Authors: E. M. Guinan, A. E. Bennett, S. L. Doyle, L. O’Neill, J. Gannon, G. Foley, J. A. Elliott, J. O’Sullivan, J. V. Reynolds, J. Hussey
Categories: Research Article, Health-related quality of life, Oesophageal cancer, Physical activity, Physical functioning, Survivorship care
Oesophagectomy remains the only curative intervention for oesophageal cancer, with defined nutritional and health-related quality of life (HR-QOL) consequences. It follows therefore that there is a significant risk of decline in physical wellbeing with oesophagectomy however this has been inadequately quantified. This study prospectively examines change in physical functioning and habitual physical activity participation, from pre-surgery through 6-months post-oesophagectomy.
Patients scheduled for oesophagectomy with curative intent were recruited. Key domains of physical functioning including exercise tolerance (six-minute walk test (6MWT)) and muscle strength (hand-grip strength), and habitual physical activity participation, including sedentary behaviour (accelerometry) were measured pre-surgery (T0) and repeated at 1-month (T1) and 6-months (T2) post-surgery. HR-QOL was measured using the EORTC-QOL C30.
Thirty-six participants were studied (mean age 62.4 (8.8) years, n = 26 male, n = 26 transthoracic oesophagectomy). Mean 6MWT distance decreased significantly from T0 to T1 (p = 0.006) and returned to T0 levels between T1 and T2 (p < 0.001). Percentage time spent sedentary increased throughout recovery (p < 0.001) and remained significantly higher at T2 in comparison to T0 (p = 0.003). In contrast, percentage time spent engaged in either light or moderate-to-vigorous intensity activity, all reduced significantly (p < 0.001 for both) and remained significantly lower at T2 in comparison to T0 (p = 0.009 and p = 0.01 respectively). Patients reported deficits in multiple domains of HR-QOL during recovery including global health status (p = 0.04), physical functioning (p < 0.001) and role functioning (p < 0.001). Role functioning remained a clinically important 33-points lower than pre-operative values at T2.
Habitual physical activity participation remains significantly impaired at 6-months post-oesophagectomy. Physical activity is a measurable and modifiable target for physical rehabilitation, which is closely aligned with patient-reported deficits in role functioning. Rehabilitation aimed at optimising physical health in oesophageal cancer survivorship is warranted.
Keywords: Physical functioning, Physical activity, Oesophageal cancer, Survivorship care, Health-related quality of life
Oesophagectomy is an exemplar model of a complex operation, with a relatively high postoperative risk of major morbidity [1], and defined nutritional and health-related quality of life (HR-QOL) implications [2, 3]. Oesophageal cancer is the eighth most common cancer globally, with an estimated 456,000 new cases in 2012 (3.2% of all cancers) and the sixth most common cause of cancer mortality (4.9% of all cancer deaths) [4]. Approximately 20% of patients diagnosed with oesophageal cancer undergo oesophagectomy with curative intent [5]. This complex procedure involving upper laparotomy usually in combination with thoracotomy and one lung anaesthesia, and is associated with significant postoperative morbidity. Postoperative pulmonary complications (PPCs), which are among the most serious postoperative morbidity, occur in 15–30% of patients post-oesophagectomy and are the primary cause of postoperative mortality, contributing to 45.5–55% of post-oesophagectomy deaths [6]. In the modern era, surgery is preceded by chemotherapy or combination chemoradiotherapy for the majority of patients who present with locally advanced disease [2]; an approach which has contributed to 5-year survival rates of up to 47% [7]. Accordingly, at a time when overall survival is improving, there is a growing emphasis on the nutritional, physical and emotional wellbeing of patients undergoing curative treatment for locally advanced disease [8].
