review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Vincenzo Sforza | Q56953948 |
Giuseppina Liguori | Q63412293 | ||
Claudia Cardone | Q87293374 | ||
P2093 | author name string | Fortunato Ciardiello | |
Alfonso Reginelli | |||
Teresa Troiani | |||
Erika Martinelli | |||
Giulio Belli | |||
Stefania Napolitano | |||
Giulia Martini | |||
Valentina Gambardella | |||
Carminia Della Corte | |||
Marianna L Ferrara | |||
P2860 | cites work | Analysis of PTEN, BRAF, and EGFR status in determining benefit from cetuximab therapy in wild-type KRAS metastatic colon cancer. | Q38934630 |
Primary and acquired resistance of colorectal cancer cells to anti-EGFR antibodies converge on MEK/ERK pathway activation and can be overcome by combined MEK/EGFR inhibition. | Q38996793 | ||
Increased TGF-α as a mechanism of acquired resistance to the anti-EGFR inhibitor cetuximab through EGFR-MET interaction and activation of MET signaling in colon cancer cells | Q39079626 | ||
Resistance to BRAF inhibition in BRAF-mutant colon cancer can be overcome with PI3K inhibition or demethylating agents | Q39224151 | ||
Inhibition of MEK and PI3K/mTOR suppresses tumor growth but does not cause tumor regression in patient-derived xenografts of RAS-mutant colorectal carcinomas | Q39384830 | ||
MEK1/2 inhibitors AS703026 and AZD6244 may be potential therapies for KRAS mutated colorectal cancer that is resistant to EGFR monoclonal antibody therapy | Q39625657 | ||
Sym004: a novel synergistic anti-epidermal growth factor receptor antibody mixture with superior anticancer efficacy. | Q39752760 | ||
Response to Cetuximab With or Without Irinotecan in Patients With Refractory Metastatic Colorectal Cancer Harboring the KRAS G13D Mutation: Australasian Gastro-Intestinal Trials Group ICECREAM Study | Q39821902 | ||
PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers | Q39859169 | ||
Prognostic Role of PIK3CA Mutation in Colorectal Cancer: Cohort Study and Literature Review | Q24289005 | ||
Oncogenic ERBB3 mutations in human cancers | Q24293022 | ||
Amplification of the MET receptor drives resistance to anti-EGFR therapies in colorectal cancer | Q24563539 | ||
Activation of ERBB2 signaling causes resistance to the EGFR-directed therapeutic antibody cetuximab | Q24600031 | ||
Deregulation of the PI3K and KRAS signaling pathways in human cancer cells determines their response to everolimus | Q24600932 | ||
Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer | Q24604601 | ||
Comprehensive molecular characterization of human colon and rectal cancer | Q24630415 | ||
The ErbB2/ErbB3 heterodimer functions as an oncogenic unit: ErbB2 requires ErbB3 to drive breast tumor cell proliferation | Q24678674 | ||
Dual Inhibition of MEK and PI3K Pathway in KRAS and BRAF Mutated Colorectal Cancers | Q26781362 | ||
Prognostic value of c-Met in colorectal cancer: a meta-analysis | Q26860232 | ||
Tumour heterogeneity and the evolution of polyclonal drug resistance | Q26866803 | ||
PIK3CA exon 20 mutations as a potential biomarker for resistance to anti-EGFR monoclonal antibodies in KRAS wild-type metastatic colorectal cancer: a systematic review and meta-analysis | Q26992267 | ||
The structure of a human p110alpha/p85alpha complex elucidates the effects of oncogenic PI3Kalpha mutations | Q27649316 | ||
A two-in-one antibody against HER3 and EGFR has superior inhibitory activity compared with monospecific antibodies | Q27675148 | ||
K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions | Q27680654 | ||
KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer. | Q27824867 | ||
Combined inhibition of MEK and mTOR signaling inhibits initiation and progression of colorectal cancer | Q39887307 | ||
Cetuximab continuation after first progression in metastatic colorectal cancer (CAPRI-GOIM): a randomized phase II trial of FOLFOX plus cetuximab versus FOLFOX. | Q39899490 | ||
Randomized trial of TAS-102 for refractory metastatic colorectal cancer | Q41741632 | ||
