Abstract
Purpose
Post-diagnostic coffee and tea consumption and prostate cancer progression is understudied.
Methods
We examined 1,557 men from the Cancer of the Prostate Strategic Urologic Research Endeavor who completed a food frequency questionnaire a median of 28 months post-diagnosis. We estimated associations between post-diagnostic coffee (total, caffeinated, decaffeinated) and tea (total, non-herbal, herbal) and risk of prostate cancer progression (recurrence, secondary treatment, bone metastases, or prostate cancer death) using Cox proportional hazards regression. We also examined whether smoking (current, former, never) modified these associations.
Results
We observed 167 progression events (median follow-up 9 years). Higher coffee intake was associated with higher risk of progression among current smokers (n = 95). The hazard ratio (HR) [95% confidence interval (CI)] for 5 vs 0 cups/day of coffee was 0.5 (CI 0.2, 1.7) among never smokers, but 4.5 (CI 1.1, 19.4) among current smokers (p-interaction: 0.001). There was no association between total coffee intake and prostate cancer progression among never and former smokers. However, we observed an inverse association between decaffeinated coffee (cups/days) and risk of prostate cancer progression in these men (HR > 0 to < 1 vs 0: 1.1 (CI 0.7, 1.8); HR1 to <2 vs 0: 0.7 (CI 0.3, 1.4); HR≥2 vs 0: 0.6 (CI 0.3, 1.1); p-trend = 0.03). There was no association between tea and prostate cancer progression, overall or by smoking status.
Conclusion
Among non-smoking men diagnosed with localized prostate cancer, moderate coffee and tea consumption was not associated with risk of cancer progression. However, post-diagnostic coffee intake was associated with increased risk of progression among current smokers.
Similar content being viewed by others
Availability of data and materials
Data may be available for replication or meta-analyses upon request.
Code availability
Code may be available for replication or meta-analyses upon request.
References
Siegel RL, Miller KD, Jemal A (2020) Cancer statistics. CA Cancer J Clin 70(1):7–30
Wilson KM, Kasperzyk JL, Rider JR, Kenfield S, van Dam RM, Stampfer MJ, Giovannucci E, Mucci LA (2011) Coffee consumption and prostate cancer risk and progression in the Health Professionals Follow-up Study. J Natl Cancer Inst 103(11):876–884
Grosso G, Godos J, Galvano F, Giovannucci EL (2017) Coffee, caffeine, and health outcomes: an umbrella review. Annu Rev Nutr 37:131–156
Pounis G, Tabolacci C, Costanzo S, Cordella M, Bonaccio M, Rago L, D’Arcangelo D, Filippo Di Castelnuovo A, de Gaetano G, Donati MB, Iacoviello L, Facchiano F, Moli-sani study i (2017) Reduction by coffee consumption of prostate cancer risk: evidence from the Moli-sani cohort and cellular models. Int J Cancer 141(1):72–82
Geybels MS, Neuhouser ML, Wright JL, Stott-Miller M, Stanford JL (2013) Coffee and tea consumption in relation to prostate cancer prognosis. Cancer Causes Control 24(11):1947–1954
Bhathena SJ, Velasquez MT (2002) Beneficial role of dietary phytoestrogens in obesity and diabetes. Am J Clin Nutr 76(6):1191–1201
Bidel S, Hu G, Sundvall J, Kaprio J, Tuomilehto J (2006) Effects of coffee consumption on glucose tolerance, serum glucose and insulin levels—a cross-sectional analysis. Horm Metab Res 38(1):38–43
Arnlov J, Vessby B, Riserus U (2004) Coffee consumption and insulin sensitivity. JAMA 291(10):1199–1201
Leung LK, Su Y, Chen R, Zhang Z, Huang Y, Chen ZY (2001) Theaflavins in black tea and catechins in green tea are equally effective antioxidants. J Nutr 131(9):2248–2251
Beltz LA, Bayer DK, Moss AL, Simet IM (2006) Mechanisms of cancer prevention by green and black tea polyphenols. Anticancer Agents Med Chem 6(5):389–406
Lin YW, Hu ZH, Wang X, Mao QQ, Qin J, Zheng XY, Xie LP (2014) Tea consumption and prostate cancer: an updated meta-analysis. World J Surg Oncol 12:38
Gregg JR, Lopez DS, Reichard C, Zheng J, Wu W, Ye Y, Chapin B, Kim J, Daniel CR, Davis J (2019) Coffee, caffeine metabolism genotype and disease progression in patients with localized prostate cancer managed with active surveillance. J Urol 201(2):308–314
Klesges RC, Ray JW, Klesges LM (1994) Caffeinated coffee and tea intake and its relationship to cigarette smoking: an analysis of the Second National Health and Nutrition Examination Survey (NHANES II). J Subst Abuse 6(4):407–418
Istvan J, Matarazzo JD (1984) Tobacco, alcohol, and caffeine use: a review of their interrelationships. Psychol Bull 95(2):301–326
Huncharek M, Haddock KS, Reid R, Kupelnick B (2010) Smoking as a risk factor for prostate cancer: a meta-analysis of 24 prospective cohort studies. Am J Public Health 100(4):693–701
