The immune checkpoint inhibitor nivolumab inhibits the programmed death 1 receptor and suppresses the immune resistance of cancer cells. This is a long‐term follow up of a single‐arm, open‐label, multicenter, phase
II
study of nivolumab in untreated Japanese patients with stage
III
/
IV
or recurrent melanoma. In addition, a post–hoc subgroup analysis stratified by melanoma types was performed. Nivolumab was administered intravenously at a dose of 3 mg/kg every 2 weeks. The primary endpoint was the overall response rate (
ORR
), and secondary endpoints included overall survival (
OS
), progression‐free survival (
PFS
), best overall response, the disease control rate and change in tumor diameter. Safety was assessed by recording treatment‐related adverse events (
TRAE
), including select immune‐related adverse events. Of the 24 patients initially included in the primary phase
II
study, 10 survived for over 3 years (41.7%). The
ORR
was 34.8% (90% confidence interval [
CI
]: 20.8, 51.9) for all patients. When analyzing by melanoma type, the
ORR
was 66.7% (90%
CI
: 34.7, 88.3) for superficial spreading, 33.3% (90%
CI
: 11.7, 65.3) for mucosal, and 28.6% (90%
CI
: 10.0, 59.1) for acral lentiginous tumors. The median
OS
was 32.9 months, the 3‐year
OS
rate was 43.5%, and the 3‐year
PFS
rate was 17.2%. A long‐term response was observed in all the tumor types. The most common
TRAE
included skin toxicity (45.8%) and endocrine disorders (29.2%). This study demonstrated the long‐term efficacy and tolerability of nivolumab in patients with advanced or recurrent melanoma, irrespective of melanoma type.