Phase I Study of Muscadine Grape Extract for Patients With Advanced Cancer
Rhonda L Bitting, Janet A Tooze, Scott Isom, W Jeffrey Petty, Stefan C Grant, Rodwige J Desnoyers, Alexandra Thomas, Christopher Y Thomas, Angela T Alistar, Shannon L Golden, Katherine Pleasant, Mark C Chappell, E Ann Tallant, Patricia E Gallagher, Heidi D Klepin, Rhonda L Bitting, Janet A Tooze, Scott Isom, W Jeffrey Petty, Stefan C Grant, Rodwige J Desnoyers, Alexandra Thomas, Christopher Y Thomas, Angela T Alistar, Shannon L Golden, Katherine Pleasant, Mark C Chappell, E Ann Tallant, Patricia E Gallagher, Heidi D Klepin
Abstract
Objective: Preclinical studies with muscadine grape extract (MGE) show antitumor activity and decreased systemic inflammation. This phase I study (NCT02583269) assessed safety and tolerability of a proprietary MGE preparation in patients with advanced solid tumors.
Methods: Patients with metastatic or unresectable cancers who were progressing on standard therapies were assigned to MGE in a standard 3+3 design. Five dose levels were tested (320 to 1600 mg total phenolics/d). Safety and maximum-tolerated dose were assessed after 4 weeks. Patients were evaluated for response at 8 weeks and continued on MGE if clinically stable. Secondary outcomes were response, survival, adherence, fatigue, and quality of life (QOL).
Results: In total, 23 patients (lung, n=7; gastrointestinal, n=7; genitourinary, n=6; other, n=3) received MGE capsules by mouth twice daily. The cohort [median age 72 years, 48% Eastern Cooperative Oncology Group (ECOG) 2] was heavily pretreated. After 4 weeks on MGE, possibly attributable adverse events grade 2 or higher were fatigue (n=1), decreased lymphocyte count (n=1), and constipation (n=2), including 1 dose-limiting toxicity for grade 3 constipation. Maximum-tolerated dose was not reached. No partial responses were observed. Median time on therapy was 8 weeks, with 29% of patients treated beyond 16 weeks and a median overall survival of 7.2 months. QOL and fatigue levels were stable from baseline to 8 weeks. Higher MGE dose was correlated with improvement in self-reported physical well-being QOL at 8 weeks (r=0.6; P=0.04).
Conclusions: MGE is safe and well-tolerated in heavily pretreated and older cancer patients. The potential anticancer properties and the effects of MGE on physical well-being and QOL metrics will be evaluated in future studies.
Conflict of interest statement
The authors declare no conflicts of interest.
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Source: PubMed