Oesophageal cancer and its treatment, particularly oesophagectomy, leads to significant anatomic and physiologic alterations of the gastrointestinal tract and thus the long-term nutritional implications of curative treatment for oesophageal cancer are well documented [9]. Up to 80% of patients are cachexic at presentation [10], with recent data demonstrating that weight loss, sarcopenia, malabsorption and altered gut hormone function persist into survivorship [11–13]. Notwithstanding the considerable survival advantages of modern multimodal treatment regimens when compared with surgery alone [2, 7], chemotherapy and chemoradiotherapy can adversely impact body composition and muscle strength [14], with emerging evidence linking loss of skeletal muscle mass during neoadjuvant therapy with chemotherapy toxicity and major postoperative complications [15].
It follows therefore that there is a significant risk of decline in physical functioning resulting from both curative treatment for oesophageal cancer and poor nutritional status. Declines in cardiopulmonary fitness, a key determinant of physical functioning [16], ability to engage in activities of daily living [17], and increased risk of postoperative complications [18] are reported with neoadjuvant chemo(radio)therapy [19–21], and associated with higher mortality risk at 1-year post oesophagectomy [21]. Physical inactivity is associated with increased postoperative risk following oesophagectomy [22] and is a defined problem among cancer survivors [23, 24], associated with HR-QOL [25] and, increasingly, survival outcomes [26]. While an acute decline in physical fitness, muscle strength and HR-QOL is described from pre-oesophagectomy to post-operative discharge [17], prospective evaluations characterising the impact of oesophagectomy on physical outcomes, particularly long-term evaluations of physical functioning, are lacking [27]. Subjectively, patients report perceived deficits in physical functioning domains of HR-QOL which persist into survivorship [28, 29]; however, the measured impact of oesophagectomy on physical functioning is inadequately quantified. We have previously described deficits in cardiorespiratory fitness and moderate-to-vigorous intensity physical activity participation in oesophageal cancer survivors at up to two years post-operatively, in comparison to age- and gender-matched controls [30], suggesting that curative treatment exerts a profound and lasting impact on physical status.
With increasing emphasis on survivorship care in oesophageal cancer, there is a recognised need to better understand the physical consequences of oesophageal cancer and its treatment in order to develop tailored rehabilitation programmes involving exercise and diet prescription to attenuate the impact of treatment on physical functioning and optimise HR-QOL in recovery [31]. Cancer survivorship models emphasise that exercise rehabilitation implemented early in the cancer continuum, particularly within the first 6-months postoperatively, is likely to have the greatest impact on HR-QOL [32]. This study therefore seeks to characterise the impact of oesophagectomy on physical functioning and habitual physical activity participation in early postoperative recovery and up to 6-months post-oesophagectomy to inform targets and priorities for exercise rehabilitation during this period.
Patients with a diagnosis of oesophageal cancer and scheduled for oesophagectomy were identified from the upper gastrointestinal clinic at the Oesophageal and Gastric Centre at St James’s Hospital (SJH), Dublin, Ireland, a high-volume national centre. Ethical approval was obtained from the SJH–Tallaght Hospital Joint Research Ethics Committee. Informed written consent was obtained prior to study commencement. Using a prospective observational design, participants were recruited pre-operatively and measurements were collected pre-surgery (T0), at 1-month post-surgery (T1) and at 6-months post-surgery (T2). Visits were conducted in the Wellcome Trust-HRB Clinical Research Facility at SJH.
All participants were treated according to standardised care pathways involving either multimodal therapy or surgery only. Patients with locally advanced disease received either pre- and postoperative chemotherapy as per the MAGIC regimen [33] or neoadjuvant chemoradiation as per the CROSS protocol [34]. Surgical resection was performed at least 6-weeks post neoadjuvant therapy. The surgical approach involved either transthoracic en-bloc oesophagectomy (2-stage or 3-stage) or transhiatial oesophagectomy following evaluation of patient demographics and comorbidities as previously described [35]. Postoperatively, patients were immediately extubated and admitted to a monitored bed, normally the high dependency unit (HDU). Patients were transferred to the ward on postoperative day (POD)3 or when medically suitable. The institutional enhanced recovery after surgery protocol included the following elements; early enteral feeding via jejunostomy, early mobilisation and airway clearance techniques from POD1, removal of chest drains on POD2 and contrast study for anastomotic integrity on POD4. Postoperative analgesia was managed using thoracic epidural analgesia. The jejunostomy remained in-situ for 4–6 weeks postoperatively and supplemental overnight enteral nutrition was continued on discharge for a planned duration of 4 weeks in all participants [36]. Patients were reviewed at regular intervals postoperatively by the specialist dietetic service.
