Literature DB >> 28533226

IGF1R Protein Expression Is Not Associated with Differential Benefit to Concurrent Trastuzumab in Early-Stage HER2+ Breast Cancer from the North Central Cancer Treatment Group (Alliance) Adjuvant Trastuzumab Trial N9831.

Monica M Reinholz1, Beiyun Chen1, Amylou C Dueck2, Kathleen Tenner3, Karla Ballman3, Darren Riehle1, Robert B Jenkins1, Xochiquetzal J Geiger4, Ann E McCullough5, Edith A Perez6.   

Abstract

Background: Preclinical evidence indicates that increased insulin-like growth factor receptor-1 (IGF1R) signaling interferes with the action of trastuzumab suggesting a possible mechanism of trastuzumab resistance. Thus, we evaluated IGF1R prevalence, relationship with demographic data, and association with disease-free survival (DFS) of patients randomized to chemotherapy alone (Arm A) or chemotherapy with sequential (Arm B) or concurrent trastuzumab (Arm C) in the prospective phase III HER2+ adjuvant N9831 trial.Experimental Design: IGF1R protein expression was determined in tissue microarray sections (three cores per block; N = 1,197) or in whole tissue sections (WS; N = 537) using IHC (rabbit polyclonal antibody against IGF1R β-subunit). A tumor was considered positive (IGF1R+) if any core or WS had ≥1+ membrane staining in >0% invasive cells. Median follow-up was 8.5 years.
Results: Of 1,734 patients, 708 (41%) had IGF1R+ breast tumors. IGF1R+ was associated with younger age (median 48 vs. 51, P = 0.007), estrogen receptor/progesterone receptor positivity (78% vs. 35%, P < 0.001), nodal positivity (89% vs. 83%, P < 0.001), well/intermediate grade (34% vs. 24%, P < 0.001), tumors ≥2 cm (72% vs. 67%, P = 0.02) but not associated with race or tumor histology. IGF1R did not affect DFS within arms. Between Arms A and C, patients with IGF1R+ and IGF1R- tumors had DFS HRs of 0.48 (P ≤ 0.001) and 0.68 (P = 0.009), respectively (Pinteraction = 0.17). Between Arms A and B, patients with IGF1R+ and IGF1R- tumors had DFS HRs of 0.83 (P = 0.25) and 0.69 (P = 0.01), respectively (Pinteraction = 0.42).Conclusions: In contrast to preclinical studies that suggest a decrease in trastuzumab sensitivity in IGF1R+ tumors, our adjuvant data show benefit of adding trastuzumab for patients with either IGF1R+ and IGF1R- breast tumors. Clin Cancer Res; 23(15); 4203-11. ©2016 AACR. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 28533226      PMCID: PMC5769872          DOI: 10.1158/1078-0432.CCR-15-0574

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  49 in total

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Authors:  Jiping Zha; Mark R Lackner
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2.  Insulin-like growth factor-I receptor/human epidermal growth factor receptor 2 heterodimerization contributes to trastuzumab resistance of breast cancer cells.

Authors:  Rita Nahta; Linda X H Yuan; Bing Zhang; Ryuji Kobayashi; Francisco J Esteva
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Review 3.  Role of the insulin-like growth factor family in cancer development and progression.

Authors:  H Yu; T Rohan
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4.  Sequential versus concurrent trastuzumab in adjuvant chemotherapy for breast cancer.

Authors:  Edith A Perez; Vera J Suman; Nancy E Davidson; Julie R Gralow; Peter A Kaufman; Daniel W Visscher; Beiyun Chen; James N Ingle; Shaker R Dakhil; Joanne Zujewski; Alvaro Moreno-Aspitia; Thomas M Pisansky; Robert B Jenkins
Journal:  J Clin Oncol       Date:  2011-10-31       Impact factor: 44.544

5.  Quantitative determination of insulin-like growth factor 1 receptor mRNA in formalin-fixed paraffin-embedded tissues of invasive breast cancer.

Authors:  Peifen Fu; Mutsuko Ibusuki; Yutaka Yamamoto; Satoko Yamamoto; Saori Fujiwara; Keiichi Murakami; Shusen Zheng; Hirotaka Iwase
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6.  Recombinant human insulin-like growth factor binding protein 3 inhibits growth of human epidermal growth factor receptor-2-overexpressing breast tumors and potentiates herceptin activity in vivo.

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Review 7.  Beyond trastuzumab: overcoming resistance to targeted HER-2 therapy in breast cancer.

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Journal:  Curr Cancer Drug Targets       Date:  2009-03       Impact factor: 3.428

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Journal:  J Mammary Gland Biol Neoplasia       Date:  2008-11-25       Impact factor: 2.673

9.  Predicting degree of benefit from adjuvant trastuzumab in NSABP trial B-31.

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Journal:  J Natl Cancer Inst       Date:  2013-11-21       Impact factor: 13.506

10.  Heterotrimerization of the growth factor receptors erbB2, erbB3, and insulin-like growth factor-i receptor in breast cancer cells resistant to herceptin.

Authors:  Xiaoping Huang; Lizhi Gao; Shuiliang Wang; James L McManaman; Ann D Thor; Xiaohe Yang; Francisco J Esteva; Bolin Liu
Journal:  Cancer Res       Date:  2010-01-26       Impact factor: 12.701

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Journal:  Cancer Genomics Proteomics       Date:  2018 Nov-Dec       Impact factor: 4.069

2.  Effect of body mass index on response to neo-adjuvant therapy in HER2-positive breast cancer: an exploratory analysis of the NeoALTTO trial.

Authors:  Serena Di Cosimo; Luca Porcu; Dominique Agbor-Tarh; Saverio Cinieri; Maria Alice Franzoi; Maria Carmen De Santis; Cristina Saura; Jens Huober; Debora Fumagalli; Miguel Izquierdo; Martine Piccart; Maria Grazia Daidone; Evandro de Azambuja
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