scholarly article | Q13442814 |
P50 | author | Yujie Yuan | Q43373168 |
P2093 | author name string | Jian Tu | |
Jin-Ning Ye | |||
Shi-Rong Cai | |||
Yu-Long He | |||
Qing-Hai Li | |||
Run Lin | |||
Wei-Ling He | |||
Ying-Zhao Wang | |||
Chu-Wei Liu | |||
P2860 | cites work | Prognostic Role of PIK3CA Mutation in Colorectal Cancer: Cohort Study and Literature Review | Q24289005 |
Oncogenic ERBB3 mutations in human cancers | Q24293022 | ||
A quantitative protein interaction network for the ErbB receptors using protein microarrays | Q24293746 | ||
Identification of the Hepatocyte Growth Factor Receptor As the c- met Proto-Oncogene Product | Q24310794 | ||
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 | ||
Comprehensive molecular characterization of human colon and rectal cancer | Q24630415 | ||
A hierarchical network of interreceptor interactions determines signal transduction by Neu differentiation factor/neuregulin and epidermal growth factor | Q24648517 | ||
EGF receptor trafficking: consequences for signaling and cancer | Q27021340 | ||
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 | ||
MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling | Q27851406 | ||
K-ras mutations and benefit from cetuximab in advanced colorectal cancer. | Q27851454 | ||
U3-1402, a Novel HER3-Targeting Antibody-Drug Conjugate, for the Treatment of Colorectal Cancer | Q92508053 | ||
Rechallenge for Patients With RAS and BRAF Wild-Type Metastatic Colorectal Cancer With Acquired Resistance to First-line Cetuximab and Irinotecan: A Phase 2 Single-Arm Clinical Trial | Q93375221 | ||
ErbB-2 amplification inhibits down-regulation and induces constitutive activation of both ErbB-2 and epidermal growth factor receptors. | Q40966152 | ||
A Phase Ib Dose-Escalation Study of the Safety, Tolerability, and Pharmacokinetics of Cobimetinib and Duligotuzumab in Patients with Previously Treated Locally Advanced or Metastatic Cancers with Mutant KRAS | Q41064400 | ||
Analysis of KRAS/NRAS Mutations in a Phase III Study of Panitumumab with FOLFIRI Compared with FOLFIRI Alone as Second-line Treatment for Metastatic Colorectal Cancer | Q41407101 | ||
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. | Q41410508 | ||
IGF2 is an actionable target that identifies a distinct subpopulation of colorectal cancer patients with marginal response to anti-EGFR therapies. | Q41511106 | ||
Heterogeneity of receptor function in colon carcinoma cells determined by cross-talk between type I insulin-like growth factor receptor and epidermal growth factor receptor | Q41998867 | ||
Rilotumumab plus epirubicin, cisplatin, and capecitabine as first-line therapy in advanced MET-positive gastric or gastro-oesophageal junction cancer (RILOMET-1): a randomised, double-blind, placebo-controlled, phase 3 trial | Q42693879 | ||
A randomised, open-label phase II trial of afatinib versus cetuximab in patients with metastatic colorectal cancer | Q42695640 | ||
Protein biomarkers predictive for response to anti-EGFR treatment in RAS wild-type metastatic colorectal carcinoma | Q42696314 | ||
Scatter factor is a fibroblast-derived modulator of epithelial cell mobility | Q42807925 | ||
All ErbB receptors other than the epidermal growth factor receptor are endocytosis impaired | Q42816057 | ||
Insulin-like growth factor 1 expression correlates with clinical outcome in K-RAS wild type colorectal cancer patients treated with cetuximab and irinotecan. | Q43184834 | ||
Intrapatient cetuximab dose escalation in metastatic colorectal cancer according to the grade of early skin reactions: the randomized EVEREST study | Q43765241 | ||
Treatment rationale and study design for a randomized, double-blind, placebo-controlled phase II study evaluating onartuzumab (MetMAb) in combination with bevacizumab plus mFOLFOX-6 in patients with previously untreated metastatic colorectal cancer | Q43840478 | ||
HER3 expression in patients with primary colorectal cancer and corresponding lymph node metastases related to clinical outcome | Q44029257 | ||
Analysis of HER-3, insulin growth factor-1, nuclear factor-kB and epidermal growth factor receptor gene copy number in the prediction of clinical outcome for K-RAS wild-type colorectal cancer patients receiving irinotecan-cetuximab. | Q44284095 | ||
