Molecular Oncology
Volume 1, Issue 4 , Pages 406-412, April 2008

Prognostic factors versus predictive factors: Examples from a clinical trial of erlotinib

  • Gary M. Clark

      Affiliations

    • Corresponding Author InformationTel.: +1 303 546 7633; fax: +1 303 546 7889.

Biostatistics and Data Management, OSI Pharmaceuticals, Inc., 2860 Wilderness Place, Boulder, CO 80301, USA

Received 11 November 2007; received in revised form 3 December 2007; accepted 4 December 2007. published online 03 January 2008.

Abstract 

It would be helpful to have factors that could identify patients who will, or will not, benefit from treatment with specific therapies. Ideally, these should be molecular-based factors. When results with molecular-based factors are disappointing, physicians often use clinical characteristics to make treatment decisions. Several characteristics have been suggested to predict sensitivity to epidermal growth factor receptor inhibitors in patients with non-small lung cancer, including gender, histology, smoking history. This report demonstrates that gender and histology are actually prognostic, rather than predictive factors. Before biomarkers or clinical characteristics are included in guidelines for selecting patients for specific treatments, it is imperative that the prognostic effects of these factors are distinguished from their ability to predict a differential clinical benefit from the specific treatment.

Keywords: Prognostic, Predictive, Epidermal growth factor receptor, Non-small lung cancer, Erlotinib, Smoking, Histology

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Presented in part at the 13th Danish Cancer Society Symposium: From the Bench to the Bedside and Back, Copenhagen, Denmark, August 27–29, 2007.

PII: S1574-7891(07)00102-0

doi:10.1016/j.molonc.2007.12.001

Molecular Oncology
Volume 1, Issue 4 , Pages 406-412, April 2008