2018
Advantages in Prognosis of Adult Patients with Ewing Sarcoma: 11-years Experiences and Current Treatment Management
ADÁMKOVÁ KRÁKOROVÁ, Dagmar, Katerina KUBACKOVA, Ladislav DUŠEK, Tomáš TOMÁŠ, Pavel JANÍČEK et. al.Základní údaje
Originální název
Advantages in Prognosis of Adult Patients with Ewing Sarcoma: 11-years Experiences and Current Treatment Management
Autoři
ADÁMKOVÁ KRÁKOROVÁ, Dagmar (203 Česká republika), Katerina KUBACKOVA (203 Česká republika), Ladislav DUŠEK (203 Česká republika, domácí), Tomáš TOMÁŠ (203 Česká republika), Pavel JANÍČEK (203 Česká republika), Štěpán TUČEK (203 Česká republika), Jana PRAUSOVA (203 Česká republika), Igor KISS (203 Česká republika) a Iva ZAMBO (203 Česká republika, garant)
Vydání
PATHOLOGY & ONCOLOGY RESEARCH, DORDRECHT, SPRINGER, 2018, 1219-4956
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30109 Pathology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.433
Kód RIV
RIV/00216224:14110/18:00103942
Organizační jednotka
Lékařská fakulta
UT WoS
000433372000023
Klíčová slova anglicky
Ewing sarcoma; Adults; Multimodal treatment; Risk factors; Prognosis
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 2. 2019 20:07, Soňa Böhmová
Anotace
V originále
Ewing sarcoma (ES) is an exceptionally rare tumor in adults. Data regarding outcomes of adult patients with ES and experiences with age-adapted therapeutic strategies are very limited. The aim of this study was to evaluate prognostic factors and clinical outcome in a cohort of adult patients treated according to pediatric protocols in the Czech Republic. The records of 58 adult ES patients diagnosed between 2002 and 2013 were reviewed and factors relevant to prognosis and survival were analyzed. The median age of study cohort was 29 years (range, 18-59). The most frequent location was axial (36.2%), followed by involvement of extraskeletal tissues (34.5%) and bones of the extremities (29.3%). Twenty-eight (48.3%) patients had metastatic disease. In cases with localized ES, the 5-year overall survival (OS) was 76.5%. Using the log-rank test, the presence of metastasis at diagnosis, local treatment without surgery and a failure to achieve complete remission were associated with significantly shorter survival. In a multivariate Cox proportional hazard analysis, the achievement of complete remission was an independent predictor of patients's survival time. Outcomes of adults with localized ES treated according to multimodal pediatric protocols are similar to children. The achievement of complete remission is an independent predictor of survival time in ES patients. Severe hematological toxicity is foreseeable and manageable. Prognosis of patients with metastases or progression remains dismal.