commerciallyAbiraterone and enzalutamide in the first line therapy of metastatic castration resistant prostate cancer
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F24%3A10001242" target="_blank" >RIV/00064190:_____/24:10001242 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.5603/rpor.99028" target="_blank" >https://doi.org/10.5603/rpor.99028</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5603/rpor.99028" target="_blank" >10.5603/rpor.99028</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
commerciallyAbiraterone and enzalutamide in the first line therapy of metastatic castration resistant prostate cancer
Popis výsledku v původním jazyce
Background: The aim was to assess therapeutic outcomes and tolerance in patients with metastatic castration resistant prostate cancer (mCRPC) treated with androgen receptor targeted agents (ARTA) treatment at one oncological center in the Czech Republic. Materials and methods: Retrospective analysis of 64 patients with mCRPC treated with abiraterone (50 patients) and enzalutamide (14 patients) in the first line of this disease was conducted. Kaplan-Meier analysis was used to calculate progression free survival (PFS) and overall survival (OS). We performed a multivariate analysis of risk factors for treatment outcomes (PFS, OS) by Cox regression analysis. Results: The median follow-up was 28.4 months. The median PFS was 15.4 months [95% confidence interval (CI): 12.3-18.5], median OS was 38.2 months (95% CI: 19.9-56.5). Regression analysis demonstrated a favorable prognostic effect on PFS in patients with reduction of PSA GREATER-THAN OR EQUAL TO 50 %, in patients with early reduction of prostate-specific antigen (PSA) GREATER-THAN OR EQUAL TO 50% within 3 months, in patients younger than 74 years and in overall performance status (PS) 0. Regression analysis demonstrated a favorable prognostic effect on OS in patients with reduction of PSA GREATER-THAN OR EQUAL TO 50 %, in patients with early reduction of PSA GREATER-THAN OR EQUAL TO 50 % within 3 months and in patients with overall PS 0. Adverse effects grade 3-4 were reported in 17 (27.9%) patients in abirateron arm and in 1 (7.1%) patient in enzalutamide arm. Conclusion: The analysis of patients with mCRPC treated with ARTA in the first line showed that ARTA represents an effective and safe therapy and contributes to longer survival. (C) 2024 Greater Poland Cancer Centre.
Název v anglickém jazyce
commerciallyAbiraterone and enzalutamide in the first line therapy of metastatic castration resistant prostate cancer
Popis výsledku anglicky
Background: The aim was to assess therapeutic outcomes and tolerance in patients with metastatic castration resistant prostate cancer (mCRPC) treated with androgen receptor targeted agents (ARTA) treatment at one oncological center in the Czech Republic. Materials and methods: Retrospective analysis of 64 patients with mCRPC treated with abiraterone (50 patients) and enzalutamide (14 patients) in the first line of this disease was conducted. Kaplan-Meier analysis was used to calculate progression free survival (PFS) and overall survival (OS). We performed a multivariate analysis of risk factors for treatment outcomes (PFS, OS) by Cox regression analysis. Results: The median follow-up was 28.4 months. The median PFS was 15.4 months [95% confidence interval (CI): 12.3-18.5], median OS was 38.2 months (95% CI: 19.9-56.5). Regression analysis demonstrated a favorable prognostic effect on PFS in patients with reduction of PSA GREATER-THAN OR EQUAL TO 50 %, in patients with early reduction of prostate-specific antigen (PSA) GREATER-THAN OR EQUAL TO 50% within 3 months, in patients younger than 74 years and in overall performance status (PS) 0. Regression analysis demonstrated a favorable prognostic effect on OS in patients with reduction of PSA GREATER-THAN OR EQUAL TO 50 %, in patients with early reduction of PSA GREATER-THAN OR EQUAL TO 50 % within 3 months and in patients with overall PS 0. Adverse effects grade 3-4 were reported in 17 (27.9%) patients in abirateron arm and in 1 (7.1%) patient in enzalutamide arm. Conclusion: The analysis of patients with mCRPC treated with ARTA in the first line showed that ARTA represents an effective and safe therapy and contributes to longer survival. (C) 2024 Greater Poland Cancer Centre.
Klasifikace
Druh
J<sub>SC</sub> - Článek v periodiku v databázi SCOPUS
CEP obor
—
OECD FORD obor
30204 - Oncology
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Reports of Practical Oncology and Radiotherapy
ISSN
1507-1367
e-ISSN
—
Svazek periodika
29
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
PL - Polská republika
Počet stran výsledku
9
Strana od-do
1-9
Kód UT WoS článku
—
EID výsledku v databázi Scopus
2-s2.0-85188792331