| Literature DB >> 33393133 |
Tom Wei-Wu Chen1,2, Angela Pang3, Mark E Puhaindran4, Myo Myint Maw5, Herbert H Loong6, Virote Sriuranpong7, Chih-Chi Chang8, Siyamol Mingmalairak7, Takeshi Hirose9, Makoto Endo9, Akira Kawai10, Mohamad Farid11, Sze Huey Tan12,13, Wei Lin Goh11, Richard Quek14, Jeffrey C H Chan15, Alex K C Leung15, Roger K C Ngan15,16.
Abstract
Angiosarcoma (AS) is a rare disease with a dismal prognosis. The treatment landscape and prognostic factors for advanced AS, including locally advanced, unresectable, and metastatic disease remain elusive. The Asian Sarcoma Consortium is an international collaborative effort to understand the sarcoma treatment landscape in Asia. We undertook a retrospective chart review of AS patients seen in 8 sarcoma academic centers across Asia. Patients with complete clinical, treatment, and follow-up data were enrolled. Overall, 276 advanced AS patients were included into this study; 84 (30%) of the patients had metachronous metastatic AS. The median age was 67 y; primary sites of AS was cutaneous in 55% and visceral in 45% of patients. In total, 143 (52%) patients received at least 1 line of systemic chemotherapy. The most common first-line chemotherapy regimen used was paclitaxel (47.6%) followed by liposomal doxorubicin (19.6%). The median overall survival (OS) was 7.8 mo. Significant prognostic factors for OS included age > 65 (hazard ratio (HR) 1.54, P = .006), male gender (HR 1.39, P = .02), and a cutaneous primary AS site (HR 0.63, P = .004). The median progression-free survival (PFS) for first-line chemotherapy was 3.4 mo. PFS for single vs combination or paclitaxel vs liposomal doxorubicin chemotherapy regimens were comparable. This study provides an insight into the treatment patterns and prognostic factors of advanced AS patients in Asia. Prognosis of advanced AS remains poor. Data from this study serve as a benchmark for future clinical study design.Entities:
Keywords: advanced disease; angiosarcoma; chemotherapy; ethnicity; prognosis
Year: 2021 PMID: 33393133 DOI: 10.1111/cas.14793
Source DB: PubMed Journal: Cancer Sci ISSN: 1347-9032 Impact factor: 6.716