OPINION article

Front. Pediatr., 14 October 2022

Sec. Pediatric Oncology

Volume 10 - 2022 | https://doi.org/10.3389/fped.2022.998337

The pediatric oncology exercise field speeds up to address important issues regarding chemotherapy-related cardiotoxicity

  • 1. Department of Pediatric, Division of Hematology and Oncology, Penn State College of Medicine, Hershey, PA, United States

  • 2. Department of Public Health Sciences, Penn State College of Medicine, Hershey, PA, United States

  • 3. School of Kinesiology and Physical Activity Sciences, Faculty of Medicine, University of Montreal, Montreal, QC, Canada

  • 4. Division of Pediatric Hematology and Oncology, Sainte-Justine University Health Center, Research Center, Montreal, QC, Canada

Introduction

Chemotherapy-related cardiotoxicity is well understood and recognized in oncology (, ). Randomized controlled trials have shown that exercise has the potential to prevent chemotherapy-induced cardiotoxicity in adults diagnosed with cancer (). Nevertheless, the pediatric oncology exercise field is in emergence comparatively to the adult oncology exercise field and has also the potential to adequately respond to the chemotherapy-related cardiotoxicity burden that several childhood cancer survivors face. Chemotherapy-related cardiotoxicity causes multiple late comorbidities and is the most common cause of late-onset post-treatment morbidity and mortality in childhood cancer survivors (). In fact, childhood cancer survivors experience a 2- to 10-fold increased risk of cardiovascular diseases relative to the general population () and are seven times more likely to die from cardiovascular complications (e.g., high-grade ectopy, impaired left ventricular contractility, late congestive heart failure, and sudden death) (, ). Through the recently published international pediatric oncology exercise guidelines, clinical and research experts in pediatric oncology have highlighted that “cardiotoxicity” is a specific condition that needs to be considered in the field of pediatric oncology exercise (). Hence, in a recent scoping review discussing the benefits of exercise at different intensities to prevent and manage cancer treatment-related cardiac dysfunction in childhood and adolescent cancer survivors, authors pointed out the necessity to do clinical research to consolidate current findings (). This opinion paper discusses the potential of exercise for childhood cancer survivors to prevent chemotherapy-related cardiotoxicity and associated cardiovascular risk factors. It also presents the primary key challenges encountered in cardio-oncology and exercise settings.

Cardiac health and exercise capacity in childhood cancer survivors

Every year, almost 10,500 children receive a diagnosis of cancer in the United-States. Among them, approximately 85% live at least 5 years post-diagnosis. As of 2019, the National Cancer Institute has reported that there are 483,000 childhood cancer survivors in the United-States (). Several childhood cancer survivors are facing chronic health problem related to their cancer treatments. A study combining the Childhood Cancer Survivor Study (CCSS) and the Surveillance Epidemiology and End Results (SEER) data reported that ∼70% of childhood cancer survivors face mild to moderate chronic condition, and 32% of them face a severe, disabling or life-threatening chronic condition (). The authors also showed that chronic health problems increase with age no later than 5 years post-diagnosis ().

Although medical research and progress have allowed to reach better survival rates, children’s exposure to chemotherapeutic agents causes several long-term adverse effects, such as cardiovascular diseases (). Studies have observed that survivors exposed to anthracycline drugs may face subclinical dysfunctions and cardiac abnormalities (). Indeed, some childhood cancer survivors have a reduced ejection fraction and impaired left ventricular contractility. Moreover, they are at high risk of developing cardiomyopathy and researchers have shown that some childhood cancer survivors are at an early stage of heart failure a few years after the end of their treatment (, ). Chemotherapy-related cardiotoxicity is a leading cause of morbidity and mortality by late congestive heart failure and sudden death (, ). Findings from the CCSS have shown that they are seven times more likely to die from late cardiovascular complications than their healthy peers ().

As a result of the treatment, they received during their cancer, childhood cancer survivors have a lower exercise capacity and cardiorespiratory fitness than their healthy peers (). A study performed as part of the St Jude Lifetime Cohort Study (1,041 people who had survived cancer ≥10 years) showed that exercise intolerance [defined by the authors as the inability to perform as expected on a measure of exercise capacity (<85% of predicted VO2 peak and maximal aerobic capacity <7.9 metabolic equivalents)] was associated with mortality (HR = 3.9; 95% CI = 1.09–14.14), global longitudinal strain (OR = 1.71; 95% CI = 1.11–2.63) and chronotropic incompetence (OR = 3.58; 95% CI = 1.75–7.31) (). Global longitudinal strain is a sensitive measure to detect subclinical left ventricular dysfunction in patients at high risk for heart failure (, ). Chronotropic incompetence, however, is a predictor of mortality in cardiac patients and has been associated with cardiac autonomic nervous system dysfunction (31). Evidence from observational studies shows that these parameters can be improved by exercise in those who are physically active compared to those who are inactive (32, 33). Indeed, in 15,450 adult survivors of childhood cancer, a multicenter cohort analysis observed that exercise exposure was significantly associated with a reduction in the cumulative incidence of all-cause mortality, relapse and health-related mortality (34). A large case-control study showed that exercising less than 3 days per week was associated with an increased risk for all-cause mortality, compared to childhood cancer survivors who exercised more than 3 days per week (35).

