Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11392
Title: Randomized phase 2 sequencing and pharmacokinetic study of gemcitabine and oxaliplatin in advanced non-small cell lung cancer.
Authors: Mitchell, Paul L R;Broad, Adam;Rosenthal, Mark A;Galettis, Peter;Abraham, Rick;Burns, Ivon;Clarke, Stephen;Milner, Alvin;Diiulio, Juliana;Links, Matthew
Affiliation: Department of Medical Oncology, Austin Hospital, Queensland, Australia. paul.mitchell@austin.org.au
Issue Date: 23-May-2011
Citation: Asia-pacific Journal of Clinical Oncology 2011; 7(4): 376-84
Abstract: This multicentre phase II trial examined the combination of gemcitabine and oxaliplatin in patients with advanced non-small cell lung cancer (NSCLC). The effect of sequence administration was randomized and pharmacokinetics (PK) assessed.Eligible patients had stage IIIB or IV or recurrent NSCLC, no prior chemotherapy, World Health Organization performance status ≤2 and measurable disease. Treatment comprised: gemcitabine (1250 mg/m(2)) and oxaliplatin (70 mg/m(2)), each given on days 1 and 8 of a 21-day cycle. Patients were randomized 1:1 to the sequencing of the two drugs for the duration of their treatment. The primary end-point was response rate (RR). Secondary end-points included progression-free survival (PFS), overall survival (OS), toxicity, PK and the effect of drug sequencing.A total of 46 patients were enrolled of whom 43 were evaluable for response. Overall 13 patients (30%) achieved a partial response, PFS was 4.2 months (95% CI 2.8-5.8 months), and OS was 6.8 months (95% CI 4.4-10.1 months). There was only one case of grade 3 neurosensory toxicity despite a median cumulative oxaliplatin dose in excess of 500 mg/m(2) . No differences in clinical or PK end-points were observed between the two different sequencing arms.This oxaliplatin and gemcitabine schedule has shown activity in advanced NSCLC with modest toxicity. Neither clinical nor PK outcomes were influenced by the sequencing of these agents, although definite conclusions are limited by small patient numbers. The favorable toxicity profile of this doublet, in light of an encouraging RR, warrants its further investigation in NSCLC.
Internal ID Number: 22151988
URI: http://ahro.austin.org.au/austinjspui/handle/1/11392
DOI: 10.1111/j.1743-7563.2011.01390.x
URL: http://www.ncbi.nlm.nih.gov/pubmed/22151988
Type: Journal Article
Subjects: Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols.administration & dosage.pharmacokinetics
Carcinoma, Non-Small-Cell Lung.drug therapy.metabolism
Deoxycytidine.administration & dosage.analogs & derivatives
Disease-Free Survival
Drug Administration Schedule
Female
Humans
Kaplan-Meier Estimate
Lung Neoplasms.drug therapy.metabolism
Male
Middle Aged
Organoplatinum Compounds.administration & dosage
Survival Analysis
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.