Lack of KRAS, NRAS, BRAF and TP53 mutations improves outcome of elderly metastatic colorectal cancer patients treated with cetuximab, oxaliplatin and UFT. | Q44526398 | ||
Role of NRAS mutations as prognostic and predictive markers in metastatic colorectal cancer. | Q44995693 | ||
Results From the Phase III Randomized Trial of Onartuzumab Plus Erlotinib Versus Erlotinib in Previously Treated Stage IIIB or IV Non-Small-Cell Lung Cancer: METLung | Q45048643 | ||
Structural basis for inhibition of the epidermal growth factor receptor by cetuximab | Q45345151 | ||
Significance of mTOR signaling and its inhibitor against cancer stem-like cells in colorectal cancer | Q45778366 | ||
A Phase Ib Dose-Escalation Study of Encorafenib and Cetuximab with or without Alpelisib in Metastatic BRAF-Mutant Colorectal Cancer | Q46091563 | ||
Gene copy number for epidermal growth factor receptor (EGFR) and clinical response to antiEGFR treatment in colorectal cancer: a cohort study | Q46465639 | ||
PTEN Regulates PI(3,4)P2 Signaling Downstream of Class I PI3K. | Q47100426 | ||
Sidedness and TP53 mutations impact OS in anti-EGFR but not anti-VEGF treated mCRC - an analysis of the KRAS registry of the AGMT (Arbeitsgemeinschaft Medikamentöse Tumortherapie). | Q47117539 | ||
Oncogenic RAS Signaling Promotes Tumor Immunoresistance by Stabilizing PD-L1 mRNA. | Q47143491 | ||
lncRNA MIR100HG-derived miR-100 and miR-125b mediate cetuximab resistance via Wnt/β-catenin signaling. | Q47648793 | ||
Association of Tumor HER3 Messenger RNA Expression With Panitumumab Efficacy in Advanced Colorectal Cancer | Q47707557 | ||
Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors: Guideline From the College of American Pathologists, the International Association for the Study of Lung Cancer, an | Q48507379 | ||
The Genetic/Non-genetic Duality of Drug 'Resistance' in Cancer | Q49835177 | ||
Combined BRAF, EGFR, and MEK Inhibition in Patients with BRAFV600E-Mutant Colorectal Cancer | Q50066241 | ||
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 | ||
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 | ||
HER2 gene copy number status may influence clinical efficacy to anti-EGFR monoclonal antibodies in metastatic colorectal cancer patients | Q27852057 | ||
The predictive value of KRAS, NRAS, BRAF, PIK3CA and PTEN for anti-EGFR treatment in metastatic colorectal cancer: A systematic review and meta-analysis | Q27852988 | ||
Predictive role of BRAF mutations in patients with advanced colorectal cancer receiving cetuximab and panitumumab: a meta-analysis | Q27853129 | ||
HER2 activating mutations are targets for colorectal cancer treatment | Q27853193 | ||
Phase II study of single-agent cetuximab in KRAS G13D mutant metastatic colorectal cancer. | Q27853212 | ||
Phase II Pilot Study of Vemurafenib in Patients With Metastatic BRAF-Mutated Colorectal Cancer | Q27853224 | ||
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 | Q27853335 | ||
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 | ||
MET-Driven Resistance to Dual EGFR and BRAF Blockade May Be Overcome by Switching from EGFR to MET Inhibition in BRAF-Mutated Colorectal Cancer. | Q27853393 | ||
Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer | Q27860681 | ||
Mutations of the BRAF gene in human cancer | Q27860760 | ||
MicroRNAs: genomics, biogenesis, mechanism, and function | Q27861070 | ||
PTEN: life as a tumor suppressor | Q28203431 | ||
Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer | Q28240089 | ||
Insulin-like growth factor-binding proteins in serum and other biological fluids: regulation and functions | Q28257453 | ||
Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer | Q28298328 | ||
Insulin-like growth factors and their binding proteins: biological actions | Q28301853 | ||
ras oncogenes in human cancer: a review | Q29547769 | ||
Epigenetics in cancer | Q29547853 | ||
CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer | Q29614277 | ||
Ras oncogenes: split personalities | Q29615405 | ||
Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer | Q29616236 | ||
