Abstract
Purpose of Review
This study aimed to summarize evidence published between 1999 and June 2020 examining diet and lifestyle after prostate cancer (PC) diagnosis in relation to risk of biochemical recurrence, PC progression, and PC-specific mortality.
Recent Findings
Secondary prevention is an important research area in cancer survivorship. A growing number of studies have reported associations between post-diagnostic modifiable behaviors and risk of PC outcomes.
Summary
Evidence on modifiable lifestyle factors and PC remains limited. Where multiple studies exist, findings are often mixed. However, studies consistently suggest that smoking and consumption of whole milk/high-fat dairy are associated with higher risk of PC recurrence and mortality. In addition, physical activity and ½ to 1 glass of red wine/day have been associated with lower risk of recurrence and PC-specific mortality. Greater inclusion of racially/ethnically diverse groups in future research is necessary to understand these relationships in populations most impacted by adverse PC outcomes.
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Introduction
Prostate cancer (PC) is the second most common malignancy diagnosed among men worldwide, with an estimated 1.3 million diagnoses worldwide in 2018 [1]. Despite its relatively high survival rate, it remains the fifth most common cause of cancer-related death among men worldwide, with 358,989 deaths reported in 2018. Moreover, it is the leading cancer-related cause of death in men in 46 countries [1]. The varying disease courses PC can take underscore its heterogeneity in presentation and prognosis and highlight the importance of secondary prevention. Over the past two decades, there has been a growing interest in identifying modifiable factors, such as diet and lifestyle factors, associated with overall health, disease progression, and mortality among men with PC.
Methods
In this review, we summarize findings from studies evaluating associations of post-diagnostic dietary and lifestyle (e.g., physical activity, body size, smoking) behaviors with PC recurrence, progression, and mortality; highlight important new research; and discuss where additional research is needed. We focused on observational studies to complement a recent review of randomized trials on this topic [2•]. Although focused on literature from the last 5 years, additional studies from the past two decades provide further context. We used the search terms “prostate cancer”, “progression”, and “mortality” in combination with each dietary or lifestyle factor (see subsection headers below) to search PubMed for articles published through June 22, 2020. Papers that examined all-cause mortality (ACM) were included if a PC-specific outcome (recurrence/progression, PC-specific mortality (PCSM)) was also evaluated. A single author (CSL) reviewed titles and abstracts of 1894 returns and identified 168 unique articles for further review. Eighty-three were deemed relevant, 33 of which were published between 2015 and 2020. Most common reasons for exclusion included exposure assessment prior to diagnosis and lacking assessment of any of the outcomes of interest.
Given known racial/ethnic disparities in PC, including a greater mortality burden among African-American/Black (AA/B) men, we assessed the race/ethnicity distributions of the populations studied. Table 1 summarizes characteristics of the studies reviewed, stratified by exposure. Table 2 summarizes the findings of all included observational studies. Where relevant, we supplement our discussion with findings from randomized trials [2•].
Diet
Fish
Five studies published between 2006 and 2020 examined post-diagnostic fish intake in relation to PC outcomes, three of which considered recurrence or progression [4, 6, 7]. One of these, a study of 1202 men with non-metastatic PC from the Health Professionals Follow-up Study (HPFS), observed evidence of an inverse association in models adjusted for pre-diagnostic fish intake (hazard ratio (HR) for 1 serving/day increase: 0.52, p = 0.006; 95% confidence interval (CI) unavailable) [7]. The other two—a study of 940 men with stage ≤ T3 PC from Washington University and a study of 1294 men with localized/regional disease from the Cancer of the Prostate Strategic Urologic Research Endeavor (CaPSURE™)—observed no association [4, 6]. However, the Washington University study reported a statistically significant inverse association for recurrence when modeling the substitution of fish/poultry for red meat [4]. The remaining two studies examined PCSM and ACM and observed no statistically significant associations for fish intake, though one of these reported a borderline statistically significant inverse trend per 1 standard deviation (SD) of greater fish intake and ACM (HR: 0.90; CI: 0.80 to 1.01; p = 0.08) [3, 5]. No study reported an elevated risk of adverse PC outcomes with fish intake. In summary, evidence that fish intake following PC diagnosis is associated with PC outcomes is very limited.
