Advertisement
Journal Home
Search for

Volume 62, Issue 1, Pages 105-112 (October 2008)


View previous. 16 of 20 View next.

Expression of excision repair cross-complementation group 1 and class III β-tubulin predict survival after chemotherapy for completely resected non-small cell lung cancer

Katsuhiro Okudaa, Hidefumi SasakiaCorresponding Author Informationemail address, Charles Dumontetb, Osamu Kawanoa, Haruhiro Yukiuea, Tomoki Yokoyamaa, Motoki Yanoa, Yoshitaka Fujiia

Received 8 January 2008; received in revised form 18 February 2008; accepted 24 February 2008. published online 07 April 2008.

Summary 

In this study, we examined the expression of excision repair cross-complementation group 1 (ERCC1) protein in 90 completely resected lung cancer samples from patients who received adjuvant or neo-adjuvant platinum-based chemotherapy. Epidermal growth factor receptor (EGFR) was also studied in these samples. We also examined class III β-tubulin protein expression in 50 patients treated with a platinum-based drug plus paclitaxel. Among 90 patients treated with platinum-based chemotherapy, the loss of ERCC1 protein expression was associated with a better prognosis (p=0.0068). The effect of ERCC1 expression on survival was not seen in a separate set of 59 patients who underwent curative resection but did not receive adjuvant chemotherapy. Among 50 patients treated with a platinum-based drug plus paclitaxel, loss of class III β-tubulin protein expression was also associated with a better prognosis (p=0.0303). When combined, patients with a tumor that was negative for both ERCC1 and class III β-tubulin had a significantly longer overall survival than those with a tumor that expressed either ERCC1 or class III β-tubulin (p=0.0230). There was no relationship between the presence of an EGFR mutation and the patients’ survival after the platinum-based chemotherapy. In conclusion, we found that the loss of ERCC1 and class III β-tubulin protein expression were predictors of better survival in patients who received a platinum-based plus taxane chemotherapy.

a Department of Oncology, Immunology and Surgery, Nagoya City University Graduate School of Medical Science, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan

b Unite Institut National de la Sante et de la Recherche Medicale 590, Laboratoire de Cytologie Analytique, Faculte de Medecine, Universite Claude Bernard, 8 Avenue Rockefeller, 69373 Lyon Cedex 08, Lyon, France

Corresponding Author InformationCorresponding author. Tel.: +81 52 853 8231; fax: +81 52 853 6440.

PII: S0169-5002(08)00108-6

doi:10.1016/j.lungcan.2008.02.021


View previous. 16 of 20 View next.