University of Colorado Cancer Center, Aurora, CO
Karl D. Lewis , Michele Maio , Mario Mandalà , Betty J Nelson , Grant R. Goodman , Dirk Schadendorf
Background: Approximately 50% of melanomas carry a mutation in the BRAF gene. The oral BRAF inhibitor vemurafenib (VEM) has demonstrated meaningful clinical benefit in BRAFV600 mutation-positive, locally advanced/unresectable or metastatic melanoma. For patients (pts) with resected melanoma, interferon alfa-2b represents the only widely approved adjuvant therapy; however, its use is limited by a modest improvement in disease recurrence and a high incidence of severe adverse effects that lead to treatment discontinuation in up to a third of pts. BRIM8 is a phase III, international, multicenter, double-blind, randomized, placebo-controlled study designed to evaluate the safety and efficacy of VEM in pts with resected cutaneous melanoma at high risk (>50%) for recurrence (stage IIC and III disease). Methods: Pts aged ≥18 yrs with histologically confirmed stage IIC or III BRAFV600mutation-positive (by cobas testing) melanoma of cutaneous origin that has been completely resected are eligible. Pts without clinical or radiologic evidence of regional lymph node involvement must undergo sentinel lymph node biopsy, and those with evidence of regional or sentinel lymph node involvement must undergo complete regional lymphadenectomy. Pts with a history of systemic therapy for treatment or prevention of melanoma (including interferon alfa-2b) are ineligible. Two cohorts (C) will enroll ~ 725 pts: C1—500 pts with completely resected stage IIC, IIIA (one or more nodal metastasis >1 mm in diameter, per Rotterdam classification), or IIIB cutaneous melanoma; C2—225 pts with stage IIIC cutaneous melanoma. Pts will be randomized 1:1 to receive VEM (960 mg bid) or placebo for 52 weeks with randomization stratified by pathologic stage and region (C1) and by region (C2). Primary efficacy outcome measure is investigator-assessed disease-free survival. Secondary efficacy outcome measures include overall and distant metastasis-free survival. Safety, pharmacokinetic, and pt-reported outcomes will also be assessed. As of 13 Jan 2014, 179/196 sites are active and 154 pts have been randomized (C1: 89; C2: 65). Clinical trial information: NCT01667419.
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