Amphiregulin Expression Is a Predictive Biomarker for


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 12 2020
Historique:
received: 14 07 2020
revised: 18 08 2020
accepted: 10 09 2020
pubmed: 19 9 2020
medline: 15 12 2021
entrez: 18 9 2020
Statut: ppublish

Résumé

Amphiregulin ( Ligand mRNA expression; Of 688 patients with available material, high High

Identifiants

pubmed: 32943459
pii: 1078-0432.CCR-20-2748
doi: 10.1158/1078-0432.CCR-20-2748
doi:

Substances chimiques

AREG protein, human 0
Amphiregulin 0
Antineoplastic Agents, Immunological 0
Biomarkers, Tumor 0
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Cetuximab PQX0D8J21J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6559-6567

Informations de copyright

©2020 American Association for Cancer Research.

Références

Holch JW, Ricard I, Stintzing S, Modest DP, Heinemann V. The relevance of primary tumour location in patients with metastatic colorectal cancer: a meta-analysis of first-line clinical trials. Eur J Cancer. 2017;70:87–98.
Arnold D, Lueza B, Douillard JY, Peeters M, Lenz HJ, Venook A, et al. Prognostic and predictive value of primary tumour side in patients with RAS wild-type metastatic colorectal cancer treated with chemotherapy and EGFR directed antibodies in six randomized trials. Ann Oncol. 2017;28:1713–29.
Carpenter BL, Chen M, Knifley T, Davis KA, Harrison SM, Stewart RL, et al. Integrin alpha6beta4 promotes autocrine epidermal growth factor receptor (EGFR) signaling to stimulate migration and invasion toward hepatocyte growth factor (HGF). J Biol Chem. 2015;290:27228–38.
Carpenter BL, Liu J, Qi L, Wang C, O'Connor KL. Integrin alpha6beta4 upregulates amphiregulin and epiregulin through base excision repair-mediated DNA demethylation and promotes genome-wide DNA hypomethylation. Sci Rep. 2017;7:6174.
Lee MS, McGuffey EJ, Morris JS, Manyam G, Baladandayuthapani V, Wei W, et al. Association of CpG island methylator phenotype and EREG/AREG methylation and expression in colorectal cancer. Br J Cancer. 2016;114:1352–61.
Bormann F, Stinzing S, Tierling S, Morkel M, Markelova MR, Walter J, et al. Epigenetic regulation of amphiregulin and epiregulin in colorectal cancer. Int J Cancer. 2019;144:569–81.
Stintzing S, Ivanova B, Ricard I, Jung A, Kirchner T, Tannapfel A, et al. Amphiregulin (AREG) and epiregulin (EREG) gene expression as predictor for overall survival (OS) in oxaliplatin/fluoropyrimidine plus bevacizumab treated mCRC patients-analysis of the phase III AIO KRK-0207 trial. Front Oncol. 2018;8:474.
Kuramochi H, Nakajima GO, Hayashi K, Araida T, Yamamoto M. Amphiregulin/epiregulin mRNA expression and primary tumor location in colorectal cancer. Anticancer Res. 2019;39:4729–36.
Khambata-Ford S, Garrett CR, Meropol NJ, Basik M, Harbison CT, Wu S, et al. Expression of epiregulin and amphiregulin and K-ras mutation status predict disease control in metastatic colorectal cancer patients treated with cetuximab. J Clin Oncol. 2007;25:3230–7.
Baker JB, Dutta D, Watson D, Maddala T, Munneke BM, Shak S, et al. Tumour gene expression predicts response to cetuximab in patients with KRAS wild-type metastatic colorectal cancer. Br J Cancer. 2011;104:488–95.
Jacobs B, De Roock W, Piessevaux H, Van Oirbeek R, Biesmans B, De Schutter J, et al. Amphiregulin and epiregulin mRNA expression in primary tumors predicts outcome in metastatic colorectal cancer treated with cetuximab. J Clin Oncol. 2009;27:5068–74.
Seligmann JF, Elliott F, Richman SD, Jacobs B, Hemmings G, Brown S, et al. Combined epiregulin and amphiregulin expression levels as a predictive biomarker for panitumumab therapy benefit or lack of benefit in patients with RAS wild-type advanced colorectal cancer. JAMA Oncol. 2016;2:633–42.
Stahler A, Heinemann V, Giessen-Jung C, Crispin A, Schalhorn A, Stintzing S, et al. Influence of mRNA expression of epiregulin and amphiregulin on outcome of patients with metastatic colorectal cancer treated with 5-FU/LV plus irinotecan or irinotecan plus oxaliplatin as first-line treatment (FIRE 1-trial). Int J Cancer. 2016;138:739–46.
Fischer von Weikersthal L, Schalhorn A, Stauch M, Quietzsch D, Maubach PA, Lambertz H, et al. Phase III trial of irinotecan plus infusional 5-fluorouracil/folinic acid versus irinotecan plus oxaliplatin as first-line treatment of advanced colorectal cancer. Eur J Cancer. 2011;47:206–14.
