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Review

Update on Taxanes in the First-Line Treatment of Advanced Non-Small-Cell Lung Cancer

by
M.A. Socinski
University of Pittsburgh Cancer Institute, Cancer Pavilion, 5150 Centre Avenue, Fifth Floor, Pittsburgh, PA 15232, USA
Curr. Oncol. 2014, 21(5), 691-703; https://doi.org/10.3747/co.21.1997
Submission received: 2 July 2014 / Revised: 3 August 2014 / Accepted: 4 September 2014 / Published: 1 October 2014

Abstract

Based on demonstrated favourable risk–benefit profiles, taxanes remain a key component in the first-line standard of care for advanced non-small-cell lung cancer (nsclc) and nsclc subtypes. In 2012, a novel taxane, nab-paclitaxel (Abraxane: Celgene Corporation, Summit, NJ, U.S.A.), was approved, in combination with carboplatin, for the first-line treatment of locally advanced or meta-static nsclc. The approval was granted because of demonstrated improved antitumour activity and tolerability compared with solvent-based paclitaxel–carboplatin in a phase iii trial. This review focuses on the evolution of first-line taxane therapy for advanced nsclc and the new options and advances in taxane therapy that might address unmet needs in advanced nsclc.
Keywords: docetaxel; elderly patients; nab-paclitaxel; paclitaxel; squamous cell carcinoma docetaxel; elderly patients; nab-paclitaxel; paclitaxel; squamous cell carcinoma

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MDPI and ACS Style

Socinski, M.A. Update on Taxanes in the First-Line Treatment of Advanced Non-Small-Cell Lung Cancer. Curr. Oncol. 2014, 21, 691-703. https://doi.org/10.3747/co.21.1997

AMA Style

Socinski MA. Update on Taxanes in the First-Line Treatment of Advanced Non-Small-Cell Lung Cancer. Current Oncology. 2014; 21(5):691-703. https://doi.org/10.3747/co.21.1997

Chicago/Turabian Style

Socinski, M.A. 2014. "Update on Taxanes in the First-Line Treatment of Advanced Non-Small-Cell Lung Cancer" Current Oncology 21, no. 5: 691-703. https://doi.org/10.3747/co.21.1997

APA Style

Socinski, M. A. (2014). Update on Taxanes in the First-Line Treatment of Advanced Non-Small-Cell Lung Cancer. Current Oncology, 21(5), 691-703. https://doi.org/10.3747/co.21.1997

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