Predicting degree of benefit from adjuvant trastuzumab in NSABP trial B-31. (Record no. 1438)

MARC details
000 -LEADER
fixed length control field 04248nam a22005657a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 130224s20132013 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0027-8874
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 24262440
245 ## - TITLE STATEMENT
Title Predicting degree of benefit from adjuvant trastuzumab in NSABP trial B-31.
251 ## - Source
Source Journal of the National Cancer Institute. 105(23):1782-8, 2013 Dec 4.
252 ## - Abbreviated Source
Abbreviated source J Natl Cancer Inst. 105(23):1782-8, 2013 Dec 4.
253 ## - Journal Name
Journal name Journal of the National Cancer Institute
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2013
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Manufacturer FY2014
266 ## - Date added to catalog
Date added to catalog 2014-02-24
501 ## - WITH NOTE
Local holdings Available online from MWHC library: 1996 - present (after 1 year), Available in print through MWHC library: 1999 - 2006
520 ## - SUMMARY, ETC.
Abstract BACKGROUND: National Surgical Adjuvant Breast and Bowel Project (NSABP) trial B-31 suggested the efficacy of adjuvant trastuzumab, even in HER2-negative breast cancer. This finding prompted us to develop a predictive model for degree of benefit from trastuzumab using archived tumor blocks from B-31.
520 ## - SUMMARY, ETC.
Abstract CONCLUSIONS: We developed a gene expression-based predictive model for degree of benefit from trastuzumab and demonstrated that HER2-negative tumors belong to the moderate benefit group, thus providing justification for testing trastuzumab in HER2-negative patients (NSABP B-47).
520 ## - SUMMARY, ETC.
Abstract METHODS: Case subjects with tumor blocks were randomly divided into discovery (n = 588) and confirmation cohorts (n = 991). A predictive model was built from the discovery cohort through gene expression profiling of 462 genes with nCounter assay. A predefined cut point for the predictive model was tested in the confirmation cohort. Gene-by-treatment interaction was tested with Cox models, and correlations between variables were assessed with Spearman correlation. Principal component analysis was performed on the final set of selected genes. All statistical tests were two-sided.
520 ## - SUMMARY, ETC.
Abstract RESULTS: Eight predictive genes associated with HER2 (ERBB2, c17orf37, GRB7) or ER (ESR1, NAT1, GATA3, CA12, IGF1R) were selected for model building. Three-dimensional subset treatment effect pattern plot using two principal components of these genes was used to identify a subset with no benefit from trastuzumab, characterized by intermediate-level ERBB2 and high-level ESR1 mRNA expression. In the confirmation set, the predefined cut points for this model classified patients into three subsets with differential benefit from trastuzumab with hazard ratios of 1.58 (95% confidence interval [CI] = 0.67 to 3.69; P = .29; n = 100), 0.60 (95% CI = 0.41 to 0.89; P = .01; n = 449), and 0.28 (95% CI = 0.20 to 0.41; P < .001; n = 442; P(interaction) between the model and trastuzumab < .001).
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element *Antibodies, Monoclonal, Humanized/tu [Therapeutic Use]
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Topical term or geographic name entry element *Antineoplastic Agents/tu [Therapeutic Use]
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Topical term or geographic name entry element *Breast Neoplasms/dt [Drug Therapy]
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Topical term or geographic name entry element *Breast Neoplasms/me [Metabolism]
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Topical term or geographic name entry element *Estrogen Receptor alpha/ge [Genetics]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element *Gene Expression Regulation, Neoplastic
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Topical term or geographic name entry element *Receptor, erbB-2/ge [Genetics]
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Topical term or geographic name entry element Chemotherapy, Adjuvant
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Topical term or geographic name entry element Cohort Studies
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Topical term or geographic name entry element Female
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Topical term or geographic name entry element Gene Expression Profiling
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Topical term or geographic name entry element Humans
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Topical term or geographic name entry element Odds Ratio
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Topical term or geographic name entry element Predictive Value of Tests
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Topical term or geographic name entry element Principal Component Analysis
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Proportional Hazards Models
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Topical term or geographic name entry element RNA, Messenger/me [Metabolism]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Treatment Outcome
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution Washington Cancer Institute
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Medline publication type Journal Article
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Medline publication type Randomized Controlled Trial
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Medline publication type Research Support, N.I.H., Extramural
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Medline publication type Research Support, Non-U.S. Gov't
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors Swain, Sandra M
790 ## - Authors
All authors Bandos H, Blackmon NL, Bohn OL, Burandt E, Costantino JP, Fehrenbacher L, Fumagalli D, Gavin PG, Geyer CE Jr, Goldstein LC, Horne ZD, Jeong JH, Kim C, Kim SI, Kim SR, Lee A, Mamounas EP, Paik S, Pogue-Geile KL, Rastogi P, Reilly ML, Remillard MY, Romond EH, Sneige N, Swain SM, Tanaka N, Taniyama Y, Wickerham DL, Wolmark N
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="http://dx.doi.org/10.1093/jnci/djt321">http://dx.doi.org/10.1093/jnci/djt321</a>
Public note http://dx.doi.org/10.1093/jnci/djt321
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Date last checked out Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 02/24/2014 1 24262440 24262440 09/26/2017 09/26/2017 02/24/2014 Journal Article

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