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Association details:
Biomarker:BRAF wild-type
Cancer:Melanoma
Drug:Opdivo (nivolumab) (PD1 inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: B - Late Trials
New
Source:
Title:

Survival Outcomes in Patients With Previously Untreated BRAF Wild-Type Advanced Melanoma Treated With Nivolumab Therapy Three-Year Follow-up of a Randomized Phase 3 Trial

Excerpt:
The median overall survival was 37.5 months (95% CI, 25.5 months–not reached) in the nivolumab group and 11.2 months (95% CI, 9.6-13.0 months) in the dacarbazine group (hazard ratio, 0.46; 95% CI, 0.36-0.59; P < .001). Complete and partial responses, respectively, were reported for 19.0% (40 of 210) and 23.8% (50 of 210) of patients in the nivolumab group compared with 1.4% (3 of 208) and 13.0% (27 of 208) of patients in the dacarbazine group....Nivolumab led to improved 3-year overall survival vs dacarbazine in patients with previously untreated BRAF wild-type advanced melanoma.
DOI:
10.1001/jamaoncol.2018.4514
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Nivolumab Plus Radiotherapy in Advanced Melanoma

Excerpt:
...BRAF status must be determinate but patient will be eligible regardless the status (BRAF wildtype and BRAF V600 mutation positive patients could be included) 9....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Go to data
Title:

Study of Nivolumab (BMS-936558) Compared With Dacarbazine in Untreated, Unresectable, or Metastatic Melanoma

Excerpt:
...- Known BRAF wild-type, as per regionally acceptable V600 mutational status testing....
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C4 – Case Studies
Source:
Title:

Long Term Administration of Nivolumab for Metastatic Melanoma: A Case Report

Published date:
06/27/2022
Excerpt:
We present the case of a 75-year-old man with metastatic melanoma who underwent 95 cycles of nivolumab...a biopsy of the dorso-lumbar spine was performed, which established that the bone lesions were metastases of melanoma, BRAF negative. Therefore, in January 2018, we decided to initiate monotherapy with nivolumab 240 mg every two weeks, and zoledronic acid 4 mg every four weeks....After six doses of nivolumab, the pain was controlled, and the patient recovered from the motor deficit....it was interpreted as partial remission.
Secondary therapy:
zoledronic acid
DOI:
10.7759/cureus.26359