Literature DB >> 33648940

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

Frank A Sinicrope1, Thomas R Viggiano2, Navtej S Buttar2, Louis M Wong Kee Song2, Kenneth W Schroeder2, Robert E Kraichely2, Mark V Larson2, Robert E Sedlack2, John B Kisiel2, Christopher J Gostout2, Abdul M Kalaiger2, Árpád V Patai2,3, Gary Della'Zanna4, Asad Umar4, Paul J Limburg2, Jeffrey P Meyers5, Nathan R Foster5, Chung S Yang6, Stephen Sontag7.   

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 (N = 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; P = 0.28); total ACF burden was also similar (-2.3% difference of means; P = 0.83). Adenoma recurrence rates at 6 months were similar by arm (P > 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.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 33648940      PMCID: PMC8102407          DOI: 10.1158/1940-6207.CAPR-20-0598

Source DB:  PubMed          Journal:  Cancer Prev Res (Phila)        ISSN: 1940-6215


  33 in total

1.  Green tea, black tea and colorectal cancer risk: a meta-analysis of epidemiologic studies.

Authors:  Can-Lan Sun; Jian-Min Yuan; Woon-Puay Koh; Mimi C Yu
Journal:  Carcinogenesis       Date:  2006-04-25       Impact factor: 4.944

2.  Aberrant crypt foci in human colons: distribution and histomorphologic characteristics.

Authors:  B Shpitz; Y Bomstein; Y Mekori; R Cohen; Z Kaufman; D Neufeld; M Galkin; J Bernheim
Journal:  Hum Pathol       Date:  1998-05       Impact factor: 3.466

3.  Effects of dosing condition on the oral bioavailability of green tea catechins after single-dose administration of Polyphenon E in healthy individuals.

Authors:  H-H Sherry Chow; Iman A Hakim; Donna R Vining; James A Crowell; James Ranger-Moore; Wade M Chew; Catherine A Celaya; Steven R Rodney; Yukihiko Hara; David S Alberts
Journal:  Clin Cancer Res       Date:  2005-06-15       Impact factor: 12.531

4.  Inhibition of intestinal tumorigenesis in Apcmin/+ mice by (-)-epigallocatechin-3-gallate, the major catechin in green tea.

Authors:  Jihyeung Ju; Jungil Hong; Jian-nian Zhou; Zui Pan; Mousumi Bose; Jie Liao; Guang-yu Yang; Ying Ying Liu; Zhe Hou; Yong Lin; Jianjie Ma; Weichung Joe Shih; Adelaide M Carothers; Chung S Yang
Journal:  Cancer Res       Date:  2005-11-15       Impact factor: 12.701

5.  Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: a preliminary report from a one-year proof-of-principle study.

Authors:  Saverio Bettuzzi; Maurizio Brausi; Federica Rizzi; Giovanni Castagnetti; Giancarlo Peracchia; Arnaldo Corti
Journal:  Cancer Res       Date:  2006-01-15       Impact factor: 12.701

6.  Phase 2 trial of daily, oral Polyphenon E in patients with asymptomatic, Rai stage 0 to II chronic lymphocytic leukemia.

Authors:  Tait D Shanafelt; Timothy G Call; Clive S Zent; Jose F Leis; Betsy LaPlant; Deborah A Bowen; Michelle Roos; Kristina Laumann; Asish K Ghosh; Connie Lesnick; Mao-Jung Lee; Chung S Yang; Diane F Jelinek; Charles Erlichman; Neil E Kay
Journal:  Cancer       Date:  2012-07-03       Impact factor: 6.860

7.  Transport by OATP1B1 and OATP1B3 enhances the cytotoxicity of epigallocatechin 3-O-gallate and several quercetin derivatives.

Authors:  Yuchen Zhang; Amanda Hays; Alexander Noblett; Mahendra Thapa; Duy H Hua; Bruno Hagenbuch
Journal:  J Nat Prod       Date:  2013-01-17       Impact factor: 4.050

8.  EGCG inhibits activation of the insulin-like growth factor (IGF)/IGF-1 receptor axis in human hepatocellular carcinoma cells.

Authors:  Masahito Shimizu; Yohei Shirakami; Hiroyasu Sakai; Hideharu Tatebe; Takayuki Nakagawa; Yukihiko Hara; I Bernard Weinstein; Hisataka Moriwaki
Journal:  Cancer Lett       Date:  2007-12-31       Impact factor: 8.679

9.  Aberrant crypt foci in patients with neoplastic and nonneoplastic colonic disease.

Authors:  H Bouzourene; P Chaubert; W Seelentag; F T Bosman; E Saraga
Journal:  Hum Pathol       Date:  1999-01       Impact factor: 3.466

10.  Endoscopic identification and quantification of aberrant crypt foci in the human colon.

Authors:  Douglas G Adler; Christopher J Gostout; Darius Sorbi; Lawrence J Burgart; Linan Wang; W Scott Harmsen
Journal:  Gastrointest Endosc       Date:  2002-11       Impact factor: 9.427

View more
  1 in total

Review 1.  Inhibition and potential treatment of colorectal cancer by natural compounds via various signaling pathways.

Authors:  Mingchuan Wang; Xianjun Liu; Tong Chen; Xianbin Cheng; Huijie Xiao; Xianglong Meng; Yang Jiang
Journal:  Front Oncol       Date:  2022-09-08       Impact factor: 5.738

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.