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- Publisher Website: 10.1016/j.lungcan.2005.03.029
- Scopus: eid_2-s2.0-22044445819
- PMID: 16022917
- WOS: WOS:000231253300012
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Article: Randomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer
Title | Randomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer |
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Authors | |
Keywords | Non-small cell lung cancer Progression-free survival Tolerance |
Issue Date | 2005 |
Citation | Lung Cancer, 2005, v. 49, n. 2, p. 233-240 How to Cite? |
Abstract | Purpose: The objective of this trial was to compare two vinorelbine-based doublets with carboplatin (CBDCA-VC) or with gemcitabine (VG) in patients with stage IIIB-IV non-small cell lung cancer (NSCLC). Patients and Methods: A total of 316 patients with advanced NSCLC previously untreated were randomized to either vinorelbine 30 mg/m2 D1,8 with carboplatin AUC 5 D1 (VC) or vinorelbine 25 mg/m2 with gemcitabine (VG) 1000 mg/m2 both given D1,8 every 3 weeks. The primary endpoint was response rate with secondary parameters being survival (OS), progression-free survival (PFS), tolerance and clinical benefit. Results: The median number of cycles was four in each arm with a total of 1268 cycles. The objective response (OR) on intent-to-treat was 20.8% in VC and 28% in VG (p = 0.15). Median PFS was 3.9 months in VC and 4.4 months (mo) in VG (p = 0.18). Median survival was significantly longer (p = 0.01) for VG with 11.5 mo compared to 8.6 mo in VC with 1 year survival at 48.9 and 34.4%, respectively. Tolerance was better in the VG arm as compared to the VC patients. Four toxic deaths were recorded in the VC group. Clinical benefit response rate was 32.4% compared to 40.9% in 111 and 110 evaluable patients in VC and VG, respectively. Conclusion: VG compared to VC resulted in a similar overall response rate, favourable median survival and a better toxicity profile. For non-cisplatin-based chemotherapy, VG is a useful alternative. © 2005 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/326450 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.761 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Tan, E. H. | - |
dc.contributor.author | Szczesna, A. | - |
dc.contributor.author | Krzakowski, M. | - |
dc.contributor.author | Macha, H. N. | - |
dc.contributor.author | Gatzemeier, U. | - |
dc.contributor.author | Mattson, K. | - |
dc.contributor.author | Wernli, M. | - |
dc.contributor.author | Reiterer, P. | - |
dc.contributor.author | Hui, R. | - |
dc.contributor.author | Von Pawel, J. | - |
dc.contributor.author | Bertetto, O. | - |
dc.contributor.author | Pouget, J. C. | - |
dc.contributor.author | Burillon, J. P. | - |
dc.contributor.author | Parlier, Y. | - |
dc.contributor.author | Abratt, R. | - |
dc.date.accessioned | 2023-03-10T02:19:22Z | - |
dc.date.available | 2023-03-10T02:19:22Z | - |
dc.date.issued | 2005 | - |
dc.identifier.citation | Lung Cancer, 2005, v. 49, n. 2, p. 233-240 | - |
dc.identifier.issn | 0169-5002 | - |
dc.identifier.uri | http://hdl.handle.net/10722/326450 | - |
dc.description.abstract | Purpose: The objective of this trial was to compare two vinorelbine-based doublets with carboplatin (CBDCA-VC) or with gemcitabine (VG) in patients with stage IIIB-IV non-small cell lung cancer (NSCLC). Patients and Methods: A total of 316 patients with advanced NSCLC previously untreated were randomized to either vinorelbine 30 mg/m2 D1,8 with carboplatin AUC 5 D1 (VC) or vinorelbine 25 mg/m2 with gemcitabine (VG) 1000 mg/m2 both given D1,8 every 3 weeks. The primary endpoint was response rate with secondary parameters being survival (OS), progression-free survival (PFS), tolerance and clinical benefit. Results: The median number of cycles was four in each arm with a total of 1268 cycles. The objective response (OR) on intent-to-treat was 20.8% in VC and 28% in VG (p = 0.15). Median PFS was 3.9 months in VC and 4.4 months (mo) in VG (p = 0.18). Median survival was significantly longer (p = 0.01) for VG with 11.5 mo compared to 8.6 mo in VC with 1 year survival at 48.9 and 34.4%, respectively. Tolerance was better in the VG arm as compared to the VC patients. Four toxic deaths were recorded in the VC group. Clinical benefit response rate was 32.4% compared to 40.9% in 111 and 110 evaluable patients in VC and VG, respectively. Conclusion: VG compared to VC resulted in a similar overall response rate, favourable median survival and a better toxicity profile. For non-cisplatin-based chemotherapy, VG is a useful alternative. © 2005 Elsevier Ireland Ltd. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Lung Cancer | - |
dc.subject | Non-small cell lung cancer | - |
dc.subject | Progression-free survival | - |
dc.subject | Tolerance | - |
dc.title | Randomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.lungcan.2005.03.029 | - |
dc.identifier.pmid | 16022917 | - |
dc.identifier.scopus | eid_2-s2.0-22044445819 | - |
dc.identifier.volume | 49 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 233 | - |
dc.identifier.epage | 240 | - |
dc.identifier.isi | WOS:000231253300012 | - |