EGFR antagonists in cancer treatment | Q29616740 | ||
EGF-ERBB signalling: towards the systems level | Q29619032 | ||
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 | ||
Regorafenib monotherapy for previously treated metastatic colorectal cancer (CORRECT): an international, multicentre, randomised, placebo-controlled, phase 3 trial | Q29620127 | ||
The RAF proteins take centre stage | Q29620153 | ||
A Randomized Phase II/III Study of Dalotuzumab in Combination With Cetuximab and Irinotecan in Chemorefractory, KRAS Wild-Type, Metastatic Colorectal Cancer | Q30316105 | ||
T-Cell Transfer Therapy Targeting Mutant KRAS in Cancer. | Q30832820 | ||
Randomized, phase II study of the insulin-like growth factor-1 receptor inhibitor IMC-A12, with or without cetuximab, in patients with cetuximab- or panitumumab-refractory metastatic colorectal cancer | Q33391425 | ||
Multicenter phase II study of tivozanib (AV-951) and everolimus (RAD001) for patients with refractory, metastatic colorectal cancer | Q33407027 | ||
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 | ||
Metastatic colorectal cancer: current state and future directions | Q38445676 | ||
K-ras oncogene mutations in sporadic colorectal cancer in The Netherlands Cohort Study | Q38452428 | ||
Antroquinonol, a Ubiquinone Derivative from the Mushroom Antrodia camphorata, Inhibits Colon Cancer Stem Cell-like Properties: Insights into the Molecular Mechanism and Inhibitory Targets | Q38725272 | ||
FOXO3a and the MAPK p38 are activated by cetuximab to induce cell death and inhibit cell proliferation and their expression predicts cetuximab efficacy in colorectal cancer. | Q38743209 | ||
Global patterns and trends in colorectal cancer incidence and mortality. | Q38915351 | ||
Emergence of Multiple EGFR Extracellular Mutations during Cetuximab Treatment in Colorectal Cancer. | Q38916276 | ||
Association of MicroRNA-31-5p with Clinical Efficacy of Anti-EGFR Therapy in Patients with Metastatic Colorectal Cancer | Q38932418 | ||
Antroquinonol blocks Ras and Rho signaling via the inhibition of protein isoprenyltransferase activity in cancer cells | Q38948117 | ||
Acquired RAS or EGFR mutations and duration of response to EGFR blockade in colorectal cancer. | Q39120801 | ||
Association of CpG island methylator phenotype and EREG/AREG methylation and expression in colorectal cancer. | Q39703372 | ||
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 | ||
Safety and Pharmacokinetics/Pharmacodynamics of the First-in-Class Dual Action HER3/EGFR Antibody MEHD7945A in Locally Advanced or Metastatic Epithelial Tumors. | Q40153403 | ||
Antibody-dependent cellular cytotoxicity mediated by cetuximab against lung cancer cell lines | Q40164557 | ||
Co-targeting the EGFR and IGF-IR with anti-EGFR monoclonal antibody ICR62 and the IGF-IR tyrosine kinase inhibitor NVP-AEW541 in colorectal cancer cells. | Q50616696 | ||
PIK3CA and PTEN gene and exon mutation-specific clinicopathologic and molecular associations in colorectal cancer. | Q51028104 | ||
Phase II Study of the Dual EGFR/HER3 Inhibitor Duligotuzumab (MEHD7945A) versus Cetuximab in Combination with FOLFIRI in Second-Line RAS Wild-Type Metastatic Colorectal Cancer. | Q52673332 | ||
A phase I study of continuous oral dosing of OSI-906, a dual inhibitor of insulin-like growth factor-1 and insulin receptors, in patients with advanced solid tumors. | Q52873936 | ||
MET amplification, expression, and exon 14 mutations in colorectal adenocarcinoma. | Q54092400 | ||
First-in-Human Phase I Study of Lumretuzumab, a Glycoengineered Humanized Anti-HER3 Monoclonal Antibody, in Patients with Metastatic or Advanced HER3-Positive Solid Tumors. | Q54240617 | ||
EGFR gene gain and PTEN protein expression are favorable prognostic factors in patients with KRAS wild-type metastatic colorectal cancer treated with cetuximab. | Q54373171 | ||
MET signaling in colon cancer stem-like cells blunts the therapeutic response to EGFR inhibitors. | Q54383135 | ||
HER2 signaling and resistance to the anti-EGFR monoclonal antibody cetuximab: a further step toward personalized medicine for patients with colorectal cancer. | Q54510894 | ||