Healthy lifestyle in childhood cancer survivors

Over the past decade, clinical and research experts in pediatric oncology have demonstrated that exercise is beneficial and safe for childhood cancer survivors. A state-of-the-art review recently highlighted the importance of exercise in childhood cancer survivors and its key role in preventing chemotherapy-related cardiotoxicity (). Indeed, chemotherapy-related cardiotoxicity leads to cardiac dysfunctions (e.g., decline in left ventricular ejection fraction), because of mitochondrial biogenesis impairment (36), whereas exercise stimulates mitochondrial biogenesis (37). Moreover, observational studies have reported that exercise in childhood cancer survivors improves left ventricular ejection fraction (38, 39) and markers of cardiovascular health (33, 40). Several other pathways also need to be taken into consideration as potential mechanisms of chemotherapy-induced cardiotoxicity, such as inhibition of topoisomerase 2B, oxidative stress, DNA damage and Ca2+ release and myocardial fibrosis (4144). Nevertheless, research on the impact of exercise on theses parameters needs to be pursued in human and animal models to strengthen the evidence (45, 46). Studies have shown, however, that chemotherapy-induced cardiotoxicity may not be reversible in animal models and observational human studies biopsies (4749) which reinforces the importance of exercising during cancer treatments.

Nevertheless, few childhood cancer survivors are physically active. The American Association for Cancer Research (AACR) has reported that almost one in two survivors are not following the physical activity guidelines and that >70% are less likely to be physically active than their healthy peers (50). In an observational cohort study of childhood acute lymphoblastic leukemia survivors, it has been reported that survivors and healthy people had a clinically equivalent level of moderate to vigorous physical activity per week, despite a substantially lower cardiorespiratory fitness level in survivors (). Long-term follow-up of childhood cancer survivors has shown that their physical activity level worsens significantly until they ultimately reach a sedentary behavior state (51). These findings are worrying because a low physical activity level is associated with lower cardiac health (33, 35) and an inactive lifestyle has been associated with cardiovascular disease in childhood cancer survivors (52). To enhance cardiac health prognoses and favor health-related benefits in cancer survivors, the American College of Sports Medicine (ACSM) guidelines recommend achieving at least 30 min per day of aerobic exercise training, in addition to doing resistance training (53). Evidence has shown promising results on cardiac function, while requiring further studies to explore the preventative effects of exercise on cardiotoxicity (41, 53, 54).

Considering the current literature, it is important to note that in several childhood cancer survivors, chemotherapy-related cardiotoxicity is reinforced by their lifestyle and behavioral risk factors adopted during and after their treatment (55, 56). It has been well demonstrated that physical inactivity and sedentary behavior favor cardiovascular diseases (57). As an example, physical inactivity has been described as the fourth cardiovascular risk factor and was pointed out to be responsible for over 5 million deaths (58, 59). Cardiovascular diseases are also associated with other risk factors, such as depressive symptoms, metabolic syndrome, weight status (abdominal obesity, overweight, obesity), dyslipidemia, diabetes, hypertension and smoking (60). These cardiovascular risk factors are commonly reported in childhood cancer survivors (61, 62). Thus, addressing childhood cancer survivors' cardiovascular risk factors could be a powerful way to prevent chemotherapy-related cardiotoxicity, in addition to adopting a preventative approach initiated at cancer diagnosis (63, 64).

Primary key challenges

In a recent scoping review, Wogksch et al. described the associations between physical activity and chronic diseases and reported that childhood cancer survivors who engage in physical activity decrease their risk of cardiovascular diseases, in addition to improving markers of cardiovascular diseases and their risk of mortality, compared to childhood cancer survivors who do not engage in physical activity (33). These findings confirm those of Slater et al., who reported in a cross-sectional study that childhood cancer survivors (n = 319) with a high physical activity level had lower percent fat mass, abdominal subcutaneous and visceral fat, and greater lean body mass and insulin sensitivity than survivors who reported having a low physical activity level (65). Considering the current literature in cardiology, physical activity has a prophylactic effect on cardiovascular risk factors and does not require for patients to engage in several hours per day of exercise (66). Several studies share the important message that physical inactivity always needs to be avoided in childhood cancer survivors, which can be achieved by engaging in regular physical activity. This also joins the international pediatric oncology exercise guidelines global message that moving is important for all pediatric patients with cancer and survivors ().

