2001
DOI: 10.1016/s0959-8049(01)80096-4
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Coexpression of EGFr, HER2, HER3 and HER4 in primary human breast carcinoma

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“…The majority of these trials, however, did not select their patients prospectively on the basis of EGFR expression status and were small, and therefore any subgroup benefit may not have been detected. We have previously shown that other members of the HER2 gene family may influence response to therapy and clinical outcome, 9,11,40,49 and results from single‐agent studies with lapatinib, a small‐molecule inhibitor of EGFR and Her2 tyrosine kinases and dimerization inhibitor, in which patients are treated on the basis of biomarker expression, are promising 50 . Given the increasing knowledge of Her family biology, similar hypothesis‐driven enrichment of patient populations to be treated with EGFR inhibitors should also be carried out, and detection and interpretation of EGFR standardized.…”
Section: Drug‐driven Tissue Biomarker Discoverymentioning
confidence: 99%
“…The majority of these trials, however, did not select their patients prospectively on the basis of EGFR expression status and were small, and therefore any subgroup benefit may not have been detected. We have previously shown that other members of the HER2 gene family may influence response to therapy and clinical outcome, 9,11,40,49 and results from single‐agent studies with lapatinib, a small‐molecule inhibitor of EGFR and Her2 tyrosine kinases and dimerization inhibitor, in which patients are treated on the basis of biomarker expression, are promising 50 . Given the increasing knowledge of Her family biology, similar hypothesis‐driven enrichment of patient populations to be treated with EGFR inhibitors should also be carried out, and detection and interpretation of EGFR standardized.…”
Section: Drug‐driven Tissue Biomarker Discoverymentioning
confidence: 99%