Angiosarcoma in the breast: a population-based cohort from Sweden

被引:5
作者
Olander, Susanne [1 ]
Wennstig, Anna-Karin [2 ,3 ]
Garmo, Hans [4 ]
Holmberg, Lars [4 ,5 ]
Nilsson, Greger [6 ,7 ,8 ]
Blomqvist, Carl [9 ,10 ]
Karlsson, Fredrik [11 ,12 ]
Wickberg, Asa [13 ]
Warnberg, Fredrik [14 ]
Sund, Malin [2 ,15 ,16 ]
Wadsten, Charlotta [2 ,17 ]
机构
[1] Sunderby Hosp, Dept Surg, Lulea, Sweden
[2] Umea Univ, Dept Surg & Perioperat Sci, Surg, Umea, Sweden
[3] Sundsvall Hosp, Dept Oncol, Sundsvall, Sweden
[4] Uppsala Univ, Reg Canc Ctr, Uppsala, Sweden
[5] Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England
[6] Uppsala Univ, Univ Hosp, Sect Expt & Clin Oncol, Dept Immunol Genet & Pathol, Uppsala, Sweden
[7] Gavle Cent Hosp, Dept Oncol, Gavle, Sweden
[8] Visby Hosp, Dept Oncol, Visby, Sweden
[9] Helsinki Univ Hosp, Dept Oncol, Helsinki, Finland
[10] Orebro Univ Hosp, Dept Oncol, Orebro, Sweden
[11] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[12] Karolinska Univ Hosp, Dept Breast Endocrine Tumours & Sarcoma, Stockholm, Sweden
[13] Orebro Univ, Fac Med & Hlth, Dept Surg, Orebro, Sweden
[14] Univ Gothenburg, Inst Clin Sci, Dept Surg, Sahlgrenska Acad, Gothenburg, Sweden
[15] Univ Helsinki, Dept Surg, Helsinki, Sweden
[16] Helsinki Univ Hosp, Helsinki, Sweden
[17] Sundsvall Hosp, Dept Surg, S-85643 Sundsvall, Sweden
关键词
CANCER; MANAGEMENT; RADIOTHERAPY; OUTCOMES; SURGERY; SARCOMA; RISK;
D O I
10.1093/bjs/znad290
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Breast angiosarcoma is a rare disease mostly observed in breast cancer (BC) patients who have previously received radiotherapy (RT). Little is known about angiosarcoma aetiology, management, and outcome. The study aim was to estimate risk and to characterize breast angiosarcoma in a Swedish population-based cohort.Methods The Swedish Cancer Registry was searched for breast angiosarcoma between 1992 and 2018 in three Swedish healthcare regions (population 5.5 million). Information on previous BC, RT, management, and outcome were retrieved from medical records.Results Overall, 49 angiosarcomas located in the breast, chest wall, or axilla were identified, 8 primary and 41 secondary to BC treatment. Median age was 51 and 73 years, respectively. The minimum latency period of secondary angiosarcoma after a BC diagnosis was 4 years (range 4-21 years). The cumulative incidence of angiosarcoma after breast RT increased continuously, reaching 1.4 & PTSTHOUSND; after 20 years. Among 44 women with angiosarcoma treated by surgery, 29 developed subsequent local recurrence. Median recurrence-free survival was 3.4 and 1.8 years for primary and secondary angiosarcoma, respectively. The 5-year overall survival probability for the whole cohort was 50 per cent (95 per cent c.i., 21 per cent-100 per cent) for primary breast angiosarcoma and 35 per cent (95 per cent c.i., 23 per cent-54 per cent) for secondary angiosarcoma.Conclusion Breast angiosarcoma is a rare disease strongly associated with a history of previous BC RT. Overall survival is poor with high rates of local recurrences and distant metastasis. The present study reports the incidence and management of primary and secondary breast angiosarcoma in a population receiving modern radiotherapy.The latency from breast cancer diagnosis to angiosarcoma ranges between 4 and 21 years with a steadily increasing incidence throughout 25 years of follow-up. Overall survival is poor with high rates of local recurrences and distant metastasis.
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收藏
页码:1850 / 1856
页数:7
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