Exercise can be a useful approach to address chemotherapy-related cardiotoxicity in pediatric patients considering that the probability to develop a cardiovascular disease is approximately 3% in childhood cancer survivors who are 30 years old, a number that increases to about 10% at 45 years old (67). The literature highlights that exercise can be an even more powerful approach when addressing cardiovascular risk factors that may have an impact on chemotherapy-related cardiotoxicity observed in childhood cancer survivors. Managing risk factors in cardio-oncology can be challenging considering that most of childhood cancer survivors are under several cardiac parameter thresholds. It is also important to remind that the cardiac challenges they face are different than those in adult patients with cancer or cardiac patients. During the first year of their follow-up, childhood cancer survivors do not have more cardiovascular risk factors than their healthy counterparts (68). While the clinical observations could be encouraging at first glance, long-term follow-ups have shown that the prevalence of cardiovascular risk factors increases with time, as well as the risk of cardiovascular diseases (67, 69). For example, an observational study showed that the impact of chemotherapy treatment was subclinical and that childhood acute lymphoblastic leukemia survivors were in the first stage of heart failure (). The authors hypothesized that these survivors were compensating for subclinical cardiac remodeling. These findings emphasize the importance of providing cardio-oncology follow-ups to survivors exposed to chemotherapy treatments even if they are not at risk of cardiac diseases at the time of their follow-up appointment. Therefore, ongoing studies are being conducted to enhance our understanding of the effect of exercise on cardiotoxicity in childhood cancer survivors, such as the HIMALAYAS Trial (NCT05023785). The HIMALAYAS trial aims to evaluate the impact of exercise on cardiovascular health in childhood, adolescent and young adult cancer survivors, and is a good example to understand how the research field of pediatric oncology exercise is evolving.

Another challenge is the diagnosis of cardiac dysfunction in childhood cancer survivors. There is no broad consensus on how cardiotoxicity should be measured in childhood cancer survivors, leading to heterogeneity between studies (7074). Indeed, cardiotoxicity can be measured by a combination of different parameters, such as reduced resting systolic function, reduced resting diastolic dysfunction, impaired hemodynamics and systolic functional reserve measured during exercise or reduced exercise capacity or cardiopulmonary fitness (VO2 peak). In this sense, clinicians and researchers need to be cautious when interpreting the reported data and findings on the associations between exercise and cardiotoxicity.

While cardiac dysfunctions can be observed at rest, research experts and clinicians have started recommending an exercise stress test coupled with cardiac imaging techniques to unmask cardiac impairments that are not observable at rest in cancer survivors (7577). It has been demonstrated that survivors can achieve a safe maximal cardiopulmonary exercise test without being limited by symptoms, potential overprotection, or musculoskeletal issues (78). Nevertheless, in clinical settings, performing a maximal cardiopulmonary exercise test can be a challenge since it requires human and financial resources. And although there are other exercise testing procedures that can be used (79), a maximal cardiopulmonary exercise test remains the gold standard in exercise physiology to measure the maximal oxygen consumption of childhood cancer survivors and their cardiorespiratory fitness, which is associated to their cardiac health. It is also important to note that not all exercise physiologists or healthcare providers are trained to perform a maximal cardiopulmonary exercise test and that not all countries authorize an exercise physiologist to perform this type of maximal exercise test, even under the supervision of a cardiologist.

Finally, to strengthen the pediatric oncology exercise field to address the cardiac health of children with cancer and childhood cancer survivors, exercise professionals should be trained to be experts in oncology and more specifically in cardio-oncology, as recommended (8082). Having expertise in these two major fields can be a real challenge since a number of factors have to be taken into consideration. For example, evidence-based medicine in pediatric cardio-oncology is different than in adult cardio-oncology. In both cases, it is important to consider patients' health status, treatment trajectory and adopt a multidisciplinary approach.

Conclusion

The pediatric oncology exercise field is in its early stages and future studies are required to explore the benefits of exercise on the cardiovascular health of childhood cancer survivors. As discussed, the evidence regarding chemotherapy-related cardiotoxicity is limited and looking at the big picture by addressing cardiovascular risk factors would be a research path to follow in order to improve our knowledge. It is also important to take into consideration that childhood cancer survivors are children, adolescents and adult patients with different needs and who are at different stages of their physiological and cardiac development. Addressing chemotherapy-related cardiotoxicity is a great challenge and we hope that this paper will generate interest and ideas.

Statements

Author contributions

MC designed and wrote the manuscript, and DC revised and contributed to the writing of the manuscript. All authors contributed to the article and approved the submitted version.

Acknowledgments

We appreciate the assistance of Ariane Levesque (Department of Psychology, University of Montreal) for her review and edit of the article in the English language.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1.

    LipshultzSEDiamondMBFrancoVIAggarwalSLegerKSantosMVet alManaging chemotherapy-related cardiotoxicity in survivors of childhood cancers. Paediatr Drugs. (2014) 16(5):37389. 10.1007/s40272-014-0085-1

  • 2.

    AvilaMSSiqueiraSRRFerreiraSMABocchiEA. Prevention and treatment of chemotherapy-induced cardiotoxicity. Methodist Debakey Cardiovasc J. (2019) 15(4):26773. 10.14797/mdcj-15-4-267

  • 3.

