MERGANCOVA, Jana, Anna LIEROVA, Oldřich COUFAL, Jan ZATECKY, Bohuslav MELICHAR, Ilona ZEDNIKOVA, Jindriska MERGANCOVA, Anna JESENKOVA, Karel STASTNY, Jiri GATEK, Otakar KUBALA, Jiri PROKOP, Daniel DYTTERT, Marian KARABA, Ivana SCHWARZBACHEROVA, Anna HUMENANSKA, Jindrich SUK, Michal VALENTA, Vladimir MOUCHA, Lukas SAKRA, Ales HLAVKA, Maria HACOVA, Radovan VOJTISEK, Marek SOCHOR, Tomas JIRASEK, Michaela ZABOJNIKOVA, Martina ZEMANOVA, Katarina MACHALEKOVA, Dominika RUSNAKOVA, Eva KUDELOVA a Marek SMOLAR. Radiation-associated angiosarcoma of the breast: An international multicenter analysis. SURGICAL ONCOLOGY-OXFORD. OXFORD: ELSEVIER SCI LTD, 2022, roč. 41, May 2022, s. 1-8. ISSN 0960-7404. Dostupné z: https://dx.doi.org/10.1016/j.suronc.2022.101726.
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Základní údaje
Originální název Radiation-associated angiosarcoma of the breast: An international multicenter analysis
Autoři MERGANCOVA, Jana (203 Česká republika), Anna LIEROVA (203 Česká republika), Oldřich COUFAL (203 Česká republika, domácí), Jan ZATECKY (203 Česká republika), Bohuslav MELICHAR (203 Česká republika), Ilona ZEDNIKOVA (203 Česká republika), Jindriska MERGANCOVA (203 Česká republika), Anna JESENKOVA (203 Česká republika), Karel STASTNY (203 Česká republika), Jiri GATEK (203 Česká republika), Otakar KUBALA (203 Česká republika), Jiri PROKOP (203 Česká republika), Daniel DYTTERT, Marian KARABA, Ivana SCHWARZBACHEROVA (203 Česká republika), Anna HUMENANSKA (203 Česká republika), Jindrich SUK (203 Česká republika), Michal VALENTA (203 Česká republika), Vladimir MOUCHA (203 Česká republika), Lukas SAKRA (203 Česká republika), Ales HLAVKA (203 Česká republika), Maria HACOVA (203 Česká republika), Radovan VOJTISEK (203 Česká republika), Marek SOCHOR (203 Česká republika), Tomas JIRASEK (203 Česká republika), Michaela ZABOJNIKOVA (203 Česká republika), Martina ZEMANOVA, Katarina MACHALEKOVA, Dominika RUSNAKOVA, Eva KUDELOVA a Marek SMOLAR (garant).
Vydání SURGICAL ONCOLOGY-OXFORD, OXFORD, ELSEVIER SCI LTD, 2022, 0960-7404.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30204 Oncology
Stát vydavatele Velká Británie a Severní Irsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 2.300
Kód RIV RIV/00216224:14110/22:00128320
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.suronc.2022.101726
UT WoS 000789993900010
Klíčová slova anglicky Radiation; Angiosarcoma; Breast; Multicenter study
Štítky 14110813, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 27. 1. 2023 11:20.
Anotace
Introduction: Radiation-associated angiosarcoma (RAAS) is a rare and serious complication of breast irradiation. Due to the rarity of the condition, clinical experience is limited and publications on this topic include only retrospective studies or case reports.Materials and methods: All patients diagnosed with RAAS between January 2000 and December 2017 in twelve centers across the Czech Republic and Slovakia were evaluated.Results: Data of 53 patients were analyzed. The median age at diagnosis was 72 (range 44-89) years. The median latency period between irradiation and diagnosis of RAAS was 78 (range 36-172) months. The median radiation dose was 57.6 (range 34-66) Gy. The whole breast radiation therapy with radiation boost to the tumor bed was the most common radiotherapy regimen. Total mastectomy due to RAAS was performed in 43 patients (81%), radical excision in 8 (15%); 2 patients were not surgically treated due to unresectable disease. Adjuvant chemotherapy followed surgical therapy of RAAS in 18 patients, 3 patients underwent adjuvant radiotherapy. The local recurrence rate of RAAS was 43% and the median time from surgery to the onset of recurrence was 7.5 months (range 3-66 months). The 3-year survival rate was 56%, the 5-year survival rate was only 33%. 46% of patients died during the follow-up period.Conclusion: The present data demonstrate that RAAS is a rare condition with high local recurrence rate (43%) and mortality (the 5-year survival rate was 33%.). Early diagnosis of RAAS based on biopsy is crucial for treatment with radical intent. Surgery with negative margins constitutes the most important part of the therapy; the role of adjuvant chemotherapy and radiotherapy is still unclear.
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