Meat, Poultry, and Eggs
Three studies conducted between 2006 and 2016 considered post-diagnostic consumption of meat, poultry, and eggs in relation to recurrence/progression and observed no associations with total poultry or total, processed, or unprocessed red meat (Table 2) [4, 6, 7]. A study of 1294 men with localized/regional PC in CaPSURE observed a positive association between poultry with skin and risk of PC progression (HRtertile3 vs 1: 2.26; CI: 1.36, 3.76; p trend = 0.003) [6]. This study also observed a borderline statistically significant association with egg intake (HRquartile 4 vs 1: 2.02; CI: 1.10, 3.72; p trend = 0.05), which was not replicated by a later study of 940 men from Washington University [4].
Three studies examined post-diagnostic intake of meat, poultry, and eggs with respect to PCSM, with mostly null results [3, 5, 8]. However, a study of 4882 men with non-metastatic PC from the Cancer Prevention Study-II Nutritional Cohort (CPS-II) reported an inverse relationship with unprocessed red meat (HRquartile 4 vs 1: 0.64; CI: 0.46, 0.91; p trend = 0.01) [3]; while a study of 926 men with non-metastatic PC from the Physicians’ Health Study (PHS) observed a higher risk per 1 SD increase in processed meats (HR: 1.32; CI: 1.06, 1.64; p = 0.01) [5].
Two studies examining PCSM also examined ACM, with mixed findings (Table 2) [3, 5]. In the PHS, there was a higher risk per 1 SD increase in intake of processed meats (HR: 1.17; CI: 1.06, 1.30; p = 0.003) and eggs (HR: 1.12; CI: 1.02, 1.24; p = 0.02), but no association with total red meat [5]. Conversely, the CPS-II study observed an association with total red meat (HRquartile 4 vs 1: 1.22; CI: 1.07, 1.39; p trend = 0.03), but not with eggs [3]. Furthermore, despite not demonstrating a statistically significant trend, each upper quartile (Q) of processed red meat intake in CPS-II had a higher risk of ACM compared to Q1 (HRQ4: 1.17; CI: 1.04, 1.33. HRQ3: 1.15; CI: 1.02, 1.30. HRQ2: 1.14; CI: 1.01, 1.28; p trend = 0.07) [3]. This study also reported an inverse association with total poultry and ACM (HRQ4: 0.84; CI: 0.75, 0.95; p trend = 0.01), which was not examined in the PHS.
In summary, recommendations on post-diagnostic meat, poultry, or egg intake specifically for PC outcomes cannot be made due to lack of concordance across a limited number of studies. However, based on national guidelines for general and cardiovascular health, it is prudent to limit consumption of processed meat and select lean choices of meat or skinless poultry [86, 87].
Dairy
Three studies conducted between 2006 and 2018 considered post-diagnostic dairy intake in relation to PC recurrence or progression [7, 9, 11]. Where there was overlap in exposures examined, studies agreed. Studies in CaPSURE and HPFS both found no association with total, high-fat, or low-fat dairy, but reported positive associations between > 4 servings/week vs 0–3 servings/month of whole milk and risk of progression (HR: 1.73; CI: 1.00, 2.98; p trend = 0.04. HR: 1.51; CI: 1.03, 2.20; p trend = 0.03) [9, 11]. Two studies from the HPFS found no association between total milk and risk of PC progression [7, 11], although one of these noted a positive association in models adjusting for pre-diagnostic intake (HRcontinuous: 1.12, p = 0.04, CI unavailable) [7]. Table 2 shows various other dairy items that were examined by a single study [9].
Three studies examined post-diagnostic dairy intake and PCSM (Table 2) [5, 10, 11]. While results for most subcategories of dairy were null, there were consistent positive associations for whole milk. One of these, a study of 3918 men with localized/locally advanced PC from the HPFS, observed a relationship with > 4 serving/week vs 0–3 servings/month of whole milk (HR: 2.15; CI: 1.28, 3.60; p trend < 0.01) [11]. A population-based study of 525 Swedish men did not observe this association in the full cohort but replicated this finding for ≥ 3 vs < 1 serving/day of high-fat milk among 230 men diagnosed with localized disease (HR: 4.86; CI: 1.52, 15.57; p trend = 0.003) [10].
