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| Profile Name | BRAF mut CD274 pos |
| Gene Variant Detail | |
| Relevant Treatment Approaches |
| Molecular Profile | Indication/Tumor Type | Response Type | Relevant Treatment Approaches | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|---|
| BRAF mut CD274 pos | lung non-small cell carcinoma | not predictive | Pembrolizumab | Clinical Study - Cohort | Actionable | In a retrospective analysis, BRAF mutant non-small cell lung cancer patients with CD274 (PD-L1) expression >/= 50% did not show a significantly different response to treatment with either Keytruda (pembrolizumab), Opdivo (nivolumab), or Tecentriq (atezolizumab) when compared to BRAF mutant patients with CD274 (PD-L1) expression, 0-49%, demonstrating an objective response rate of 36% (4/11) vs 14% (1/7) (p=0.59) and median progression-free survival of 5.3 mo vs 2.2 mo (p=0.73) (PMID: 29723688). | 29723688 | |
| BRAF mut CD274 pos | lung non-small cell carcinoma | not predictive | Nivolumab | Clinical Study - Cohort | Actionable | In a retrospective analysis, BRAF mutant non-small cell lung cancer patients with CD274 (PD-L1) expression >/= 50% did not show a significantly different response to treatment with either Keytruda (pembrolizumab), Opdivo (nivolumab), or Tecentriq (atezolizumab) when compared to BRAF mutant patients with CD274 (PD-L1) expression, 0-49%, demonstrating an objective response rate of 36% (4/11) vs 14% (1/7) (p=0.59) and median progression-free survival of 5.3 mo vs 2.2 mo (p=0.73) (PMID: 29723688). | 29723688 | |
| BRAF mut CD274 pos | lung non-small cell carcinoma | not predictive | Atezolizumab | Clinical Study - Cohort | Actionable | In a retrospective analysis, BRAF mutant non-small cell lung cancer patients with CD274 (PD-L1) expression >/= 50% did not show a significantly different response to treatment with either Keytruda (pembrolizumab), Opdivo (nivolumab), or Tecentriq (atezolizumab) when compared to BRAF mutant patients with CD274 (PD-L1) expression, 0-49%, demonstrating an objective response rate of 36% (4/11) vs 14% (1/7) (p=0.59) and median progression-free survival of 5.3 mo vs 2.2 mo (p=0.73) (PMID: 29723688). | 29723688 |