    TranchitaEMurriAGrazioliECerulliCEmerenzianiGPCeciRet alThe beneficial role of physical exercise on anthracyclines induced cardiotoxicity in breast cancer patients. Cancers. (2022) 14(9):2288. 10.3390/cancers14092288

  • 4.

    ScottJMNilsenTSGuptaDJonesLW. Exercise therapy and cardiovascular toxicity in cancer. Circulation. (2018) 137(11):117691. 10.1161/CIRCULATIONAHA.117.024671

  • 5.

    KirkhamAAEvesNDShaveREBlandKABovardJGelmonKAet alThe effect of an aerobic exercise bout 24 h prior to each doxorubicin treatment for breast cancer on markers of cardiotoxicity and treatment symptoms: a RCT. Breast Cancer Res Treat. (2018) 167(3):71929. 10.1007/s10549-017-4554-4

  • 6.

    HowdenEJBigaranABeaudryRFraserSSeligSFoulkesSet alExercise as a diagnostic and therapeutic tool for the prevention of cardiovascular dysfunction in breast cancer patients. Eur J Prev Cardiol. (2019) 26(3):30515. 10.1177/2047487318811181

  • 7.

    LipshultzSEAdamsMJColanSDConstineLSHermanEHHsuDTet alLong-term cardiovascular toxicity in children, adolescents, and young adults who receive cancer therapy: pathophysiology, course, monitoring, management, prevention, and research directions: a scientific statement from the American heart association. Circulation. (2013) 128(17):192795. 10.1161/CIR.0b013e3182a88099

  • 8.

    KhannaAPequenoPGuptaSThavendiranathanPLeeDSAbdel-QadirHet alIncreased risk of all cardiovascular disease subtypes among childhood cancer survivors. Circulation. (2019) 140(12):10413. 10.1161/CIRCULATIONAHA.119.041403

  • 9.

    GrenierMALipshultzSE. Epidemiology of anthracycline cardiotoxicity in children and adults. Semin Oncol. (1998) 25(4 Suppl 10):7285. 10.1053/j.seminoncol.2006.04.019

  • 10.

    KremerLCvan DalenECOffringaMOttenkampJVoutePA. Anthracycline-induced clinical heart failure in a cohort of 607 children: long-term follow-up study. J Clin Oncol. (2001) 19(1):1916. 10.1200/JCO.2001.19.1.191

  • 11.

    WurzAMcLaughlinELateganCChamorro ViñaCGrimshawSLHamariLet alThe international pediatric oncology exercise guidelines (iPOEG). Transl Behav Med. (2021) 11(10):191522. 10.1093/tbm/ibab028

  • 12.

    KendallSJLangleyJEAghdamMCrooksBNGiacomantonioNHeinze-MilneSet alThe impact of exercise on cardiotoxicity in pediatric and adolescent cancer survivors: a scoping review. Curr Oncol. (2022) 29(9):635063. 10.3390/curroncol29090500

  • 13.

    National cancer Institute. Childhood cancer survivor study: An overview United-States. Bethesda, Maryland: U.S. Department of Health and Human Services (2021). Available from:https://www.cancer.gov/types/childhood-cancers/ccss.

  • 14.

    PhillipsSMPadgettLSLeisenringWMStrattonKKBishopKKrullKRet alSurvivors of childhood cancer in the United States: prevalence and burden of morbidity. Cancer Epidemiol, Biomarkers Prev. (2015) 24(4):65363. 10.1158/1055-9965.EPI-14-1418

  • 15.

    LeerinkJMde BaatECFeijenEABellersenLvan DalenECGrotenhuisHBet alCardiac disease in childhood cancer survivors: risk prediction, prevention, and surveillance: JACC cardiooncology state-of-the-art review. Cardio Oncol. (2020) 2(3):36378. 10.1016/j.jaccao.2020.08.006

  • 16.

    ArmstrongGTPlanaJCZhangNSrivastavaDGreenDMNessKKet alScreening adult survivors of childhood cancer for cardiomyopathy: comparison of echocardiography and cardiac magnetic resonance imaging. J Clin Oncol. (2012) 30(23):287684. 10.1200/JCO.2011.40.3584

  • 17.

    LipshultzSEColanSDGelberRDPerez-AtaydeARSallanSESandersSP. Late cardiac effects of doxorubicin therapy for acute lymphoblastic leukemia in childhood. N Engl J Med. (1991) 324(12):80815. 10.1056/NEJM199103213241205

  • 18.

    LipshultzSELipsitzSRSallanSEDaltonVMMoneSMGelberRDet alChronic progressive cardiac dysfunction years after doxorubicin therapy for childhood acute lymphoblastic leukemia. J Clin Oncol. (2005) 23(12):262936. 10.1200/JCO.2005.12.121

  • 19.