Two studies examining PCSM also examined ACM; both observed an association with high-fat dairy intake (HR1 SD increase: 1.18; CI: 1.07, 1.30; p = 0.001. HR ≥ 4.5 serv/day : 1.04; CI: 0.73, 1.49; HR3–< 4.5 serv/day: 0.82; CI: 0.58, 1.17; HR1–< 3 serv/day: 0.75; CI: 0.53 to 1.04 vs < 1 serv/day; p trend = 0.05) [5, 10]. Effect modification was observed in the Swedish cohort based on stage at diagnosis and milk type. There was a positive association for servings/day of high-fat milk (HR ≥ 3 vs < 1: 3.32; CI: 1.85, 5.97; p trend = 0.001) among men diagnosed with localized PC, while low-fat milk was positively associated with ACM among 295 men diagnosed with advanced PC (HR ≥ 2 vs < 1: 1.72; CI: 1.14, 2.57; p trend = 0.02) [10].
In summary, men should limit whole milk to < 4 servings/week following a PC diagnosis to minimize risk of progression and PCSM. Limiting high-fat dairy is also advised, and consistent with heart-healthy diet recommendations, to decrease risk of ACM following PC diagnosis.
Dietary Fats
Five studies examined post-diagnostic dietary fats in relation to PC outcomes, with only one published in the last 5 years [12,13,14,15,16]. Only one, a study of 390 men who underwent radical prostatectomy (RP), examined risk of recurrence and reported a higher risk associated with saturated fat (HRQ4 vs Q1–3: 1.90; CI: 1.16, 3.11; p value unavailable) [15].
Four studies examined specific types of dietary fat (Table 2) with respect to PCSM [12,13,14, 16]. Studies agreed that there was no association with monounsaturated, polyunsaturated, trans, or animal fat intake. Two studies also examined total dietary fat and found no association, although one—a Swedish study of 525 men—reported a positive trend between total dietary fat and risk of PCSM among the subgroup of men diagnosed with localized PC (HRQ4 vs Q1: 2.07; CI: 0.93, 4.59; p trend = 0.03) [14, 16]. There was mixed evidence regarding saturated and vegetable fat intake. Two studies—a Canadian study of 384 men and a study of 926 men with non-metastatic PC in the PHS—observed a relationship with saturated fat intake (HRtertile 3 vs 1: 3.1; CI: 1.3, 7.7; p trend = 0.008; HR for 5% caloric exchange of saturated fat for carbohydrates: 2.78; CI: 1.01, 7.64; p = 0.05) [12, 16]. Two other studies reported no statistically significant relationships between post-diagnostic saturated fat and risk of PCSM [13, 14]. Regarding vegetable fat, a study of 4577 men with non-metastatic PC from the HPFS observed an inverse relationship with PCSM (HR for 10% caloric exchange of vegetable fat for carbohydrate: 0.71; CI: 0.51, 0.98; p = 0.04), whereas the PHS analysis did not observe a statistically significant association [12, 13].
Two studies considered ACM with mixed results [12, 13]. Both observed no association with monounsaturated or animal fat, but an inverse association with vegetable fat (PHS HRQ4 v Q1: 0.65; CI: 0.45, 0.93; p trend = 0.03; HPFS HRquintile5 vs 1: 0.65; CI: 0.52, 0.83; p trend < 0.001) and a positive association with saturated fat (PHS HR for 5% caloric exchange of saturated fat for carbohydrate: 1.81; CI: 1.20, 2.74; p = 0.005; HPFS HR for 5% caloric exchange of saturated fat for carbohydrate: 1.30; CI: 1.05, 1.60; p = 0.02) [12, 13]. The HPFS also observed an inverse relationship between polyunsaturated fat and ACM (HRquintile 5 vs 1: 0.73; CI: 0.57, 0.94; p trend = 0.004) and a positive association with trans fat (HRquintile 5 vs 1: 1.51; CI: 1.14, 2.01; p trend = 0.002) [13]. The PHS observed no associations with polyunsaturated or trans fats [12].
