First-cycle rash and survival in patients with advanced non-small-cell lung cancer receiving cetuximab in combination with first-line chemotherapy : a subgroup analysis of data from the FLEX phase 3 study


Autoria(s): Gatzemeier, U.; von Pawel, J.; Vynnychenko, I.; Zatloukal, P.; de Marinis, F.; Eberhardt, W. E. E.; Paz-Ares, L.; Schumacher, K. M.; Goddemeier, T.; O'Byrne, Kenneth J.; Pirker, R.
Data(s)

2011

Resumo

Background: The randomised phase 3 First-Line Erbitux in Lung Cancer (FLEX) study showed that the addition of cetuximab to cisplatin and vinorelbine significantly improved overall survival compared with chemotherapy alone in the first-line treatment of advanced non-small-cell lung cancer (NSCLC). The main cetuximab-related side-effect was acne-like rash. Here, we assessed the association of this acne-like rash with clinical benefit. Methods: We did a subgroup analysis of patients in the FLEX study, which enrolled patients with advanced NSCLC whose tumours expressed epidermal growth factor receptor. Our landmark analysis assessed if the development of acne-like rash in the first 21 days of treatment (first-cycle rash) was associated with clinical outcome, on the basis of patients in the intention-to-treat population alive on day 21. The FLEX study is registered with ClinicalTrials.gov, number NCT00148798. Findings: 518 patients in the chemotherapy plus cetuximab group-290 of whom had first-cycle rash-and 540 patients in the chemotherapy alone group were alive on day 21. Patients in the chemotherapy plus cetuximab group with first-cycle rash had significantly prolonged overall survival compared with patients in the same treatment group without first-cycle rash (median 15·0 months [95% CI 12·8-16·4] vs 8·8 months [7·6-11·1]; hazard ratio [HR] 0·631 [0·515-0·774]; p<0·0001). Corresponding significant associations were also noted for progression-free survival (median 5·4 months [5·2-5·7] vs 4·3 months [4·1-5·3]; HR 0·741 [0·607-0·905]; p=0·0031) and response (rate 44·8% [39·0-50·8] vs 32·0% [26·0-38·5]; odds ratio 1·703 [1·186-2·448]; p=0·0039). Overall survival for patients without first-cycle rash was similar to that of patients that received chemotherapy alone (median 8·8 months [7·6-11·1] vs 10·3 months [9·6-11·3]; HR 1·085 [0·910-1·293]; p=0·36). The significant overall survival benefit for patients with first-cycle rash versus without was seen in all histology subgroups: adenocarcinoma (median 16·9 months, [14·1-20·6] vs 9·3 months [7·7-13·2]; HR 0·614 [0·453-0·832]; p=0·0015), squamous-cell carcinoma (median 13·2 months [10·6-16·0] vs 8·1 months [6·7-12·6]; HR 0·659 [0·472-0·921]; p=0·014), and carcinomas of other histology (median 12·6 months [9·2-16·4] vs 6·9 months [5·2-11·0]; HR 0·616 [0·392-0·966]; p=0·033). Interpretation: First-cycle rash was associated with a better outcome in patients with advanced NSCLC who received cisplatin and vinorelbine plus cetuximab as a first-line treatment. First-cycle rash might be a surrogate clinical marker that could be used to tailor cetuximab treatment for advanced NSCLC to those patients who would be most likely to derive a significant benefit. Funding: Merck KGaA. © 2011 Elsevier Ltd.

Identificador

http://eprints.qut.edu.au/65072/

Publicador

The Lancet Publishing Group

Relação

DOI:10.1016/S1470-2045(10)70278-3

Gatzemeier, U., von Pawel, J., Vynnychenko, I., Zatloukal, P., de Marinis, F., Eberhardt, W. E. E., Paz-Ares, L., Schumacher, K. M., Goddemeier, T., O'Byrne, Kenneth J., & Pirker, R. (2011) First-cycle rash and survival in patients with advanced non-small-cell lung cancer receiving cetuximab in combination with first-line chemotherapy : a subgroup analysis of data from the FLEX phase 3 study. The Lancet Oncology, 12(1), pp. 30-37.

Direitos

Copyright 2011 The Lancet Publishing Group

Fonte

School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #cetuximab #cisplatin #epidermal growth factor receptor #navelbine #acne #adult #advanced cancer #aged #article #cancer combination chemotherapy #cancer survival #clinical effectiveness #controlled clinical trial #disease association #disease marker #drug efficacy #drug eruption #drug potentiation #female #human #lung adenocarcinoma #lung carcinoma #lung non small cell cancer #lung squamous cell carcinoma #major clinical study #male #multiple cycle treatment #overall survival #phase 1 clinical trial #priority journal #progression free survival #protein expression #survival rate #survival time #Antibodies #Monoclonal #Antineoplastic Combined Chemotherapy Protocols #Carcinoma #Non-Small-Cell Lung #Exanthema #Humans #Lung Neoplasms #Middle Aged
Tipo

Journal Article