Targeting the human epidermal growth factor receptor 2 (HER2) oncogene in colorectal cancer. | Q54962247 | ||
Insulin-like growth factors and cancer | Q56336667 | ||
Tivantinib for second-line treatment of MET-high, advanced hepatocellular carcinoma (METIV-HCC): a final analysis of a phase 3, randomised, placebo-controlled study | Q56384328 | ||
Vaccination with mutant ras peptides and induction of T-cell responsiveness in pancreatic carcinoma patients carrying the corresponding RAS mutation | Q56815463 | ||
Biomarker Analyses and Final Overall Survival Results From a Phase III, Randomized, Open-Label, First-Line Study of Gefitinib Versus Carboplatin/Paclitaxel in Clinically Selected Patients With Advanced Non–Small-Cell Lung Cancer in Asia (IPASS) | Q57908992 | ||
Requirement for intrinsic protein tyrosine kinase in the immediate and late actions of the EGF receptor | Q59054268 | ||
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries | Q60142201 | ||
Receptor tyrosine kinase-dependent PI3K activation is an escape mechanism to vertical suppression of the EGFR/RAS/MAPK pathway in KRAS-mutated human colorectal cancer cell lines | Q61808208 | ||
Expression of epiregulin and amphiregulin and K-ras mutation status predict disease control in metastatic colorectal cancer patients treated with cetuximab | Q80704669 | ||
Epidermal growth factor receptor gene copy number and clinical outcome of metastatic colorectal cancer treated with panitumumab | Q80704675 | ||
Pilot study of mutant ras peptide-based vaccine as an adjuvant treatment in pancreatic and colorectal cancers | Q80765497 | ||
Immunization with mutant p53- and K-ras-derived peptides in cancer patients: immune response and clinical outcome | Q81897940 | ||
Prognostic value of cetuximab-related skin toxicity in metastatic colorectal cancer patients and its correlation with parameters of the epidermal growth factor receptor signal transduction pathway: results from a randomized trial of the GERMAN AIO C | Q84243064 | ||
Molecular Landscape of ERBB2/ERBB3 Mutated Colorectal Cancer | Q88541726 | ||
Predictive biomarkers for response to EGFR-directed monoclonal antibodies for advanced squamous cell lung cancer | Q89113396 | ||
HER2-targeted therapy: an emerging strategy in advanced colorectal cancer | Q90247451 | ||
Encorafenib, Binimetinib, and Cetuximab in BRAF V600E-Mutated Colorectal Cancer | Q90362927 | ||
The KRASG12C Inhibitor MRTX849 Provides Insight toward Therapeutic Susceptibility of KRAS-Mutant Cancers in Mouse Models and Patients | Q90974072 | ||
The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity | Q91013772 | ||
MicroRNA-425-5p Expression Affects BRAF/RAS/MAPK Pathways In Colorectal Cancers | Q91046328 | ||
Adaptive mutability of colorectal cancers in response to targeted therapies | Q91172844 | ||
Trametinib in the treatment of multiple malignancies harboring MEK1 mutations | Q91246711 | ||
The current state of molecular testing in the treatment of patients with solid tumors, 2019 | Q92214210 | ||
Mechanisms of Receptor Tyrosine-Protein Kinase ErbB-3 (ERBB3) Action in Human Neoplasia | Q92224118 | ||
Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway): an updated report from a multicentre, open-label, phase 2a, multiple basket study | Q92280751 | ||
Binimetinib, Encorafenib, and Cetuximab Triplet Therapy for Patients With BRAF V600E-Mutant Metastatic Colorectal Cancer: Safety Lead-In Results From the Phase III BEACON Colorectal Cancer Study | Q92502573 | ||
Differential endocytic routing of homo- and hetero-dimeric ErbB tyrosine kinases confers signaling superiority to receptor heterodimers | Q33888963 | ||
Addition of cetuximab to oxaliplatin-based first-line combination chemotherapy for treatment of advanced colorectal cancer: results of the randomised phase 3 MRC COIN trial | Q33922925 | ||
Patient and tumor characteristics and BRAF and KRAS mutations in colon cancer, NCCTG/Alliance N0147 | Q33947880 | ||
Ras in cancer and developmental diseases | Q34202697 | ||
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 | ||
Epigenetic Alterations in Colorectal Cancer: Emerging Biomarkers | Q34487177 | ||