Overall, diets with higher saturated fat may increase risk of PC recurrence and mortality. Replication of findings for vegetable, polyunsaturated, and trans fats with mortality outcomes is needed, though findings are consistent with recommendations for overall health [86, 87].
Vegetables: Tomato (Lycopene), Cruciferous
We identified three studies that considered post-diagnostic tomato intake in relation to PC outcomes [5, 7, 17]. Two of these evaluated tomatoes in relation to risk of PC progression with inconsistent findings. The first, a study of 1560 men with non-metastatic PC from CaPSURE, found no statistically significant association with either fresh tomatoes or tomato sauce [17]. In contrast, a study of 1202 men with localized/regional PC from the HPFS reported an inverse association with tomato sauce (HR1 serving/day: 0.46, p = 0.04, CI unavailable) and a positive association with fresh tomato intake (HR1 serving/day: 1.27, p = 0.02, CI unavailable) [7]. However, associations were attenuated and neither was statistically significant when pre-diagnostic intake was excluded from the models [7]. Clinical trials have reported that supplemental lycopene is associated with return to normal PSA and normal bone scans in men with metastatic PC treated with orchiectomy [2]. Lycopene concentrations are higher in cooked than raw tomatoes, which may explain why a protective association is only observed for cooked tomatoes.
A single study of 926 men with non-metastatic disease in the PHS examined PCSM and ACM and found no association between tomato intake as part of a prudent diet and risk of PCSM or ACM [5].
Two observational studies examined cruciferous vegetables [5, 17]. CaPSURE reported an inverse association between cruciferous vegetable intake and risk of PC progression (HRQ4 vs Q1: 0.41; CI: 0.22, 0.76; p trend = 0.003) [17]. The PHS found no association with either PCSM or ACM [5].
Recent findings from the Men’s Eating and Living (MEAL) trial warrant discussion. MEAL randomized 443 men with low-risk PC on active surveillance to receive counseling promoting consumption of ≥ 7 vegetable-fruit servings/day, including at least two servings each of cruciferous vegetables and tomatoes [88]. During the 2-year intervention, 245 events of progression were observed. Though the intervention modestly increased daily servings of cruciferous vegetables (between group difference at 24 months: 0.49; CI: 0.33 to 0.64; p < 0.01) and tomatoes (between group differences at 24 months: 0.14; CI: 0.03, 0.26; p = 0.02), it did not affect risk of disease progression.
Overall, results for post-diagnostic intake of tomatoes/lycopene and cruciferous vegetables and PC outcomes are inconsistent. Nonetheless, it is prudent to encourage PC survivors to include a wide variety of vegetables in their diet for weight management and risk reduction for many chronic diseases, including diabetes and cardiovascular disease [86, 87].
Alcohol
Two studies examined post-diagnostic alcohol consumption and PC outcomes [18, 19]. Only one, a Canadian study of 829 men with ≥ T2 disease, considered recurrence, and observed no association with total alcohol [19].
When examining PCSM, the two studies agreed there was no association for overall trend of total alcohol or liquor intake. However, the Canadian study observed a positive association with moderate intake of liquor in analyses excluding non-drinkers (HR≥ 3.7 vs > 0–< 0.9 drinks/week: 2.41; CI: 1.20, 4.84; p trend = 0.01) [19]. Conflicting findings were reported for other types of alcohol. A study of 5182 men with non-metastatic PC from the HPFS observed a borderline statistically significant positive association with beer intake (HR≥ 7 vs 0 serving/week: 2.64; CI: 0.58, 12.06; p trend = 0.05) and an inverse association with moderate total wine intake (HR3–< 7 vs 0 serving/week: 0.53; CI: 0.26, 1.07; p trend = 0.03), which appeared to be driven by red wine (HR3–< 7 vs 0: 0.49; CI: 0.25, 0.97; p trend = 0.05) [18]. Notably, the inverse association was not observed among men with higher levels of wine intake. The Canadian study found no evidence that total wine or beer were associated with PCSM [19].
