Routine versus aggressive upstream rhythm control for prevention of early atrial fibrillation in heart failure: background, aims and design of the RACE 3 study

The RACE 3 study (ClinicalTrials.gov Identifier NCT00877643) is a prospective, randomised, open-label, multinational, multicenter, superiority trial designed to compare two rhythm-control strategies in patients with short-lasting (i.e. early) persistent AF. The study is initiated and coordinated by the Interuniversity Cardiology Institute of the Netherlands, the University Medical Center Groningen, and the Working Group on Cardiovascular Research the Netherlands. The trial is funded by major grants from the Netherlands Heart Foundation (NHS B 2008 035), the Interuniversity Cardiology Institute Netherlands and the Working Group on Cardiovascular Research the Netherlands and by unrestricted educational grants from pharmaceutical and device companies. None of the sponsors are involved in the study design and data collection, data analysis, or manuscript preparation. The steering committee (see Appendix) designed the study and is responsible for the conduct of the study, data analyses and reporting, and manuscript preparation. Study monitoring, data management and validation are independently performed at the Trial Coordination Center (University Medical Center Groningen, the Netherlands). The study was approved by the institutional review boards of all participating centers. All patients are asked to give written informed consent.

Study recruitment started in 2009, and randomisation is expected to be concluded in the summer of 2014. Follow-up for the primary endpoint will be 1 year. In addition, an exploratory randomised long-term extension of the RACE 3 study will be performed to study the long-term effects of the two treatment strategies. Total follow-up will be 5 years. The study is being conducted in 15 centers in the Netherlands and five centers in the United Kingdom. At present, 168 patients have been included.

The primary objective is to investigate whether in patients with early AF and mild-to-moderate early systolic or diastolic heart failure an aggressive upstream rhythm-control approach, including ACEIs and/or ARBs, MRAs, statins, cardiac rehabilitation therapy, counselling, and dietary restrictions, increases persistence of sinus rhythm compared with conventional rhythm control.

Secondary objectives will investigate whether aggressive upstream rhythm control improves persistence of sinus rhythm without the need for class III ion-channel antiarrhythmic drugs or pulmonary vein ablation, quality of life, left ventricular function, and exercise capacity, and decreases the number of patients with permanent AF, number of electrical cardioversions, numbers of pulmonary vein and atrioventricular node ablations, hospitalisations for heart failure or other cardiovascular reasons, and all-cause mortality. Cost-effectiveness will also be studied. In addition, the association of biomarkers of processes related to remodelling and thrombosis, and the role of genetic factors in AF recurrences, the development of heart failure hospitalisations and other cardiovascular morbidity and mortality will be investigated.

The study population consists of patients with early symptomatic persistent AF and mild-to-moderate early heart failure who are to undergo an electrical cardioversion and who are otherwise stable. A total of 250 patients are to be included. Early symptomatic persistent AF is defined as a total history of AF <5 years before randomisation and a total persistent AF duration of >7 days but <6 months (more than one episode is allowed), with a maximum of one previous electrical cardioversion during the last 2 years; neither electrical nor chemical cardioversion ≥2 years ago are allowed. Mild-to-moderate early heart failure is defined as a total heart failure history <1 year and either diastolic heart failure (left ventricular ejection fraction [LVEF] ≥45 %, New York Heart Association [NYHA] functional class II-III, and additional criteria consisting of echo parameters and/or elevated N-terminal pro-brain natriuretic peptide [NTproBNP]), or systolic heart failure (LVEF 25–45 % and NYHA class I–III). The most important exclusion criteria include severe heart failure, i.e. NYHA class IV or LVEF <25 %, left atrial size >50 mm, severe valvular disease, and present MRA use. A list of inclusion and exclusion criteria is provided in Table 1.

Patients are randomised to either aggressive upstream rhythm control or conventional rhythm control. Randomisation is performed 3 weeks prior to electrical cardioversion in order to start upstream therapy 3 weeks before cardioversion (Fig. 2).

Aggressive upstream rhythm control consists of: 1) Rhythm control for AF including electrical cardioversion and antiarrhythmic treatment as in routine clinical practice, according to the guidelines [2, 38]. The first ECV will be performed without institution of class III ion-channel antiarrhythmic drugs but with a beta-blocker. In addition, patients are started on upstream medication to prevent AF (i.e. ACEIs and/or ARBs, and MRAs, and statins); 2) Optimal medication for heart failure according to the guidelines; 3) Dietary (salt and fluid) restrictions; 4) Counselling by heart failure/rhythm nurse (visits every 6 weeks); and 5) Cardiac rehabilitation. Treatment with upstream therapy is started at randomisation and continued during follow-up. Every effort is made to titrate each patient to the highest dose free from unacceptable side effects for all upstream drugs. Counselling by the heart failure/rhythm nurse is performed every 6 weeks to check and stimulate physical activity and drug adherence and to make patients aware of dietary factors that can reduce disease burden. Heart rhythm is assessed on ECG. Furthermore, patients will be stimulated to quit smoking. Cardiac rehabilitation aims to stimulate patients to be physically active. Cardiac rehabilitation starts immediately after inclusion and lasts 9–11 weeks (at least 6–8 weeks after electrical cardioversion, even if cardioversion needs to be postponed). Supervised physical training takes place at least two, but preferably three times a week. Training is performed according to perceived exertion, in which patients are stimulated to exercise at the highest pace or intensity that still allows for comfortable conversation.

