Impact of dietary patterns and the main food groups on mortality and recurrence in cancer survivors: a systematic review of current epidemiological literature

Sylvia H J Jochems, Frits H M Van Osch, Richard T Bryan, Anke Wesselius, Frederik J van Schooten, Kar Keung Cheng, Maurice P Zeegers, Sylvia H J Jochems, Frits H M Van Osch, Richard T Bryan, Anke Wesselius, Frederik J van Schooten, Kar Keung Cheng, Maurice P Zeegers

Abstract

Objective: To determine whether there is an association between dietary patterns/indices and foods from the main food groups (highest vs lowest intakes) prior to or after cancer diagnosis and mortality and cancer recurrence in cancer survivors.

Participants: Survivors of common cancers with a 10-year survival rate of ≥50%: bladder, bowel, breast, cervical, kidney, laryngeal, prostate, testicular, uterine cancer, malignant melanoma and (non-)Hodgkin's lymphoma.

Outcome measures: Mortality (overall, cancer-specific, from other causes) and cancer recurrence.

Information sources: PubMed, Embase and the Cochrane Library were searched from inception to April 2017. Additional studies were identified by searching reference lists. Two authors independently screened titles and abstracts, assessed study quality and extracted the data.

Results: A total of 38 studies were included. The risk of bias was rated low for the included randomised controlled trials (RCTs) and moderate for the cohort studies. The quality of evidence was assessed with the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) approach and was rated moderate (RCTs), and (very)low (cohort studies). Reducing the amount of fat after diagnosis appears to decrease the risk of breast cancer recurrence. Adherence to a high-quality diet and prudent diet after diagnosis appears to decrease the risk of death from other causes (and overall mortality for high-quality diet) in breast cancer survivors. Adherence to a Western diet, before and after diagnosis, appears to increase the risk of overall mortality and death from other causes among breast cancer survivors. Evidence from studies among other cancer survivors was too limited or could not be identified.

Conclusion: For many cancer survivors, there is little evidence to date to indicate that particular dietary behaviours influence outcomes with regard to recurrence and mortality. Notwithstanding, limited evidence suggests that a low-fat diet, a high-quality diet and a prudent diet are beneficial for breast cancer survivors, while a Western diet is detrimental for breast cancer survivors.

Keywords: cancer recurrence; cancer survivors; diet; dietary pattern; food; mortality.

Conflict of interest statement

Competing interests: None declared.

© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

References

    1. Schwingshackl L, Schwedhelm C, Hoffmann G, et al. . Food groups and risk of all-cause mortality: a systematic review and meta-analysis of prospective studies. Am J Clin Nutr 2017;105:ajcn153148 10.3945/ajcn.117.153148
    1. Schwingshackl L, Hoffmann G. Adherence to Mediterranean diet and risk of cancer: an updated systematic review and meta-analysis of observational studies. Cancer Med 2015;4:1933–47. 10.1002/cam4.539
    1. Leenders M, Sluijs I, Ros MM, et al. . Fruit and vegetable consumption and mortality: European prospective investigation into cancer and nutrition. Am J Epidemiol 2013;178:590–602. 10.1093/aje/kwt006
    1. Nguyen CT, Pham NM, Lee AH, et al. . Prevalence of and risk factors for Type 2 diabetes mellitus in Vietnam: a systematic review. Asia Pac J Public Health 2015;27:588–600. 10.1177/1010539515595860
    1. Bours MJ, Beijer S, Winkels RM, et al. . Dietary changes and dietary supplement use, and underlying motives for these habits reported by colorectal cancer survivors of the Patient Reported Outcomes Following Initial Treatment and Long-Term Evaluation of Survivorship (PROFILES) registry. Br J Nutr 2015;114:286–96. 10.1017/S0007114515001798
    1. Humpel N, Magee C, Jones SC. The impact of a cancer diagnosis on the health behaviors of cancer survivors and their family and friends. Support Care Cancer 2007;15:621–30. 10.1007/s00520-006-0207-6
    1. Zhang FF, Liu S, John EM, et al. . Diet quality of cancer survivors and noncancer individuals: results from a national survey. Cancer 2015;121:4212–21. 10.1002/cncr.29488
    1. D’Avanzo B, La Vecchia C, Negri E, et al. . Attributable risks for bladder cancer in Northern Italy. Ann Epidemiol 1995;5:427–31. 10.1016/1047-2797(95)00057-7
    1. Rock CL, Doyle C, Demark-Wahnefried W, et al. . Nutrition and physical activity guidelines for cancer survivors. CA Cancer J Clin 2012;62:242–74. 10.3322/caac.21142
    1. World Cancer Research Fund International, American Institute for Cancer Research. 2014. Diet, nutrition, physical activity, and breast cancer survivors. (accessed 2 Jun 2017).
    1. Schwedhelm C, Boeing H, Hoffmann G, et al. . Effect of diet on mortality and cancer recurrence among cancer survivors: a systematic review and meta-analysis of cohort studies. Nutr Rev 2016;74:737–48. 10.1093/nutrit/nuw045
    1. Cancer Research UK. Cancer survival statistics. (accessed 10 Jun 2017).
    1. Reedy J, Wirfält E, Flood A, et al. . Comparing 3 dietary pattern methods--cluster analysis, factor analysis, and index analysis-With colorectal cancer risk: The NIH-AARP Diet and Health Study. Am J Epidemiol 2010;171:479–87. 10.1093/aje/kwp393
    1. Guenther PM, Reedy J, Krebs-Smith SM. Development of the Healthy Eating Index-2005. J Am Diet Assoc 2008;108:1896–901. 10.1016/j.jada.2008.08.016
    1. Guenther PM, Reedy J, Krebs-Smith SM, et al. . Evaluation of the Healthy Eating Index-2005. J Am Diet Assoc 2008;108:1854–64. 10.1016/j.jada.2008.08.011
    1. Chiuve SE, Fung TT, Rimm EB, et al. . Alternative dietary indices both strongly predict risk of chronic disease. J Nutr 2012;142:1009–18. 10.3945/jn.111.157222
    1. Inoue-Choi M, Lazovich D, Prizment AE, et al. . Adherence to the World Cancer Research Fund/American Institute for Cancer Research recommendations for cancer prevention is associated with better health-related quality of life among elderly female cancer survivors. J Clin Oncol 2013;31:1758–66. 10.1200/JCO.2012.45.4462
    1. Catsburg C, Miller AB, Rohan TE. Adherence to cancer prevention guidelines and risk of breast cancer. Int J Cancer 2014;135:2444–52. 10.1002/ijc.28887
