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   <subfield code="a">The impact of a fourteen-gene molecular assay on physician treatment decisions in non-small-cell lung cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Shane Dormady, Michael Broder, Girish Putcha, Robert Dumanois, Alison DeCristofaro, Eunice Chang, Paul Billings, Thierry Jahan]</subfield>
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   <subfield code="a">Background: Five-year survival in early-stage, non-squamous, non-small-cell lung cancer (NSCLC) remains poor compared with other solid tumors, even after complete resection. Post-operative management depends on prognostic staging to identify individuals at highest risk for death, and therefore with the greatest need for further intervention. A 14-gene quantitative RT-PCR test successfully differentiates stage I-III NSCLC patients who are at high-, intermediate-, or low-risk for 5-year mortality. This study assesses the impact of the assay's prognostic information on physician decisions regarding adjuvant chemotherapy. Methods: We invited 115 physicians who ordered the test to participate in an on-line survey. The primary outcome measure was the proportion of patients with different pre- and post-test chemotherapy recommendations. Results: Fifty-eight physicians (50%) completed the survey on 120 stage I or II NSCLC patients. Ninety-one patients (76%) had stage I lung cancer; 27 (23%), 39 (33%), and 54 (45%) patients had low-, intermediate-, and high-risk scores, respectively. Physicians' chemotherapy recommendations were changed post-testing in 37 patients (30.8%, 95% CI 22.7-39.9%). High-risk patients were more likely to have a change in treatment recommendation (44.4%, 95% CI 30.9-58.6%) than low risk patients (3.7%, 95% CI 0.1-19.0%); a substantial number of changes were observed in both stage I (33.0%, 95% CI 23.5-43.6%) and stage II (24.1%, 95% CI 10.3-43.5%). Conclusions: Our data show that the assay resulted in a significant impact on physician treatment decisions in early-stage NSCLC, and that the nature of treatment changes generally correlated with the test's assessment of risk.</subfield>
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   <subfield code="a">Japan Society of Clinical Oncology, 2014</subfield>
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   <subfield code="a">Lung cancer</subfield>
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   <subfield code="a">Dormady</subfield>
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   <subfield code="u">Valley Medical Oncology Consultants, 2940 Whipple Ave., Redwood City, CA, USA</subfield>
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   <subfield code="a">Broder</subfield>
   <subfield code="D">Michael</subfield>
   <subfield code="u">Partnership for Health Analytic Research, LLC, 280 South Beverly Drive, Suite 404, 90212, Beverly Hills, CA, USA</subfield>
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   <subfield code="u">Life Technologies Corporation, 5791 Van Allen Way, 92008, Carlsbad, CA, USA</subfield>
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   <subfield code="u">Partnership for Health Analytic Research, LLC, 280 South Beverly Drive, Suite 404, 90212, Beverly Hills, CA, USA</subfield>
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   <subfield code="u">Partnership for Health Analytic Research, LLC, 280 South Beverly Drive, Suite 404, 90212, Beverly Hills, CA, USA</subfield>
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   <subfield code="u">Life Technologies Corporation, 5791 Van Allen Way, 92008, Carlsbad, CA, USA</subfield>
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   <subfield code="u">Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco, Box 1724, 94143-1724, San Francisco, CA, USA</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">International Journal of Clinical Oncology</subfield>
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   <subfield code="g">20/1(2015-02-01), 59-69</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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