Both studies also examined ACM and found no association with post-diagnostic total alcohol, beer, or liquor intake [18, 19]. However, the Canadian study observed an association with total alcohol (HR≥ 2 vs > 0–< 2 drinks/day: 1.45; CI: 1.06, 2.00; p = 0.02) and liquor (HR≥ 3.7 vs > 0–< 0.9 drinks/week: 1.82; CI: 1.20, 2.79; p trend = 0.01) in analyses excluding non-drinkers [19]. The HPFS found an inverse association with 3–< 7 vs 0 servings/week of red wine (HR: 0.64; CI: 0.45, 0.90; p trend = 0.007) and total wine (HR: 0.57; CI: 0.40, 081; p trend = 0.08), though overall trend for the latter did not reach statistical significance [18]. The Canadian study also observed an inverse association with moderate total wine intake (HR0.2–< 0.9 vs 0 drinks/week: 0.60; CI: 0.46, 0.79; p trend = 0.01) that was not observed at higher levels of wine consumption [19].
The limited data among PC survivors suggests a potential benefit of red wine at modest intake levels (1/2–1 serving/day). Men should limit total alcohol consumption to ≤ 2 drinks/day, as excess alcohol damages the heart, liver, and pancreas; increases risk of other cancers (including head and neck, esophageal, liver, and colorectal); and weakens the immune system [89]. This aligns with recommendations from many cancer control agencies [1, 90, 91].
Supplements or Single-Nutrient Intake from Diet
Selenium
A single study within the HPFS examined selenium supplements (mg/day) and PC outcomes and found an increased risk of PCSM (HR≥ 140: 2.60; CI: 1.44, 4.70. HR25–139: 1.33; CI: 0.77, 2.30. HR1–24: 1.18; CI: 0.73, 1.91 vs 0; p trend = 0.001), but no association with recurrence or ACM [21].
Vitamin D
Three studies examined vitamin D (dietary intake or serum level) and PC outcomes [10, 20, 22]. Only one, a study of 1476 men from Seattle, examined recurrence/progression and found no association with serum 25(OH)D [22]. All three studies examined PCSM and reported no association with serum level or dietary vitamin D intake [10, 20, 22]. Two of the studies examined ACM outcomes [10, 20]. One, a study of 1119 men from New South Wales, reported an increased risk of ACM among men with higher levels of 1,25(OH)2D (HRQ4 vs Q1: 0.45; CI: 0.29, 0.69; p trend = 0.005) [20]. The other, a study of 525 Swedish men, observed no association between dietary intake of vitamin D and ACM [10].
Calcium and Phosphorous
A single study from Sweden considered both dietary calcium and phosphorous intake and observed no association with either PCSM or ACM [10].
Overall, evidence on dietary supplement use or single-nutrient intake and risk of PC recurrence or mortality is limited. Additional studies are needed to confirm the finding that selenium supplementation is associated with an increased risk of PCSM. Men with PC should follow the recommendations of the American Institute for Cancer Research and the World Cancer Research Fund and aim to meet nutritional needs through diet alone [90, 91].
Obesity
Obesity is among the most extensively studied potential risk factor among men with PC, and the evidence is inconsistent. Regarding recurrence/progression outcomes reported between 2015 and 2020, six studies observed no association with body mass index (BMI) [25,26,27, 31,32,33], while three reported a positive association [28, 30, 34]. A report by our team attempted to clarify the discrepancies in past studies by examining adjustment for clinical and, separately, pathological characteristics in a population of men undergoing RP from CaPSURE [27]. We hypothesized that residual confounding by disease stage may partially explain positive associations reported between BMI at the time of diagnosis and risk of recurrence. We observed that with adjustment for disease severity using metrics from diagnosis (biopsy) only, there was evidence of a positive relationship between very obese men (BMI ≥ 35 kg/m2) and risk of recurrence [27]. However, when we controlled for surgical pathology characteristics, the observed association was no longer statistically significant. Consistent with our finding, two of the three studies that found an association between BMI and risk of recurrence did not adjust for pathologic features [30, 34]. Four of the six studies that reported no association adjusted for pathologic features [25,26,27, 32]. Such data suggest that obesity influences tumor aggressiveness earlier in the natural history of prostate cancer and are consistent with a larger body of evidence implicating pre-diagnosis BMI in healthy populations and risk of fatal prostate cancer [92].