Conventional rhythm control consists of: 1) Rhythm control for AF including electrical cardioversion and antiarrhythmic treatment as in routine clinical practice, according to the guidelines [2, 38]. The first ECV will be performed without institution of class III ion-channel antiarrhythmic drugs but with a beta-blocker; 2) Optimal medication for heart failure according to the guidelines; 3) Follow-up visits (without counselling) every 6 weeks for documentation of heart rhythm with ECG only.

The difference between upstream rhythm control and conventional rhythm control consists of the aggressive institution of upstream drugs (ACEIs and/or ARBs, and MRAs, and statins), dietary restrictions, counselling visits, and cardiac rehabilitation.

Background therapy in both treatment arms: In both treatment arms re-electrical cardioversion is performed after a recurrence with institution of ion-channel antiarrhythmic drugs and/or pulmonary vein ablation according to the guidelines [2].

Follow-up visits take place at one, three, six, nine, and 12 months after the first study electrical cardioversion. Thereafter in the long-term extension, patient visits are twice a year in the aggressive group, alternated with telephone counselling by the research nurse every 6 months between the visits, and once a year in the conventional group. Total follow-up will be 5 years. A blood sample for biomarker and genetic analyses, 24-h urine to assess sodium secretion, echocardiogram, bicycle exercise testing and questionnaires testing quality of life and costs are collected at baseline and at 1 year of follow-up. During follow-up in both treatment arms every effort is made to keep the patient in a rhythm-control strategy. An electrocardiogram is conducted every 6 weeks to aid documentation of recurrent AF. Recurrence of persistent AF is defined as documented, symptomatic AF episodes lasting longer than 7 days or that do not terminate spontaneously. The persistence of AF is preferably verified by 24-h Holter monitoring to show continuous (and not paroxysmal) AF. Cardiovascular hospitalisations and mortality are carefully documented and monitored. A committee of experts who are unaware of the treatment assignments will adjudicate cardiovascular morbidity and mortality.

Permanent AF is defined as accepted AF [2]. Hospitalisation for heart failure is defined as a hospitalisation (≥1 overnight stay) for heart failure requiring intravenous diuretics. Stroke is defined as a disabling haemorrhagic, ischaemic or undetermined stroke confirmed by a neurologist on the basis of computerised tomography or magnetic resonance imaging and necessitating hospitalisation. Systemic emboli must be confirmed by a physician and necessitate hospitalisation. Bleeding is defined as bleeding with a decrease in the haemoglobin value of >20 g/l or requiring blood transfusion, or symptomatic bleeding in a critical organ or area (intra-cranial, retroperitoneal, spinal, ocular, pericardial, atraumatic articular), or as a fatal bleeding. Syncope is defined as sudden temporary loss of consciousness with spontaneous recovery accompanied by trauma necessitating hospital admission (≥1 overnight stay). Life-threatening adverse effects of antiarrhythmic drugs include drug-induced heart failure, conduction disturbances and ventricular arrhythmias necessitating hospital admission (≥1 overnight stay). Myocardial infarction requires at least two of the following: 1) typical chest pain for at least 20 min; 2) electrocardiogram showing signs of acute myocardial infarction; 3) cardiac enzyme elevation more than twice the upper limit of normal. Life-threatening arrhythmias are defined as those arrhythmias requiring hospitalisation. All-cause mortality is categorised by means of blinded adjudication into four categories: death from cardiac arrhythmia, death from non-arrhythmic cardiac causes, death from non-cardiac vascular causes, and death from non-cardiovascular causes.

The presence of the primary endpoint requires that: 1) the patient is still in a rhythm-control strategy according to the attending physician, and 2) that sinus rhythm is maintained after 1 year of follow-up, defined as sinus rhythm during ≥6/7th of the assessable time of continuous 7-day Holter monitoring during the last week of the study. Failure to fulfil these requirements is considered therapy failure. The primary endpoint therefore requires that a 7-day Holter is performed during the last 7 days of follow-up. At least 5/7th of the continuous 7-day Holter monitoring should be assessable; otherwise, the 7-day Holter monitoring is to be repeated.

