TY - JOUR
T1 - Green Tea Extract to Prevent Colorectal Adenomas, Results of a Randomized, Placebo-Controlled Clinical Trial
AU - Seufferlein, Thomas
AU - Ettrich, Thomas J.
AU - Menzler, Stefan
AU - Messmann, Helmut
AU - Kleber, Gerhard
AU - Zipprich, Alexander
AU - Frank-Gleich, Stefanie
AU - Algül, Hana
AU - Metter, Klaus
AU - Odemar, Frank
AU - Heuer, Theodor
AU - Hügle, Ulrich
AU - Behrens, Rüdiger
AU - Berger, Andreas W.
AU - Scholl, Catharina
AU - Schneider, Katharina L.
AU - Perkhofer, Lukas
AU - Rohlmann, Friederike
AU - Muche, Rainer
AU - Stingl, Julia C.
N1 - Publisher Copyright:
© 2022 by The American College of Gastroenterology. Unauthorized reproduction of this article is prohibited.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - INTRODUCTION:Preclinical, epidemiological, and small clinical studies suggest that green tea extract (GTE) and its major active component epigallocatechingallate (EGCG) exhibit antineoplastic effects in the colorectum.METHODS:A randomized, double-blind trial of GTE standardized to 150 mg of EGCG b.i.d. vs placebo over 3 years was conducted to prevent colorectal adenomas (n = 1,001 with colon adenomas enrolled, 40 German centers). Randomization (1:1, n = 879) was performed after a 4-week run-in with GTE for safety assessment. The primary end point was the presence of adenoma/colorectal cancer at the follow-up colonoscopy 3 years after randomization.RESULTS:The safety profile of GTE was favorable with no major differences in adverse events between the 2 well-balanced groups. Adenoma rate in the modified intention-to-treat set (all randomized participants [intention-to-treat population] and a follow-up colonoscopy 26-44 months after randomization; n = 632) was 55.7% in the placebo and 51.1% in the GTE groups. This 4.6% difference was not statistically significant (adjusted relative risk 0.905; P = 0.1613). The respective figures for the per-protocol population were 54.3% (151/278) in the placebo group and 48.3% (129/267) in the GTE group, indicating a slightly lower adenoma rate in the GTE group, which was not significant (adjusted relative risk 0.883; P = 0.1169).DISCUSSION:GTE was well tolerated, but there was no statistically significant difference in the adenoma rate between the GTE and the placebo groups in the whole study population.
AB - INTRODUCTION:Preclinical, epidemiological, and small clinical studies suggest that green tea extract (GTE) and its major active component epigallocatechingallate (EGCG) exhibit antineoplastic effects in the colorectum.METHODS:A randomized, double-blind trial of GTE standardized to 150 mg of EGCG b.i.d. vs placebo over 3 years was conducted to prevent colorectal adenomas (n = 1,001 with colon adenomas enrolled, 40 German centers). Randomization (1:1, n = 879) was performed after a 4-week run-in with GTE for safety assessment. The primary end point was the presence of adenoma/colorectal cancer at the follow-up colonoscopy 3 years after randomization.RESULTS:The safety profile of GTE was favorable with no major differences in adverse events between the 2 well-balanced groups. Adenoma rate in the modified intention-to-treat set (all randomized participants [intention-to-treat population] and a follow-up colonoscopy 26-44 months after randomization; n = 632) was 55.7% in the placebo and 51.1% in the GTE groups. This 4.6% difference was not statistically significant (adjusted relative risk 0.905; P = 0.1613). The respective figures for the per-protocol population were 54.3% (151/278) in the placebo group and 48.3% (129/267) in the GTE group, indicating a slightly lower adenoma rate in the GTE group, which was not significant (adjusted relative risk 0.883; P = 0.1169).DISCUSSION:GTE was well tolerated, but there was no statistically significant difference in the adenoma rate between the GTE and the placebo groups in the whole study population.
UR - http://www.scopus.com/inward/record.url?scp=85131702288&partnerID=8YFLogxK
U2 - 10.14309/ajg.0000000000001706
DO - 10.14309/ajg.0000000000001706
M3 - Article
C2 - 35213393
AN - SCOPUS:85131702288
SN - 0002-9270
VL - 117
SP - 884
EP - 894
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 6
ER -