Correction: CDK1 Is a Synthetic Lethal Target for KRAS Mutant Tumours | Q42876061 | ||
PIK3CA, BRAF, and PTEN status and benefit from cetuximab in the treatment of advanced colorectal cancer--results from NCIC CTG/AGITG CO.17. | Q43562170 | ||
A randomized phase IIIB trial of chemotherapy, bevacizumab, and panitumumab compared with chemotherapy and bevacizumab alone for metastatic colorectal cancer | Q44093928 | ||
Association of KRAS G13D tumor mutations with outcome in patients with metastatic colorectal cancer treated with first-line chemotherapy with or without cetuximab | Q45102101 | ||
PTEN expression and KRAS mutations on primary tumors and metastases in the prediction of benefit from cetuximab plus irinotecan for patients with metastatic colorectal cancer. | Q46034442 | ||
Fluorouracil, leucovorin, and irinotecan plus cetuximab treatment and RAS mutations in colorectal cancer | Q46233566 | ||
A phase II study of farnesyl transferase inhibitor R115777 in pancreatic cancer: a Southwest oncology group (SWOG 9924) study | Q46679647 | ||
Phase III randomized, placebo-controlled study of cetuximab plus brivanib alaninate versus cetuximab plus placebo in patients with metastatic, chemotherapy-refractory, wild-type K-RAS colorectal carcinoma: the NCIC Clinical Trials Group and AGITG CO | Q50976831 | ||
Primary and Acquired Resistance of Colorectal Cancer to Anti-EGFR Monoclonal Antibody Can Be Overcome by Combined Treatment of Regorafenib with Cetuximab. | Q50993154 | ||
Blockade of EGFR and MEK intercepts heterogeneous mechanisms of acquired resistance to anti-EGFR therapies in colorectal cancer. | Q51752412 | ||
Effects of atropine and glycopyrrolate on cognitive function following anaesthesia and electroconvulsive therapy (ECT). | Q51802723 | ||
FOLFOX4 plus cetuximab treatment and RAS mutations in colorectal cancer. | Q53520406 | ||
Heterogeneity of KRAS, NRAS, BRAF and PIK3CA mutations in metastatic colorectal cancer and potential effects on therapy in the CAPRI GOIM trial. | Q54279287 | ||
Clinical activity of FOLFIRI plus cetuximab according to extended gene mutation status by next-generation sequencing: findings from the CAPRI-GOIM trial. | Q54343844 | ||
Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study | Q57152185 | ||
RAF/RAS oncogenes and mismatch-repair status | Q57281056 | ||
ESMO Consensus Guidelines for management of patients with colon and rectal cancer. A personalized approach to clinical decision making | Q57758061 | ||
Phase I Pharmacokinetic and Pharmacodynamic Dose-Escalation Study of RG7160 (GA201), the First Glycoengineered Monoclonal Antibody Against the Epidermal Growth Factor Receptor, in Patients With Advanced Solid Tumors | Q58614658 | ||
Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice | Q71803596 | ||
Overexpression and amplification of the met/HGF receptor gene during the progression of colorectal cancer | Q77555522 | ||
High concordance of KRAS status between primary colorectal tumors and related metastatic sites: implications for clinical practice | Q82839912 | ||
More on influenza vaccine in young children | Q84470306 | ||
Open-label phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer | Q27851407 | ||
K-ras mutations and benefit from cetuximab in advanced colorectal cancer. | Q27851454 | ||
Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer | Q27851456 | ||
PIK3CA mutations in colorectal cancer are associated with clinical resistance to EGFR-targeted monoclonal antibodies | Q27851465 | ||
Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis | Q27851573 | ||
Association of KRAS p.G13D mutation with outcome in patients with chemotherapy-refractory metastatic colorectal cancer treated with cetuximab | Q27851587 | ||
KRAS, BRAF, PIK3CA, and PTEN mutations: implications for targeted therapies in metastatic colorectal cancer. | Q27851616 | ||
