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[HTML][HTML] Rare epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer
Epidermal growth factor receptor (EGFR) mutations are the second most common oncogenic
driver event in non-small cell lung cancer (NSCLC). Classical activating mutations (exon 19 …
driver event in non-small cell lung cancer (NSCLC). Classical activating mutations (exon 19 …
[HTML][HTML] Overview of current systemic management of EGFR-mutant NSCLC
Front-line epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI) therapy is
the standard of care for lung cancer patients with sensitising EGFR mutations (exon 19 …
the standard of care for lung cancer patients with sensitising EGFR mutations (exon 19 …
[HTML][HTML] ESMO expert consensus statements on the management of EGFR mutant non-small-cell lung cancer
Highlights•A virtual consensus on the management of EGFR-mutant NSCLC was organized
by the ESMO, including 34 experts from 18 countries.•The experts compiled …
by the ESMO, including 34 experts from 18 countries.•The experts compiled …
Osimertinib for patients with non–small-cell lung cancer harboring uncommon EGFR mutations: a multicenter, open-label, phase II trial (KCSG-LU15-09)
JH Cho, SH Lim, HJ An, KH Kim, KU Park… - Journal of Clinical …, 2020 - ascopubs.org
PURPOSE Approximately 10% of patients with epidermal growth factor receptor (EGFR)
mutation–positive non–small-cell lung cancer (NSCLC) harbor uncommon mutations. Here …
mutation–positive non–small-cell lung cancer (NSCLC) harbor uncommon mutations. Here …
[HTML][HTML] Recent advances on the role of EGFR tyrosine kinase inhibitors in the management of NSCLC with uncommon, non exon 20 insertions, EGFR mutations
The first-line treatment of choice for patients with epidermal growth factor receptor (EGFR)
mutation-positive non-small cell lung cancer (NSCLC) is an EGFR tyrosine kinase inhibitor …
mutation-positive non-small cell lung cancer (NSCLC) is an EGFR tyrosine kinase inhibitor …
First-line osimertinib for previously untreated patients with NSCLC and uncommon EGFR mutations: the UNICORN phase 2 nonrandomized clinical trial
Y Okuma, K Kubota, M Shimokawa, K Hashimoto… - JAMA …, 2024 - jamanetwork.com
Importance Non–small cell lung cancer (NSCLC) with uncommonEGFRmutations is a rare
subgroup, composing 14% of allEGFRmutations. Objective To determine the usefulness of …
subgroup, composing 14% of allEGFRmutations. Objective To determine the usefulness of …
[HTML][HTML] Afatinib for the treatment of NSCLC harboring uncommon EGFR mutations: a database of 693 cases
JCH Yang, M Schuler, S Popat, S Miura… - Journal of Thoracic …, 2020 - Elsevier
Introduction Limited clinical data are available regarding the efficacy of EGFR tyrosine
kinase inhibitors (EGFR TKIs) in patients with NSCLC harboring uncommon EGFR …
kinase inhibitors (EGFR TKIs) in patients with NSCLC harboring uncommon EGFR …
Not all epidermal growth factor receptor mutations in lung cancer are created equal: perspectives for individualized treatment strategy
Somatic mutations in the epidermal growth factor receptor (EGFR) gene are present in
approximately 20%(in Caucasians) to 40%(in East Asians) of adenocarcinomas of the lung …
approximately 20%(in Caucasians) to 40%(in East Asians) of adenocarcinomas of the lung …
[HTML][HTML] UNcommon EGFR mutations: international case series on efficacy of osimertinib in real-life practice in first-LiNe setting (UNICORN)
Introduction Approximately 10% of EGFR mutations (EGFRmuts) are uncommon
(ucEGFRmuts). We aimed to collect real-world data about osimertinib for patients with …
(ucEGFRmuts). We aimed to collect real-world data about osimertinib for patients with …
[HTML][HTML] Driven by mutations: the predictive value of mutation subtype in EGFR-mutated non–small cell lung cancer
E Castellanos, E Feld, L Horn - Journal of thoracic oncology, 2017 - Elsevier
EGFR-mutated NSCLC is a genetically heterogeneous disease that includes more than 200
distinct mutations. The implications of mutational subtype for both prognostic and predictive …
distinct mutations. The implications of mutational subtype for both prognostic and predictive …