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Subject Areas on Research
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A phase 3 trial of whole brain radiation therapy and stereotactic radiosurgery alone versus WBRT and SRS with temozolomide or erlotinib for non-small cell lung cancer and 1 to 3 brain metastases: Radiation Therapy Oncology Group 0320.
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A phase I study of bevacizumab (B) in combination with everolimus (E) and erlotinib (E) in advanced cancer (BEE).
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A phase II study of induction chemotherapy followed by thoracic radiotherapy and erlotinib in poor-risk stage III non-small-cell lung cancer: results of CALGB 30605 (Alliance)/RTOG 0972 (NRG).
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A phase II study of isoflavones, erlotinib, and gemcitabine in advanced pancreatic cancer.
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Adjuvant chemotherapy for non-small cell lung cancer.
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An innovative, multi-arm, complete phase 1b study of the novel anti-cancer agent tasisulam in patients with advanced solid tumors.
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Beta-blockers alprenolol and carvedilol stimulate beta-arrestin-mediated EGFR transactivation.
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CIP2A mediates erlotinib-induced apoptosis in non-small cell lung cancer cells without EGFR mutation.
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Capillary isoelectric-focusing immunoassays to study dynamic oncoprotein phosphorylation and drug response to targeted therapies in non-small cell lung cancer.
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Circulating mutational portrait of cancer: manifestation of aggressive clonal events in both early and late stages.
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Crizotinib and erlotinib inhibits growth of c-Met+/EGFRvIII+ primary human glioblastoma xenografts.
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Development of bilateral acquired toxoplasmic retinochoroiditis during erlotinib therapy.
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Direct Evidence of Target Inhibition with Anti-VEGF, EGFR, and mTOR Therapies in a Clinical Model of Wound Healing.
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Does radiologic response correlate to pathologic response in patients undergoing neoadjuvant therapy for borderline resectable pancreatic malignancy?
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Downstaging in pancreatic cancer: a matched analysis of patients resected following systemic treatment of initially locally unresectable disease.
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Dynamic contrast-enhanced MRI in head-and-neck cancer: the impact of region of interest selection on the intra- and interpatient variability of pharmacokinetic parameters.
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EGF promotes mammalian cell growth by suppressing cellular senescence.
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EGFRvIII and c-Met pathway inhibitors synergize against PTEN-null/EGFRvIII+ glioblastoma xenografts.
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Efficacy of bevacizumab plus erlotinib for advanced hepatocellular carcinoma and predictors of outcome: final results of a phase II trial.
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Efficacy of bevacizumab plus erlotinib versus erlotinib alone in advanced non-small-cell lung cancer after failure of standard first-line chemotherapy (BeTa): a double-blind, placebo-controlled, phase 3 trial.
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Epidermal Growth Factor Receptor Mutational Testing and Erlotinib Treatment Among Veterans Diagnosed With Lung Cancer in the United States Department of Veterans Affairs.
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Epidermal growth factor receptor inhibitors and their role in non-small-cell lung cancer.
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Epidermal growth factor regulates hematopoietic regeneration after radiation injury.
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Erlotinib-mediated inhibition of EGFR signaling induces metabolic oxidative stress through NOX4.
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Gefitinib for refractory advanced non-small-cell lung cancer.
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Glioblastoma multiforme and the epidermal growth factor receptor.
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Inhibition of the epidermal growth factor receptor in combined modality treatment for locally advanced non-small cell lung cancer.
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Inhibition of the mammalian target of rapamycin (mTOR) in advanced pancreatic cancer: results of two phase II studies.
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NOX4 mediates cytoprotective autophagy induced by the EGFR inhibitor erlotinib in head and neck cancer cells.
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Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants.
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Phase 1 trial of dasatinib plus erlotinib in adults with recurrent malignant glioma.
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Phase 2 study of erlotinib in patients with unresectable hepatocellular carcinoma.
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Phase 2 trial of erlotinib plus sirolimus in adults with recurrent glioblastoma.
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Phase I and pharmacokinetic study of erlotinib for solid tumors in patients with hepatic or renal dysfunction: CALGB 60101.
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Phase II study of stereotactic radiosurgery for the treatment of patients with oligoprogression on erlotinib.
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Phase II trial of bevacizumab and erlotinib in patients with recurrent malignant glioma.
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Phase II trial of erlotinib in gastroesophageal junction and gastric adenocarcinomas: SWOG 0127.
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Phase II trial of the combination of bevacizumab and erlotinib in patients who have advanced hepatocellular carcinoma.
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Phase Ib Study of Telisotuzumab Vedotin in Combination With Erlotinib in Patients With c-Met Protein-Expressing Non-Small-Cell Lung Cancer.
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Potentiation of the effect of erlotinib by genistein in pancreatic cancer: the role of Akt and nuclear factor-kappaB.
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Prospective trial of synchronous bevacizumab, erlotinib, and concurrent chemoradiation in locally advanced head and neck cancer.
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Randomized phase II study of gefitinib versus erlotinib in patients with advanced non-small cell lung cancer who failed previous chemotherapy.
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Randomized phase II trial of erlotinib alone or with carboplatin and paclitaxel in patients who were never or light former smokers with advanced lung adenocarcinoma: CALGB 30406 trial.
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Results of the NRG Oncology/RTOG 0848 Adjuvant Chemotherapy Question-Erlotinib+Gemcitabine for Resected Cancer of the Pancreatic Head: A Phase II Randomized Clinical Trial.
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SOX2 expression is an early event in a murine model of EGFR mutant lung cancer and promotes proliferation of a subset of EGFR mutant lung adenocarcinoma cell lines.
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Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review.
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TD-19, an erlotinib derivative, induces epidermal growth factor receptor wild-type nonsmall-cell lung cancer apoptosis through CIP2A-mediated pathway.
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Targeted therapies for cancer 2004.
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Targeted therapy in rectal cancer.
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Targeting the future in head and neck cancer.
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The addition of erlotinib to gemcitabine and cisplatin does not appear to improve median survival in metastatic pancreatic cancer.
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The past, present, and future management of brain metastases in EGFR-mutant non-small cell lung cancer.
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The rexinoid LG100268 and the synthetic triterpenoid CDDO-methyl amide are more potent than erlotinib for prevention of mouse lung carcinogenesis.