Exercise Training in Elderly Cancer Patients: A Systematic Review
Abstract
:Simple Summary
Abstract
1. Introduction
2. Elderly Population: When an Epidemiological Shift Turns into a New Model of Care
3. Exercise and Cancer: Pathophysiological Basis
4. Exercise in Older Cancer Patients
Authors, Year. | Cancer Type | Mean Age | Follow-Up | Intervention and Methods | Main Results |
---|---|---|---|---|---|
Focht et al., 2019, [78] | Prostate | 66 | 3 months | Single-blind, 2-arm, randomized controlled Individualized trial, 32 prostate cancer patients undergoing androgen deprivation therapy were randomly assigned to a 12-week of group-mediated cognitive behavioral exercise and dietary intervention (n = 16) or standard care treatment (n = 16) | Lifestyle intervention yielded more favorable improvements in relevant social cognitive outcomes relative to standard care |
Galvão et al., 2021, [79] | Prostate | 69 | 12 months | A total of 135 prostate cancer patients aged 43–90 years on androgen deprivation therapy were randomized to twice weekly supervised impact loading and resistance exercise, supervised aerobic and resistance exercise, and usual care | Various supervised exercise modes (aerobic, resistance, and impact loading are effective in reducing psychological distress in men with prostate cancer. |
Poh Loh et al., 2019, [80] | Solid cancer | 68 | 6 weeks | Exploratory secondary analysis of a randomized controlled trial. Patients were randomized to exercise (home-based, low-to-moderate intensity progressive walking and resistance training program) or usual care (control) for the first six weeks of chemotherapy. | Among older cancer patients receiving chemotherapy, a 6-week structured exercise program improved anxiety and mood, especially among those participants with worse baseline symptoms |
Winters-Stone et al., 2016, [115] | Prostate | 70 | 6 months | Single-blind randomized controlled trial comparing exercise together (patients and his/her spouse, 32 couples) to usual care (32 couples). The exercise consisted of a progressive strength training program. | Men exercising together became stronger in the upper body (p < 0.01) and more physically active (p < 0.01) than usual care. Women in Exercising Together increased muscle mass (p = 0.05) and improved upper (p < 0.01) and lower body (p < 0.01) strength and physical performance battery scores (p = 0.01) more than usual care |
Winters-Stone et al., 2021, [76] | Breast | 72 | 18 months | Early-stage, post-treatment, older (≥65 years) breast cancer survivors (n = 114) were randomized to 12 months of supervised aerobic (n = 37), resistance (n = 39), or stretching (active control; n = 38) training followed by 6 months of unsupervised home-based training | Supervised exercise can improve strength and physical functioning among older breast cancer survivors. Resistance training may lead to better improvements compared to aerobic or flexibility training, whether in a supervised or unsupervised setting |
Galvão et al., 2017, [81] | Prostate with bone metastases | 70 | 3 months | A total of 57 prostate cancer patients with bone metastases (pelvis, 75.4%; femur, 40.4%; rib/thoracic spine, 66.7%; lumbar spine, 43.9%; humerus, 24.6%; other sites, 70.2%) were randomized to multimodal supervised aerobic, resistance, and flexibility exercises undertaken thrice weekly (n = 28) or usual care (n = 29) | Multimodal modular exercise in prostate cancer patients with bone metastases led to self-reported improvements in physical function and objectively measured lower body muscle strength with no skeletal complications or increased bone pain |
Scott et al., 2021, [82] | Lung | 65 | 17 weeks | A total of 90 lung cancer survivors with poor cardiorespiratory fitness were randomly allocated to receive 48 consecutive supervised sessions thrice weekly of Aerobic training [27], Resistance Training [26], Combination training [23], Stretching control [26] | Aerobic training and combination training significantly improved VO2 peak in lung cancer survivors |