Identification of a mutation in the extracellular domain of the Epidermal Growth Factor Receptor conferring cetuximab resistance in colorectal cancer | Q27851708 | ||
Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR. | Q27851711 | ||
A molecularly annotated platform of patient-derived xenografts ("xenopatients") identifies HER2 as an effective therapeutic target in cetuximab-resistant colorectal cancer | Q27851787 | ||
Pilot trial of combined BRAF and EGFR inhibition in BRAF-mutant metastatic colorectal cancer patients | Q27853121 | ||
Predictive role of BRAF mutations in patients with advanced colorectal cancer receiving cetuximab and panitumumab: a meta-analysis | Q27853129 | ||
Phase II study of single-agent cetuximab in KRAS G13D mutant metastatic colorectal cancer. | Q27853212 | ||
Combined BRAF and MEK Inhibition With Dabrafenib and Trametinib in BRAF V600-Mutant Colorectal Cancer. | Q27853216 | ||
Phase II Pilot Study of Vemurafenib in Patients With Metastatic BRAF-Mutated Colorectal Cancer | Q27853224 | ||
Meta-analysis comparing the efficacy of anti-EGFR monoclonal antibody therapy between KRAS G13D and other KRAS mutant metastatic colorectal cancer tumours. | Q27853329 | ||
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 | Q27853380 | ||
Global cancer statistics, 2012 | Q27860501 | ||
Mutations of the BRAF gene in human cancer | Q27860760 | ||
Untangling the ErbB signalling network | Q27860884 | ||
Panitumumab versus cetuximab in patients with chemotherapy-refractory wild-type KRAS exon 2 metastatic colorectal cancer (ASPECCT): a randomised, multicentre, open-label, non-inferiority phase 3 study | Q28238311 | ||
Raf kinase as a target for anticancer therapeutics | Q28244900 | ||
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency | Q28262647 | ||
Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer | Q28271324 | ||
The biology and clinical relevance of the PTEN tumor suppressor pathway | Q28272157 | ||
Aspirin use, tumor PIK3CA mutation, and colorectal-cancer survival | Q28277824 | ||
KRAS gene amplification in colorectal cancer and impact on response to EGFR-targeted therapy | Q28285473 | ||
Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer | Q28298328 | ||
Chemotherapy, bevacizumab, and cetuximab in metastatic colorectal cancer | Q28308193 | ||
The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers | Q29395525 | ||
ras oncogenes in human cancer: a review | Q29547769 | ||
Detection of circulating tumor DNA in early- and late-stage human malignancies | Q29615778 | ||
The causes and consequences of genetic heterogeneity in cancer evolution | Q29615848 | ||
Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer | Q29616236 | ||
EGFR antagonists in cancer treatment | Q29616740 | ||
ERBB receptors and cancer: the complexity of targeted inhibitors | Q29619520 | ||
Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status | Q29619648 | ||
Randomized, phase III trial of panitumumab with infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX4) versus FOLFOX4 alone as first-line treatment in patients with previously untreated metastatic colorectal cancer: the PRIME study | Q29619653 | ||
Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA | Q29620083 | ||
PI3K and cancer: lessons, challenges and opportunities | Q30080017 | ||
A phase Ib study of linsitinib (OSI-906), a dual inhibitor of IGF-1R and IR tyrosine kinase, in combination with everolimus as treatment for patients with refractory metastatic colorectal cancer | Q33418329 | ||
Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: pooled analysis of the CRYSTAL and OPUS randomised clinical trials | Q34263478 | ||
Cetuximab shows activity in colorectal cancer patients with tumors that do not express the epidermal growth factor receptor by immunohistochemistry. | Q34554584 | ||
Randomized phase III study of panitumumab with fluorouracil, leucovorin, and irinotecan (FOLFIRI) compared with FOLFIRI alone as second-line treatment in patients with metastatic colorectal cancer. | Q34624122 | ||
