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Real-world outcomes of immunotherapy with or without chemotherapy in first-line treatment of advanced non-small cell lung cancer
ID
Pelicon, Veronika
(
Avtor
),
ID
Čufer, Tanja
(
Avtor
),
ID
Knez, Lea
(
Avtor
)
PDF - Predstavitvena datoteka,
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(1,07 MB)
MD5: B847C44E30D48C33961AEBB044BA0D68
URL - Izvorni URL, za dostop obiščite
https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1182748/full
Galerija slik
Izvleček
Background: Immunotherapy alone (mono-IT) or combined with chemotherapy (chemo-IT) has recently become the cornerstone of first-line treatment for advanced non-small cell lung cancer (NSCLC) patients. Here, real-world outcomes of first-line mono-IT and chemo-IT of advanced NSCLC treated within routine clinical practice at a single academic center in the Central Eastern European (CEE) region are presented. Materials and methods: A total of 176 consecutive patients with advanced NSCLC treated with mono-IT (118 patients) or chemo-IT (58 patients) were included. At the participating institution, all medical data relevant for providing oncology care are collected prospectively and in a standardized manner using purposely created pro-forms. Adverse events (AEs) were recorded and graded according to Common Terminology Criteria for Adverse Events (CTCAE). The Kaplan−Meier method was used to estimate median overall survival (mOS) and median duration of treatment (mDOT). Results: The 118 patients in the mono-IT cohort had a median age of 64 years, most were male (59%), 20% had ECOG PS ≥2, and 14% had controlled CNS metastases at baseline. With a median follow-up time (mFU) of 24.1 months, the mOS was 19.4 months (95% CI, 11.1-27.6), and the mDOT was 5.0 months (95% CI, 3.5-6.5). The 1-year OS was 62%. The 58 patients in the chemo-IT cohort had a median age of 64 years, most were male (64%), 9% had ECOG PS ≥2, and 7% had controlled CNS metastases at baseline. With a mFU of 15.5 months, the mOS was 21.3 months (95% CI, 15.9-26.7), and the mDOT was 12.0 months (95% CI, 8.3-15.6). The 1-year OS was 75%. Adverse events of severe grade were recorded in 18% and 26% of patients, and immunotherapy discontinuation due to AEs occurred in 19% and 9% in the mono-IT and chemo-IT groups, respectively. No treatment-related deaths were recorded. Conclusion: The results from the present real-world observational study from a CEE country suggest similar effectiveness and safety of first-line mono-IT and chemo-IT in patients with advanced NSCLC to those observed in randomized clinical trials. However, continuous follow-up will offer better insight into the magnitude of long-term benefits in routine clinical practice.
Jezik:
Angleški jezik
Ključne besede:
non-small cell lung cancer
,
immunotherapy
,
chemo-immunotherapy
,
realworld outcomes
,
first line
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
MF - Medicinska fakulteta
Različica publikacije:
Objavljena publikacija
Leto izida:
2023
Št. strani:
11 str.
Številčenje:
Vol. 13, art. 1182748
PID:
20.500.12556/RUL-147298
UDK:
616-085.37:616.24-006
ISSN pri članku:
2234-943X
DOI:
10.3389/fonc.2023.1182748
COBISS.SI-ID:
157113347
Datum objave v RUL:
29.06.2023
Število ogledov:
554
Število prenosov:
70
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Frontiers in oncology
Skrajšan naslov:
Front. oncol.
Založnik:
Frontiers Editorial Office
ISSN:
2234-943X
COBISS.SI-ID:
1601583
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
nedrobnocelični pljučni rak
,
kemo-imunoterapija
,
realni rezultati
,
prva linija
,
imunoterapija
,
kemoterapija
,
rak (medicina)
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0189
Naslov:
Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0360
Naslov:
Celostna obravnava alergijskih bolezni in astme v Sloveniji: od epidemiologije do genetike
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