Seven studies published between 2015 and 2020 examined BMI and PCSM [23, 24, 26, 29,30,31, 34]. Only one—a study of 1442 men treated with intensity modulated radiation therapy for localized disease, and therefore lacking pathologic measures of disease severity—observed an association (HRcontinuous: 1.15; CI: 1.07, 1.23; p < 0.001) [34]. Three additional studies published before 2015 also reported a positive association, only one of which controlled for pathologic metrics [57,58,59]. The two studies that considered waist circumference and waist-to-hip ratio found no association [23, 29].
Five studies published between 2015 and 2020 examined BMI and ACM with mixed results [23, 24, 27, 29, 34]. Three of these reported a higher risk associated with higher BMI (HR≥ 35 vs 18.5–25: 1.70 (1.12, 2.60), p trend = 0.001. HRcontinuous: 1.05; CI: 1.02, 1.08; p = 0.004. HRper 5-unit: 1.07; CI; 1.02, 1.12; p = 0.01) [24, 27, 34]. The two others observed no associations with BMI, waist circumference, or waist-to-hip ratio [23, 29]. There were numerous older studies that reported similarly null findings between BMI and ACM among men with PC (Table 2).
Evidence is mixed regarding if obesity measured following a PC diagnosis is associated with worse PC outcomes, and further research is warranted regarding whether weight loss among PC survivors who are obese offers PC-specific benefits. Nonetheless, given the relationship of obesity with other chronic diseases, including other malignancies and heart disease, men should be counseled to reach and maintain a healthy weight.
Physical Activity
Multiple studies have examined various forms of post-diagnostic physical activity (PA) in relation to PC outcomes (Table 2). Only three of these considered recurrence/progression outcomes with mixed results [37, 40, 42]. Two examined different types of PA in the same cohort of 237 Canadian men on active surveillance [37, 40]. These studies demonstrated a lower odds of disease reclassification (OR > 92.27 vs < 46.62: 0.43; CI: 0.21, 0.88; p trend = 0.027) but not risk of progression, with higher MET-hour/week of total PA, as well as lower odds associated with vigorous PA (OR > 0 vs 0: 0.42; CI: 0.20, 0.85; p = 0.016) [37, 40]. In contrast, a CaPSURE analysis of 1455 men with localized disease found no association between vigorous PA and risk of PC progression. However, few men engaged in vigorous activity in this population, and brisk walking pace was associated with a statistically significant 57% lower risk of progression [42].
Six studies examined PA and PCSM with generally consistent findings of benefits for PA (Table 2) [35, 36, 38, 39, 41, 43]. A HPFS study of 2705 men with non-metastatic PC and a US-based study of 1354 men with localized disease reported an inverse association with vigorous PA (HR≥ 3 vs < 1 h/week: 0.39; CI: 0.18, 0.84; p trend = 0.03. HR≥ 1 vs < 1 time/week: 0.63; CI: 0.42, 0.95; p = 0.029) [36, 43]. A Canadian study of 830 men with stage ≥ T2 PC reported a 44% decreased risk for recreational PA and PCSM (> 26 vs ≤ 4 MET-hours/week, CI: 10–65%) [39]. An additional study in the CPS-II cohort similarly reported a statistically significant 31% decreased risk of PCSM associated with recreational PA [38]. A 2015 study of 4623 Swedish men with localized PC reported a 32% reduction in risk of PCSM for ≥ 1 vs < 1 h/week of exercise after diagnosis (CI 6–52%); a similar benefit was reported for walking/biking ≥ 20 vs < 20 min/day, but not for total recreational physical activity or household work [41]. While there has been variability in the type, duration, or intensity of PA associated with PCSM benefits, these reports suggest that PA offers benefit for reducing risk of PCSM.
Five studies examining PCSM also examined ACM and overwhelmingly reported an inverse relationship with PA [35, 38, 39, 41, 43]. The risk reduction comparing the highest to lowest PA categories were as follows: 42–62% for total PA, 35–49% for vigorous PA, 14–37% recreational PA, and 7–30% for walking/biking [38, 39, 41, 43].
In summary, there is strong evidence that increased PA following PC diagnosis is associated with lower risk of PCSM and ACM. The 2018 National PA Guidelines in the USA recommend that adults do ≥ 150 min/week of moderate-intensity or ≥ 75 min/week of vigorous-intensity aerobic PA. These guidelines report lower risk of PC mortality as a health benefit associated with regular PA for PC survivors [93•]. In addition, clinical trials have shown that PA improves bone mineral density and quality-of-life among men undergoing androgen deprivation therapy for PC [2•]. Considering the totality of evidence, we recommend that PC survivors engage in regular PA. Trials are underway to develop interventions to help men with PC meet PA goals, while considering a man’s current capabilities and health-related concerns (see Table 2 in ref. [2•]).
Smoking
Multiple studies have examined the relationship between smoking and PC recurrence/progression and PCSM (Table 2). There is overall agreement that men reporting smoking following diagnosis are at higher risk of recurrence/progression and PCSM compared to never smokers [44, 46, 47, 51,52,53, 55].
Some evidence exists that the duration of smoking cessation may affect the risk of PC outcomes among former smokers. Specifically, an Austrian study of 6538 men with localized PC reported that former smokers who had quit ≥ 10 years prior had a similar risk of recurrence as never smokers, but those who had quit < 10 years prior were at increased risk of recurrence [47]. Results from a US-based study of 752 men for the outcome of PCSM support this conclusion, though results did not reach statistical significance [52]. Limited data on former smoking duration and dose may account for the mixed evidence regarding whether former smokers are at an increased risk for poor PC outcomes [44, 46, 47, 51,52,53,54].
Fewer studies examined ACM outcomes [44, 48, 53, 56]. A Canadian study of 434 men with localized disease found no association between former or current smokers and ACM, though it was limited by a short follow-up period (median 70 months) [53]. As expected, all other studies found a statistically significant increased risk of death associated with smoking [44, 48, 56].
In summary, current smokers are at an increased risk of disease recurrence/progression, PCSM, and ACM. Men who smoke should be provided with resources to help them quit to improve their PC-specific prognosis and overall health.
Diversity of Study Populations
Race/Ethnicity
AA/B men experience higher rates of PC incidence and mortality than men of any other race/ethnicity. In the USA, the rate of PCSM is more than twofold higher in AA/B vs White men (40.8 vs 18.2 per 100,000 in AA/B and White men, respectively) [94]. Despite this fact, existing evidence on post-diagnostic modifiable risk factors has been collected almost exclusively in White populations. Characteristics of 33 recently published (2015–2020) studies are shown in Table 1; 13 did not report the racial/ethnic distribution of their study sample [10, 19, 21, 29, 32, 34, 35, 37, 38, 41, 45,46,47]. An additional seven dichotomized race as White/Caucasian vs other (all ≥ 92% White) [4, 5, 12, 18, 24, 31, 39]. Only six included ≥ 10% AA/B/African-Caribbean men [23, 26, 28, 30, 33, 44].
Few studies have examined whether the associations between lifestyle factors and risk of PC outcomes vary by race/ethnicity. The two that provided results stratified by race (AA/B vs White) both examined BMI as the primary exposure [26, 33]. The first was a study of 5929 (33% AA/B) men treated via RP that observed no association between BMI and PCSM or recurrence, overall or in either race/ethnicity stratum [26]. The other was a study of 647 men that reported a positive association between BMI ≥ 30 vs BMI < 30 with PC recurrence among the 363 White men (HR: 1.80; CI: 1.09, 2.96) but not among the 284 AA/B men (HR: 1.10; CI: 0.69, 1.76) [33].