Demographic and clinicopathologic data was gathered from medical charts and from the institutional upper gastrointestinal cancer database. Postoperative data included in-hospital mortality, hospital and critical care length of stay (LOS) and postoperative complications.
Weight (kg) was recorded using a calibrated Seca scale. Height (cm) was measured barefoot using a Seca stadiometer. Body mass index (BMI) was calculated as weight (kg)/height (m^2^). Mid-arm circumference (MAC) was measured in cm at the halfway point between the olecranon process of the ulna and the acromion process of the scapula. Waist circumference (cm) was measured at the mid-point between the iliac crest and the 12th rib following gentle expiration. MAC and waist circumference were taken in duplicate and averaged for data entry. Bioimpedance analysis was used to determine body composition and was performed using the Seca mBCA 515 (Seca, Hamburg, Germany).
Functional exercise performance was measured using the 6-min walk test (6MWT). Participants walked at their fastest pace for 6 min along a 30 m walkway with the aim of achieving the furthest distance possible with standardised verbal encouragement [37]. Isometric hand grip strength (HGS) (kg) was measured using a handheld digital dynamometer (Jamar). Measures were taken in triplicate, bilaterally and the highest measure recorded.
Physical activity was measured using the ActiGraph GT3X+ triaxial accelerometer (Actigraph Pensacola, FL). The accelerometer was worn on the hip, secured with an elastic belt, during waking hours for 7 days following all study visits. Data were analysed using the Actilife software using standardised algorithms to analyse time in physical activity domains and adherence to physical activity guidelines (150 min moderate-to-vigorous intensity physical activity (MVPA)/week, accumulated in bouts ≥10 min [38]). The following cut-points were used to define activity sedentary 0–99 counts per minute (CPM), light 100–2019 CPM, moderate 2020–5998 and vigorous ≥5999 [39]. A valid data was defined as one with 10 h of data and at least four consecutive days were required for analysis.
QOL was assessed using the European Organisation for Research and Treatment of Cancer (EORTC) Core QOL Questionnaire, the QLQ-C30 (version 3.0). This validated instrument assessed QOL in functional, symptom and global domains. Scores for each question were calculated according to the EORTC QLQ-C30 manual and linearly transformed into a 0–100 scale [40].
This is an exploratory descriptive study, which considers the impact of oesophagectomy on clinically important outcomes using a patient-centred, multifaceted approach. Using previous literature to estimate an effect size of 0.5 for the effect of treatment for oesophageal cancer on physical status [14] a significance level of 0.05 and a power of 0.8, a sample size of 33 was calculated for repeated measures. This sample estimate is consistent with other publications in this field [17].
SPSS version 22.0 was used for analyses. Variables were tested for normality using the Shapiro-Wilks test. Normally distributed variables were summarised as mean and standard deviation (SD). Non-normally distributed data were summarised as median and interquartile range (IQR). Categorical variables are presented as frequency (percentage).
A mixed between-within subjects analysis of variance (ANOVA) was conducted to assess the change in outcomes across three timepoints in consideration of the impact of treatment regimen (CROSS, MAGIC or surgery only). Data was tested to ensure that the assumptions of homogeneity of variance (Levene’s test for equal variances) and homogeneity of intercorrelations (Box’s M statistic) were not violated. Multivariate statistics were interpreted. Interaction effects were examined and reported where significant. Differences between the groups were presented as partial eta squared *(*η^2^) effect sizes. The strength of the differences was interpreted as small (η^2^ < 0.01), medium (η^2^ = 0.01–0.06) or large (η^2^ = 0.06–0.138). Post-hoc pairwise comparison for comparison of main effects were examined using Bonferroni analysis. A Friedman test was used to examine changes in non-parametric outcomes over the three timepoints. Associations between measures of anthropometry and measures of functional performance were assessed using Pearson Product Moment Correlation Coefficients. Statistical significance was taken at p < 0.05.