Moosmann N, von Weikersthal LF, Vehling-Kaiser U, Stauch M, Hass HG, Dietzfelbinger H, et al. Cetuximab plus capecitabine and irinotecan compared with cetuximab plus capecitabine and oxaliplatin as first-line treatment for patients with metastatic colorectal cancer: AIO KRK-0104–a randomized trial of the German AIO CRC study group. J Clin Oncol. 2011;29:1050–8.
Heinemann V, von Weikersthal LF, Decker T, Kiani A, Vehling-Kaiser U, Al-Batran SE, et al. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014;15:1065–75.
Neumann J, Wehweck L, Maatz S, Engel J, Kirchner T, Jung A. Alterations in the EGFR pathway coincide in colorectal cancer and impact on prognosis. Virchows Arch. 2013;463:509–23.
Jonker DJ, Karapetis CS, Harbison C, O'Callaghan CJ, Tu D, Simes RJ, et al. Epiregulin gene expression as a biomarker of benefit from cetuximab in the treatment of advanced colorectal cancer. Br J Cancer. 2014;110:648–55.
Cushman SM, Jiang C, Hatch AJ, Shterev I, Sibley AB, Niedzwiecki D, et al. Gene expression markers of efficacy and resistance to cetuximab treatment in metastatic colorectal cancer: results from CALGB 80203 (Alliance). Clin Cancer Res. 2015;21:1078–86.
Moroni M, Veronese S, Benvenuti S, Marrapese G, Sartore-Bianchi A, Di Nicolantonio F, et al. Gene copy number for epidermal growth factor receptor (EGFR) and clinical response to antiEGFR treatment in colorectal cancer: a cohort study. Lancet Oncol. 2005;6:279–86.
Sartore-Bianchi A, Moroni M, Veronese S, Carnaghi C, Bajetta E, Luppi G, et al. Epidermal growth factor receptor gene copy number and clinical outcome of metastatic colorectal cancer treated with panitumumab. J Clin Oncol. 2007;25:3238–45.
Sartore-Bianchi A, Trusolino L, Martino C, Bencardino K, Lonardi S, Bergamo F, et al. Dual-targeted therapy with trastuzumab and lapatinib in treatment-refractory, KRAS codon 12/13 wild-type, HER2-positive metastatic colorectal cancer (HERACLES): a proof-of-concept, multicentre, open-label, phase 2 trial. Lancet Oncol. 2016;17:738–46.
Meric-Bernstam F, Hurwitz H, Raghav KPS, McWilliams RR, Fakih M, VanderWalde A, et al. Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway): an updated report from a multicentre, open-label, phase 2a, multiple basket study. Lancet Oncol. 2019;20:518–30.
Sartore-Bianchi A, Amatu A, Porcu L, Ghezzi S, Lonardi S, Leone F, et al. HER2 positivity predicts unresponsiveness to EGFR-targeted treatment in metastatic colorectal cancer. Oncologist. 2019;24:1395–402.
Pentheroudakis G, Kotoula V, De Roock W, Kouvatseas G, Papakostas P, Makatsoris T, et al. Biomarkers of benefit from cetuximab-based therapy in metastatic colorectal cancer: interaction of EGFR ligand expression with RAS/RAF, PIK3CA genotypes. BMC Cancer. 2013;13:49.
Llovet P, Sastre J, Ortega JS, Bando I, Ferrer M, Garcia-Alfonso P, et al. Prognostic value of BRAF, PI3K, PTEN, EGFR copy number, amphiregulin and epiregulin status in patients with KRAS codon 12 wild-type metastatic colorectal cancer receiving first-line chemotherapy with anti-EGFR therapy. Mol Diagn Ther. 2015;19:397–408.
Tejpar S, Stintzing S, Ciardiello F, Tabernero J, Van Cutsem E, Beier F, et al. Prognostic and predictive relevance of primary tumor location in patients with RAS wild-type metastatic colorectal cancer: retrospective analyses of the CRYSTAL and FIRE-3 trials. JAMA Oncol. 2017;3:194–201.
Salem ME, Weinberg BA, Xiu J, El-Deiry WS, Hwang JJ, Gatalica Z, et al. Comparative molecular analyses of left-sided colon, right-sided colon, and rectal cancers. Oncotarget. 2017;8:86356–68.
Guinney J, Dienstmann R, Wang X, de Reynies A, Schlicker A, Soneson C, et al. The consensus molecular subtypes of colorectal cancer. Nat Med. 2015;21:1350–6.
Van Cutsem E, Cervantes A, Adam R, Sobrero A, Van Krieken JH, Aderka D, et al. ESMO consensus guidelines for the management of patients with metastatic colorectal cancer. Ann Oncol. 2016;27:1386–422.
Clinical practice guidelines in oncology (NCCN Guidelines) colon cancer version 4.2020. 2020.
Chiorean EG, Nandakumar G, Fadelu T, Temin S, Alarcon-Rozas AE, Bejarano S, et al. Treatment of patients with late-stage colorectal cancer: ASCO Resource-Stratified Guideline. JCO Glob Oncol. 2020;6:414–38.
Price T, Shen L, Ma B, Esser R, Chen W, Gibbs P, et al. Phase II APEC trial: the impact of primary tumor side on outcomes of first-line cetuximab plus FOLFOX or FOLFIRI in patients with RAS wild-type metastatic colorectal cancer. Asia Pac J Clin Oncol. 2019;15:225–30.
Weisenberger DJ, Siegmund KD, Campan M, Young J, Long TI, Faasse MA, et al. CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet. 2006;38:787–93.

