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dc.contributor.authorMüller, Jörg Andreas-
dc.contributor.authorDelank, Karl-Stefan-
dc.contributor.authorLaudner, Kevin-
dc.contributor.authorWittenberg, Ian-
dc.contributor.authorZeh, Alexander-
dc.contributor.authorVordermark, Dirk-
dc.contributor.authorMedenwald, Daniel-
dc.date.accessioned2023-11-30T09:46:56Z-
dc.date.available2023-11-30T09:46:56Z-
dc.date.issued2023-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/114067-
dc.identifier.urihttp://dx.doi.org/10.25673/112109-
dc.description.abstractPurpose: Sarcomas are a heterogeneous group of malignant neoplasms with a wide range of histological types and occur in almost any anatomic site and side. This study evaluated the prognostic factors in sarcoma patients based on German clinical cancer registry data. Methods: The German clinical cancer register of Saxony-Anhalt was used for all data analyses. Sarcoma cases of all clinical or pathological T-stages (T1a–T4c), all N-stages (N0-3) and M-stages (0–1b) corresponding to the Union for International Cancer Control (UICC) stages I to IVB were considered. In our analyses, 787 cases diagnosed between 2005 and 2022 were included. Further, we assessed the association of cancer-related parameters with mortality and hazard ratios (HR) from the Cox proportional hazard models. We included sex, age at diagnosis, histological grade, T-, N- and M-stages, tumor size, tumor localization and tumor side as parameters in our regression models. Results: The majority of sarcoma patients were diagnosed with leiomyosarcoma (12%), liposarcoma (11%), angiosarcoma (5.3%) and myxofibrosarcoma (2.7%). In our univariate regression models, tumors localized in more than one location, head, face and neck region as well as the pelvis and lower extremity were associated with increased mortality risk (more than one location: HR 7.10, 95% CI 2.20–22.9; head, face and neck: HR 1.35, 95% CI 0.89–2.06; pelvis: HR 1.27, 95% CI 0.86–1.89; lower extremity: HR 1.44, 95% CI 1.05–1.96). Higher histological grades, UICC-grades and TNM-stages were related to a higher mortality risk. Differing histological subtypes had significant influence on overall survival and progression-free survival. Patients diagnosed with fibromyxoid sarcoma, rhabdomyosarcoma and angiosarcoma were related to higher mortality risk compared to other histological subtypes (fibromyxoid sarcoma: HR 5.2, 95% CI 0.71–38.1; rhabdomyosarcoma: HR 2.93, 95% CI 1.44–6.00; angiosarcoma: HR 1.07, 95% CI 0.53–2.18). Conclusions: Histological grade, tumor size, nodal and distant metastasis, tumor localization and histological subtype were determined as prognostic factors in terms of survival.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titleClinical characteristics of sarcoma patients: a population-based data analysis from a German clinical cancer registryeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleJournal of cancer research and clinical oncology-
local.bibliographicCitation.volume149-
local.bibliographicCitation.pagestart17051-
local.bibliographicCitation.pageend17069-
local.bibliographicCitation.publishernameSpringer-
local.bibliographicCitation.publisherplaceBerlin-
local.bibliographicCitation.doi10.1007/s00432-023-05350-5-
local.subject.keywordsSoft tisse sarcoma · Cancer registry · Prognostic factors · Overall survival · Progression-free survival-
local.openaccesstrue-
dc.identifier.ppn1871690676-
cbs.publication.displayform2023-
local.bibliographicCitation.year2023-
cbs.sru.importDate2023-11-30T09:46:19Z-
local.bibliographicCitationEnthalten in Journal of cancer research and clinical oncology - Berlin : Springer, 1904-
local.accessrights.dnbfree-
Enthalten in den Sammlungen:Open Access Publikationen der MLU

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