    1. Kant AK, Schatzkin A, Graubard BI, et al. . A prospective study of diet quality and mortality in women. JAMA 2000;283:2109–15. 10.1001/jama.283.16.2109
    1. Haines PS, Siega-Riz AM, Popkin BM. The Diet Quality Index revised: a measurement instrument for populations. J Am Diet Assoc 1999;99:697–704. 10.1016/S0002-8223(99)00168-6
    1. Fung TT, Chiuve SE, McCullough ML, et al. . Adherence to a DASH-style diet and risk of coronary heart disease and stroke in women. Arch Intern Med 2008;168:713 10.1001/archinte.168.7.713
    1. Olsen A, Egeberg R, Halkjær J, et al. . Healthy aspects of the Nordic diet are related to lower total mortality. J Nutr 2011;141:639–44. 10.3945/jn.110.131375
    1. Fung TT, Kashambwa R, Sato K, et al. . Post diagnosis diet quality and colorectal cancer survival in women. PLoS One 2014;9:e115377 10.1371/journal.pone.0115377
    1. Kim EH, Willett WC, Fung T, et al. . Diet quality indices and postmenopausal breast cancer survival. Nutr Cancer 2011;63:381–8. 10.1080/01635581.2011.535963
    1. McCullough ML, Willett WC. Evaluating adherence to recommended diets in adults: the Alternate Healthy Eating Index. Public Health Nutr 2006;9:152–7. 10.1079/PHN2005938
    1. Sofi F, Macchi C, Abbate R, et al. . Mediterranean diet and health status: an updated meta-analysis and a proposal for a literature-based adherence score. Public Health Nutr 2014;17:2769–82. 10.1017/S1368980013003169
    1. Schwingshackl L, Hoffmann G. Diet quality as assessed by the Healthy Eating Index, the Alternate Healthy Eating Index, the dietary approaches to stop hypertension score, and health outcomes: a systematic review and meta-analysis of cohort studies. J Acad Nutr Diet 2015;115:780–800. 10.1016/j.jand.2014.12.009
    1. Public Health England. The eatwell guide. 2017. (accessed 10 Jun 2017).
    1. Higgins JPT, Savović J, Hróbjartsson A, et al. . A revised tool for assessing risk of bias in randomized trials. Cochrane Database Syst Rev 2016:1–21. 10.1002/14651858.CD201601
    1. Sterne JA, Hernán MA, Reeves BC, et al. . ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ 2016;355:i4919 10.1136/bmj.i4919
    1. Guyatt GH, Oxman AD, Vist GE, et al. . GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ 2008;336:924–6. 10.1136/
    1. Moher D. PRISMA checklist PRISMA 2009 checklist. PLoS Med 2009;6:e1000097.
    1. Higgins JP, Savovic J, Page MJ, et al. . Revised Cochrane risk of bias tool for randomized trials (RoB 2.0). 2016;52.
    1. Sterne J, Higgins J, Reeves B, et al. . A tool for evaluating risk of bias in non- randomized studies of interventions (ROBINS-I): development and applications. 2015.
    1. Tang L, Zirpoli GR, Guru K, et al. . Intake of cruciferous vegetables modifies bladder cancer survival. Cancer Epidemiol Biomarkers Prev 2010;19:1806–11. 10.1158/1055-9965.EPI-10-0008
    1. Meyerhardt JA, Niedzwiecki D, Hollis D, et al. . Association of dietary patterns with cancer recurrence and survival in patients with stage III colon cancer. JAMA 2007;298:754 10.1001/jama.298.7.754
    1. Zhu Y, Wu H, Wang PP, et al. . Dietary patterns and colorectal cancer recurrence and survival: a cohort study. BMJ Open 2013;3:e002270 10.1136/bmjopen-2012-002270
    1. Pelser C, Arem H, Pfeiffer RM, et al. . Prediagnostic lifestyle factors and survival after colon and rectal cancer diagnosis in the National Institutes of Health (NIH)-AARP Diet and Health Study. Cancer 2014;120:1540–7. 10.1002/cncr.28573
    1. Ratjen I, Schafmayer C, di Giuseppe R, et al. . Postdiagnostic mediterranean and healthy nordic dietary patterns are inversely associated with all-cause mortality in long-term colorectal cancer survivors. J Nutr 2017;147:636–44. 10.3945/jn.116.244129