Zimmer et al., 2017, [83] | Colorectal | 68 | 4 weeks | Thirty patients (stage IV) undergoing outpatient palliative treatment were randomly assigned to an intervention or control group (IG, n = 17; CG, n = 13). The IG participated in an eight-week supervised exercise program including endurance, resistance, and balance training (2×/week for 60 min) whereas the CG received written standard recommendations to obtain physical fitness. | Positive effects of a multimodal exercise program on chemotherapy-induced peripheral neuropathy, balance, and strength on patients with colorectal cancer in a palliative setting, thereby consequently increasing patients’ quality of life. |
Mikkelsen et al., 2022, [84] | Advanced pancreatic, biliary tract, or non-small cell-lung cancer | 72 (median) | 12 weeks | Eighty-four older adults (≥65 years) with advanced pancreatic, biliary tract, or non-small cell lung cancer who received systemic oncological treatment were randomized 1:1 to an intervention group or a control group. The intervention was a 12-week multimodal exercise-based program including supervised exercise twice weekly followed by a protein supplement, a home-based walking program, and nurse-led support and counseling | A 12-week multimodal exercise intervention with targeted support proved effective in improving physical function in older patients with advanced cancer during oncological treatment |
Owusu et al., 2022, [85] | Breast | 72 | 1 year | Randomized controlled trial. The interventions included 20 weeks of supervised moderate-intensity aerobic and resistance training followed by 32 weeks of unsupervised exercise (n = 108) and a 20-week support group program followed by 32 weeks of unsupervised activity (n = 105) | Combined aerobic and resistance exercise appears to improve physical performance in older breast cancer survivor |
Mardani et al., 2020, [86] | Prostate | 69 | 12 weeks | 80 patients were randomly allocated to intervention (exercise program, n = 40) and control (n = 40) groups in a single-blind, parallel, randomized controlled trial | In the intervention group, statistically significant improvements in physical, emotional, social, and sexual function were reported. Moreover, the patients in this group reported reduced fatigue, insomnia, constipation, diarrhea, urinary, bowel, and hormonal treatment-related symptoms in comparison with before the exercise program |
Taaffe et al., 2017, [87] | Prostate | 69 | 1 year | 163 prostate cancer patients aged on androgen deprivation therapy were randomized to exercise targeting the musculoskeletal system (impact loading + resistance training; n = 58), the cardiovascular and muscular systems (aerobic + resistance training; n = 54), or to usual care/delayed exercise (n = 51) | Different exercise modes have comparable effects on reducing fatigue and enhancing vitality during ADT. Patients with the highest levels of fatigue and lowest vitality had the greatest benefits |
Wall et al., 2017 [88] | Prostate | 69 | 6 months | Ninety-seven men with localized prostate cancer receiving ADT were randomized to either exercise (n = 50) or usual care (n = 47). The supervised exercise was undertaken twice weekly at moderate to high intensity. | Combined aerobic and resistance exercise program has a significant favorable effect on cardiorespiratory capacity, resting fat oxidation, glucose, and body composition despite the adverse effects of hormone suppression. |
Gaskin et al., 2016, [89] | Prostate | 67 | 12 weeks | Secondary analysis on data from a multicentre cluster randomized controlled trial in which 15 clinicians were randomly assigned to refer eligible patients to an exercise training intervention (n = 8) or to provide usual care (n = 7). Data from 119 patients (intervention n = 53, control n = 66) were available for this analysis | Men with prostate cancer who act upon clinician referrals to community-based exercise training programs can improve their strength, physical functioning, and, potentially, cardiovascular health, irrespective of whether they are treated with ADT |
Maréchal et al., 2018, [90] | Prostate and breast | 69 | 12 weeks | Fourteen participants completed 12 weeks of a mixed exercise program (n = 6) or stretching (n = 8) while they were under cancer treatment | Exercise program led to significant improvements in physical capacity and may reduce sedentary behavior time |