HGF rescues colorectal cancer cells from EGFR inhibition via MET activation | Q34550898 | ||
Cetuximab shows activity in colorectal cancer patients with tumors that do not express the epidermal growth factor receptor by immunohistochemistry. | Q34554584 | ||
Lack of correlation between epidermal growth factor receptor status and response to Panitumumab monotherapy in metastatic colorectal cancer | Q34618161 | ||
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 | ||
Addition of aflibercept to fluorouracil, leucovorin, and irinotecan improves survival in a phase III randomized trial in patients with metastatic colorectal cancer previously treated with an oxaliplatin-based regimen | Q34642136 | ||
Effectors of epidermal growth factor receptor pathway: the genetic profiling ofKRAS, BRAF, PIK3CA, NRAS mutations in colorectal cancer characteristics and personalized medicine | Q35067570 | ||
Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing. | Q35133788 | ||
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 | ||
MiR-199a-5p and miR-375 affect colon cancer cell sensitivity to cetuximab by targeting PHLPP1. | Q35672735 | ||
EGFR-mediated re-activation of MAPK signaling contributes to insensitivity of BRAF mutant colorectal cancers to RAF inhibition with vemurafenib | Q35841043 | ||
Does overexpression of HER-2 correlate with clinicopathological characteristics and prognosis in colorectal cancer? Evidence from a meta-analysis | Q35957036 | ||
Epigenetics and colorectal cancer | Q36081553 | ||
Alterations in the human epidermal growth factor receptor 2-phosphatidylinositol 3-kinase-v-Akt pathway in gastric cancer | Q36450457 | ||
DNA methylation status as a biomarker of anti-epidermal growth factor receptor treatment for metastatic colorectal cancer | Q36467389 | ||
The genomic landscape of response to EGFR blockade in colorectal cancer. | Q36930106 | ||
Targeting the epidermal growth factor receptor in metastatic colorectal cancer | Q37002166 | ||
Deficient mismatch repair system in patients with sporadic advanced colorectal cancer | Q37081098 | ||
TP53 mutations predict disease control in metastatic colorectal cancer treated with cetuximab-based chemotherapy | Q37177918 | ||
Assessment of somatic k-RAS mutations as a mechanism associated with resistance to EGFR-targeted agents: a systematic review and meta-analysis of studies in advanced non-small-cell lung cancer and metastatic colorectal cancer | Q37274280 | ||
A randomized, placebo-controlled, phase 1/2 study of tivantinib (ARQ 197) in combination with irinotecan and cetuximab in patients with metastatic colorectal cancer with wild-type KRAS who have received first-line systemic therapy | Q37352435 | ||
MET signalling: principles and functions in development, organ regeneration and cancer | Q37811895 | ||
Risk of venous and arterial thromboembolic events associated with anti-EGFR agents: a meta-analysis of randomized clinical trials | Q37975484 | ||
The predictive role of skin rash with cetuximab and panitumumab in colorectal cancer patients: a systematic review and meta-analysis of published trials | Q38074290 | ||
Treatment related severe and fatal adverse events with cetuximab in colorectal cancer patients: a meta-analysis | Q38115675 | ||
BRAF mutation is associated with distinct clinicopathological characteristics in colorectal cancer: a systematic review and meta-analysis | Q38151250 | ||
Resistance to anti-EGFR therapy in colorectal cancer: from heterogeneity to convergent evolution | Q38257912 | ||
Heterogeneity of Acquired Resistance to Anti-EGFR Monoclonal Antibodies in Patients with Metastatic Colorectal Cancer. | Q38377594 | ||
Amphiregulin and epiregulin mRNA expression in primary tumors predicts outcome in metastatic colorectal cancer treated with cetuximab | Q38420145 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P921 | main subject | metastatic colon cancer | Q108566365 |
P304 | page(s) | 179-191 | |
P577 | publication date | 2020-06-23 | |
P1433 | published in | Gastroenterology report | Q27725210 |
P1476 | title | Anti-EGFR therapy in metastatic colorectal cancer: mechanisms and potential regimens of drug resistance | |
P478 | volume | 8 |