    1. Dik VK, Murphy N, Siersema PD, et al. . Prediagnostic intake of dairy products and dietary calcium and colorectal cancer survival--results from the EPIC cohort study. Cancer Epidemiol Biomarkers Prev 2014;23:1813–23. 10.1158/1055-9965.EPI-14-0172
    1. Romaguera D, Ward H, Wark PA, et al. . Pre-diagnostic concordance with the WCRF/AICR guidelines and survival in European colorectal cancer patients: a cohort study. BMC Med 2015;13:107 10.1186/s12916-015-0332-5
    1. Ward HA, Norat T, Overvad K, et al. . Pre-diagnostic meat and fibre intakes in relation to colorectal cancer survival in the European Prospective Investigation into Cancer and Nutrition. Br J Nutr 2016;116:316–25. 10.1017/S0007114516001859
    1. Yang B, McCullough ML, Gapstur SM, et al. . Calcium, vitamin D, dairy products, and mortality among colorectal cancer survivors: the Cancer Prevention Study-II Nutrition Cohort. J Clin Oncol 2014;32:2335–43. 10.1200/JCO.2014.55.3024
    1. Skeie G, Braaten T, Olsen A, et al. . Whole grain intake and survival among Scandinavian colorectal cancer patients. Nutr Cancer 2014;66:6–13. 10.1080/01635581.2014.847472
    1. Carr PR, Jansen L, Walter V, et al. . Associations of red and processed meat with survival after colorectal cancer and differences according to timing of dietary assessment. Am J Clin Nutr 2016;103:192–200. 10.3945/ajcn.115.121145
    1. McCullough ML, Gapstur SM, Shah R, et al. . Association between red and processed meat intake and mortality among colorectal cancer survivors. J Clin Oncol 2013;31:2773–82. 10.1200/JCO.2013.49.1126
    1. Chlebowski RT, Blackburn GL, Thomson CA, et al. . Dietary fat reduction and breast cancer outcome: interim efficacy results from the Women’s Intervention Nutrition Study. J Natl Cancer Inst 2006;98:1767–76. 10.1093/jnci/djj494
    1. Pierce JP, Natarajan L, Caan BJ, et al. . Influence of a diet very high in vegetables, fruit, and fiber and low in fat on prognosis following treatment for breast cancer. JAMA 2007;298:289–98. 10.1001/jama.298.3.289
    1. George SM, Irwin ML, Smith AW, et al. . Postdiagnosis diet quality, the combination of diet quality and recreational physical activity, and prognosis after early-stage breast cancer. Cancer Causes Control 2011;22:589–98. 10.1007/s10552-011-9732-9
    1. George SM, Ballard-Barbash R, Shikany JM, et al. . Better postdiagnosis diet quality is associated with reduced risk of death among postmenopausal women with invasive breast cancer in the women’s health initiative. Cancer Epidemiol Biomarkers Prev 2014;23:575–83. 10.1158/1055-9965.EPI-13-1162
    1. Izano MA, Fung TT, Chiuve SS, et al. . Are diet quality scores after breast cancer Diagnosis associated with improved breast cancer survival? Nutr Cancer 2013;65:820–6. 10.1080/01635581.2013.804939
    1. McCullough ML, Gapstur SM, Shah R, et al. . Pre- and postdiagnostic diet in relation to mortality among breast cancer survivors in the CPS-II Nutrition Cohort. Cancer Causes Control 2016;27:1303–14. 10.1007/s10552-016-0802-x
    1. Kroenke CH, Fung TT, Hu FB, et al. . Dietary patterns and survival after breast cancer diagnosis. J Clin Oncol 2005;23:9295–303. 10.1200/JCO.2005.02.0198
    1. Kwan ML, Weltzien E, Kushi LH, et al. . Dietary patterns and breast cancer recurrence and survival among women with early-stage breast cancer. J Clin Oncol 2009;27:919–26. 10.1200/JCO.2008.19.4035
    1. Vrieling A, Buck K, Seibold P, et al. . Dietary patterns and survival in German postmenopausal breast cancer survivors. Br J Cancer 2013;108:188–92. 10.1038/bjc.2012.521
