Adjuvant Ipilimumab in High-Risk Uveal Melanoma.
Eric FountainRoland L BassettSuzanne CainLiberty PosadaDan S GombosPatrick HwuAgop BedikianSapna Pradyuman PatelPublished in: Cancers (2019)
Uveal melanoma is a common intraocular malignant tumor that is uniformly fatal once metastatic. No effective adjuvant therapy currently exists to reduce the risk of distant metastasis after definitive treatment of the primary lesion. Immunotherapy has been used effectively in the adjuvant setting in locally advanced cutaneous melanoma. We performed a Phase I/II clinical trial of adjuvant ipilimumab in high-risk primary uveal melanoma with distant metastasis-free survival (DMFS) as the primary objective. A total of 10 patients with genomically high-risk disease were treated: three at a dose of 3 mg/kg and seven at 10 mg/kg. Two of the seven patients at the higher dose had to discontinue therapy secondary to grade 3 toxicity. At 36 months follow-up, 80% of patients had no evidence of distant disease (95% CI, 58.7⁻100). With recent advancements in CTLA-4 inhibition, PD-1 inhibition, and combined checkpoint blockade, immunotherapy is a promising avenue of treatment in uveal melanoma. Further clinical trials are needed to elucidate the role of immunotherapy in the adjuvant setting.
Keyphrases
- clinical trial
- early stage
- locally advanced
- skin cancer
- free survival
- squamous cell carcinoma
- lymph node
- newly diagnosed
- end stage renal disease
- dna damage
- basal cell carcinoma
- stem cells
- rectal cancer
- oxidative stress
- phase ii
- study protocol
- radiation therapy
- combination therapy
- open label
- cell cycle
- bone marrow
- mesenchymal stem cells
- double blind
- patient reported outcomes
- placebo controlled