^
Evidence Level:
Sensitive: A1 - Approval

[EGFR exon 19 deletion-Non Small Cell Lung Cancer-gefitinib]

Source:
Excerpt:
IRESSA is a tyrosine kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test.
Evidence Level:
Sensitive: A1 - Approval

[EGFR L858R-Non Small Cell Lung Cancer-gefitinib]

Source:
Excerpt:
IRESSA is a tyrosine kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test.
Evidence Level:
Sensitive: A1 - Approval

[EGFR L858R-Non Small Cell Lung Cancer-dacomitinib]

Source:
Excerpt:
VIZIMPRO is a kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as detected by an FDA-approved test.
Evidence Level:
Sensitive: A1 - Approval

[EGFR exon 19 deletion-Non Small Cell Lung Cancer-dacomitinib]

Source:
Excerpt:
VIZIMPRO is a kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as detected by an FDA-approved test.
Evidence Level:
Sensitive: C3 – Early Trials

[EGFR T790M-Non Small Cell Lung Cancer-rociletinib]

Title:
Rociletinib in EGFR-Mutated Non–Small-Cell Lung Cancer
Excerpt:
...T790M-positive patients treated with rociletinib in our study had a sustained clinical benefit. A response rate of 59% with prolonged disease control was noted. Although the best responses were observed among those with T790M-positive cancers, rociletinib showed some antitumor activity in patients without a documented T790M mutation.
DOI:
10.1056/NEJMoa1413654