Between January 2014 and October 2016, 52 patients were recruited and tested pre-surgery, of whom 43 returned for repeat measures 1-month post-surgery and 36 returned at 6-months post-surgery. The mean time between a pre-surgery assessment and a 1-month post-surgery assessment was 66 (21) days. The mean time between 1-month and 6-months post-surgery assessments was 157 (42) days. Reasons for not completing follow-up measurements disease progression (n = 6); prolonged postoperative morbidity (n = 3); participant death (n = 2) and participant drop-out (n = 5) (Fig. 1). Demographic characteristics are presented in Table 1. Demographic characteristics of the final sample were comparable to those lost to follow-up.
Fig. 1 Participant Recruitment and Retention. Flow of participants through the study
Body weight, BMI, fat mass, body fat percentage, fat free mass (FFM), skeletal muscle mass, waist circumference and MAC all reduced significantly over the study period (Table 2). Pre-operatively, participants had a mean body weight of 81.9 (16.4) kg and a mean BMI of 27.8 (4.3 kg/m^2^. Male participants had a pre-operative waist circumference of 98.6 (12.3) cm and female participants had a mean waist circumference of 91.38 (9.8) cm. Percentage weight loss from pre-surgery to 1-month (− 6.2 (4.3) %) and to 6-months (− 8.9 (7.4) %) post-surgery was clinically significant. There was no impact of treatment approach on weight (p = 0.356, η^2^ = 0.069), BMI (p = 0.963, η^2^ = 0.003), fat mass (p = 0.0.78, η^2^ = 0.225), body fat percentage (p = 0.375, η^2^ = 0.082), skeletal muscle mass (p = 0.102, η^2^ = 0.188), waist circumference (p = 0.306, η^2^ = 0.102) or MAC (p = 0.399, η^2^ = 0.088).
Pre-operatively, male participants walked a mean distance of 513.7 (73.6)m and female participants walked a mean distance of 477.6 (76.0)m during the 6MWT. Significant changes in 6MWT distance were observed over the study period (p < 0.001, η^2^ = 0.51) (Table 3). Mean 6MWT distance decreased significantly from pre-surgery (502.6 (76.7)m) to 1-month post-surgery (463.5 (98.4)m) (mean change − 39.1 (95%CI − 68.3 to − 9.9)m, p = 0.006), and then increased from 1-month post-surgery to 6-months post-surgery (507.8 (87.8)m) (mean change 44.3 (95%CI 23.0 to 65.5)m, p < 0.001) (Fig. 2a). There was no difference between the distance walked pre-surgery and at 6 months post-surgery (p = 1.00). There was no impact of treatment approach on 6MWT distance (p = 0.639, η^2^ = 0.033). Distance walked during the 6MWT did not correlate with any measure of body composition at any timepoint.
Fig. 2 Functional Exercise Tolerance and Physical Activity Levels Pre-Surgery and at 1-Month and 6-Months Post-Surgery. Box-plots depicting distance walked during the six-minute walk test distance (Fig. 1a), percentage walking hours spent sedentary (Fig. 1b) and in light intensity activity (Fig. 1c) and minutes per day spent in moderate-to-vigorous intensity activity (Fig. 1d) at each timepoint. All participants experienced significant acute decreases in walk distance and activity levels from pre-surgery to 1-month post-surgery which improved again to 6-months post-surgery, however all domains of physical activity, including sedentary behaviour, remained impaired at 6-months post-surgery in comparison to pre-surgery values
Preoperatively, mean HGS was 38.4 (8.0) kg in males and 23.6 (4.8) kg in females. Mean HGS did not change over time from pre-surgery (35.5 (9.9) kg); neither to 1-month post-surgery (33.9 (9.9) kg) nor to 6-months post-surgery (35.8 (10.9) kg) (p = 0.91, η^2^ = 0.15) (Table 3). There was no impact of treatment approach on HGS (p = 0.706, η^2^ = 0.025). HGS correlated positively and strongly with skeletal muscle mass at T0 (r = 0.78, p < 0.001), T1 (r = 0.73, p < 0.001) and T3 (r = 0.68, p < 0.001).