Secondary endpoints include: 1) The presence of sinus rhythm during 7-day Holter monitoring after 1 year of follow-up with or without antiarrhythmic drugs; 2) Sinus rhythm after 1 year of follow-up during 7-day Holter monitoring without the need for pulmonary vein isolation; 3) Permanent AF; 4) Number of electrical cardioversions; 5) Pulmonary vein ablations; 6) Atrioventricular node ablation; 7) Left ventricular systolic and diastolic function; 8) Exercise capacity; 9) Hospitalisations for heart failure; 10) Hospitalisations for other cardiovascular reasons and 11) All-cause mortality. Additional analyses include quality of life, biomarker and genetic analyses and costs and cost-effectiveness assessment. Quality of life assessment includes the Short Form Health Survey (SF)-36, Multidimensional Fatigue Index (MVI)-20, Eysenck Personality Questionnaire (EPQ), Toronto AF Questionnaire, Center for Epidemiologic Studies Questionnaire (CES-D), Minnesota Questionnaire, European Heart Failure Self-Care Behaviour Scale, Hospital Anxiety and Depression Scale (HADS), and the Ladder of Life. Biomarker analyses will include markers associated with collagen metabolism, inflammation, dedifferentiation, thrombosis, neurohumoral factors and proteomic profiles in order to study the association between severity of remodelling, heart failure and activation of thrombosis and outcome of AF. In addition, genetic analyses will be performed. Costs will be calculated from a societal perspective. All relevant costs inside and outside the health care system are taken into account. Direct medical costs, direct non-medical costs, and indirect non-medical costs will be calculated. The time horizon of the economic evaluation will be equal to that of the clinical study. For the exploratory randomised long-term extension all the above-mentioned endpoints will be assessed as secondary endpoints after 5 years of follow-up.

All data are recorded electronically and are transferred to the server holding the central database at the Trial Coordination Center, which is regularly backed up and password protected. The electronic case record forms are monitored at regular times by the study monitor.

A data safety monitoring board (DSMB) has been established to perform on-going safety surveillance and to perform interim analyses on the safety data, in addition to assessing scientific content. The DSMB is an independent committee that meets on a regular basis to evaluate (serious) adverse events and clinical endpoints.

A committee of experts, masked to the treatment assignments, will adjudicate all possible (clinical) endpoints.

The RACE 3 study is a superiority trial; the null hypothesis (H₀) is that the number of patients in sinus rhythm in the upstream rhythm-control arm will be equal to the number of patients in sinus rhythm in the conventional rhythm-control arm. The alternative hypothesis (H_a) is that there will be more patients in sinus rhythm in the upstream rhythm-control arm than in the conventional rhythm-control arm. To test these hypotheses, chi-square analysis and logistic regression (univariate and multivariate) will be conducted.

The primary efficacy population (intent-to-treat) consists of all randomised patients. Patients will be analysed according to treatment received. The number of subjects who enrol and are randomised will be summarised by treatment group. The number of subjects withdrawing from the study will be tabulated by reason for withdrawal and by treatment group. The time of withdrawal and reason for withdrawal will be listed by treatment group. Potential biases due to withdrawal of subjects will be investigated. Patients’ demographics and disease characteristics at baseline will be tabulated and evaluated for treatment group differences. If differences are found, caution will be taken when interpreting the results of the analyses between groups and the methods may be modified to adjust for these differences.

Unless stated otherwise, all secondary analyses will be performed using the same patients included in the primary analysis. Secondary variables will be analysed using an appropriate statistical test, depending on the nature of the variable. Changes in parameters over time in the different treatment groups will be analysed using repeated measurement analysis or techniques that evaluate the timing of endpoints, when appropriate.

The sample size is based on data of other studies. Persistence of sinus rhythm has been observed in 20 % to 50 % of patients 1 year after electrical cardioversion. These numbers approach 20 % to 30 % when patients have a history of heart failure [39‐42]. In a treatment strategy using electrical cardioversions and amiodarone, persistence of sinus rhythm was observed in 50 % after 1 year of follow-up [43]. Therefore, we expect that after 1 year of follow-up, persistence of sinus rhythm will be observed in 50 % of patients randomised to conventional rhythm control versus 70 % of patients randomised to upstream rhythm control. Based on a type 1 error of 0.05 and a power of 80 %, we calculated an estimated sample size of 100 patients in each study group. Taking into account a dropout rate of 20 %, the sample size should be 250 patients in total. Stratification is done for LVEF< and ≥45 %. An interim analysis consisting of a preliminary open assessment of the primary endpoint will be conducted by an independent data monitoring committee after 100 patients have completed the protocol. This will be done in order to have the option to adapt the sample size if the incidence rates at the interim analyses of the two treatment arms are different than originally expected to find the predefined treatment effect.