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Inge J. Stijleman
Researcher at University of Utah
Publications - 13
Citations - 5075
Inge J. Stijleman is an academic researcher from University of Utah. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 9, co-authored 13 publications receiving 4376 citations. Previous affiliations of Inge J. Stijleman include Huntsman Cancer Institute.
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Journal ArticleDOI
Supervised Risk Predictor of Breast Cancer Based on Intrinsic Subtypes
Joel S. Parker,Michael Mullins,Maggie C.U. Cheang,Samuel Leung,David Voduc,Tammi L. Vickery,Sherri R. Davies,Christiane Fauron,Xiaping He,Zhiyuan Hu,John Quackenbush,Inge J. Stijleman,Juan P. Palazzo,James Stephen Marron,Andrew B. Nobel,Elaine R. Mardis,Torsten O. Nielsen,Matthew J. Ellis,Charles M. Perou,Philip S. Bernard +19 more
TL;DR: D diagnosis by intrinsic subtype adds significant prognostic and predictive information to standard parameters for patients with breast cancer.
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A Comparison of PAM50 Intrinsic Subtyping with Immunohistochemistry and Clinical Prognostic Factors in Tamoxifen-Treated Estrogen Receptor–Positive Breast Cancer
Torsten O. Nielsen,Joel S. Parker,Samuel Leung,K. David Voduc,Mark T. W. Ebbert,Tammi L. Vickery,Sherri R. Davies,Jacqueline E. Snider,Inge J. Stijleman,Jerry S. Reed,Maggie C.U. Cheang,Maggie C.U. Cheang,Elaine R. Mardis,Charles M. Perou,Philip S. Bernard,Matthew J. Ellis +15 more
TL;DR: The PAM50 gene expression test for intrinsic biological subtype can be applied to large series of formalin-fixed, paraffin-embedded breast cancers, and gives more prognostic information than clinical factors and IHC using standard cut points.
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Responsiveness of intrinsic subtypes to adjuvant anthracycline substitution in the NCIC.CTG MA.5 randomized trial
Maggie C.U. Cheang,K. David Voduc,Dongsheng Tu,Shan Jiang,Samuel Leung,Stephen Chia,Lois E. Shepherd,Mark Levine,Kathleen I. Pritchard,Sherri R. Davies,Inge J. Stijleman,Carole Davis,Mark T. W. Ebbert,Joel S. Parker,Matthew J. Ellis,Philip S. Bernard,Charles M. Perou,Torsten O. Nielsen +17 more
TL;DR: The HER2-E showed the greatest benefit from CEF versus CMF, with absolute 5-year RFS and OS differences exceeding 20%, whereas the chemotherapy-sensitive basal-like tumors showed no added benefit for CEF overCMF, suggesting that nonanthracycline regimens may be adequate in this subtype although further investigation is required.
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Intrinsic Subtypes from PAM50 Gene Expression Assay in a Population-Based Breast Cancer Cohort: Differences by Age, Race, and Tumor Characteristics
Carol Sweeney,Philip S. Bernard,Rachel E. Factor,Marilyn L. Kwan,Laurel A. Habel,Charles P. Quesenberry,Kaylynn Shakespear,Erin Weltzien,Inge J. Stijleman,Carole Davis,Mark T. W. Ebbert,Adrienne Castillo,Lawrence H. Kushi,Bette J. Caan +13 more
TL;DR: It is indicated that over 50% of breast cancers treated in the community have luminal A subtype, and Gene expression–based classification shifted some tumors categorized as low risk by surrogate clinicopathologic criteria to higher-risk subtypes.
Journal ArticleDOI
PAM50 proliferation score as a predictor of weekly paclitaxel benefit in breast cancer
Miguel Martin,Aleix Prat,Álvaro Rodríguez-Lescure,Rosalía Caballero,Mark T. W. Ebbert,Blanca Munárriz,Manuel Ruiz-Borrego,Roy R. L. Bastien,C. Crespo,Carole Davis,César A. Rodríguez,J. M. López-Vega,V. Furio,Ana M. García,Maribel Casas,Matthew J. Ellis,Donald A. Berry,Brandelyn N. Pitcher,Lyndsay Harris,Amparo Ruiz,Eric P. Winer,Clifford A. Hudis,Inge J. Stijleman,David Tuck,Eva Carrasco,Charles M. Perou,Philip S. Bernard +26 more
TL;DR: The PAM50 proliferation score identifies a subset of patients with a low proliferation status that may derive a larger benefit from weekly paclitaxel and results were obtained in the CALGB data set, although the interaction test did not reach statistical significance.