In the week before surgery, participants spent 7.2 (1.6) hours/day sedentary, 4.1 (1.5) hours/day engaged in light intensity activity and a median of 11.5 (31.6) minutes/day engaging in moderate-to-vigorous intensity activity. There were significant effects for time for sedentary behaviour (p < 0.002, η^2^ = 0.46), light intensity activity (p < 0.001, η^2^ = 0.69), and daily MVPA (p < 0.001) (Table 3). There was no impact of treatment approach on either sedentary behaviour (p = 0.766, η^2^ = 0.028) or light intensity activity participation (p = 0.694, η^2^ = 0.038).
On post-hoc analysis, sedentary behaviour increased from pre-surgery (7.2 (1.6) hours/day) to 1-month post-surgery (8.7 (1.7) hours per day) (mean change (1.5 (0.39–2.7 h per day), p < 0.05) and remained elevated at six-months post-surgery (8.46 (1.7) hours/day) (Fig. 2b). At 6-months post-surgery, sedentary behaviour was significantly higher than pre-operative levels (mean difference 1.3 (0.4–2.2 h/day), p = 0.05). Sedentary behaviour did not correlate with skeletal muscle mass at any timepoint.
In contrast, light intensity activity decreased from pre-surgery (4.1 (1.5) hours/day) to 1-month post-surgery (2.3 (0.9) hours per day (mean change − 1.8 (95%CI 2.5 to − 1.1) (p < 0.05) and increased from 1-month post-surgery to six months post-surgery (3.5 (1.4) hours/day (mean change 1.2 (95%CI 0.5 to 1.9) hours/day, p < 0.05) (Fig. 2c). Minutes spent engaging in light intensity activity did not correlate with skeletal muscle mass at any timepoint.
Similarly, daily minutes spent engaging in MVPA, decreased from a median of 11.5 (31.6) minutes/day pre-surgery to 4.7 (12.9) minutes/day at 1-month post-surgery (p < 0.001), and increased from 1-month postoperative to 6-months postoperatively (12.5 (24.6) minutes/day (p = 0.001) (Fig. 2c). At 6-months post-surgery, daily minutes spent engaging in MVPA was significantly lower than preoperative levels (p = 0.01).
Health-related quality of life scores are detailed in Table 4**.** There were significant changes over time in multiple domains of quality of life on the QLQ-C30 including global health status (p = 0.04), physical functioning (p < 0.001), role functioning (p < 0.001), fatigue (p < 0.001), pain (p < 0.001), dyspnoea (p < 0.001), appetite loss (p = 0.002) and diarrhoea (p = 0.004). Clinically important (> 10-point) change in physical function and role function was reported from pre-surgery to 1-month post-surgery. Role functioning remained impaired (33-points lower) at 6-months post-surgery in comparison with pre-operative values.
This study provides a novel prospective evaluation of measured and perceived change in physical functioning following oesophagectomy. It demonstrates that habitual physical activity participation and perceived role functioning remain significantly impaired at 6-months post-surgery, despite exercise capacity recovering to preoperative levels. Consistent with previous reports, symptom scores worsened postoperatively [41] and percentage weight loss was clinically significant at 6-months [13]. This significant and clinically relevant pattern of deterioration highlights the challenges of transitioning from active treatment to survivorship post-oesophagectomy and adjusting to the ‘new normal’ after cancer.