    YlänenKPoutanenTSavikurki-HeikkiläPRinta-KiikkaIEerolaAVettenrantaK. Cardiac magnetic resonance imaging in the evaluation of the late effects of anthracyclines among long-term survivors of childhood cancer. J Am Coll Cardiol. (2013) 61(14):153947. 10.1016/j.jacc.2013.01.019

  • 20.

    CaruMCorbinDPerieDLemayVDelfrateJDrouinSet alDoxorubicin treatments induce significant changes on the cardiac autonomic nervous system in childhood acute lymphoblastic leukemia long-term survivors. Clin Res Cardiol. (2019) 108(9):10008. 10.1007/s00392-019-01427-9

  • 21.

    De CaroESmeraldiATrocchioGCalevoMHanauGPongiglioneG. Subclinical cardiac dysfunction and exercise performance in childhood cancer survivors. Pediatr Blood Cancer. (2011) 56(1):1226. 10.1002/pbc.22606

  • 22.

    LipshultzSEFrancoVIMillerTLColanSDSallanSE. Cardiovascular disease in adult survivors of childhood cancer. Annu Rev Med. (2015) 66:16176. 10.1146/annurev-med-070213-054849

  • 23.

    ArmstrongGTLiuQYasuiYNegliaJPLeisenringWRobisonLLet alLate mortality among 5-year survivors of childhood cancer: a summary from the childhood cancer survivor study. J Clin Oncol. (2009) 27(14):232838. 10.1200/JCO.2008.21.1425

  • 24.

    CaruMSamoilenkoMDrouinSLemayVKernLRomoLet alChildhood acute lymphoblastic leukemia survivors have a substantially lower cardiorespiratory fitness level than healthy Canadians despite a clinically equivalent level of physical activity. J Adolesc Young Adult Oncol. (2019) 8(6):67483. 10.1089/jayao.2019.0024

  • 25.

    NessKKPlanaJCJoshiVMLuepkerRVDurandJBGreenDMet alExercise intolerance, mortality, and organ system impairment in adult survivors of childhood cancer. J Clin Oncol. (2020) 38(1):29. 10.1200/JCO.19.01661

  • 26.

    MillerAMLopez-MitnikGSomarribaGLipsitzSRHinkleASConstineLSet alExercise capacity in long-term survivors of pediatric cancer: an analysis from the cardiac risk factors in childhood cancer survivors study. Pediatr Blood Cancer. (2013) 60(4):6638. 10.1002/pbc.24410

  • 27.

    PlanaJCGalderisiMBaracAEwerMSKyBScherrer-CrosbieMet alExpert consensus for multimodality imaging evaluation of adult patients during and after cancer therapy: a report from the American society of echocardiography and the European association of cardiovascular imaging. J Am Soc Echocardiogr. (2014) 27(9):91139. 10.1016/j.echo.2014.07.012

  • 28.

    FeiLKeelingPJSadoulNCopieXMalikMMcKennaWJet alDecreased heart rate variability in patients with congestive heart failure and chronotropic incompetence. Pacing Clin Electrophysiol. (1996) 19(4 Pt 1):47783. 10.1111/j.1540-8159.1996.tb06519.x

  • 29.

    KawasakiTKaimotoSSakataniTMikiSKamitaniTKuribayashiTet alChronotropic incompetence and autonomic dysfunction in patients without structural heart disease. Europace. (2010) 12(4):5616. 10.1093/europace/eup433

  • 30.

    PaolilloSAgostoniPDe MartinoFFerrazzanoFMarsicoFGargiuloPet alHeart rate during exercise: mechanisms, behavior, and therapeutic and prognostic implications in heart failure patients with reduced ejection fraction. Heart Fail Rev. (2018) 23(4):53745. 10.1007/s10741-018-9712-1

  • 31.

    BertrandÉCaruMLemayVAndelfingerGLaverdiereCKrajinovicMet alHeart rate response and chronotropic incompetence during cardiopulmonary exercise testing in childhood acute lymphoblastic leukemia survivors. Pediatr Hematol Oncol. (2021) 38(6):56480. 10.1080/08880018.2021.1894279

  • 32.

    NaaktgeborenWRGroenWGJacobseJNStegginkLCWalenkampAMvan HartenWHet alPhysical activity and cardiac function in long-term breast cancer survivors: a cross-sectional study. JACC CardioOncol. (2022) 4(2):18391. 10.1016/j.jaccao.2022.02.007.

  • 33.

    WogkschMDGoodenoughCGFinchERPartinRENessKK. Physical activity and fitness in childhood cancer survivors: a scoping review. Aging and Cancer. (2021) 2(4):11228. 10.1002/aac2.12042

  • 34.

    ScottJMLiNLiuQYasuiYLeisenringWNathanPCet alAssociation of exercise with mortality in adult survivors of childhood cancer. JAMA Oncol. (2018) 4(10):13528. 10.1001/jamaoncol.2018.2254

  • 35.

    CoxCLNolanVGLeisenringWYasuiYOggSWMertensACet alNoncancer-related mortality risks in adult survivors of pediatric malignancies: the childhood cancer survivor study. J Cancer Surviv. (2014) 8(3):46071. 10.1007/s11764-014-0353-7

  • 36.

