Anyone has experience with muscadine grape skin capsules for prostate cancer.
Muscadine Grapes: Anyone has experience... - Advanced Prostate...
Muscadine Grapes
I’ve got a lot of vines in my mini backyard vineyard… these are two species of muscadine. I’ve eaten them seasonally for over 20 years. Tasty but doesn’t seem like they had any impact on my getting PCa ….. dunno.
I found a study that the skin is the best to inhibit growth. Dosage might need to be higher. Google MKSE
I’ll check them out …thanks.
Hey Kaliber
For maximum effect, you should mash then ferment the grapes. Might not help PCA but should make you feel better right away
Phase 1 trial not specific to PCa but it's a start.
"Higher MGE dose was correlated with improvement in self-reported physical well-being QOL at 8 weeks (r=0.6; P=0.04)."
"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."
Phase I Study of Muscadine Grape Extract for Patients With Advanced CancerBitting, Rhonda L. MD*,†; Tooze, Janet A. PhD*,‡; Isom, Scott MS*,‡; Petty, W. Jeffrey MD*,†; Grant, Stefan C. MD*,†; Desnoyers, Rodwige J. MD*,†; Thomas, Alexandra MD*,†; Thomas, Christopher Y. MD*,†; Alistar, Angela T. MD*,†; Golden, Shannon L. MA§; Pleasant, Katherine BA§; Chappell, Mark C. PhD§; Tallant, E. Ann PhD*,§; Gallagher, Patricia E. PhD*,§; Klepin, Heidi D. MD*,†Author Information
American Journal of Clinical Oncology: June 2021 - Volume 44 - Issue 6 - p 239-246
doi: 10.1097/COC.0000000000000814
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.