Park et al., 2012, [91] | Prostate | 69.1 | 12 weeks | A total of 66 patients were randomized to an exercise or a control group. The exercise group received a combined exercise intervention (resistance, flexibility, and Kegel exercises) twice a week for 12 weeks, and the control group received only Kegel exercises | A 12-week combined exercise intervention after radical prostatectomy results in improvement of physical function, continence rate, and quality of life |
Winters-Stone et al., 2015, [92] | Prostate | 70 | 1 year | A total of 51 prostate cancer survivors were randomized to moderate to vigorous intensity resistance training or stretching (placebo) | One year of resistance training improved muscle strength in androgen-deprived prostate cancer survivors. Strengthening muscles using functional movement patterns may be an important feature of exercise programs designed to improve perceptions of physical function and disability |
Pysizora et al., 2017 [93] | Advanced cancer | 72 | 2 weeks | Sixty patients diagnosed with advanced cancer receiving palliative care were randomized into two groups: the treatment group (n = 30) and the control group (n = 30). The therapy took place three times a week for 2 weeks. The 30-min physiotherapy session included active exercises, myofascial release, and proprioceptive neuromuscular facilitation (PNF) techniques. The control group did not exercise | The physiotherapy program, which included active exercises, myofascial release, and proprioceptive neuromuscular facilitation techniques, had beneficial effects on cancer-related fatigue and other symptoms in patients with advanced cancer who received palliative care |
Stuecher et al., 2019, [94] | Advanced gastrointestinal | 67 | 12 weeks | Participants (n = 44) were randomly assigned to a home-based physical activity program of 150 min moderate walking per week or a control group (CG) | A home-based physical activity improves postural sway and body composition and might stabilize functional capacity in patients with advanced gastrointestinal cancer during chemotherapy. Although the other outcomes did not differ between groups, the aforementioned effects might contribute to the maintenance of independence in ADL and a better treatment tolerance and thus enhance patients’ quality of life |
5. Prehabilitation: Exercise Training First
6. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
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---|---|---|---|---|
Xie L et al., 2007. [44] | Comparing the effects of weight loss by dietary calories restriction-fed or exercise-trained mice on Ras-MAPK and PI3K- Akt cascades | Sustaining proliferative signaling | Impact on Plasma IGF-1 and skin tissue IGF-1R levels -Impact on Ras-MAPK Pathway -Impact on PI3K Pathway -Effects on Plasma leptin levels -Effect on activated caspase-3 levels in skin tissues -Effects of gene expression relevant to RAS and -PI3K signaling pathways | Body weight significantly decreased, with a 20% dietary calories restriction, which corresponded to a decrease of body fat and plasma IGF-1 levels. Treadmill exercise with pair-feeding selectively reduced the PI3K-Akt pathway |
Ouyang P et al., 2010. [45] | Impact of exercise with dietary consideration on the phospholipid profile in TPA-induced mouse skin tissues | Sustaining proliferative signaling | Impact on PI3K Pathway | Exercise with controlled diet interventions significantly reduced body weight and body fat as well as modified the phospholipid profile. This modified profile might provide potential cancer prevention benefits, perhaps via reducing TPA-induced PIs and PI-related PI3K expression. |
Leung PS et al., 2004. [46] | Effect of exercise on serum-stimulated p53 protein content in the LNCaP prostate cell line. | Sustaining proliferative signaling | Effects on circulating IGF-1 levels and p53 expression | Serum from men who regularly exercise does increase the p53 protein in LNCaP tumor cells and that this is likely important for the reduced cell growth and the induction of apoptosis. |
Yu M et al., 2016. [47] | Female SENCAR mice were pair-fed an AIN-93 diet with or without 10-week treadmill exercise at 20 m/min, 60 min/day and 5 days/week. | Evading growth suppressor | Effects of exercise on MDM2 and p53 expression Effects of exercise on the expression of p53-transcripted proteins (p21, IGFBP-3, PTEN) | Exercise appeared to activate p53, resulting in enhanced expression of p21, IGFBP-3, and PTEN that might induce a negative regulation of IGF-1 pathway and thus contribute to the observed cancer prevention by exercise in this skin cancer model |
