Abstract

PurposeThe aim of this study is to compare the therapeutic effect between endostar plus adjuvant chemotherapy and adjuvant chemotherapy alone in the patients with completely resected non-small cell lung cancer (NSCLC) at stage IB to IIIA.Experimental DesignThis is an open, multicenter, randomized (1:1) study with 250 NSCLC patients. Completely resected NSCLC patients at stages IB to IIIA were randomized to receive adjuvant NP plus endostar (Vinorelbine 25 mg/m2 on day 1 and day 8 plus Cisplatin 75 mg/m2 on day 1, and plus endostar 7.5 mg/m2 per day iv for consecutive 14 days) or NP regimen alone. Every 21 days were set as one cycle for 4 cycles. The primary endpoint was disease-free survival (DFS). Secondary endpoints included tumor response rate, overall survival and safety.ResultsThe two groups had no significant difference in the incidence of toxicity reaction. Endostar plus NP prolonged the DFS of patients with completely resected NSCLC at stage IIIA (19.33±3.73 vs 17.10±9.68 months) but with no statistical difference compared to NP alone. In the endostar plus NP group, those cases with high expression of vascular endothelial growth factor (VEGF) showed a significantly better DFS than those with low VEGF expression (48.45±3.52 vs 40.18±4.54 months, P<0.05).ConclusionsVascular targeted therapy with endostar plus NP prolongs the DFS of patients with complete resectable NSCLC in stage IIIA and significantly extends the DFS of NSCLC patients with high VEGF expression, but does not show benefits in OS for stage IB−IIIA.

Highlights

  • Lung cancer is the leading cause of cancerrelated death worldwide [1]

  • Endostar was approved by SFDA in 2005 and has been used as the first-line therapy for advanced Non-small cell lung cancer (NSCLC) combined with chemotherapy in China

  • It has been demonstrated that the combination of chemotherapy plus anti-angiogenesis based therapy such as bevacizumab, a recombinant humanized monoclonal antibody against vascular endothelial growth factor A (VEGF-A), increased www.impactjournals.com/oncotarget the response rate and progression-free survival of patients with NSCLC [25, 26]

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Summary

Introduction

Lung cancer is the leading cause of cancerrelated death worldwide [1]. Non-small cell lung cancer (NSCLC) accounts for approximately 85% of lung cancers and its five-year survival rate is below 20% [2, 3]. Chemotherapy is one of the standard therapeutic approaches for advanced NSCLC. Cisplatin-based treatment is the first line chemotherapy for lung cancer. Advances in cisplatin-based chemotherapy have resulted in improvement of survival rate, the therapeutic efficacy is limited due to the development of cisplatin resistance. For NSCLC patients suitable for tumor resection, postoperative adjuvant chemotherapy could extend the time to recurrence and increase the survival rate of NSCLC patients [4, 5]. Drug-resistance and over-treatment phenomena are present in most patients receiving conventional postoperative adjuvant chemotherapy [6,7,8], it is important to develop novel postoperative adjuvant chemotherapies to improve the survival rate of operable NSCLC patients

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