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Association details:
Evidence:
Evidence Level:
Sensitive: A2 - Guideline
Source:
Published date:
12/07/2021
Excerpt:
Non-Small Cell Lung Cancer...BRAF V600E MUTATION POSITIVE...Single-agent Vemurafenib or dabrafenib are treatment options if the combination of dabrafenib + trametinib is not tolerated.
Evidence Level:
Sensitive: C1 - Off-label
  (Approved for Melanoma)
New
Excerpt:
TAFINLAR is a kinase inhibitor indicated as a single agent for the treatment of patients with unresectable or metastatic melanoma with BRAF V600E mutation as detected by an FDA-approved test.
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Go to data
Title:

Study of Selective BRAF Kinase Inhibitor Dabrafenib Monotherapy Twice Daily and in Combination With Dabrafenib Twice Daily and Trametinib Once Daily in Combination Therapy in Subjects With BRAF V600E Mutation Positive Metastatic (Stage IV) Non-small Cell Lung Cancer.

Excerpt:
...Presence of a BRAF V600E mutation in lung cancer tissue.
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Clinical characteristics and treatment outcomes of 65 patients with BRAF-mutated non-small cell lung cancer (NSCLC).

Published date:
05/28/2020
Excerpt:
Of 30 V600E-mutated patients who received anti-BRAF therapy during the course of disease, the median PFS of vemurafenib, dabrafenib, and dabrafenib plus trametinib was 7.8 months, 5.8 months and 6.0 months, respectively (P = 0.970)….Our data demonstrated the clinical benefit of anti-BRAF targeted therapy in Chinese NSCLC patients harboring BRAF-V600E mutation.
DOI:
10.1200/JCO.2020.38.15_suppl.e21745
Evidence Level:
Sensitive: C3 – Early Trials
New
Title:

Dabrafenib in BRAF V600E–Mutant Advanced Non-Small Cell Lung Cancer: an Open-label, Single arm, Multicenter, Phase 2 Trial

Excerpt:
...increased response rates, longer PFS, and promising survival with acceptable toxicity makes this a reasonable treatment option for patients with BRAF V600E NSCLC....In conclusion, this study is, to our knowledge, the first trial of BRAF inhibition to focus on BRAF V600E–mutant NSCLC. Dabrafenib induced durable clinical responses in a significant number of patients and had an acceptable safety profile.
DOI:
10.1016/S1470-2045(16)00077-2
Trial ID:
Evidence Level:
Sensitive: C4 – Case Studies
New
Title:

Molecular characterization of acquired resistance to the BRAF inhibitor dabrafenib in a patient with BRAF-mutant non-small-cell lung cancer

Excerpt:
Identification of the driver BRAF mutation prompted use of a targeted therapy that led to a major objective response and substantial, though transient, 8-month symptomatic improvement. The second biopsy defined a probable mechanism of acquired resistance of particular relevance to lung cancer. 
DOI:
10.1097/JTO.0b013e31828bb1b3