Piguet AC et al., 2015. [48] | Mice were fed a standardized 10% fat diet and were randomly divided into exercise or sedentary groups. The exercise group ran on a motorized treadmill for 60 min/day, 5 days/week for 32 weeks | Evading growth suppressor | Exercise can stimulate the phospshorylation of AMPK and its substrate raptor, which decrease the kinase activity of mTOR | After 32 weeks of regular exercise, 71% of exercised mice developed nodules larger than 15 mm3 vs. 100% of mice in the sedentary group. The mean number of tumors per liver was reduced by exercise, as well as the total tumoral volume per liver |
Jiang Wet al, 2009. [49] | Effects on mammary carcinogenesis of physical activity in rats. | Evading growth suppressor | Effects of exercise on caspase-3 activity and AMPK signaling | Cell proliferation associated proteins were reduced and caspase 3 activity and pro-apoptotic proteins were elevated by PA or RE relative to SC (p < 0.05). It was observed that these effects may be mediated, in part, by activation of AMP-activated protein kinase and down regulation of protein kinase B and the mammalian target of rapamycin. |
Zhu Z el al., 2008. [50] | Identify circulating growth factors, hormones, and cellular and molecular mechanisms that account for the effects of physical activity on mammary carcinogenesis in rats. | Evading growth suppressor | Effects of physical exercise on activation of AMP-activated protein kinase, and down-regulation of protein kinase B, which collectively down-regulate the activity of the mammalian target of rapamycin | Cancer incidence (98.1 versus 84.6%; p < 0.01) and average number of cancers per rat (3.72 versus 2.67, respectively; p < 0.01) were reduced by physical activity. The average cancer mass per rat was 0.62 g in the physically active group and 1.16 g in the sedentary control group (p = 0.17) |
Zhu Z el al., 2008. [50] | Identify circulating growth factors, hormones, and cellular and molecular mechanisms that account for the effects of physical activity on mammary carcinogenesis in rats. | Evading growth suppressor | Effects of physical exercise on activation of AMP-activated protein kinase, and down-regulation of protein kinase B, which collectively down-regulate the activity of the mammalian target of rapamycin | Cancer incidence (98.1 versus 84.6%; p < 0.01) and average number of cancers per rat (3.72 versus 2.67, respectively; p < 0.01) were reduced by physical activity. The average cancer mass per rat was 0.62 g in the physically active group and 1.16 g in the sedentary control group (p = 0.17) |
Khori V et al., 2015. [51] | Forty-eight female BALB/c mice were equally divided into six groups to investigate the effects of interval exercise training with tamoxifen on miR-21 expression and its possible assumed mechanisms in an estrogen receptor-positive breast cancer model | Evading growth suppressor | Exercise training and tamoxifen reduced tumor IL-6 levels, NF-kB and STAT3 expressions, and up-regulated TPM1 and PDCD4 expressions (p < 0.05). Both exercise and tamoxifen had synergistic effects in reducing miR-21 and Bcl-2, and up-regulating PDCD4 expression | Results showed that interval exercise training may reduce mammary tumor burden in mice through possible underlying pathway of miR-21 |
Zheng X et al., 2008. [52] | Effect of voluntary exercise on the formation and growth of human pancreas Panc-1 and prostate PC-3 tumors in immunodeficient mice | Resisting cell death | Effects of voluntary running wheel exercise on mitosis and apoptosis in Panc-1 and PC-3 tumors | Voluntary running wheel exercise inhibited the growth of human pancreas and prostate tumors in immunodeficient SCID mice, and these effects of exercise were paralleled by decreased proliferation and increased apoptosis |
Hojman P et al., 2011. [53] | Incubation of mamary cancer cells with conditioned serum from exercising mice | Resisting cell death | Effect of exercise on caspase activation | Post exercise serum inhibits mammary cancer cell proliferation and induces apoptosis |
