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1.
Sci Rep ; 10(1): 9710, 2020 06 16.
Artigo em Inglês | MEDLINE | ID: mdl-32546796

RESUMO

Cardiorespiratory fitness is an independent risk factor for cardiovascular disease and shortened life expectancy in breast cancer survivors. This randomised controlled trial (n = 153) was designed for patients with a physically inactive lifestyle prediagnosis and concurrently referred to adjuvant chemotherapy. We compared two 12-week exercise interventions aimed at physiological and patient-reported outcomes (cardiorespiratory fitness, muscle strength, metabolic markers, physical activity, pain, fatigue), including a 39-week follow-up. A supervised hospital-based moderate to high intensity group exercise intervention was compared to an instructed home-based individual pedometer intervention. The two 12-week interventions included oncologists' recommendations and systematic health counselling. Outcomes were measured at baseline and week 6, 12 and 39. Primary outcome cardiorespiratory fitness declined significantly during chemotherapy and was restored in both interventions at follow-up. The interventions effectively engaged breast cancer patients in sustaining physical activities during and following adjuvant treatment. A composite metabolic score improved significantly. Positive cardiorespiratory fitness responders had improved clinical effects on fatigue, pain and dyspnoea versus negative responders. We conclude that a loss of cardiorespiratory fitness among physically inactive breast cancer patients may be restored by early initiated interventions and by adapting to physical activity recommendations, leading to a decreased cardiovascular risk profile in breast cancer survivors.


Assuntos
Terapia por Exercício/métodos , Fadiga/etiologia , Aptidão Física/fisiologia , Adjuvantes Imunológicos/uso terapêutico , Adjuvantes Farmacêuticos/efeitos adversos , Adjuvantes Farmacêuticos/uso terapêutico , Adulto , Mama/patologia , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/fisiopatologia , Sobreviventes de Câncer , Aptidão Cardiorrespiratória/fisiologia , Quimioterapia Adjuvante/efeitos adversos , Exercício Físico/fisiologia , Feminino , Humanos , Pessoa de Meia-Idade , Força Muscular/fisiologia , Aptidão Física/psicologia , Qualidade de Vida , Comportamento Sedentário
2.
BMJ Open Sport Exerc Med ; 1(1): e000021, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-27900123

RESUMO

INTRODUCTION: Anti-neoplastic treatment is synonymous with an inactive daily life for a substantial number of patients. It remains unclear what is the optimal setting, dosage and combination of exercise and health promoting components that best facilitate patient adherence and symptom management in order to support cardio-respiratory fitness and lifestyle changes in an at-risk population of pre-illness physically inactive cancer patients. METHODS: Patients with breast or colon cancer referred to adjuvant chemotherapy and by the oncologists pre-screening verified as physically inactive were eligible to enter a randomised three-armed feasibility study comparing a 12-week supervised hospital-based moderate to high intensity exercise intervention or alternate an instructive home-based12-week pedometer intervention, with usual care. RESULTS: Using a recommendation based physical activity screening instrument in order to correspond with cardio-respiratory fitness (VO2 peak) proved to be an applicable method to identify pre-illness physically inactive breast and colon cancer patients. The study demonstrated convincing recruitment (67%), safety and intervention adherence among breast cancer patients; while the attendance rate for colon cancer patients was notably lower (33%). VO2-peak declined on average 12% across study groups from baseline to 12 weeks though indices towards sustaining watt performance and reduce fat mass favoured the hospital-based intervention. Pedometer use was well adapted in both breast and colon cancer patients. CONCLUSIONS: Despite a fair adherence and safety, the current study calls into question whether aerobic exercise, regardless of intensity, is able to increase VO2-peak during texane-based chemotherapy in combination with Neulasta in physically inactive breast cancer patients. TRIAL REGISTRATION: ISRCTN24901641.

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