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Article: Randomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer

TitleRandomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer
Authors
KeywordsNon-small cell lung cancer
Progression-free survival
Tolerance
Issue Date2005
Citation
Lung Cancer, 2005, v. 49, n. 2, p. 233-240 How to Cite?
AbstractPurpose: 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 Identifierhttp://hdl.handle.net/10722/326450
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.761
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTan, E. H.-
dc.contributor.authorSzczesna, A.-
dc.contributor.authorKrzakowski, M.-
dc.contributor.authorMacha, H. N.-
dc.contributor.authorGatzemeier, U.-
dc.contributor.authorMattson, K.-
dc.contributor.authorWernli, M.-
dc.contributor.authorReiterer, P.-
dc.contributor.authorHui, R.-
dc.contributor.authorVon Pawel, J.-
dc.contributor.authorBertetto, O.-
dc.contributor.authorPouget, J. C.-
dc.contributor.authorBurillon, J. P.-
dc.contributor.authorParlier, Y.-
dc.contributor.authorAbratt, R.-
dc.date.accessioned2023-03-10T02:19:22Z-
dc.date.available2023-03-10T02:19:22Z-
dc.date.issued2005-
dc.identifier.citationLung Cancer, 2005, v. 49, n. 2, p. 233-240-
dc.identifier.issn0169-5002-
dc.identifier.urihttp://hdl.handle.net/10722/326450-
dc.description.abstractPurpose: 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.languageeng-
dc.relation.ispartofLung Cancer-
dc.subjectNon-small cell lung cancer-
dc.subjectProgression-free survival-
dc.subjectTolerance-
dc.titleRandomized study of vinorelbine-gemcitabine versus vinorelbine-carboplatin in patients with advanced non-small cell lung cancer-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.lungcan.2005.03.029-
dc.identifier.pmid16022917-
dc.identifier.scopuseid_2-s2.0-22044445819-
dc.identifier.volume49-
dc.identifier.issue2-
dc.identifier.spage233-
dc.identifier.epage240-
dc.identifier.isiWOS:000231253300012-

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