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Verfasst von:Matrood, Sami [VerfasserIn]   i
 Apostolidis, Leonidas [VerfasserIn]   i
 Schrader, Jörg [VerfasserIn]   i
 Krug, Sebastian [VerfasserIn]   i
 Lahner, Harald [VerfasserIn]   i
 Ramaswamy, Annette [VerfasserIn]   i
 Librizzi, Damiano [VerfasserIn]   i
 Kender, Zoltán [VerfasserIn]   i
 Kröcher, Anke [VerfasserIn]   i
 Kreutzfeldt, Simon [VerfasserIn]   i
 Gress, Thomas Matthias [VerfasserIn]   i
 Rinke, Anja [VerfasserIn]   i
Titel:Multicenter analysis of presacral neuroendocrine neoplasms
Titelzusatz:clinicopathological characterization and treatment outcomes of a rare disease
Verf.angabe:Sami Matrood, Leonidas Apostolidis, Jörg Schrader, Sebastian Krug, Harald Lahner, Annette Ramaswamy, Damiano Librizzi, Zoltan Kender, Anke Kröcher, Simon Kreutzfeldt, Thomas Matthias Gress and Anja Rinke
E-Jahr:2021
Jahr:06 October 2021
Umfang:16 S.
Fussnoten:Gesehen am 29.01.2022
Titel Quelle:Enthalten in: Frontiers in endocrinology
Ort Quelle:Lausanne : Frontiers Research Foundation, 2010
Jahr Quelle:2021
Band/Heft Quelle:12(2021), Artikel-ID 709256, Seite 1-16
ISSN Quelle:1664-2392
Abstract:Background and AimsNeuroendocrine neoplasms (NENs) of the presacral space are an extremely rare disease entity with largely unknown outcome and no established standard of care treatment. Therefore, we wanted to analyze clinical presentation, histopathological findings, treatment outcomes, and prognosis in a multicentric patient cohort.MethodsWe searched local databases of six German NEN centers for patients with presacral NEN. Retrospective descriptive analyses of age, sex, stage at diagnosis, symptoms, grade, immunohistochemical investigations, biomarkers, treatment, and treatment outcome were performed. Kaplan-Meier analysis was used to determine median overall survival.ResultsWe identified 17 patients (11 female, 6 male) with a median age of 50 years (range, 35-66) at diagnosis. Twelve cases presented initially with distant metastases including bone metastases in nine cases. On pathological review the majority of patients had well-differentiated G2 tumors. Immunohistochemical profile resembled rectal NENs. All but one patient had non-functioning tumors. Somatostatin receptor imaging was positive in 14 of 15 investigated cases. Eight patients were treated surgically including palliative resections; 14 patients received somatostatin analogs with limited efficacy. With 14 PRRTs completed, 79% showed clinical benefit, whereas only one patient with neuroendocrine carcinoma (NEC) responded to chemotherapy. Treatment with everolimus in three patients was not successful, whereas cabozantinib resulted in a disease stabilization in a heavily pretreated patient. During a median observation period of 44.5 months, 6 patients died. Median overall survival was not reached.ConclusionPresacral NEN are histopathologically similar to rectal NENs. Presacral NEN should be considered as possible primary in NEN of unknown primary. The majority of tumors is non-functioning and somatostatin receptor positive. PRRT demonstrated promising activity; tyrosine kinase inhibitors warrant further investigations. Further molecular characterization and prospective evaluation of this rare tumor entity are needed.
DOI:doi:10.3389/fendo.2021.709256
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kostenfrei: Volltext: https://www.frontiersin.org/article/10.3389/fendo.2021.709256
 kostenfrei: Resolving-System: http://dx.doi.org/10.3389/fendo.2021.709256
 DOI: https://doi.org/10.3389/fendo.2021.709256
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1787760693
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