to the infiltrating nature of this disease, complete resection is often not possible. Despite optimal management, the outcome of patients with localised disease remains poor. The role of (neo)adjuvant chemotherapy in angiosarcomas remains undefined. The aim of this study is to document the outcome of patients treated with (neo)adjuvant chemotherapy and assess the feasibility of performing a prospective trial by evaluating the number of patients treated at sarcoma referral centres. Methods A retrospective search within participating EORTC (European Organisation for Research and Treatment of Cancer) sites for patients treated with (neo)adjuvant chemotherapy was made. Patients treated between January 2007 and January 2016 were included. Results A total of 15 institutions participated and 86 patients were evaluable, 43 were treated with neoadjuvant, 27 with adjuvant chemotherapy and 16 with both. At the time of analysis, the median follow-up from diagnosis was 4.6 years. Median overall survival (OS) was 4.9 years (2.9 N) and the percentage alive at 4 years was 57.9 (45.5 to 68.4). The median disease-free survival was 1.4 years (0.9 to 1.7) and the percentage disease-free at 4 years was 26.8% (17.9 to 36.5). Conclusion The outcome of angiosarcoma patients treated with (neo)adjuvant chemotherapy in this case series compares favourably with previously published data. Due to the aggressive nature of angiosarcoma, a prospective trial of neoadjuvant chemotherapy should be considered.
AB - Introduction Angiosarcomas constitute approximately 2% to 3% of all soft tissue sarcomas, are characterised by an aggressive clinical behaviour and poor outcome. Optimal management of localised angiosarcomas consists of complete surgical resection with or without radiation. However, due to the infiltrating nature of this disease, complete resection is often not possible. Despite optimal management, the outcome of patients with localised disease remains poor. The role of (neo)adjuvant chemotherapy in angiosarcomas remains undefined. The aim of this study is to document the outcome of patients treated with (neo)adjuvant chemotherapy and assess the feasibility of performing a prospective trial by evaluating the number of patients treated at sarcoma referral centres. Methods A retrospective search within participating EORTC (European Organisation for Research and Treatment of Cancer) sites for patients treated with (neo)adjuvant chemotherapy was made. Patients treated between January 2007 and January 2016 were included. Results A total of 15 institutions participated and 86 patients were evaluable, 43 were treated with neoadjuvant, 27 with adjuvant chemotherapy and 16 with both. At the time of analysis, the median follow-up from diagnosis was 4.6 years. Median overall survival (OS) was 4.9 years (2.9 N) and the percentage alive at 4 years was 57.9 (45.5 to 68.4). The median disease-free survival was 1.4 years (0.9 to 1.7) and the percentage disease-free at 4 years was 26.8% (17.9 to 36.5). Conclusion The outcome of angiosarcoma patients treated with (neo)adjuvant chemotherapy in this case series compares favourably with previously published data. Due to the aggressive nature of angiosarcoma, a prospective trial of neoadjuvant chemotherapy should be considered.
KW - adjuvant
KW - angiosarcoma
KW - angiosarcoma surgery
KW - neoadjuvant
KW - sarcoma chemotherapy
UR - http://www.scopus.com/inward/record.url?scp=85089972955&partnerID=8YFLogxK
U2 - 10.1136/esmoopen-2020-000787
DO - 10.1136/esmoopen-2020-000787
M3 - Article
C2 - 32847839
AN - SCOPUS:85089972955
SN - 2059-7029
VL - 5
JO - ESMO open
JF - ESMO open
IS - 4
M1 - e000787
ER -