2016
Outcomes for Patients with Metastatic Renal Cell Carcinoma Achieving a Complete Response on Targeted Therapy: A Registry-based Analysis.
BUCHLER, Tomas; Zbyněk BORTLÍČEK; Alexandr POPRACH; Tomáš PAVLÍK; Veronika VESKRNOVA et al.Základní údaje
Originální název
Outcomes for Patients with Metastatic Renal Cell Carcinoma Achieving a Complete Response on Targeted Therapy: A Registry-based Analysis.
Autoři
BUCHLER, Tomas; Zbyněk BORTLÍČEK; Alexandr POPRACH; Tomáš PAVLÍK; Veronika VESKRNOVA; Michaela HONZIRKOVA; Milada ZEMANOVA; Ondrej FIALA; Kateřina KUBÁČKOVÁ; Ondřej SLABÝ; Marek SVOBODA; Rostislav VYZULA; Ladislav DUŠEK a Bohuslav MELICHAR
Vydání
European Urology, Amsterdam, Elsevier Science Inc. 2016, 0302-2838
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 16.265
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/16:00088841
Organizační jednotka
Lékařská fakulta
UT WoS
000380754000024
EID Scopus
2-s2.0-84960933937
Klíčová slova anglicky
Renal cell carcinoma; Targeted therapy; Complete response; Survival
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 27. 9. 2016 11:33, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
BACKGROUND: It is currently not known whether treatment with anti-vascular endothelial growth factor agents for metastatic renal cell carcinoma (mRCC) can be safely discontinued in patients achieving a complete response (CR). OBJECTIVE: To assess outcomes for patients with mRCC achieving CR on targeted therapy (TT) and the survival of patients discontinuing TT after CR. DESIGN, SETTING, AND PARTICIPANTS: A national registry was used to identify patients achieving CR during first-line TT using bevacizumab, sunitinib, sorafenib, or pazopanib. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Relationships with outcomes were analysed using a log-rank test. RESULTS AND LIMITATIONS: A total of 100 patients achieving CR were identified out of 2803 patients. The median time to CR was 10.1 mo. Median progression-free survival (PFS) from TT initiation was 3.8 yr (95% confidence interval [CI] 2.9-4.6 yr) and the 5-yr overall survival (OS) was 80% (95% CI 70-91%). Patients discontinuing TT within 1 mo after achieving CR and those continuing TT beyond CR had similar OS (CI for difference in 2-yr post-CR OS -13% to 19%; p=0.3) and PFS (CI for difference in 2-yr post-CR PFS -29% to 17%; p=0.7). The limitations include the retrospective, registry-based data analysis. CONCLUSIONS: Achievement of CR on TT for mRCC was associated with excellent long-term prognosis. No significant differences in post-CR survival were observed between patients discontinuing TT after the date of CR and those who continued on TT, although the wide CIs cannot exclude important differences between the groups. PATIENT SUMMARY: According to this registry-based analysis, patients with metastatic renal cancer with no signs of disease (complete response) after treatment with targeted agents experience excellent long-term survival even if the treatment does not continue beyond the date of complete response.
Návaznosti
| NV15-34678A, projekt VaV |
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