2024
The outcome in patients with BRAF-mutated metastatic melanoma treated with anti-programmed death receptor-1 monotherapy or targeted therapy in the real-world setting
KOPECKY, Jindrich, Marek PASEK, Radek LAKOMÝ, Bohuslav MELICHAR, Ivona MRAZOVA et. al.Základní údaje
Originální název
The outcome in patients with BRAF-mutated metastatic melanoma treated with anti-programmed death receptor-1 monotherapy or targeted therapy in the real-world setting
Autoři
KOPECKY, Jindrich (203 Česká republika), Marek PASEK (203 Česká republika), Radek LAKOMÝ (203 Česká republika, domácí), Bohuslav MELICHAR (203 Česká republika), Ivona MRAZOVA (203 Česká republika), Ondrej KUBECEK (203 Česká republika), Monika ARENBERGEROVA (203 Česká republika), Radmila LEMSTROVA (203 Česká republika), Alzbeta SVANCAROVA (203 Česká republika), Vojtech TRETERA (203 Česká republika), Alzbeta HLODAKOVA (203 Česká republika) a Kamila ZVACKOVA (203 Česká republika)
Vydání
Cancer Medicine, HOBOKEN, WILEY, 2024, 2045-7634
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.000 v roce 2022
Organizační jednotka
Lékařská fakulta
UT WoS
001185868200001
Klíčová slova anglicky
BRAF mutation; immunotherapy; real-world data; targeted therapy
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 7. 2024 09:33, Mgr. Tereza Miškechová
Anotace
V originále
Background: Immunotherapy and targeted therapy are currently two alternative backbones in the therapy of BRAF-mutated malignant melanoma. However, predictive biomarkers that would help with treatment selection are lacking. Methods: This retrospective study investigated outcomes of anti-programmed death receptor-1 monotherapy and targeted therapy in the first-line setting in patients with metastatic BRAF-mutated melanoma, focusing on clinical and laboratory parameters associated with treatment outcome. Results: Data from 174 patients were analysed. The median progression-free survival (PFS) was 17.0 months (95% CI; 8-39) and 12.5 months (95% CI; 9-14.2) for immunotherapy and targeted therapy, respectively. The 3-year PFS rate was 39% for immunotherapy and 25% for targeted therapy. The objective response rate was 72% and 51% for targeted therapy and immunotherapy. The median overall (OS) survival for immunotherapy has not been reached and was 23.6 months (95% CI; 16.1-38.2) for targeted therapy, with a 3-year survival rate of 63% and 40%, respectively. In a univariate analysis, age < 70 years, a higher number of metastatic sites, elevated serum LDH and a neutrophil-lymphocyte ratio above the cut-off value were associated with inferior PFS regardless of the therapy received, but only serum LDH level and the presence of lung metastases remained significant predictors of PFS in a multivariate analysis. Conclusions: Present real-world data document the high effectiveness of immunotherapy and targeted therapy. Although targeted therapy had higher response rates, immunotherapy improved PFS and OS. While the prognostic value of LDH was confirmed, the potential use of blood cell count-derived parameters to predict outcomes needs further investigation.