Barnard RJ et al., 2007. [54] | Serum from sedentary controls or men with regular (5 days/week) aerobic exercise was used to stimulate lymph node cancer of the prostate (LNCaP) tumor cells in vitro | Resisting cell death | Effect of exercise on the activity of p53, p21 and Bcl-2 | Exercise training alters serum insulin-like growth factor axis factors in vivo that increase LNCaP cellular p53 protein content in vitro leading to reduced growth via p21 and induced apoptosis via the mitochondrial pathway |
Higgins KA et al., 2014. [55] | Luciferase-tagged A549 lung adenocarcinoma cells were injected through the tail vein of nude male mice. After lung tumors were identified, the mice were randomized to daily wheel running versus no wheel running | Resisting cell death | Effect of exercise on p53 levels and mediators of apoptosis including Bax and active caspase 3 | Lung tumors in exercising mice grew significantly more slowly relative to sedentary mice |
Betof AS et al., 2015. [56] | Estrogen receptor–negative (ER-, 4T1) and ER+ (E0771) tumor cells were implanted orthotopically into syngeneic mice (BALB/c, N = 11–12 per group) randomly assigned to exercise or sedentary control | Resisting cell death | Effect of exercise on apoptosis | Exercise plus chemotherapy prolonged growth delay compared with chemotherapy alone (p < 0.001) in the orthotopic 4T1 model (n = 17 per group). Exercise is a potential novel adjuvant treatment of breast cancer |
Jones LW et al., 2010. [57] | Athymic female mice fed a high-fat diet were orthotopically (direct into the mammary fat pad) implanted with human breast cancer cells into the right dorsal mammary fat pad and randomly assigned [1:1] to voluntary wheel running (n = 25) or a nonintervention (sedentary) control group (n = 25). | Inducing angiogenesis | Activity of VEGF and hypoxia-inducible factor (HIF-1) Activity of AMPK and peroxisome proliferator-activated receptor-γ coactivator (PGC)-1α | Aerobic exercise can significantly increase intratumoral vascularization, leading to “normalization” of the tissue microenvironment in human breast tumors |
Jones LW et al., 2012. [58] | C57BL/6 male mice (6–8 wk of age) were orthotopically injected with transgenic adenocarcinoma of mouse prostate C-1 cells (5 × 105) and randomly assigned to exercise (n = 28) or a non-intervention control (n = 31) group | Inducing angiogenesis | Effects of primary tumor growth and metastasis; -Effects of prometastatic gene expression; -Effects on tumor MAPK and PI3K signaling; Effects on HIF-1, metabolism, and angiogenesis; -Effects on tumor perfusion/diffusion and vessel function and maturation | Exercise promote stabilization of HIF-1α with subsequent upregulation of a proangiogenic phenotype stimulating “productive” tumor perfusion (vascularization) with a shift toward reduced metastasis in an orthotopic model of murine prostate cancer |
McCullough DJ et al., 2014. [59] | Prostate tumor blood flow, vascular resistance, patent vessel number, and hypoxia were measured in vivo in conscious rats at rest and during treadmill exercise, and vasoconstrictor responsiveness of resistance arterioles was investigated in vitro | Inducing angiogenesis | Effect of exercise on tumor blood flow | During exercise there is enhanced tumor perfusion and diminished tumor hypoxia due, in part, to a diminished vasoconstriction. The clinical relevance of these findings is that exercise may enhance the delivery of tumor-targeting drugs as well as attenuate the hypoxic microenvironment within a tumor and lead to a less aggressive phenotype |
Almeida PW et al., 2009. [60] | Effect of training protocol in Swiss Mice inoculated with Ehrlich tumor cells | Evading immune destruction | Accumulation in tumor tissue of immunocompetent cells | Moderate swim training markedly reduced the growth of Ehrlich tumors in mice and suppressed macrophage infiltration and neutrophil accumulation in tumor tissue |