Lubeck DP, Litwin MS, Henning JM, Stier DM, Mazonson P, Fisk R, Carroll PR (1996) The CaPSURE database: a methodology for clinical practice and research in prostate cancer. CaPSURE Research Panel. Cancer of the Prostate Strategic Urologic Research Endeavor. Urology 48(5):773–777
Hu FB, Rimm E, Smith-Warner SA, Feskanich D, Stampfer MJ, Ascherio A, Sampson L, Willett WC (1999) Reproducibility and validity of dietary patterns assessed with a food-frequency questionnaire. Am J Clin Nutr 69(2):243–249
Rimm EB, Giovannucci EL, Stampfer MJ, Colditz GA, Litin LB, Willett WC (1992) Reproducibility and validity of an expanded self-administered semiquantitative food frequency questionnaire among male health professionals. Am J Epidemiol 135(10):1114–1126; discussion 1127–1136
Feskanich D, Rimm EB, Giovannucci EL, Colditz GA, Stampfer MJ, Litin LB, Willett WC (1993) Reproducibility and validity of food intake measurements from a semiquantitative food frequency questionnaire. J Am Diet Assoc 93(7):790–796
Richman EL, Stampfer MJ, Paciorek A, Broering JM, Carroll PR, Chan JM (2010) Intakes of meat, fish, poultry, and eggs and risk of prostate cancer progression. Am J Clin Nutr 91(3):712–721
Cao S, Liu L, Yin X, Wang Y, Liu J, Lu Z (2014) Coffee consumption and risk of prostate cancer: a meta-analysis of prospective cohort studies. Carcinogenesis 35(2):256–261
Discacciati A, Orsini N, Wolk A (2014) Coffee consumption and risk of nonaggressive, aggressive and fatal prostate cancer—a dose-response meta-analysis. Ann Oncol 25(3):584–591
Kenfield SA, Stampfer MJ, Chan JM, Giovannucci E (2011) Smoking and prostate cancer survival and recurrence. JAMA 305(24):2548–2555
Furstenberger G, Senn HJ (2002) Insulin-like growth factors and cancer. Lancet Oncol 3(5):298–302
Hammarsten J, Hogstedt B (2005) Hyperinsulinaemia: a prospective risk factor for lethal clinical prostate cancer. Eur J Cancer 41(18):2887–2895
Lehrer S, Diamond EJ, Stagger S, Stone NN, Stock RG (2002) Increased serum insulin associated with increased risk of prostate cancer recurrence. Prostate 50(1):1–3
Hsing AW, Chua S Jr, Gao YT, Gentzschein E, Chang L, Deng J, Stanczyk FZ (2001) Prostate cancer risk and serum levels of insulin and leptin: a population-based study. J Natl Cancer Inst 93(10):783–789
Alpha-Tocopherol BCCPSG (1994) The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med 330(15):1029–1035
Substance Abuse and Mental Health Services Administration, Results from the 2016 National Survey on Drug Use and Health: Detailed Tables. https://www.samhsa.gov/data/sites/default/files/NSDUH-DetTabs-2016/NSDUH-DetTabs-2016.pdf. Published 2017. Accessed 8 Apr 2020
Fryar CD, Kruszon-Moran D, Gu Q, Ogden CL (2018) Mean body weight, height, waist circumference, and body mass index among adults: United States, 1999–2000 through 2015–2016. National Health Statistics Reports; no 122. National Center for Health Statistics, Hyattsville, MD
Acknowledgements
The authors would like to thank the participants of CaPSURE, who made this research possible, and the research team who diligently worked to ensure data quality.
Funding
CSL is supported by the National Institutes of Health/National Cancer Institute (F31CA247093) and the UCSF Prostate Cancer Program Pilot Award. JMC is funded by the Steven & Christine Burd-Safeway Distinguished Professorship award. SAK is funded by the Helen Diller Family Chair in Population Science for Urologic Cancer. EVB is supported by the National Institutes of Health/National Cancer Institute (K07CA197077). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. CaPSURE is funded by the United States Department of Defense Prostate Cancer Research Program (W81XWH-13-2-0074 and W81XWH-04-1-0850).
Author information
Authors and Affiliations
Contributions
Conceptualization: CSL, JMC, SAK, ELVB; Data Curation: JEC, JMB; Formal Analysis: CSL; Funding Acquisition: JMC, PC, ELVB; Methodology: CSL, JMC, SAK, REG, ELVB; Supervision: ELVB; Visualization; CSL, JMC, SAK, REG, ELVB; Writing-Original Draft: CSL; Writing-Review & Editing: All authors.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
The study obtained institutional review board (IRB) approval and the study was conducted in accordance with the Belmont Report and U.S. Common Rule under local IRB supervision.
Informed consent
Informed consent was obtained from all individual participants included in the study.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Langlais, C.S., Chan, J.M., Kenfield, S.A. et al. Post-diagnostic coffee and tea consumption and risk of prostate cancer progression by smoking history. Cancer Causes Control 32, 635–644 (2021). https://doi.org/10.1007/s10552-021-01417-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10552-021-01417-1