PEAK: a randomized, multicenter phase II study of panitumumab plus modified fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) or bevacizumab plus mFOLFOX6 in patients with previously untreated, unresectable, wild-type KRAS exon 2 metastatic color | Q34660907 | ||
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 | Q34663697 | ||
Metastatic colorectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up | Q34664272 | ||
Drug development of MET inhibitors: targeting oncogene addiction and expedience | Q34782774 | ||
Genomic analysis reveals that immune function genes are strongly linked to clinical outcome in the North Central Cancer Treatment Group n9831 Adjuvant Trastuzumab Trial. | Q35102480 | ||
Randomized phase Ib/II trial of rilotumumab or ganitumab with panitumumab versus panitumumab alone in patients with wild-type KRAS metastatic colorectal cancer | Q35212113 | ||
The role of HER-3 expression in the prediction of clinical outcome for advanced colorectal cancer patients receiving irinotecan and cetuximab. | Q35584314 | ||
Panitumumab in patients with KRAS wild-type colorectal cancer after progression on cetuximab | Q35705200 | ||
Mutation of the PIK3CA oncogene in human cancers | Q36383360 | ||
Sensitivity of KRAS-Mutant Colorectal Cancers to Combination Therapy That Cotargets MEK and CDK4/6. | Q36471372 | ||
PTEN loss of expression predicts cetuximab efficacy in metastatic colorectal cancer patients | Q36611365 | ||
Primary resistance to cetuximab therapy in EGFR FISH-positive colorectal cancer patients | Q36755257 | ||
Panitumumab and irinotecan versus irinotecan alone for patients with KRAS wild-type, fluorouracil-resistant advanced colorectal cancer (PICCOLO): a prospectively stratified randomised trial | Q36977022 | ||
PIK3CA mutation is associated with poor prognosis among patients with curatively resected colon cancer | Q37137091 | ||
Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition | Q37331610 | ||
Anti-epidermal growth factor receptor monoclonal antibodies in cancer therapy. | Q37593624 | ||
Anti-epidermal growth factor receptor monoclonal antibody-based therapy for metastatic colorectal cancer: a meta-analysis of the effect of PIK3CA mutations in KRAS wild-type patients | Q37636844 | ||
Safety and efficacy of panitumumab therapy after progression with cetuximab: experience at two institutions | Q37826270 | ||
Extended RAS mutations and anti-EGFR monoclonal antibody survival benefit in metastatic colorectal cancer: a meta-analysis of randomized, controlled trials | Q38239192 | ||
Resistance to anti-EGFR therapy in colorectal cancer: from heterogeneity to convergent evolution | Q38257912 | ||
Recent therapeutic advances in the treatment of colorectal cancer | Q38262231 | ||
PIK3CA mutation/PTEN expression status predicts response of colon cancer cells to the epidermal growth factor receptor inhibitor cetuximab | Q38584695 | ||
Safety and Activity of the First-in-Class Sym004 Anti-EGFR Antibody Mixture in Patients with Refractory Colorectal Cancer. | Q38876494 | ||
Enhanced Targeting of the EGFR Network with MM-151, an Oligoclonal Anti-EGFR Antibody Therapeutic | Q38882465 | ||
Clinical Acquired Resistance to RAF Inhibitor Combinations in BRAF-Mutant Colorectal Cancer through MAPK Pathway Alterations | Q38910529 | ||
Emergence of Multiple EGFR Extracellular Mutations during Cetuximab Treatment in Colorectal Cancer. | Q38916276 | ||
P433 | issue | 28 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | colorectal cancer | Q188874 |
colorectal carcinoma | Q25493920 | ||
metastatic colon cancer | Q108566365 | ||
P304 | page(s) | 6345-6361 | |
P577 | publication date | 2016-07-01 | |
P1433 | published in | World Journal of Gastroenterology | Q15708885 |
P1476 | title | Mechanisms of resistance to anti-epidermal growth factor receptor inhibitors in metastatic colorectal cancer | |
P478 | volume | 22 |
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