    KangDWWilsonRLChristopherCNNormannAJBarnesOLesanseeJDet alExercise cardio-oncology: exercise as a potential therapeutic modality in the management of anthracycline-induced cardiotoxicity. Front Cardiovasc Med. (2021) 8:805735. 10.3389/fcvm.2021.805735

  • 37.

    FreyssenetDBerthonPDenisC. Mitochondrial biogenesis in skeletal muscle in response to endurance exercises. Arch Physiol Biochem. (1996) 104(2):12941. 10.1076/apab.104.2.129.12878

  • 38.

    SmithWANessKKJoshiVHudsonMMRobisonLLGreenDM. Exercise training in childhood cancer survivors with subclinical cardiomyopathy who were treated with anthracyclines. Pediatr Blood Cancer. (2013) 61(5): 9425. 10.1002/pbc.24850

  • 39.

    JärveläLSSarasteMNiinikoskiHHannukainenJCHeinonenOJLähteenmäkiPMet alHome-based exercise training improves left ventricle diastolic function in survivors of childhood ALL: a tissue Doppler and velocity vector imaging study. Pediatr Blood Cancer. (2016) 63(9):162935. 10.1002/pbc.26051

  • 40.

    MoralesJSValenzuelaPLHerrera-OlivaresAMBaño-RodrigoACastillo-GarcíaARincón-CastanedoCet alExercise interventions and cardiovascular health in childhood cancer: a meta-analysis. Int J Sports Med. (2020) 41(3):14153. 10.1055/a-1073-8104

  • 41.

    ChenJJWuPTMiddlekauffHRNguyenKL. Aerobic exercise in anthracycline-induced cardiotoxicity: a systematic review of current evidence and future directions. Am J Physiol Heart Circ Physiol. (2017) 312(2):H213h22. 10.1152/ajpheart.00646.2016

  • 42.

    CarrascoRCastilloRLGormazJGCarrilloMThavendiranathanP. Role of oxidative stress in the mechanisms of anthracycline-induced cardiotoxicity: effects of preventive strategies. Oxid Med Cell Longev. (2021) 2021:8863789. 10.1155/2021/8863789

  • 43.

    BhatiaS. Genetics of anthracycline cardiomyopathy in cancer survivors: JACC: cardioOncology state-of-the-art review. JACC CardioOncol. (2020) 2(4):53952. 10.1016/j.jaccao.2020.09.006

  • 44.

    MurabitoAHirschEGhigoA. Mechanisms of anthracycline-induced cardiotoxicity: is mitochondrial dysfunction the answer?Front Cardiovasc Med. (2020) 7:35. 10.3389/fcvm.2020.00035

  • 45.

    YenCJHungCHTsaiWMChengHCYangHLLuYJet alEffect of exercise training on exercise tolerance and level of oxidative stress for head and neck cancer patients following chemotherapy. Front Oncol. (2020) 10:1536. 10.3389/fonc.2020.01536

  • 46.

    HahnVSLenihanDJKyB. Cancer therapy–induced cardiotoxicity: basic mechanisms and potential cardioprotective therapies. J Am Heart Assoc. (2014) 3(2):e000665. 10.1161/JAHA.113.000665

  • 47.

    MackayBEwerMSCarrascoCHBenjaminRS. Assessment of anthracycline cardiomyopathy by endomyocardial biopsy. Ultrastruct Pathol. (1994) 18(1-2):20311. 10.3109/01913129409016291

  • 48.

    JensenBVSkovsgaardTNielsenSL. Functional monitoring of anthracycline cardiotoxicity: a prospective, blinded, long-term observational study of outcome in 120 patients. Ann Oncol. (2002) 13(5):699709. 10.1093/annonc/mdf132

  • 49.

    TimmKNPereraCBallVHenryJAMillerJJKerrMet alEarly detection of doxorubicin-induced cardiotoxicity in rats by its cardiac metabolic signature assessed with hyperpolarized MRI. Commun Biol. (2020) 3(1):110. 10.1038/s42003-019-0734-6

  • 50.

    FlorinTAFryerGEMiyoshiTWeitzmanMMertensACHudsonMMet alPhysical inactivity in adult survivors of childhood acute lymphoblastic leukemia: a report from the childhood cancer survivor study. Cancer Epidemiol Biomarkers Prev. (2007) 16(7):135663. 10.1158/1055-9965.EPI-07-0048

  • 51.

    SmithWANolanVGRobisonLLHudsonMMNessKK. Physical activity among cancer survivors and those with no history of cancer- a report from the national health and nutrition examination survey 2003–2006. Am J Transl Res. (2011) 3(4):34250.

  • 52.

    ShankarSMMarinaNHudsonMMHodgsonDCAdamsMJLandierWet alMonitoring for cardiovascular disease in survivors of childhood cancer: report from the cardiovascular disease task force of the Children’s oncology group. Pediatrics. (2008) 121(2):e38796. 10.1542/peds.2007-0575

  • 53.

