Three-arm, randomized, phase 2 study of carboplatin and paclitaxel in combination with cetuximab, cixutumumab, or both for advanced non-small cell lung cancer (NSCLC) patients who will not receive bevacizumab-based therapy: An Eastern Cooperative Oncology Group (ECOG) study (E4508)
dc.contributor.author | Hanna, Nasser H. | |
dc.contributor.author | Dahlberg, Suzanne E. | |
dc.contributor.author | Kolesar, Jill M. | |
dc.contributor.author | Aggarwal, Charu | |
dc.contributor.author | Hirsch, Fred R. | |
dc.contributor.author | Ramalingam, Suresh S. | |
dc.contributor.author | Schiller, Joan H. | |
dc.contributor.department | Department of Medicine, IU School of Medicine | en_US |
dc.date.accessioned | 2017-04-12T15:41:43Z | |
dc.date.available | 2017-04-12T15:41:43Z | |
dc.date.issued | 2015-07-01 | |
dc.description.abstract | BACKGROUND: Preclinical evidence supports the clinical investigation of inhibitors to the insulin-like growth factor receptor (IGFR) and the epidermal growth factor receptor (EGFR) either alone or in combination as treatment for patients with non-small cell lung cancer (NSCLC). METHODS: Patients with chemotherapy-naïve, advanced NSCLC who had an Eastern Cooperative Oncology Group performance status of 0 or 1 were eligible. Patients were randomized to receive carboplatin intravenously at an area under the plasma drug concentration-time curve of 6.0 plus paclitaxel 200 mg/m(2) intravenously on day 1 every 3 weeks combined with either intravenous cetuximab weekly (arm A), intravenous cixutumumab every 2 weeks (arm B), or both (arm C). Patients who had nonprogessing disease after 12 weeks of therapy were permitted to continue on maintenance antibody therapy until they developed progressive disease. The primary endpoint was progression-free survival (PFS). The study design required 180 eligible patients and had 88% power to detect a 60% increase in median PFS for either comparison (arm A vs arm C or arm B vs arm C) using the log-rank test. RESULTS: From September 2009 to December 2010, 140 patients were accrued. The study was closed to accrual early because of an excessive number of grade 5 events reported on arms A and C. Thirteen patients died during treatment (6 patients on arm A, 2 patients on arm B, and 5 patients on arm C), including 9 within approximately 1 month of starting therapy. The estimated median PFS for arms A, B, and C were similar at 3.4 months, 4.2 months, and 4 months, respectively. CONCLUSIONS: On the basis of the apparent lack of efficacy and excessive premature deaths, the current results do not support the continued investigation of carboplatin, paclitaxel, and cixutumumab either alone or in combination with cetuximab for patients with advanced NSCLC. | en_US |
dc.eprint.version | Author's manuscript | en_US |
dc.identifier.citation | Hanna, N. H., Dahlberg, S. E., Kolesar, J., Aggarwal, C., Hirsch, F. R., Ramalingam, S. S., & Schiller, J. H. (2015). Three-arm randomized phase II study of carboplatin and paclitaxel in combination with cetuximab, cixutumumab, or both for advanced non-small cell lung cancer (NSCLC) patients who will not receive bevacizumab-based therapy: An Eastern Cooperative Oncology Group (ECOG) study (E4508). Cancer, 121(13), 2253–2261. http://doi.org/10.1002/cncr.29308 | en_US |
dc.identifier.issn | 1097-0142 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/12226 | |
dc.language.iso | en_US | en_US |
dc.publisher | Wiley Blackwell (John Wiley & Sons) | en_US |
dc.relation.isversionof | 10.1002/cncr.29308 | en_US |
dc.relation.journal | Cancer | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | PMC | en_US |
dc.subject | Antineoplastic Combined Chemotherapy Protocols | en_US |
dc.subject | therapeutic use | en_US |
dc.subject | Carcinoma, Non-Small-Cell Lung | en_US |
dc.subject | drug therapy | en_US |
dc.subject | Lung Neoplasms | en_US |
dc.title | Three-arm, randomized, phase 2 study of carboplatin and paclitaxel in combination with cetuximab, cixutumumab, or both for advanced non-small cell lung cancer (NSCLC) patients who will not receive bevacizumab-based therapy: An Eastern Cooperative Oncology Group (ECOG) study (E4508) | en_US |
dc.type | Article | en_US |