Pregled bibliografske jedinice broj: 1156258
Real-world safety and efficacy of nivolumab for ≥ 2nd line treatment of metastatic renal cell carcinoma: A retrospective cohort study in Croatia, Hungary, and Malta
Real-world safety and efficacy of nivolumab for ≥ 2nd line treatment of metastatic renal cell carcinoma: A retrospective cohort study in Croatia, Hungary, and Malta // Neoplasma, 68 (2021), 1; 208-215 doi:10.4149/neo_2020_200512N519 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1156258 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Real-world safety and efficacy of nivolumab for ≥ 2nd line treatment of metastatic renal cell carcinoma:
A retrospective cohort study in Croatia, Hungary, and Malta
(Real-world safety and efficacy of nivolumab for ≥
2nd line treatment of metastatic renal cell
carcinoma: A retrospective cohort study in
Croatia, Hungary, and Malta)
Autori
Vrdoljak, Eduard ; Magri, Claude ; Gamulin, Marija ; Bošković, Lidija ; Omrčen, Tomislav ; Bajić, Žarko ; Dienes, Tamas ; Geczi, Lajos
Izvornik
Neoplasma (0028-2685) 68
(2021), 1;
208-215
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
metastatic renal carcinoma ; PD-1 immune checkpoint inhibitor ; nivolumab ; immunotherapy
Sažetak
The objective of our study was to assess the real- world safety and efficacy of nivolumab in the second- or later-line treatment of metastatic renal cell carcinoma (mRCC). We conducted a multicenter, retrospective, observational study of real-world data from patients who were treated with nivolumab under a patient expanded access program from 2015 to 2017 in Croatia, Hungary, and Malta. The primary safety endpoint was the discontinuation of therapy because of adverse events. The primary efficacy endpoint was overall survival (OS). We collected data from 87 patients with a median (interquartile range (IQR)) age of 63 (57-68) years, and 21% were women. The median (IQR) follow-up was 11 (5-31) months. Treatment was discontinued because of toxicity in 4 (5%) patients. Four (5%) patients experienced treatment-related adverse events of grade 3 or 4. The OS was 18.0 (95% CI: 11.0 to 28.6) months, and the PFS was 8.5 (95% CI: 4.9 to 12.1) months. Our study indicated a good safety and efficacy profile of nivolumab in the second- or later-line treatment of mRCC patients in a real-world clinical practice environment, which is comparable with the findings of the registrational trial.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
KBC Split,
Klinički bolnički centar Zagreb,
Medicinski fakultet, Split,
Psihijatrijska bolnica "Sveti Ivan" Zagreb
Profili:
Marija Gamulin
(autor)
Eduard Vrdoljak
(autor)
Tomislav Omrčen
(autor)
Lidija Bošković
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE