Background The WHO recommends moderate physical activity to combat the increasing risk of death from chronic diseases. We conducted a meta-analysis to assess the association between physical activity and cancer mortality and the WHO recommendations to reduce the latter.
Methods MEDLINE and EMBASE were searched up until May 2014 for cohort studies examining physical activity and cancer mortality in the general population and cancer survivors. Combined HRs were estimated using fixed-effect or random-effect meta-analysis of binary analysis. Associated HRs with defined increments and recommended levels of recreational physical activity were estimated by two-stage random-effects dose–response meta-analysis.
Results A total of 71 cohort studies met the inclusion criteria and were analysed. Binary analyses determined that individuals who participated in the most physical activity had an HR of 0.83 (95% CI 0.79 to 0.87) and 0.78 (95% CI 0.74 to 0.84) for cancer mortality in the general population and among cancer survivors, respectively. There was an inverse non-linear dose–response between the effects of physical activity and cancer mortality. In the general population, a minimum of 2.5 h/week of moderate-intensity activity led to a significant 13% reduction in cancer mortality. Cancer survivors who completed 15 metabolic equivalents of task (MET)-h/week of physical activity had a 27% lower risk of cancer mortality. A greater protective effect occurred in cancer survivors undertaking physical activity postdiagnosis versus prediagnosis, where 15 MET-h/week decreased the risk by 35% and 21%, respectively.
Conclusions Our meta-analysis supports that current physical activity recommendations from WHO reduce cancer mortality in both the general population and cancer survivors. We infer that physical activity after a cancer diagnosis may result in significant protection among cancer survivors.
- Physical activity
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Cancer is a leading disease burden in developed and developing countries with 8.2 million cancer deaths in 2012 as estimated by the WHO.1 The World Cancer Research Fund (WCRF) recently reaffirmed that the risk of cancer is affected by our lifestyles and that an active lifestyle is protective against cancer mortality.2 Specifically, an inverse association between physical activity and mortality has been discovered for breast,3 colorectal4 and prostate cancers.5 The association was further validated by meta-analyses in breast and colorectal cancers.6 ,7 However, the magnitude and intensity of physical activity most beneficial against cancer mortality is unclear. The most recent guidelines promoted by the WHO recommend a minimum of 2.5 h of moderate intensity physical activity (3 to <6 metabolic equivalents of task (MET)) or 1.25 h of vigorous intensity physical activity (≥6 METs) per week or any equivalent combination for health benefits, and 5.0 h of moderate intensity physical activity or 2.5 h of vigorous intensity physical activity per week for additional health benefits.8–11 Specific recommendations to prevent cancer mortality are still lacking.12 Accordingly, we conducted a meta-analysis of prospective studies to assess the association of physical activity with cancer mortality and to explore whether the current WHO recommendations are optimal.
Search strategy and study selection
This meta-analysis was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.13 MEDLINE and EMBASE databases were searched up to 30 May 2014 for cohort studies published in English that investigated the association between physical activity and cancer mortality. The search terms were as follows: (‘exercise’, ‘physical activity’, ‘walking’ or ‘motor activity’ with ‘cancer’, ‘neoplasm’ or ‘carcinoma’). Duplicate studies were removed, and the reference lists of relevant literature and previous relevant reviews and meta-analyses were checked for additional publications of interest.
Included studies fulfilled the following criteria: (1) cohort study design, (2) physical activity (eg, leisure-time physical activity, recreational physical activity, exercise and sports, routine activity of daily living, physical activity of transportation, etc) included as a variable, (3) investigated the association between physical activity and cancer mortality (defined as deaths due to cancer) in the general population or among cancer survivors and (4) provided relative risk (RR) or HR estimates and 95% CIs or sufficient data to calculate them. Studies were excluded if they: (1) studied a population with a chronic disease (eg, cardiovascular disease or diabetes mellitus), (2) measured physical fitness but not physical activity, (3) focused on cancer risk not cancer mortality or (4) measured only work-related physical activity. Two authors independently read the full text of all included articles to determine whether each study met the eligibility criteria outlined above.
Data collection and extraction were conducted independently by two investigators, and all discordances were resolved by discussion. For each study, the following information was extracted: first author's name, publication year, cohort name, study location, study design, age at baseline, gender, number of cases or participants, number of cancer deaths, domains of physical activity, when physical activity was measured (prediagnosis (in the general population study), prediagnosis or postdiagnosis (in the cancer survival study)), amounts of physical activity at each level in different units (eg, MET-h/week, h/week, kcal/week and km/h), cancer type, duration of follow-up, estimate of effect (reported as a RR, HR) and the corresponding 95% CI for the association of physical activity with cancer mortality, and adjustment variables (eg, age, body mass index (BMI) and stage). We extracted the binary estimate of the most comprehensive domain of physical activity from each study for a pooled assessment of the most active group compared with the least active group. The effect and 95% CI were inverted for study in which the most active group was used as the reference group. Estimates from each level of recreational physical activity, the most commonly measured domain and main modifiable form of energy expenditure, were extracted for dose–response analysis.14 Lifetime results were used if a study reported the effect of physical activity at both multiple ages and over a lifetime. When a study reported separately on males and females, both risk estimates were included in the primary analysis. Additionally, in the case of multiple publications, we included the most up-to-date or comprehensive information.
Assessment of risk of bias in individual studies
We used the Newcastle-Ottawa quality assessment scale15 to assess the risk of bias in each individual study based on the following: representativeness of the exposed cohort, selection of the unexposed cohort, methods of measuring physical activity, comparability of cohorts based on design or analysis, adjustment for confounding factors (age, BMI, stage, tumour differentiation, etc), duration and adequacy of follow-up, and study end points (cancer mortality). High-quality responses earned a star with up to nine stars in total.
Binary analysis, and fixed-effect or random-effect models were used to estimate the summary HRs for associations between physical activity and cancer mortality when appropriate.16 Dose–response analyses were conducted for studies with three or more quantitative activity levels in MET-h/week and h/week, the most applicable measures of physical activity, using non-linear random effect models.17 For each activity level, the median or mean amount of physical activity was assigned to the corresponding HR estimate. If the median or mean value was not reported, we used the midpoint of the upper and lower boundaries of each category. For studies reporting open upper boundaries for the highest category (eg, >200 min/week), we multiplied the reported lower boundary by 1.25 and used this value (eg, 250 min/week) as the midpoint.18 Heterogeneity in the relationship between physical activity and cancer mortality was assessed by Q test and quantified by I2 statistic.19 In order to assess the effect of the study characteristics and quality on the reported estimates, heterogeneity was analysed by comparing the effect estimate summary from subgroup analyses. Subgroup analyses were conducted in topics that had at least three original studies and were by cancer type, gender, study location, follow-up duration (<10 years, ≥10 years) and when physical activity was measured (prediagnosis or postdiagnosis). To test for statistically significant potential confounders (eg, publication year, study location, follow-up duration, cancer type, when physical activity was measured, measurement of physical activity, study design and quality), meta-regression analysis20 was used to calculate ratios of risk. Publication bias was examined using Begg's test and Egger's test.21 We performed sensitivity analyses by omitting one study at a time from the initial meta-analysis. All statistical tests were two-sided and p values <0.05 were considered statistically significant. All analyses were conducted using Stata software (V.12.0; StataCorp, College Station, Texas, USA).
In total, 16 980 articles were initially identified in the literature search; and 10 619 articles were left after removing duplicates, of which 10 422 studies were not relevant to the main topic and excluded. Thirty of the remaining 197 studies were excluded due to a focus on occupational physical activity, 91 for not fulfilling the inclusion criteria and 7 for providing information from overlapping studies. Two additional articles were identified in a manual search of reference lists. Overall, 71 studies were included in the primary meta-analysis (figure 1).
Characteristics of the studies
Of the 71 prospective studies reporting on the association between physical activity and cancer mortality, 36 were general population-based studiesS[1–36] and 35 studies were conducted among cancer survivors.S[37–71] The major characteristics of these studies and reference list are shown in online supplementary table S1. In total, 3 985 164 participants were included in the general population-based studies and 66 995 cancer deaths were observed. Nine studies were done in North America,S[1 2 8 16 23 28 32 34 35] 9 in AsiaS[7 12–14 25–27 31 33] and 18 in Europe.S[3–6 9–11 15 17–22 24 29 30 36] Twenty-two studies provided data on the relationship between physical activity and mortality from various cancer,S[1–6 9 11 14–16 19 21–23 26 29–31 33 35 36] with five on colorectal cancer,S[12 24 26 27 34] four on pancreatic cancerS[8 13 18 25] and three on breast cancer.S[26 32 34] In the 35 cancer survival studies, 69 011 patients with cancer were included with 9516 cancer deaths. Twenty-five of these studies were conducted in North America,S[38–41 43 44 48–52 54 57–65 68–71] and six in Europe.S[45–47 53 55 67] Nineteen studies were on breast cancer survivalS[37–41 44 47 50–55 57 60 61 67–69] and nine on colorectal cancer survival.S[42 43 49 56 59 62 65 66 70] Of these, 24 studies,S[37–43 45–47 51 53–55 57 61–65 67 68 70 71] 14 studiesS[40 43 44 49 50 56–60 62 65 66 69] and five studiesS[40 43 57 62 65] reported on the association between prediagnosis, postdiagnostic or both prediagnostic and postdiagnostic physical activity, respectively, and cancer mortality. The overall quality score ranged from 6 to 9 based on the Newcastle-Ottawa scale with 16 studies scoring 6 stars, 10 scoring 9 stars and the rest 7–8 stars.
The role of physical activity in reducing cancer mortality in the general population
As shown in table 1, compared to the lowest amount of physical activity, the highest amount of physical activity presented significant protection against death from cancer, with a pooled HR of 0.83 (95% CI 0.79 to 0.87, I2=65.6%). Consistent associations were confirmed by subanalyses of gender, study location, duration of follow-up and cancer type. The highest levels of physical activity reduced cancer mortality by 17% in males and females. Similarly, studies conducted in North America, Europe and Asia found a 17–19% protective effect. Cancer mortality presented a 17% and 16% reduction in studies, respectively, with a follow-up of less than or at least 10 years. Besides, high level of physical activity reduced the mortality of colorectal cancer by 21%. The heterogeneity of binary comparison was significant (I2=65.6%), which, based on subgroup analysis, was mainly from North American studies. Besides study location, meta-regression did not find new sources of heterogeneity. Begg's test (p=0.32) and Egger's test (p=0.09) indicated no evidence for publication bias. Also, sensitivity analysis found that the pooled results did not overtly change even on omission of the most influential study (online supplementary figures S1 and S2).
Figure 2 shows evidence of a non-linear association between recreational physical activity and cancer mortality by MET-h/week in general population. The HRs of cancer mortality following 5, 10, 15, 20 and 25 MET-h/week of recreational physical activity were 0.88, 0.86, 0.86, 0.85 and 0.84, respectively, when compared with inactivity. The dose–response curve steeply sloped below 7.5 MET-h/week, the minimum energy expenditure of 2.5 h moderate physical activity per week recommended by the WHO, and then gently declined. Individuals who met the lower limit of the WHO guidelines, 7.5 MET-h/week, had a 14% lower risk of cancer mortality. An approximate 2% reduction in cancer mortality for every 1 MET-h/week increase below 7.5 MET-h/week occurred compared to a 1% reduction in cancer mortality by every 10 over 7.5 MET-h/week. Pooled results indicate a similar inverse relation between recreational physical activity and cancer mortality in Asians (online supplementary table S2 and figure S3). The HRs of cancer death for 5, 10, 15, 20 and 25 MET-h/week of recreational physical activity were 0.91, 0.87, 0.86, 0.85 and 0.84, respectively, when compared with the lowest amount of physical activity in the Asian population. This curve shows a significant reduction below 12 MET-h/week and over 22 MET-h/week with a 1% reduction in cancer mortality for every 1 MET-h/week. A similar relationship was observed in studies within 10 years of follow-up. Other subgroups could not be analysed due to insufficient data.
The HRs of cancer mortality for 2, 3, 4, 6 and 8 h/week of recreational physical activity were 0.94, 0.92, 0.91, 0.91 and 0.90, respectively, compared to inactivity (online supplementary table S2). As shown in figure 2, the curve trended a decline with continuously increasing levels of recreational physical activity. Individuals who engaged in 2.5 h/week of recreational physical activity compared to none had a 7% lower cancer mortality. A further 2% reduction in cancer mortality was seen for every additional 6 h/week activity over 2.5 h/week. Subgroup analyses are presented in online supplementary figure S3. Cancer mortality decreased rapidly below 2 h/week and then declined steadily over 2 h/week in North Americans. A similar effect was observed in individuals following up over 10 years. Other subgroups could not be analysed due to insufficient data.
The role of physical activity in reducing cancer mortality in cancer survivors
A strong association between high levels of physical activity and cancer mortality was observed in cancer survivors with an HR of 0.78 (95% CI 0.72 to 0.84, I2=56.9%) (table 2). The highest levels of physical activity reduced cancer mortality by 21% in female cancer survivors. However, we did not observe a similar association in males. The protection by physical activity against cancer death was further observed in North American studies with reduced 25% cancer mortality, but not in European. The association between physical activity and cancer mortality was not affected by duration of follow-up, which showed a 20% and 30% lower risk in participants followed up for less than and at least 10 years, respectively. A more pronounced protection from postdiagnostic physical activity (HR=0.60, 95% CI 0.50 to 0.71, I2=53.8%) than prediagnostic physical activity (HR=0.86, 95% CI 0.80 to 0.92, I2=16.7%) was observed among cancer survivors. This inverse association between physical activity and cancer mortality was confirmed in breast cancer survivors and colorectal cancer survivors. There was evidence of heterogeneity between cancer survival studies of highest versus lowest levels of physical activity (I2=56.9%). On the basis of subgroup analyses, the studies conducted in North America are responsible for most of the observed heterogeneity. Meta-regression analysis indicated that how physical activity was measured (p=0.01) was statistically signiﬁcant in a multivariate model, while Egger's test suggests publication bias (p<0.001). Results from the sensitivity analysis did not change even if the most influential study was omitted (online supplementary figures S1 and S2).
The pooled results show the expected inverse relationship between recreational physical activity and cancer mortality. The cancer mortality declined rapidly with a 2% reduction for every 1 MET-h/week below 10 MET-h/week followed by a plateau over 15 MET-h/week (figure 3). Compared with no recreational physical activity, 5, 10, 15, 30 and 50 MET-h/week reduced the overall cancer mortality by 18%, 25%, 27% 30% and 35%, respectively. Subgroup analyses demonstrated that similar trends occurred in all studies included (online supplementary table S3 and figure S4). An inverse association between recreational physical activity and cancer mortality was found in females. The cancer mortality dropped rapidly with a 2% reduction for each added 1 MET-h/week below 10 MET-h/week and then stabilised at 70% for activity over 15 MET-h/week. Similarly, a protective role for recreational physical activity was observed in North Americans and cancer survivors within 10 years of follow-up. In particular, stronger protection occurred against cancer mortality with postdiagnostic physical activity compared with prediagnostic physical activity. Cancer mortality quickly decreased by 35% when individuals participated in 15 MET-h/week of recreational physical activity after diagnosis and a further 5% reduction in cancer mortality occurred with every additional 10 MET-h/week. In comparison, the cancer mortality decreased by 21% at 15 MET-h/week of prediagnostic physical activity with no further reduction on increasing the amount of recreational physical activity (figure 4). We further explored the association between recreational physical activity and breast cancer mortality and the results were similar to the analysis of the female subgroup; the results stabilised at a 2.5% reduction in cancer mortality for every additional 1 MET-h/week below 10 MET-h/week. An inverse linear relationship was found between recreational physical activity and colorectal cancer mortality (pfor non-linearity=0.772), which was statistically significant over 10 MET-h/week with a 1% reduction in cancer mortality with every additional 1 MET-h/week online supplementary figure S4. Furthermore, we conducted subset analysis among breast cancer survivors, and a more pronounced benefit was found from postdiagnostic physical activity than prediagnostic physical activity. Compared with no recreational physical activity, 5, 10, 15 and 20 MET-h/week of prediagnostic physical activity reduced breast cancer mortality by 24%, 28%, 29% and 30%, respectively. Meanwhile, breast cancer mortality reduced by 24%, 32%, 39% and 40% when individuals participated in 5, 10, 15 and 20 MET-h/week of recreational physical activity after diagnosis, respectively. Similarly, the decreasing trend in colorectal cancer mortality occurred in postdiagnostic physical activity as in overall physical activity (online supplementary figure S5).
This relatively large meta-analysis summarises the contribution of physical activity to reducing cancer mortality and quantifies the reduction in cancer mortality with incremental increases in recreational physical activity. In summary, we found that a high level of physical activity lowered the risk of cancer mortality in the general population and cancer survivors compared to inactivity. Dose–response analyses estimated the benefits for different levels of recreational physical activity by measuring MET-h/week and h/week. The results primarily showed consistent non-linear relationships between recreational physical activity and cancer mortality in the general population and among cancer survivors.
Our findings based on the general population showed that individuals undergoing the highest levels of physical activity had a 17% reduction in cancer mortality. This effect was not influenced by gender, study location or duration of follow-up. Dose–response analyses further revealed that the cancer mortality decreased significantly by 13% and 7% in the general population that undertook 7.5 MET-h/week and 2.5 h/week recreational physical activity, respectively. Recent meta-analyses confirmed a similar inverse relationship between high levels of physical activity and all-cause mortality.18 ,22 In particular, one meta-analysis quantified the dose–response of all-cause mortality to non-vigorous physical activity and demonstrated that adhering to the WHO's recommendations contributed to a 19% reduction.22 A recent dose–response analysis based on six studies from the National Cancer Institution Cohort Consortium found that compared with individuals reporting no leisure time physical activity, 21% lower cancer mortality was steadily observed among those performing 1–3 times of the WHO's recommendation (7.5 to <22.5 MET-h/week).23 Similarly, our study, based on extensive original publications, confirmed that moderate intensity activity was associated with cancer mortality benefit in the general population as well.
The inverse relationship between physical activity and cancer mortality was also confirmed in cancer survivors. Basically, cancer survivors undertaking the highest level of physical activity had a 22% reduction in cancer mortality. In particular, evidence from the meta-analysis suggests a non-linear dose–response of cancer mortality to recreational physical activity. Our findings confirmed and extend previous qualitative evidence,6 ,7 which reported a correlation between physical activity and cancer mortality in breast and colorectal cancers, respectively. In addition, our findings are consistent with recent published quantitative meta-analysis by Zhong et al,24 which revealed a similar non-linear dose–response relationship between physical activity and breast cancer mortality. The effect of recreational physical activity within a female subgroup analysis was very similar to that within the breast cancer subgroup, which suggests that they came out of similar data sources. The benefit of recreational physical activity was evident for North Americans and strongly supports the 2008 Physical Activity Guidelines for Americans, which endorses 2.5 h/week of moderate activity.25
Several mechanisms potentially explain the protection afforded by physical activity against cancer mortality. Studies cite the metabolic effects of high physical activity, including lower BMI, lower sex hormones, reduced adiposity, insulin and c-peptide levels and possibly effects on inflammation or the immune system.26–29 However, the proposed mechanisms may differ based on the type of cancer. For instance, physical activity increases insulin sensitivity.30 Higher circulating insulin and insulin-like growth factor-1 and lower insulin-binding protein level have been associated with colorectal risk in epidemiology studies.31–33 A previous study showed higher colorectal cancer mortality among individuals with metabolic abnormalities related to insulin metabolism compared with those without hyperinsulinaemia and insulin resistance.34 In a similar way, insulin resistance may influence the risk of breast cancer recurrence and mortality,35 and physical activity is known to lower insulin levels and improve insulin sensitivity.36 ,37 Furthermore, exercise intervention studies have measured improvements in insulin-like growth factor 1 (IGF-I) and insulin-like growth factor binding protein 3 (IGFBP-3) and biomarkers related to cancer progression and recurrence among breast cancer survivors following high levels of exercise.38 ,39
Interestingly, we found that the inverse association between physical activity and cancer mortality was more pronounced in postdiagnostic physical activity than prediagnostic physical activity with a 26% difference. Previous meta-analyses conducted in breast and colorectal cancer survival studies clearly supported that postdiagnosis physical activity was associated with lower cancer mortality than prediagnosis physical activity.7 ,40 The finding was also supported by a recently published dose–response meta-analysis in breast cancer.23 On the basis of the studies described above, there is convincing evidence that recreational physical activity after diagnosis is slightly more beneficial against cancer mortality. A possibility is that individuals who participate in physical activity after a cancer diagnosis may be motivated to change their behaviour and adopt a healthier lifestyle following a cancer diagnosis.41 Furthermore, a longitudinal study focusing on breast cancer and changes in physical activity before and after diagnosis showed that women who increased physical activity to 9 or more MET-h/week after diagnosis had lower mortality due to breast cancer even if they were inactive before diagnosis,42 and encouraged women diagnosed with breast cancer to initiate and maintain a programme of physical activity. Systematic reviews in randomised controlled trials43 ,44 and reviews45–47 have concluded that physical activity interventions during and after cancer therapies often result in meaningful and reliable improvements in several supportive care outcomes. These benefits include observed changes in physiological measures, objective performance indicators, self-reported functioning and symptoms, psychological well-being and overall quality of life. These findings may prompt the importance of participating in physical activity, especially after a cancer diagnosis, to gain maximum survival benefits.
Strengths of the meta-analysis
This is a large-scale meta-analysis based on 71 prospective studies. The comprehensiveness of our study is its primary strength. Besides, we provide quantified binary assessments, as well as dose–response relationships between recreational physical activity and cancer mortality. Overall, our results clarify and provide evidence for the WHO guidelines on physical activity at preventing cancer mortality for the general population and also cancer survivors. Our stratified results in the general population study further strengthen our finding by indicating consistent benefits of physical activity in different genders, study locations and durations of follow-up. In addition, we examined the difference between postdiagnostic and prediagnostic physical activity in relation to cancer mortality among cancer survivors in order to better understand the protection against cancer mortality by physical activity at different time points. Various comparisons were conducted to assess the association between physical activity and cancer mortality.
Limitations of the meta-analysis
This meta-analysis has several limitations. First, despite the inclusion of 71 studies in our meta-analysis, we were unable to assess whether the association between physical activity and cancer mortality differed by race, age or cancer type due to insufficient variation among studies in dose–response analyses. In this meta-analysis, the dose–response associations were only explored in subgroup analyses of female, North America, and breast and colorectal cancers. Second, there was significant heterogeneity for several outcomes that could not be explained by geography. The methods of how physical activity was assessed also contributed as physical activity is a complex behaviour with many components, and therefore it is difficult to accurately measure and classify the type of physical activity and its characteristics (ie, intensity, duration and frequency). Third, conclusion related to the associations between high levels of physical activity and cancer mortality in dose–response analyses should be interpreted with caution, especially in the association curve with an upward tail due to the incomplete extreme value (online supplementary figure S6), even though the the tail of the curve became flattened after omitting outliers. Furthermore, a large portion of the physical activity was self-reported; therefore, some misclassification of activity level was probable and quantitative characterisations should therefore be considered approximate in nature. Moreover, for postdiagnostic physical activity, it is possible that the sickest patients are the ones who are unable to exercise and more likely to die. However, to minimise the possibility of survival bias, the original studies conducted by Meyerhardt et al41 ,48 and Irwin et al42 excluded patients with cancer who either died or recurred within 1 or 2 years of physical activity assessment in their analyses, and the results were not materially altered by that procedure. Besides, all reported outcomes for postdiagnostic physical activity in this meta-analysis have been adjusted for known prognostic variables such as age and stage to reduce the influence of survival bias. Although we used adjusted estimates from included prospective studies, we cannot totally rule out potential residual confounding or confounding by unmeasured factors, such as information on treatment and more details of tumour characteristics, and those unaccounted factors may have an influence on the final results. Finally, our study suggests associations, rather than cause and effect, because of the observational nature of data.
In summary, this systematic review and meta-analysis suggests an inverse association between physical activity and cancer mortality. Quantitative data concerning the general population supports the current recommendation of physical activity equivalent to 2.5 h/week of moderate-intensity (3–6 MET-h/week), which could have substantial health benefits for individuals. We also found that a minimum 2.5 h/week of moderate-intensity recreational physical activity conferred protection against cancer mortality among cancer survivors. Therefore, we conclude that the current recommendations concerning physical activity are generally sufficient for reducing cancer mortality. Furthermore, our study displays that physical activity performed before or after cancer diagnosis is related to reduced mortality among cancer survivors. Thus, we infer that physical activity after a cancer diagnosis may result in significant protection among cancer survivors. Future randomised controlled trials are needed to verify the role of physical activity in patients with cancer. More high-quality studies are required to clarify the biological mechanisms underlying this association between physical activity and lower cancer mortality.
What are the new findings?
By this meta-analysis based on 71 prospective studies, binary analyses determined that individuals who participated in the most physical activity had an HR of 0.83 (95% CI 0.79 to 0.87) and 0.78 (95% CI 0.74 to 0.84) for cancer mortality in the general population and among cancer survivors, respectively.
Pooled results indicate the expected inverse non-linear dose–response relationship between recreational physical activity and cancer mortality.
Our meta-analysis supports that the current recommendation of physical activity (equivalent to 2.5 h/week of moderate intensity) reduces cancer mortality in both the general population and cancer survivors. We infer that physical activity after a cancer diagnosis may result in significant protection among cancer survivors.
How might it impact on clinical practice in the future?
Our results might be helpful to inform updates on recommendation concerning the advisable amount of physical activity to reduce cancer mortality in the general population and among cancer survivors.
Future randomised controlled trials could be conducted to verify the role of physical activity in improving cancer mortality.
Physical activity after diagnosis presents significant protection against cancer mortality. Therefore, physicians may consider to adopt physical active into the clinical practice of cancer treatments.
Review history and Supplementary material
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
TL and SW contributed equally.
Contributors TL, SW (Shaozhong Wei) and LL were involved in the design of the study; TL, YS, SP, QQ, JY, YD and QC acquired data from selected studies; all authors were involved in the analysis and interpretation of the data; TL, SW (Shaozhong Wei), and LL drafted the manuscript; all authors provided critical revision of the manuscript for important intellectual content; TL, YS, SP, SW (Sheng Wei) and SN carried out the statistical analyses. All authors read and approved the manuscript. LL and TL had full access to all of the data in the study and can take responsibility for the integrity of the data and the accuracy of the data analysis. SN and LL are the guarantors.
Funding This work was supported by the National Natural Science Foundation of China (NSFC-81172754 to SW (Sheng Wei) and NSFC-81302491 to LL) and Independent Innovation Fund of Huazhong University of Science and Technology (2013QN001 to LL).
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
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