NFM-07. SPRINT: PHASE II STUDY OF THE MEK 1/2 INHIBITOR SELUMETINIB (AZD6244, ARRY-142886) IN CHILDREN WITH NEUROFIBROMATOSIS TYPE 1 (NF1) AND INOPERABLE PLEXIFORM NEUROFIBROMAS (PN)

Abstract PN in NF1 cause substantial morbidity. In a phase I trial of selumetinib, 17/24 patients had a partial response (PR). This study evaluates the PR rate of PN to selumetinib and changes in PN-related morbidities. Patients 2-18 years with NF1, inoperable PN and ≥ 1 PN-related morbidity received continuous 28-day cycles of selumetinib (25 mg/m2 PO BID). Response (volumetric MRI analysis; PR = PN volume decrease ≥20%) and PN-related morbidities were assessed after every 4 cycles. Fifty children (30 male, median age 10.2 years, range 3.5, 17.4) enrolled. Disfigurement (n=44), motor dysfunction (n=33) and pain (n=28) were the most frequent PN-related morbidities. As of November 5, 2017: median cycle number 19.5 (range 0, 29); median change in PN volume -27.7% (range -50.6%, 2.2%). Best response PR (36 patients, 72%), stable disease (12 patients, 24%); 2 (4%) had no re-staging evaluations. Of the 36 PR, 32 were confirmed on ≥ two consecutive restaging studies. Pain intensity and interference scores improved significantly (p