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Association details:
Evidence:
Evidence Level:
Sensitive: C4 – Case Studies
New
Title:

A Rare Case of Lung Adenocarcinoma with EGFR L833V/H835L Co-mutation and Literature Review

Published date:
11/22/2023
Excerpt:
...we reported a case of NSCLC patient with a rare gene compound mutation EGFR L833V/H835L, who responded to Afatinib in combination with Anilotinib treatment well after 5 months of treatment, and computed tomography (CT) showed shrinkage of lung lesions.
DOI:
10.3779/j.issn.1009-3419.2023.102.36