Multicenter Randomized Phase 2 Clinical Trial of a Recombinant Human Endostatin Adenovirus in Patients with Advanced Head and Neck Carcinoma

A randomized, open-label, phase 2, multicenter clinical trial was conducted to evaluate the efficacy and safety of the addition of a recombinant human endostatin adenovirus (E10A) to cisplatin and paclitaxel in patients with advanced head and neck squamous cell carcinoma or nasopharyngeal carcinoma....

Full description

Saved in:
Bibliographic Details
Published inMolecular therapy Vol. 22; no. 6; pp. 1221 - 1229
Main Authors Ye, Wen, Liu, Ranyi, Pan, Changchuan, Jiang, Wenqi, Zhang, Li, Guan, Zhongzhen, Wu, Jiangxue, Ying, Xiaofang, Li, Lixia, Li, Su, Tan, Wen, Zeng, Musheng, Kang, Tiebang, Liu, Qing, Thomas, George R, Huang, Manli, Deng, Wuguo, Huang, Wenlin
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.06.2014
Elsevier Limited
Nature Publishing Group
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A randomized, open-label, phase 2, multicenter clinical trial was conducted to evaluate the efficacy and safety of the addition of a recombinant human endostatin adenovirus (E10A) to cisplatin and paclitaxel in patients with advanced head and neck squamous cell carcinoma or nasopharyngeal carcinoma. Patients with locally advanced or metastatic head and neck squamous cell carcinoma or nasopharyngeal carcinoma not suitable for operation or radiotherapy were randomly assigned to receive E10A plus chemotherapy every 3 weeks for a maximum of six cycles or to receive chemotherapy only. One hundred and thirty-six eligible patients were randomly assigned. The addition of E10A did not significantly improve the objective response rate (29.9 versus 39.7%, P = 0.154). However, patients who received endostatin had longer progression-free survival (7.03 versus 3.60 months, P = 0.006; hazard ratio: 0.55). The combination of E10A with chemotherapy benefited prior chemotherapy-treated patients and those who received three to four treatment cycles (6.50 versus 3.43 months, P = 0.003; 8.27 versus 4.27 months, P = 0.018; respectively). The overall disease control rate significantly increased from 80.6% in the control group to 92.6% in the test group (P = 0.034). Except for fever, no adverse events were associated with the E10A treatment. In summary, E10A plus chemotherapy is a safe and effective therapeutic approach in patients with advanced head and neck squamous cell carcinoma or nasopharyngeal carcinoma.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1525-0016
1525-0024
DOI:10.1038/mt.2014.53