Zielinski MR et al., 2004. [61] | Female BALB/c mice were randomly assigned to sedentary control or daily exercised groups | Evading immune destruction | -Effects of exhaustive exercise on EL-4 tumor progression and regression; -Exercise-induced changes in intratumoral cellular composition; -Effects of exercise on markers of cell proliferation and death | Intense exercise influences the microenvironment of a subcutaneously transplanted allogeneic tumor. Daily intense, prolonged exercise caused a delay in tumor growth, a decrease in the number of inflammatory cells (macrophages and neutrophils), and a decrease in the number of blood vessels within the tumors |
Baltgalvis KA, et al., 2008. [62] | The effect of exercise on biological pathways in Apc Min mouse intestinal polyps | Evading growth suppressor | Effect of exercise on apoptosis, b-Catenin, growth signaling, | Exercise can regulate ApcMin mouse intestinal polyp composition |
Abdalla DR et al., 2013. [63] | Cytokine synthesis by lymphocytes in the presence of mammary tumors and the interaction with physical activity | Evading immune destruction | Assessing of cluster of differentiation (CD)3, CD4, and CD8 markers and the expression of interferon-γ, interleukin (IL)-2, IL-4, IL-10, IL-12, transforming growth factor β, and tumor necrosis factor α cytokines | Physical activity promoted reductions in the incidence of tumor development and promoted immune system polarization toward an antitumor Th1 response pattern profile |
Abdalla DR et al., 2014. [64] | Effect of exercise on female BALB/c virgin mice | Evading immune destruction | Effect of exercise on effector of immunity | Practicing physical activity in the presence of a tumor promoted a reduction in tumor development and polarized the immunological response in the direction of the antitumor M1 profile |
Pedersen L et al., 2016. [65] | Effect of exercise on tumor-bearing mice | Evading immune destruction | Training-Dependent Reduction in Tumor Growth Is Associated with Induction of Immune-Related Pathways; -Training Regulates Tumor Growth through Intratumoral NK Cell Infiltration | Voluntary wheel running inhibits tumor onset and progression across a range of tumor models and anatomical locations |
Glasner A et al., 2012. [66] | All experiments were performed using 6- to 8-wk-old mice of the C57BL/6 background | Evading immune destruction | B16 and D122 cells express a ligand or ligands for NKp46/NCR1; NKp46/NCR1-dependent NK degranulation following incubation with B16 and D122 | Enhancing NKp46/NCR1 activity either through the elevation of its expression or by cytokine activation might be beneficial for the treatment of tumor metastasis |
Hampras SS et al., 2012. [68] | Epidemiological study to evaluate predictors of Treg levels in a cohort of healthy women | Evading immune destruction | Effect of a wide range of factors on Treg function | Exercise (3 or more days/week) was found be significant negative predictors of Treg cell levels |
Aoi W et al., 2013. [70] | DNA microarrays were used to compare the transcriptome of muscle tissue in sedentary and exercised young and old mice | Myokines and cancer | Effect of exercise on level of circulating secreted protein acidic and rich in cysteine (SPARC) | Exercise stimulates SPARC secretion from muscle tissues and that SPARC inhibits colon tumorigenesis by increasing apoptosis |
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Giallauria, F.; Testa, C.; Cuomo, G.; Di Lorenzo, A.; Venturini, E.; Lauretani, F.; Maggio, M.G.; Iannuzzo, G.; Vigorito, C. Exercise Training in Elderly Cancer Patients: A Systematic Review. Cancers 2023, 15, 1671. https://doi.org/10.3390/cancers15061671
Giallauria F, Testa C, Cuomo G, Di Lorenzo A, Venturini E, Lauretani F, Maggio MG, Iannuzzo G, Vigorito C. Exercise Training in Elderly Cancer Patients: A Systematic Review. Cancers. 2023; 15(6):1671. https://doi.org/10.3390/cancers15061671
Chicago/Turabian StyleGiallauria, Francesco, Crescenzo Testa, Gianluigi Cuomo, Anna Di Lorenzo, Elio Venturini, Fulvio Lauretani, Marcello Giuseppe Maggio, Gabriella Iannuzzo, and Carlo Vigorito. 2023. "Exercise Training in Elderly Cancer Patients: A Systematic Review" Cancers 15, no. 6: 1671. https://doi.org/10.3390/cancers15061671
APA StyleGiallauria, F., Testa, C., Cuomo, G., Di Lorenzo, A., Venturini, E., Lauretani, F., Maggio, M. G., Iannuzzo, G., & Vigorito, C. (2023). Exercise Training in Elderly Cancer Patients: A Systematic Review. Cancers, 15(6), 1671. https://doi.org/10.3390/cancers15061671