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National Incidence, Management and Survival of Urachal Carcinoma.
Collins, Dearbhaile C; Velázquez-Kennedy, Kyra; Deady, Sandra; Brady, Adrian P; Sweeney, Paul; Power, Derek G.
Affiliation
  • Collins DC; Department of Medical Oncology, Cork University Hospital , Cork, Ireland.
  • Velázquez-Kennedy K; Department of Medical Oncology, Cork University Hospital , Cork, Ireland.
  • Deady S; National Cancer Registry Ireland , Cork, Ireland.
  • Brady AP; Department of Radiology, Mercy University Hospital , Cork, Ireland.
  • Sweeney P; Department of Uro-Oncological Surgery, Mercy University Hospital , Cork, Ireland.
  • Power DG; Department of Medical Oncology, Cork University Hospital , Cork, Ireland.
Rare Tumors ; 8(3): 6257, 2016 Sep 05.
Article in En | MEDLINE | ID: mdl-27746878
Urachal carcinoma is an uncommon cancer whose rarity has precluded its study and evidence-based management strategies are lacking. This study assessed all urachal carcinomas in Ireland and clinical parameters in order to improve understanding. Urachal carcinomas diagnosed from 1994 to 2011 were identified from the National Cancer Registry in Ireland. Data obtained included patient age, gender, diagnostic year, pathology, tumor stage, patient treatment strategies and survival. Twenty-six urachal carcinomas were identified, the majority being adenocarcinoma. This comprised 0.3% of all invasive bladder tumors. Patients were predominantly male (62%) and over 50 years of age (58%). Twenty-two patients (85%) underwent surgery, with only six (23%) undergoing chemotherapy. On average, median overall survival was 2.6 years (range 0-15.2 yrs). Survival was longer in women (5 vs. 1.9 yrs), patients under 50 years of age (3.6 vs. 1.9 yrs), those without confirmed metastasis (4.1 vs. 0.7 yrs) and those who received chemotherapy (3.6 vs. 2.6 yrs). The overall survival of urachal carcinoma in Ireland is less than expected from published literature. This study highlights the need for centralization of rare tumors with international collaboration to identify the optimal treatment strategy and improve outcome.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Incidence_studies / Risk_factors_studies Language: En Journal: Rare Tumors Year: 2016 Type: Article Affiliation country: Ireland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Incidence_studies / Risk_factors_studies Language: En Journal: Rare Tumors Year: 2016 Type: Article Affiliation country: Ireland