    CampbellKLWinters-StoneKMWiskemannJMayAMSchwartzALCourneyaKSet alExercise guidelines for cancer survivors: consensus statement from international multidisciplinary roundtable. Med Sci Sports Exercise. (2019) 51(11):237590. 10.1249/MSS.0000000000002116

  • 54.

    CostelloBTRobertsTJHowdenEJBigaranAFoulkesSJBeaudryRIet alExercise attenuates cardiotoxicity of anthracycline chemotherapy measured by global longitudinal strain. JACC CardioOncol. (2019) 1(2):298301. 10.1016/j.jaccao.2019.09.002

  • 55.

    CardinaleDIacopoFCipollaCM. Cardiotoxicity of anthracyclines. Front Cardiovasc Med. (2020) 7:26. 10.3389/fcvm.2020.00026

  • 56.

    ZamoranoJLLancellottiPRodriguez MuñozDAboyansVAsteggianoRGalderisiMet al2016 ESC position paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC committee for practice guidelines: the task force for cancer treatments and cardiovascular toxicity of the European society of cardiology (ESC). Eur Heart J. (2016) 37(36):2768801. 10.1093/eurheartj/ehw211

  • 57.

    ChomistekAKMansonJEStefanickMLLuBSands-LincolnMGoingSBet alRelationship of sedentary behavior and physical activity to incident cardiovascular disease: results from the Women’s health initiative. J Am Coll Cardiol. (2013) 61(23):234654. 10.1016/j.jacc.2013.03.031

  • 58.

    WenCPWuX. Stressing harms of physical inactivity to promote exercise. Lancet. (2012) 380(9838):1923. 10.1016/S0140-6736(12)60954-4

  • 59.

    YusufSHawkenSOunpuuSDansTAvezumALanasFet alEffect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. (2004) 364(9438):93752. 10.1016/S0140-6736(04)17018-9

  • 60.

    World Health Organization. Cardiovascular diseases (CVDs): World Health Organization (2021). Available at:http://www.who.int/mediacentre/factsheets/fs317/en/.

  • 61.

    LemayVCaruMSamoilenkoMDrouinSAlosNLefebvreGet alPrevention of long-term adverse health outcomes with cardiorespiratory fitness and physical activity in childhood acute lymphoblastic leukemia survivors. J Pediatr Hematol Oncol. (2019) 41(7):e450e8. 10.1097/MPH.0000000000001426

  • 62.

    LuongoCRandazzoEIughettiLDI IorgiNLocheSMaghnieMet alCardiometabolic risk in childhood cancer survivors. Minerva Pediatr. (2021) 73(6):588605. 10.23736/S2724-5276.21.06544-7

  • 63.

    CaruMDuhamelGMarcilVSultanSMelocheCBouchardIet alThe VIE study: feasibility of a physical activity intervention in a multidisciplinary program in children with cancer. Support Care Cancer. (2020) 28(6):262736. 10.1007/s00520-019-05085-5

  • 64.

    BélangerVDelormeJNapartukMBouchardIMelocheCCurnierDet alEarly nutritional intervention to promote healthy eating habits in pediatric oncology: a feasibility study. Nutrients. (2022) 14(5):102445. 10.3390/nu14051024

  • 65.

    SlaterMERossJAKellyASDengelDRHodgesJSSinaikoARet alPhysical activity and cardiovascular risk factors in childhood cancer survivors. Pediatr Blood Cancer. (2015) 62(2):30510. 10.1002/pbc.25276

  • 66.

    CaruMKernLBousquetMCurnierD. Preventive fraction of physical fitness on risk factors in cardiac patients: retrospective epidemiological study. World J Cardiol. (2018) 10(4):2634. 10.4330/wjc.v10.i4.26

  • 67.

    FaberJWingerterANeuMAHenningerNEckerleSMünzelTet alBurden of cardiovascular risk factors and cardiovascular disease in childhood cancer survivors: data from the German CVSS-study. Eur Heart J. (2018) 39(17):155562. 10.1093/eurheartj/ehy026

  • 68.

    LipshultzERChowEJDoodyDRArmenianSHAsselinBLBakerKSet alCardiometabolic risk in childhood cancer survivors: a report from the Children’s oncology group. Cancer Epidemiol Biomarkers Prev. (2022) 31(3):53642. 10.1158/1055-9965.EPI-21-0360

  • 69.

    ArmstrongGTOeffingerKCChenYKawashimaTYasuiYLeisenringWet alModifiable risk factors and major cardiac events among adult survivors of childhood cancer. J Clin Oncol. (2013) 31(29):367380. 10.1200/JCO.2013.49.3205

  • 70.

    HarakeDFrancoVIHenkelJMMillerTLLipshultzSE. Cardiotoxicity in childhood cancer survivors: strategies for prevention and management. Future Cardiol. (2012) 8(4):64770. 10.2217/fca.12.44

  • 71.

