Literature DB >> 11588128

A randomized, double blind, Phase III trial using oral beta-carotene supplementation for women with high-grade cervical intraepithelial neoplasia.

K A Keefe1, M J Schell, C Brewer, M McHale, W Brewster, J A Chapman, G S Rose, D S McMeeken, W Lagerberg, Y M Peng, S P Wilczynski, H Anton-Culver, F L Meyskens, M L Berman.   

Abstract

To evaluate the effect of daily beta-carotene (30 mg) versus placebo over a 2-year period on cervical intraepithelial neoplasia (CIN) 2 and 3 lesions. Human papillomavirus (HPV) typing was done to determine whether lesion regression was related to HPV. Micronutrient levels were measured to determine whether levels were predictive of regression. Variables that influence the risk of HPV infection and CIN, such as cigarette smoking and sexual behavior, were evaluated. Women were randomized to beta-carotene or placebo, with cytology and colposcopy every 3 months. Cervical biopsies were performed before treatment and after 6 and 24 months to evaluate response. Persistence of or progression to CIN 3 resulted in removal from the study, whereas treatment continued for 2 years on all others. The presence and type of HPV was determined by PCR. Response was defined as an improvement in CIN by 2 grades. Mantel-Haenszel chi(2) test was used to analyze response to treatment. Fisher's exact test was used to determine the effect of HPV and CIN grade on response Wilcoxon's rank-sum tests were used to compare micronutrient levels between groups. Twenty-one of 124 enrolled women were not randomized because they either moved, became pregnant, voluntarily withdrew, or the pathological review of their initial cervical biopsies did not confirm CIN 2 or 3. Of the remaining 103 women, 33 experienced lesion regression, 45 had persistent or progressive disease, and 25 women did not complete the study and were considered nonresponders in the final analysis. The overall regression rate (32%) was similar between treatment arms and when stratified for CIN grade. Data on 99 women with HPV typing showed that 77% were HPV-positive and 23% HPV-negative at enrollment. HPV-positive lesions were subdivided into indeterminate-, low-, and high-risk categories; the response rate was highest for women with no HPV detected (61%), lower for indeterminate/low-risk (30%), and lowest for high-risk (18%; P =.001). CIN regression was negatively correlated with retinol levels. In conclusion, beta-carotene does not enhance the regression of high-grade CIN, especially in HPV-positive subjects.

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Year:  2001        PMID: 11588128

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


  16 in total

1.  Spontaneous regression of high-grade cervical dysplasia: effects of human papillomavirus type and HLA phenotype.

Authors:  Cornelia L Trimble; Steven Piantadosi; Patti Gravitt; Brigitte Ronnett; Ellen Pizer; Andrea Elko; Barbara Wilgus; William Yutzy; Richard Daniel; Keerti Shah; Shiwen Peng; Chienfu Hung; Richard Roden; Tzyy Choou Wu; Drew Pardoll
Journal:  Clin Cancer Res       Date:  2005-07-01       Impact factor: 12.531

Review 2.  Dynamic behavioural interpretation of cervical intraepithelial neoplasia with molecular biomarkers.

Authors:  J P A Baak; A-J Kruse; S J Robboy; E A M Janssen; B van Diermen; I Skaland
Journal:  J Clin Pathol       Date:  2006-05-05       Impact factor: 3.411

3.  Association between carotenoids and outcome of cervical intraepithelial neoplasia: a prospective cohort study.

Authors:  Takuma Fujii; Naoyoshi Takatsuka; Chisato Nagata; Koji Matsumoto; Akinori Oki; Reiko Furuta; Hiroo Maeda; Toshiharu Yasugi; Kei Kawana; Akira Mitsuhashi; Yasuo Hirai; Tsuyoshi Iwasaka; Nobuo Yaegashi; Yoh Watanabe; Yutaka Nagai; Tomoyuki Kitagawa; Hiroyuki Yoshikawa
Journal:  Int J Clin Oncol       Date:  2012-10-25       Impact factor: 3.402

4.  An updated natural history model of cervical cancer: derivation of model parameters.

Authors:  Nicole G Campos; Emily A Burger; Stephen Sy; Monisha Sharma; Mark Schiffman; Ana Cecilia Rodriguez; Allan Hildesheim; Rolando Herrero; Jane J Kim
Journal:  Am J Epidemiol       Date:  2014-07-31       Impact factor: 4.897

5.  Heat shock fusion protein-based immunotherapy for treatment of cervical intraepithelial neoplasia III.

Authors:  Mark H Einstein; Anna S Kadish; Robert D Burk; Mimi Y Kim; Scott Wadler; Howard Streicher; Gary L Goldberg; Carolyn D Runowicz
Journal:  Gynecol Oncol       Date:  2007-06-22       Impact factor: 5.482

Review 6.  Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases.

Authors:  Goran Bjelakovic; Dimitrinka Nikolova; Lise Lotte Gluud; Rosa G Simonetti; Christian Gluud
Journal:  Cochrane Database Syst Rev       Date:  2012-03-14

7.  Clearance of persistent HPV infection and cervical lesion by therapeutic DNA vaccine in CIN3 patients.

Authors:  Tae Jin Kim; Hyun-Tak Jin; Soo-Young Hur; Hyun Gul Yang; Yong Bok Seo; Sung Ran Hong; Chang-Woo Lee; Suhyeon Kim; Jung-Won Woo; Ki Seok Park; Youn-Young Hwang; Jaehan Park; In-Ho Lee; Kyung-Taek Lim; Ki-Heon Lee; Mi Seon Jeong; Charles D Surh; You Suk Suh; Jong Sup Park; Young Chul Sung
Journal:  Nat Commun       Date:  2014-10-30       Impact factor: 14.919

Review 8.  Medical treatment of cervical intraepithelial neoplasia II, III: an update review.

Authors:  Chumnan Kietpeerakool; Jatupol Srisomboon
Journal:  Int J Clin Oncol       Date:  2009-02-20       Impact factor: 3.850

9.  Evidence for frequent regression of cervical intraepithelial neoplasia-grade 2.

Authors:  Philip E Castle; Mark Schiffman; Cosette M Wheeler; Diane Solomon
Journal:  Obstet Gynecol       Date:  2009-01       Impact factor: 7.623

10.  HPV infection and number of lifetime sexual partners are strong predictors for 'natural' regression of CIN 2 and 3.

Authors:  J K Chan; B J Monk; C Brewer; K A Keefe; K Osann; S McMeekin; G S Rose; M Youssef; S P Wilczynski; F L Meyskens; M L Berman
Journal:  Br J Cancer       Date:  2003-09-15       Impact factor: 7.640

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