Low-Fat Dietary Pattern and Breast Cancer Mortality in the Women's Health Initiative Randomized Controlled Trial.

Linda Snetselar, Ross L Prentice, Fridtjof Thomas, Lifang Hou, Lihong Qi, Catherine Womack, Mara Z Vitolins, Wendy Barrington, Dorothy Lane, Rowan T Chlebowski, Thomas E Rohan, Barbara V Howard, Michael S Simon, JoAnn E Manson, Cynthia A Thomson, Garnet L Anderson, Aaron K Aragaki

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2017;35(25):2919-2926

PMID: 28654363

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In the Women’s Health Initiative Dietary Modification (WHI DM) trial, 48,835 postmenopausal women were randomly assigned to a dietary modification group or usual diet comparison group to assess low-fat dietary pattern effects on breast cancer incidence. The aim of this study was to present results of dietary modification influence on deaths as a result of breast cancer and on the more general outcome of deaths after breast cancer (breast cancer followed by death as a result of any cause). The study recruited postmenopausal women between 50 and 79 years of age with no record of previous breast cancer. The participants were randomly assigned to a low-fat dietary pattern intervention group or a usual diet comparison group. Results indicate that with long-term follow-up of the WHI DM trial, deaths after breast cancer were significantly reduced in the low-fat dietary group both during the dietary intervention period and throughout the 16.1-year cumulative follow-up period. Authors conclude that women assigned to a low-fat dietary pattern had a significantly reduced risk of death from breast cancer.

Abstract

Purpose Earlier Women's Health Initiative Dietary Modification trial findings suggested that a low-fat eating pattern may reduce breast cancers with greater mortality. Therefore, as a primary outcome-related analysis from a randomized prevention trial, we examined the long-term influence of this intervention on deaths as a result of and after breast cancer during 8.5 years (median) of dietary intervention and cumulatively for all breast cancers diagnosed during 16.1 years (median) of follow-up. Patients and Methods The trial randomly assigned 48,835 postmenopausal women with normal mammograms and without prior breast cancer from 1993 to 1998 at 40 US clinical centers to a dietary intervention with goals of a reduction of fat intake to 20% of energy and an increased intake of fruits, vegetables, and grains (40%; n = 19,541) or to a usual diet comparison (60%; n = 29,294). Results In the dietary group, fat intake and body weight decreased (all P < .001). During the 8.5-year dietary intervention, with 1,764 incident breast cancers, fewer deaths occurred as a result of breast cancer in the dietary group, which was not statistically significant (27 deaths [0.016% per year] v 61 deaths [0.024% per year]; hazard ratio [HR], 0.67; 95% CI, 0.43 to 1.06; P = .08). During the same period, deaths after breast cancer (n = 134) were significantly reduced (40 deaths [0.025% per year] v 94 deaths [0.038% per year]; HR, 0.65; 95% CI, 0.45 to 0.94; P = .02) by the dietary intervention. During the 16.1-year follow-up, with 3,030 incident breast cancers, deaths after breast cancer also were significantly reduced (234 deaths [0.085% per year] v 443 deaths [0.11% per year]; HR, 0.82; 95% CI, 0.70 to 0.96; P = .01) in the dietary group. Conclusion Compared with a usual diet comparison group, a low-fat dietary pattern led to a lower incidence of deaths after breast cancer.

Address: Rowan T. Chlebowski, Los Angeles Biomedical Research Institute, Torrance; Lihong Qi, University of California, Davis, Davis, CA; Aaron K. Aragaki, Garnet L. Anderson, Wendy Barrington, and Ross L. Prentice, Fred Hutchinson Cancer Research Center, Seattle, WA; Cynthia A. Thomson, University of Arizona Cancer Center, Tucson, AZ; JoAnn E. Manson, Brigham and Women's Hospital, Boston, MA; Michael S. Simon, Wayne State University, Detroit, MI; Barbara V. Howard, MedStar Health Research Institute; Barbara V. Howard, Georgetown-Howard Universities Center for Clinical and Translational Sciences, Washington, DC; Thomas E. Rohan, Albert Einstein College of Medicine, New York City; Dorothy Lane, Stony Brook University, Stony Brook, NY; Linda Snetselar, University of Iowa, Iowa City, IA; Catherine Womack, Methodist Healthcare; Fridtjof Thomas, University of Tennessee Health Science Center, Memphis, TN; Mara Z. Vitolins, Wake Forest School of Medicine, Winston-Salem, NC; and Lifang Hou, Northwestern University, Chicago, IL.

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