Pharmacogenetic testing in the face of unclear clinical efficacy: Lessons from cytochrome P450 2D6 for tamoxifen. Issue 20 (24th July 2013)
- Record Type:
- Journal Article
- Title:
- Pharmacogenetic testing in the face of unclear clinical efficacy: Lessons from cytochrome P450 2D6 for tamoxifen. Issue 20 (24th July 2013)
- Main Title:
- Pharmacogenetic testing in the face of unclear clinical efficacy: Lessons from cytochrome P450 2D6 for tamoxifen
- Authors:
- Peppercorn, Jeffrey
Hamilton, Erika
Marcom, Paul Kelly
Beskow, Laura
Lyman, Gary H. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr28263-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>This study evaluated self‐reported knowledge, practice, and attitudes toward commercially available cytochrome P450 2D6 (CYP2D6) pharmacogenomic testing for patients on tamoxifen for breast cancer (CYPT) among US oncologists while evidence for the use of the test was evolving.</p> </sec> <sec id="cncr28263-sec-0002" sec-type="section"> <title>METHODS</title> <p>A self‐administered survey of medical oncology breast cancer specialists at National Comprehensive Cancer Network (NCCNO) centers and a random sample of community‐based oncologists (CBOs) was undertaken. The survey evaluated knowledge and use of the CYP2D6 test and response to hypothetical test results.</p> </sec> <sec id="cncr28263-sec-0003" sec-type="section"> <title>RESULTS</title> <p>In total, 201 of 459 (44%) oncologists responded. At a time when CYPT remained experimental, 31% of oncologists reported use of CYPT and 56% reported willingness to order CYPT outside of a clinical trial if requested by a patient. Compared to oncologists specializing in breast cancer, oncologists in community‐based practice were more likely to use CYPT routinely (21% versus 11%, <italic>P</italic> &lt; .06), to order CYPT on patient request (66% versus 44%, <italic>P</italic> &lt; .001), and to change management for premenopausal women with intermediate metabolism (34% CBO<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr28263-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>This study evaluated self‐reported knowledge, practice, and attitudes toward commercially available cytochrome P450 2D6 (CYP2D6) pharmacogenomic testing for patients on tamoxifen for breast cancer (CYPT) among US oncologists while evidence for the use of the test was evolving.</p> </sec> <sec id="cncr28263-sec-0002" sec-type="section"> <title>METHODS</title> <p>A self‐administered survey of medical oncology breast cancer specialists at National Comprehensive Cancer Network (NCCNO) centers and a random sample of community‐based oncologists (CBOs) was undertaken. The survey evaluated knowledge and use of the CYP2D6 test and response to hypothetical test results.</p> </sec> <sec id="cncr28263-sec-0003" sec-type="section"> <title>RESULTS</title> <p>In total, 201 of 459 (44%) oncologists responded. At a time when CYPT remained experimental, 31% of oncologists reported use of CYPT and 56% reported willingness to order CYPT outside of a clinical trial if requested by a patient. Compared to oncologists specializing in breast cancer, oncologists in community‐based practice were more likely to use CYPT routinely (21% versus 11%, <italic>P</italic> &lt; .06), to order CYPT on patient request (66% versus 44%, <italic>P</italic> &lt; .001), and to change management for premenopausal women with intermediate metabolism (34% CBO versus 8% NCCN, <italic>P</italic> &lt; .001). Oncologists cited data from randomized trials and professional guidelines as most influential when considering use of a genetic test.</p> </sec> <sec id="cncr28263-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>Prior to definitive evidence, a minority of oncologists reported using the CYP2D6 test routinely, and many indicated willingness to change management of patients based on test results. There is a need to educate clinicians and the public regarding the uncertain benefits of commercially available genetic tests in clinical practice when evidence from ongoing trials is still emerging. <bold><italic>Cancer</italic> 2013;119:3703–3709</bold>. © <italic>2013 American Cancer Society</italic>.</p> </sec> </abstract> … (more)
- Is Part Of:
- Cancer. Volume 119:Issue 20(2013)
- Journal:
- Cancer
- Issue:
- Volume 119:Issue 20(2013)
- Issue Display:
- Volume 119, Issue 20 (2013)
- Year:
- 2013
- Volume:
- 119
- Issue:
- 20
- Issue Sort Value:
- 2013-0119-0020-0000
- Page Start:
- 3703
- Page End:
- 3709
- Publication Date:
- 2013-07-24
- Subjects:
- Cancer -- Periodicals
Cancer -- Cytopathology -- Periodicals
616.99405 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cncr.28263 ↗
- Languages:
- English
- ISSNs:
- 0008-543X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.450000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4035.xml