2015
Adjuvant Chemotherapy in Patients with Resected Non-Small-Cell- Lung Cancer Treated with Carboplatin and Oral Vinorelbine - SWITCH I Study
KOLEK, Vitezslav; Ivona GRYGARKOVA; Leona KOUBKOVA; Jana SKŘIČKOVÁ; Lenka OSTRIZKOVA et al.Základní údaje
Originální název
Adjuvant Chemotherapy in Patients with Resected Non-Small-Cell- Lung Cancer Treated with Carboplatin and Oral Vinorelbine - SWITCH I Study
Autoři
KOLEK, Vitezslav; Ivona GRYGARKOVA; Leona KOUBKOVA; Jana SKŘIČKOVÁ; Lenka OSTRIZKOVA; Jirina SVECOVA a Dimka SIXTOVA
Vydání
16th World Conference on Lung Cancer, 2015
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30203 Respiratory systems
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 5.040
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/15:00084853
Organizační jednotka
Lékařská fakulta
ISSN
Klíčová slova anglicky
non small cell lung cancer; adjuvant chemotherapy; vinorelbine; carboplatin
Štítky
Změněno: 24. 11. 2015 14:33, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Background: Adjuvant cisplatinum-based chemotherapy is recommended in patients with stages IB (> 4 cm), IIA, IIB, and IIIA of non small-cell lung cancer (NSCLC) after radical resection. Vinorelbine with cisplatin are preferable drugs in this indication, but the side effects of this treatment were not negligible in big adjuvant trials. Carboplatin with vinorelbine given intravenously switched to orally were applied in a multicentre prospective study SWITCH I to give better comfort, higher tolerability and comparable effectivenes as standard adjuvant chemotherapy. The recruitment period started in January 12th, 2005 and lasted till September 5th, 2008. Conclusion: Adjuvant chemotherapy with carboplatinum and vinorelbine given intravenously on the day 1 and orally on the day 8 in 21 day regimen appears to be a comfortable and tolerable therapy in radically resected NSCLC. It provides higher dose intensity and more of acomplished treatments compared to big adjuvant trials and LACE meta-analysis, in which these parametres varied between 50 % to 76 % only. Survival results are comparable to LACE (3-year survival 70,3% vs 64.3%), 5-year survival 56,2% vs 55.1%) and MOS 5.9 vs 5.15 y).