    StoneJRKannegantiRAbbasiMAkhtariM. Monitoring for chemotherapy-related cardiotoxicity in the form of left ventricular systolic dysfunction: a review of current recommendations. JCO Oncol Prac. (2021) 17(5):22836. 10.1200/OP.20.00924

  • 72.

    WolfCMReinerBKühnAHagerAMüllerJMeierhoferCet alSubclinical cardiac dysfunction in childhood cancer survivors on 10-years follow-up correlates with cumulative anthracycline dose and is best detected by cardiopulmonary exercise testing, circulating serum biomarker, speckle tracking echocardiography, and tissue Doppler imaging. Front Pediatr. (2020) 8:123. 10.3389/fped.2020.00123

  • 73.

    SofiaRMelitaVDe VitaARuggieroARomanoAAttinàGet alCardiac surveillance for early detection of late subclinical cardiac dysfunction in childhood cancer survivors after anthracycline therapy. Front Oncol. (2021) 11:1649. 10.3389/fonc.2021.624057

  • 74.

    RyersonABBorderWLWasilewski-MaskerKGoodmanMMeachamLAustinHet alAssessing anthracycline-treated childhood cancer survivors with advanced stress echocardiography. Pediatr Blood Cancer. (2015) 62(3):5028. 10.1002/pbc.25328

  • 75.

    KirkhamAAViraniSACampbellKL. The utility of cardiac stress testing for detection of cardiovascular disease in breast cancer survivors: a systematic review. Int J Womens Health. (2015) 7:12740. 10.2147/IJWH.S68745

  • 76.

    KearneyMCGallop-EvansECockcroftJRStöhrEJLeeEBackxKet alCardiac dysfunction in cancer survivors unmasked during exercise. Eur J Clin Invest. (2017) 47(3):21320. 10.1111/eci.12720

  • 77.

    FoulkesSCostelloBTHowdenEJJanssensKDillonHToroCet alExercise cardiovascular magnetic resonance reveals reduced cardiac reserve in pediatric cancer survivors with impaired cardiopulmonary fitness. J Cardiovasc Magn Reson. (2020) 22(1):64. 10.1186/s12968-020-00658-4

  • 78.

    CaruMLaverdièreCLemayVDrouinSBertoutLKrajinovicMet alMaximal cardiopulmonary exercise testing in childhood acute lymphoblastic leukemia survivors exposed to chemotherapy. Support Care Cancer. (2021) 29(2):98796. 10.1007/s00520-020-05582-y

  • 79.

    MizrahiDFardellJECohnRJPartinREHowellCRHudsonMMet alThe 6-minute walk test is a good predictor of cardiorespiratory fitness in childhood cancer survivors when access to comprehensive testing is limited. Int J Cancer. (2019) 47(3):84755. 10.1002/ijc.32819

  • 80.

    GevaertSAHalvorsenSSinnaevePRSambolaAGulatiGLancellottiPet alEvaluation and management of cancer patients presenting with acute cardiovascular disease: a consensus document of the Acute CardioVascular Care (ACVC) association and the ESC council of cardio-oncology-part 1: acute coronary syndromes and acute pericardial diseases. Eur Heart J Acute Cardiovasc Care. (2021) 10(8):94759. 10.1093/ehjacc/zuab056

  • 81.

    CuomoAMercurioVVarricchiGGaldieroMRRossiFWCarannanteAet alImpact of a cardio-oncology unit on prevention of cardiovascular events in cancer patients. ESC Heart Fail. (2022) 9(3):166676. 10.1002/ehf2.13879

  • 82.

    HammLFSandersonBKAdesPABerraKKaminskyLARoitmanJLet alCore competencies for cardiac rehabilitation/secondary prevention professionals: 2010 update: position statement of the American association of cardiovascular and pulmonary rehabilitation. J Cardiopulm Rehabil Prev. (2011) 31(1):210. 10.1097/HCR.0b013e318203999d

Summary

Keywords

physical activity, prevention, cardio-oncology, Childhood Cancer Survivors, survivorship, doxorubicin-related cardiotoxicity, healthy lifestyle, cardiovascular risk factors

Citation

Caru M and Curnier D (2022) The pediatric oncology exercise field speeds up to address important issues regarding chemotherapy-related cardiotoxicity. Front. Pediatr. 10:998337. doi: 10.3389/fped.2022.998337

Received

19 July 2022

Accepted

28 September 2022

Published

14 October 2022

Volume

10 - 2022

Edited by

David Mizrahi, The University of Sydney, Australia

Reviewed by

Stephen Foulkes, Baker Heart and Diabetes Institute, Australia Willeke Naaktgeboren, The Netherlands Cancer Institute (NKI), Netherlands

Updates

Copyright

*Correspondence: Maxime Caru

Specialty Section: This article was submitted to Pediatric Oncology, a section of the journal Frontiers in Pediatrics

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics