Login / Signup

Phase II study of ipilimumab and nivolumab in leptomeningeal carcinomatosis.

Priscilla K BrastianosMatthew R StricklandEudocia Quant LeeNancy WangJustine V CohenUgonma ChukwuekeDeborah Anne ForstApril EichlerBeth OvermoyerNancy U LinWendy Y ChenAditya BardiaDejan JuricIbiayi Dagogo-JackMichael D WhiteJorg DietrichNaema NayyarAlbert E KimChristopher Alvarez-BreckenridgeMaura MaharJoana Liliana MoraBrian V NahedPamela S JonesHelen A ShihElizabeth R GerstnerAnita Giobbie-HurderScott L CarterKevin OhDaniel P CahillRyan J Sullivan
Published in: Nature communications (2021)
Leptomeningeal disease (LMD) is a common complication from solid tumor malignancies with a poor prognosis and limited treatment options. We present a single arm Phase II study of 18 patients with LMD receiving combined ipilimumab and nivolumab until progression or unacceptable toxicity (NCT02939300). The primary end point is overall survival at 3 months (OS3). Secondary end points include toxicity, cumulative time-to-progression at 3 months, and progression-free survival. A Simon two-stage design is used to compare a null hypothesis OS3 of 18% against an alternative of 44%. Median follow up based on patients still alive is 8.0 months (range: 0.5 to 15.9 months). The study has met its primary endpoint as 8 of 18 (OS3 0.44; 90% CI: 0.24 to 0.66) patients are alive at three months. One third of patients have experienced one (or more) grade-3 or higher adverse events. Two patients have discontinued protocol treatment due to unacceptable toxicity (hepatitis and colitis, respectively). The most frequent adverse events include fatigue (N = 7), nausea (N = 6), fever (N = 6), anorexia (N = 6) and rash (N = 6). Combined ipilimumab and nivolumab has an acceptable safety profile and demonstrates promising activity in LMD patients. Larger, multicenter clinical trials are needed to validate these results.
Keyphrases