Randomized Phase II Trial of Polyphenon E versus Placebo in Patients at High Risk of Recurrent Colonic Neoplasia.

Christopher J Gostout, Stephen Sontag, Chung S Yang, Nathan R Foster, Jeffrey P Meyers, Paul J Limburg, Asad Umar, Gary Della'Zanna, Árpád V Patai, Abdul M Kalaiger, Frank A Sinicrope, John B Kisiel, Robert E Sedlack, Mark V Larson, Robert E Kraichely, Kenneth W Schroeder, Louis M Wong Kee Song, Navtej S Buttar, Thomas R Viggiano

Journal: Cancer prevention research (Philadelphia, Pa.) 2022;14(5):573-580

PMID: 33648940

Abstract

Polyphenon E (Poly E) is a green tea polyphenol preparation whose most active component is epigallocatechin gallate (EGCG). We studied the cancer preventive efficacy and safety of Poly E in subjects with rectal aberrant crypt foci (ACF), which represent putative precursors of colorectal cancers. Eligible subjects had prior colorectal advanced adenomas or cancers, and had ≥5 rectal ACF at a preregistration chromoendoscopy. Subjects ( = 39) were randomized to 6 months of oral Poly E (780 mg EGCG) daily or placebo. Baseline characteristics were similar by treatment arm (all P >0.41); 32 of 39 (82%) subjects completed 6 months of treatment. The primary endpoint was percent reduction in rectal ACF at chromoendoscopy comparing before and after treatment. Among 32 subjects (15 Poly E, 17 placebo), percent change in rectal ACF number (baseline vs. 6 months) did not differ significantly between study arms (3.7% difference of means; = 0.28); total ACF burden was also similar (-2.3% difference of means; = 0.83). Adenoma recurrence rates at 6 months were similar by arm ( > 0.35). Total drug received did not differ significantly by study arm; 31 (79%) subjects received ≥70% of prescribed Poly E. Poly E was well tolerated and adverse events (AE) did not differ significantly by arm. One subject on placebo had two grade 3 AEs; one subject had grade 2 hepatic transaminase elevations attributed to treatment. In conclusion, Poly E for 6 months did not significantly reduce rectal ACF number relative to placebo. Poly E was well tolerated and without significant toxicity at the dose studied. PREVENTION RELEVANCE: We report a chemoprevention trial of polyphenon E in subjects at high risk of colorectal cancer. The results show that polyphenon E was well tolerated, but did not significantly reduce the number of rectal aberrant crypt foci, a surrogate endpoint biomarker of colorectal cancer.

©2021 American Association for Cancer Research.

Address: Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. [email protected].; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.; Department of Internal Medicine and Hematology, Semmelweis University, Budapest, Hungary.; Gastrointestinal and Other Cancers Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland.; Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.; Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers University, The State University of New Jersey, Piscataway, New Jersey.; Section of Gastroenterology, Edward Hines, Jr. VA Hospital, Hines, Illinois.
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