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A cost-effectiveness analysis of a chemoresponse assay for treatment of patients with recurrent epithelial ovarian cancer.

Identifieur interne : 004209 ( Ncbi/Merge ); précédent : 004208; suivant : 004210

A cost-effectiveness analysis of a chemoresponse assay for treatment of patients with recurrent epithelial ovarian cancer.

Auteurs : Victoria Plamadeala [États-Unis] ; Joseph L. Kelley [États-Unis] ; John K. Chan [États-Unis] ; Thomas C. Krivak [États-Unis] ; Michael J. Gabrin [États-Unis] ; Stacey L. Brower [États-Unis] ; Matthew A. Powell [États-Unis] ; Thomas J. Rutherford [États-Unis] ; Robert L. Coleman [États-Unis]

Source :

RBID : pubmed:25462203

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English descriptors

Abstract

Clinical validation of a chemoresponse assay was recently published, demonstrating a significant increase in overall survival in recurrent ovarian cancer patients treated with therapies to which their tumor was sensitive in the assay. The current study investigates the cost effectiveness of using the assay at the time of ovarian cancer recurrence from the payer's perspective.

DOI: 10.1016/j.ygyno.2014.11.019
PubMed: 25462203

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pubmed:25462203

Le document en format XML

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<term>Gynecologic Surgical Procedures (economics)</term>
<term>Humans</term>
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<term>Proportional Hazards Models</term>
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<front>
<div type="abstract" xml:lang="en">Clinical validation of a chemoresponse assay was recently published, demonstrating a significant increase in overall survival in recurrent ovarian cancer patients treated with therapies to which their tumor was sensitive in the assay. The current study investigates the cost effectiveness of using the assay at the time of ovarian cancer recurrence from the payer's perspective.</div>
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<Month>03</Month>
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<Day>30</Day>
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<Year>2015</Year>
<Month>Jan</Month>
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<Title>Gynecologic oncology</Title>
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<ArticleTitle>A cost-effectiveness analysis of a chemoresponse assay for treatment of patients with recurrent epithelial ovarian cancer.</ArticleTitle>
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<MedlinePgn>94-8</MedlinePgn>
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<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">Clinical validation of a chemoresponse assay was recently published, demonstrating a significant increase in overall survival in recurrent ovarian cancer patients treated with therapies to which their tumor was sensitive in the assay. The current study investigates the cost effectiveness of using the assay at the time of ovarian cancer recurrence from the payer's perspective.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Using a Markov state transition model, patient characteristics and survival data from the recent clinical study, the cumulative costs over the study horizon (71 months) for both the baseline (no assay) and intervention (assay consistent, hypothetical) cohorts were evaluated.</AbstractText>
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<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The use of a chemoresponse assay to inform treatment decisions in recurrent ovarian cancer patients has the potential to be cost-effective in both platinum-sensitive and platinum-resistant patients.</AbstractText>
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<ForeName>Victoria</ForeName>
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