Oral vinorelbine versus etoposide with cisplatin and chemo-radiation as treatment in patients with stage III non-small cell lung cancer: A randomized phase II (RENO study).
Administration, Oral
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Chemoradiotherapy
Cisplatin
/ administration & dosage
Etoposide
/ administration & dosage
Female
Humans
Lung Neoplasms
/ drug therapy
Male
Middle Aged
Neoplasm Staging
Patient Safety
Survival Rate
Vinorelbine
/ administration & dosage
Clinical trial
Disease-free survival
Etoposide
Neoplasm metastasis
Non-small cell lung cancer
Phase II
Vinorelbine
Journal
Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
31
08
2018
revised:
31
10
2018
accepted:
30
11
2018
entrez:
27
8
2019
pubmed:
27
8
2019
medline:
18
6
2020
Statut:
ppublish
Résumé
Concomitant chemo-radiation is the standard treatment for unresectable stage III non-small cell lung cancer (LA-NSCLC). The aim of this study was to assess the safety and efficacy of oral vinorelbine and cisplatin (OVP) compared with etoposide and cisplatin (EP), both in combination with radiotherapy, in this setting. An open-label, randomized phase II trial was undertaken including 23 hospitals in Spain. Adults with untreated unresectable stage III NSCLC were randomized1:1 to receive: oral vinorelbine (days 1 and 8 with cisplatin on day 1 in 3-week cycles; 2 cycles of induction, 2 cycles in concomitance) or etoposide (days 1-5 and 29-32 with cisplatin on days 1 and 8 in 4-week cycles; 2 cycles in concomitance). Both groups received concomitant radiotherapy 2 Gy/day (66 Gy). The primary endpoint was progression free survival (PFS). One hundred and forty patients were enrolled. Sixty-nine patients received OVP and 71 received EP. Globally adverse events grade 3/4 per cycle were fewer in the vinorelbine arm (19.4%) than in the etoposide arm (62.6%) (p < 0.001). One patient (1.5%) in the OVP arm and 12 pts (17.6%) in the EP arm presented esophagitis grade 3/4 (p = 0.002). Median PFS was similar in both groups (10.8 [95% CI 7.7-13.8] and 9.6 months [95% CI 4.4-14.8]; p = 0.457, respectively). Preliminary median overall survival was 30 months in the OVP arm and 31.9 months in the EP arm (p = 0.688). Our findings show that OVP could be considered a standard combination with similar efficacy and better safety profile for the treatment of LA-NSCLC patients.
Identifiants
pubmed: 31446990
pii: S0169-5002(18)30681-0
doi: 10.1016/j.lungcan.2018.11.041
pii:
doi:
Substances chimiques
Etoposide
6PLQ3CP4P3
Cisplatin
Q20Q21Q62J
Vinorelbine
Q6C979R91Y
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
161-168Informations de copyright
Copyright © 2018. Published by Elsevier B.V.