Although limited, a few studies have identified mortality disparities among other underrepresented racial/ethnic minority populations. For example, Puerto Rican and Mexican American men may have an increased risk of PCSM compared to White men [95, 96]. Future studies should report race/ethnicity for their study population and test for effect modification by race/ethnicity when numbers allow. Deliberate and targeted recruitment of AA/B men and other high-risk populations into PC-related studies is crucial. In the interim, it should be a priority to identify existing data sources with a sufficient proportion of AA/B men and other underrepresented racial/ethnic minorities to begin to address these questions.
Education
We intended to examine educational attainment as a measure of socioeconomic status; however, only 10 of the 33 recent studies (2015–2020) reported education levels of their study populations [3, 9, 19, 23, 24, 33, 35, 36, 39, 41].
Cohorts
Most of what we know regarding diet and lifestyle following a PC diagnosis comes from a limited number of cohorts. Table 1 displays literature by exposure, consisting of 64 (non-unique) studies. The HPFS, CaPSURE, and PHS-II account for one-third (n = 22) of these (note, EVB, SAK, and JMC were authors on many of these papers). An additional 15% (n = 10) are from CPS-II, the Shared Equal Access Regional Cancer Hospital (SEARCH) database, and Royal Marsden Hospital. Finally, many of the exposures were examined by only a single study (Table 2), highlighting areas where replication and confirmation is needed.
Future Direction
In summary, research to date on post-diagnostic lifestyle factors and risk of PC recurrence and mortality has been limited to a few cohorts of predominately White men. Large cohorts that are racially/ethnically, geographically, and socio-demographically diverse are necessary to advance this field of research.
Conclusions
In this review, we focused on observational evidence of post-diagnostic modifiable diet and lifestyle factors in relation to PC outcomes. Though randomized trials are the gold standard for determining causation, many diet and lifestyle behaviors are not suitable/ethical (e.g., smoking) to randomization. Furthermore, long-term and slow-acting exposures may require extended follow-up periods to observe outcomes of interest, which may preclude study in a randomized setting. Overall, the evidence reviewed suggests that following a PC diagnosis, men should be counseled to increase physical activity and quit smoking, consistent with general health recommendations. Additionally, it may be prudent for men with PC to minimize whole milk/high-fat dairy intake; for those who consume alcohol, consider moderate consumption of red wine (e.g., ½ to 1 glass/day) over other types of alcohol, and aim to meet nutritional needs through food rather than supplements. Future research that includes more diverse populations, particularly AA/B men, is needed.
References
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This work was funded by the National Cancer Institute of the National Institutes of Health (NCI/NIH) under awards R01CA181802 (REG, EVB, JMC, SAK), R01CA207749 (REG, EVB, JMC, SAK), K07CA197077 (EVB), and K01CA211965 (NRP), as well as funding from the UCSF Prostate Cancer Program (CSL, REG) and the Movember Foundation (REG, JMC, SAK). CSL is also supported by NCI/NIH award F31CA247093. REG is also supported through a Prostate Cancer Foundation Young Investigator Award. NRP is the Helen Diller Family Chair in Community Education and Outreach for Urologic Cancer, which provides professional funds to be used for university-based teaching, service, or research in the area of urologic cancer. JMC is also supported by the Steven & Christine Burd-Safeway Distinguished Professorship, which provides professional funds to be used for university-based teaching, service, or research in the area of prostate cancer. SAK is the Helen Diller Family Chair in Population Science for Urologic Cancer, which provides professional funds to be used for university-based teaching, service, or research in the area of urologic cancer.
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SAK has received compensation from Fellow Health Inc. for service as a consultant and advisory board member. All other authors report no conflicts of interest.
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Langlais, C.S., Graff, R.E., Van Blarigan, E.L. et al. Post-Diagnostic Dietary and Lifestyle Factors and Prostate Cancer Recurrence, Progression, and Mortality. Curr Oncol Rep 23, 37 (2021). https://doi.org/10.1007/s11912-021-01017-x
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DOI: https://doi.org/10.1007/s11912-021-01017-x