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Histology classification is not a predictor of clinical outcomes in advanced non-small cell lung cancer (NSCLC) treated with vinorelbine or gemcitabine combinations

L. Trania, J. Myersonb, S. Ashleyb, K. Youngb, A. Sherib, R. Hubnerb, M. Puglisia, S. Popatb, M.E.R. O’BrienbCorresponding Author Informationemail address

Received 7 December 2009; received in revised form 1 February 2010; accepted 6 February 2010. published online 15 March 2010.
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Abstract 

Background

Until recently, histology has not been clearly or consistently described in the literature as a prognostic or predictive variable in advanced NSCLC studies. We have categorised patients treated with vinorelbine and gemcitabine based first line chemotherapy regimes for advanced NSCLC as either squamous or non-squamous, and also as either adenocarcinoma and non-adenocarcinoma, and compared outcome.

Material and methods

420 patients treated with platinum/gemcitabine, platinum/vinorelbine or single agent gemcitabine or vinorelbine as first line chemotherapy for advanced NSCLC were identified. The influence of pathology on progression free survival (PFS) and overall survival (OS) has been investigated by means of a Cox regression analysis. Hazard ratios with 95% CIs have been given for each pathological type after adjusting for the effects of age, gender, stage (III vs. IV), PS (0/1 vs. 2/3) and treatment type (platinum doublet vs. single agent).

Results

Neither univariate nor multivariate analysis suggested that there was a significant difference in the response rates for adenocarcinoma vs. non-adenocarcinoma or between squamous and non-squamous pathology. There was no difference in PFS between adenocarcinoma and non-adenocarcinoma pathologies until 8 months (p=0.98), and there was a statistically significant advantage in PFS for squamous vs. non-squamous pathologies (p=0.04). Using multivariate Cox regression analysis to adjust for the effects of age, gender, stage, PS, and treatment type, the pathology subtype was not significant. There was no difference in OS in any group.

Conclusions

These results suggest that histology may not be considered as a predictor of clinical outcome using these drugs.

a Department of Experimental Medicine, “La Sapienza” University of Rome, Viale Regina Elena 324, 00161 Rome, Italy

b Lung Unit, The Royal Marsden Hospital, Downs Road, Sutton, Surrey SM2 5PT, United Kingdom

Corresponding Author InformationCorresponding author at: Royal Marsden Hospital, Department of Medicine, Downs Road, Sutton, Surrey SM2 5PT, United Kingdom. Tel.: +44 2086613278; fax: +44 2086430373.

PII: S0169-5002(10)00068-1

doi:10.1016/j.lungcan.2010.02.003