2015
DOI: 10.1016/s0959-8049(15)30068-x
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3BA A phase II trial of erlotinib (E) and bevacizumab (B) in patients with advanced non-small-cell lung cancer (NSCLC) with activating epidermal growth factor receptor (EGFR) mutations with and without T790M mutation. The Spanish Lung Cancer Group (SLCG) and the European Thoracic Oncology Platform (ETOP) BELIEF trial

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Cited by 31 publications
(23 citation statements)
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“…The primary endpoints are toxicity and disease-free survival. 6 is a randomized phase II study of erlotinib alone or combined with bevacizumab in EGFRmutant NSCLC. Patients without brain metastases and without previous chemotherapy or tyrosine kinase inhibitor treatment will be randomized to erlotinib alone or erlotinib with bevacizumab.…”
Section: Alliance For Clinical Trials In Oncologymentioning
confidence: 99%
“…The primary endpoints are toxicity and disease-free survival. 6 is a randomized phase II study of erlotinib alone or combined with bevacizumab in EGFRmutant NSCLC. Patients without brain metastases and without previous chemotherapy or tyrosine kinase inhibitor treatment will be randomized to erlotinib alone or erlotinib with bevacizumab.…”
Section: Alliance For Clinical Trials In Oncologymentioning
confidence: 99%
“…A European single-arm phase II trial of bevacizumab-erlotinib (BELIEF; ETOP 2-11) in EGFR common mutations demonstrated a less impressive median PFS of 13.8 months, with no difference in outcome between del19 or L858R, but more prolonged PFS in those with T790M detected at baseline by an ultrasensitive method (PCR-PNA) than without (16 versus 10.5 months, respectively) [Stahel et al 2015]. The European Medicines Agency (EMA) has recently approved this combination and a confirmatory randomized European trial is recruiting (BEVERLY [ClinicalTrials.gov identifier: NCT02633189]).…”
Section: Can We Delay the Development Of Acquired Resistance To Firstmentioning
confidence: 99%
“…The results of such study showed a significant longer median PFS (16 vs 9.7 months), with about 50% reduction of the risk of progression (HR: 0.54 (95%CI: 0.36-0.79)) in favour of the combination arm (Seto et al, 2014). Interestingly the preliminary results of the European BELIEF trial have recently revealed that patients with EGFR-T790M positive tumors would benefit more from erlotinib plus bevacizumab combination with a median PFS of 16 months compared to 10.5 months of patients without T790M, suggesting a new potential strategy to overcome T790M-mediated acquired resistance (Stahel et al, 2015). The major concern for clinical use is represented by the cumulative toxicity, whit about 60% of G3-4 hypertension and 8% of G3-4 proteinuria reported in the combination arm, while no differences in drug-discontinuation rate have been observed between the two treatments.…”
Section: Anti-angiogenic Agentsmentioning
confidence: 99%