Auteurs

Arndt Stahler (A)

Department of Internal Medicine III and Comprehensive Cancer Centre Munich, University Hospital Grosshadern, Ludwig-Maximilian-Universitaet Muenchen, Munich, Germany. arndt.stahler@gmail.com.

Sebastian Stintzing (S)

Medical Department, Division of Hematology, Oncology and Tumor Immunology (CCM), Charité Universitaetsmedizin Berlin, Berlin, Germany.
DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.

Dominik P Modest (DP)

DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Medical Department, Division of Hematology, Oncology and Tumor Immunology (CVK), Charité Universitaetsmedizin Berlin, Berlin, Germany.

Ingrid Ricard (I)

Department of Internal Medicine III and Comprehensive Cancer Centre Munich, University Hospital Grosshadern, Ludwig-Maximilian-Universitaet Muenchen, Munich, Germany.

Clemens Giessen-Jung (C)

Department of Internal Medicine III and Comprehensive Cancer Centre Munich, University Hospital Grosshadern, Ludwig-Maximilian-Universitaet Muenchen, Munich, Germany.

Christine Kapaun (C)

Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.

Boryana Ivanova (B)

Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.

Florian Kaiser (F)

VK&K Studien GbR, Landshut, Germany.

Ludwig Fischer von Weikersthal (L)

Klinikum St. Marien, Oncology, Amberg, Germany.

Nicolas Moosmann (N)

Department for Hematology and Oncology, Klinikum Barmherzige Brüder, Regensburg, Germany.

Andreas Schalhorn (A)

Department of Internal Medicine III and Comprehensive Cancer Centre Munich, University Hospital Grosshadern, Ludwig-Maximilian-Universitaet Muenchen, Munich, Germany.

Martina Stauch (M)

Onkologische Praxis, Kronach, Germany.

Alexander Kiani (A)

Department of Medicine IV, Klinikum Bayreuth GmbH, Bayreuth, Germany.

Swantje Held (S)

ClinAssess GmbH, Leverkusen, Germany.

Thomas Decker (T)

Onkologische Praxis, Ravensburg, Germany.

Markus Moehler (M)

I. Department of Internal Medicine, University Medical Center Mainz, Mainz, Germany.

Jens Neumann (J)

DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.

Thomas Kirchner (T)

DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.

Andreas Jung (A)

DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.

Volker Heinemann (V)

Department of Internal Medicine III and Comprehensive Cancer Centre Munich, University Hospital Grosshadern, Ludwig-Maximilian-Universitaet Muenchen, Munich, Germany.
DKTK, German Cancer Consortium, German Cancer Research Centre (DKFZ), Heidelberg, Germany.

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