    1. McEligot AJ, Largent J, Ziogas A, et al. . Dietary fat, fiber, vegetable, and micronutrients are associated with overall survival in postmenopausal women diagnosed with breast cancer. Nutr Cancer 2006;55:132–40. 10.1207/s15327914nc5502_3
    1. Dal Maso L, Zucchetto A, Talamini R, et al. . Effect of obesity and other lifestyle factors on mortality in women with breast cancer. Int J Cancer 2008;123:2188–94. 10.1002/ijc.23747
    1. Nechuta S, Caan BJ, Chen WY, et al. . Postdiagnosis Cruciferous vegetable consumption and breast cancer outcomes: a report from the after breast cancer pooling project. Cancer Epidemiol Biomarkers Prev 2013;22:1451–6. 10.1158/1055-9965.EPI-13-0446
    1. Holmes MD, Stampfer MJ, Colditz GA, et al. . Dietary factors and the survival of women with breast carcinoma. Cancer 1999;86:826–35. 10.1002/(SICI)1097-0142(19990901)86:5<826::AID-CNCR19>;2-0
    1. Kroenke CH, Kwan ML, Sweeney C, et al. . High- and low-fat dairy intake, recurrence, and mortality after breast cancer diagnosis. J Natl Cancer Inst 2013;105:616–23. 10.1093/jnci/djt027
    1. Beasley JM, Newcomb PA, Trentham-Dietz A, et al. . Post-diagnosis dietary factors and survival after invasive breast cancer. Breast Cancer Res Treat 2011;128:229–36. 10.1007/s10549-010-1323-z
    1. Buck K, Zaineddin AK, Vrieling A, et al. . Estimated enterolignans, lignan-rich foods, and fibre in relation to survival after postmenopausal breast cancer. Br J Cancer 2011;105:1151–7. 10.1038/bjc.2011.374
    1. Hebert JR, Hurley TG, Ma Y. The effect of dietary exposures on recurrence and mortality in early stage breast cancer. Breast Cancer Res Treat 1998;51:17–28. 10.1023/A:1006056915001
    1. Crosignani P, Russo A, Tagliabue G, et al. . Tobacco and diet as determinants of survival in male laryngeal cancer patients. Int J Cancer 1996;65:308–13. 10.1002/(SICI)1097-0215(19960126)65:3<308::AID-IJC5>;2-3
    1. Han X, Zheng T, Foss F, et al. . Vegetable and fruit intake and non-Hodgkin lymphoma survival in Connecticut women. Leuk Lymphoma 2010;51:1047–54. 10.3109/10428191003690364
    1. Leo QJ, Ollberding NJ, Wilkens LR, et al. . Nutritional factors and non-Hodgkin lymphoma survival in an ethnically diverse population: the Multiethnic Cohort. Eur J Clin Nutr 2016;70:41–6. 10.1038/ejcn.2015.139
    1. Yang M, Kenfield SA, Van Blarigan EL, et al. . Dietary Patterns after Prostate cancer diagnosis in relation to disease-specific and total mortality. Cancer Prev Res 2015;8:545–51. 10.1158/1940-6207.CAPR-14-0442
    1. Kenfield SA, DuPre N, Richman EL, et al. . Mediterranean diet and prostate cancer risk and mortality in the Health Professionals Follow-up Study. Eur Urol 2014;65:887–94. 10.1016/j.eururo.2013.08.009
    1. Chavarro JE, Stampfer MJ, Hall MN, et al. . A 22-y prospective study of fish intake in relation to prostate cancer incidence and mortality. Am J Clin Nutr 2008;88:1297–303.
    1. Yang M, Kenfield SA, Van Blarigan EL, et al. . Dairy intake after prostate cancer diagnosis in relation to disease-specific and total mortality. Int J Cancer 2015;137:2462–9. 10.1002/ijc.29608
    1. Wiseman M. The second World Cancer Research Fund/American Institute for Cancer Research expert report. Food, nutrition, physical activity, and the prevention of cancer: a global perspective. Proc Nutr Soc 2008;67:253–6. 10.1017/S002966510800712X
    1. Hardy TM, Tollefsbol TO. Epigenetic diet: impact on the epigenome and cancer. Epigenomics 2011;3:503–18. 10.2217/epi.11.71
    1. Daniel M, Tollefsbol TO. Epigenetic linkage of aging, cancer and nutrition. J Exp Biol 2015;218:59–70. 10.1242/jeb.107110

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