The significant short-term and long-term impairments in global HR-QOL, and specifically in physical functioning and symptom burden, that arise following oesophagectomy are well-reported [3, 29, 41–43]. Consistent with the pattern of deterioration in HR-QOL reported by others [41, 42], we observed the largest postoperative impact in the physical functioning domain, specifically in the physical function and role function scales, of the EORTC QOQ-C30. While both scales had improved by 6-months post-surgery, role function remained a clinically relevant 33-points lower in comparison with pre-operative values. Clinically important deteriorations in physical functioning are reported with all curative interventions for oesophageal cancer, including neoadjuvant therapy, minimally invasive surgery and open surgical resection [29]. Importantly however, despite improvements in the majority of HR-QOL domains over time, patient-perceived physical functioning remains impaired at 1-year [41], 2-years [44] and up to 3-years post oesophagectomy [43]. Uniquely, we demonstrate that this profound patient-perceived deterioration in physical health is matched by clinically relevant changes in habitual activity participation.
Functional decline associated with cancer treatment is typically examined using validated, objective measures of physical functioning [16]. Using this approach, we observed an acute deterioration in physical activity participation, as measured by accelerometry, at 1-month post-oesophagectomy, with physical activity levels and sedentary behaviour remaining impaired at 6-months. Consistent with this, we have previously reported that moderate-to-vigorous intensity activity participation is significantly lower at 2-years post-oesophagectomy in comparison with age- and gender-matched controls [30]. Importantly, accelerometry captures habitual activity participation during waking hours and therefore, engagement in activities of daily living, a construct that is well-aligned with the role functioning domain of the EORTC QLQ-C30 [45], which was were perceived by participants to remain considerably impaired in survivorship. Role functioning considers an individual’s ability to engage in activities that are typical for their age and social setting [45]. In patients with cancer, physical activity levels are known to reduce at cancer diagnosis and rarely return to baseline levels following treatment completion [24]. Compared to those who are inactive or sub-optimally active, cancer survivors who exercise to recommended levels consistently report higher HR-QOL scores, particularly in physical and role functioning domains [25], hypothesised to be driven by the positive effects of physical fitness on mental wellbeing and social engagement [46], making physical activity an important and influential target in survivorship care.
Cardiopulmonary fitness, the primary measure of physical functioning [16], is impaired by the iterative attritional impact of multimodal treatment regimens in oesophageal cancer [27]. We observed a large, clinically important reduction (− 39.10 (95%CI − 68.28 to − 9.92) m) in 6MWT distance at 1-month post-oesophagectomy, consistent with the decline previously reported in a Japanese cohort from pre-surgery (563.3 (73.2) m) to pre-hospital discharge (485.3 (85.6) m) [17]. In colorectal resection, 6MWT distance at 4-weeks post-surgery is discriminative of older age, poorer physical status, open resection and occurrence of postoperative complications, and therefore is a valuable indicator of early physical recovery [47]. While the 6MWT provides a valid measure of functional exercise status in patients with cancer [48], reliability and reproducibility data is lacking [16], and walking distances correlate poorly with cardiopulmonary fitness in comparison with incremental walking protocols [49]. In contrast to our observation that 6MWT distance returned to preoperative values at 6-months postoperatively, suggesting an element of natural recovery in this cohort, a study in a Japanese cohort, utilising the highly sensitive cardiopulmonary exercise test, reported a reduction in exercise capacity from 1186.6 (300.30) ml/min pre-oesophagectomy to 916.1 (238.6) ml/min 3-months postoperatively (p < 0.0001) following open resection [50]. Furthermore, we previously reported significantly lower walking distance in disease-free patients up to 2-years post-oesophagectomy (558.33 (146.43)m) in comparison with age- and gender-matched controls (773.48 (114.00)m) using a progressive, incremental walking protocol [30]. Therefore, it is likely that cardiopulmonary fitness remains impaired in oesophageal cancer survivorship; however further prospective evaluations using sensitive measures of fitness are required.
The nutritional challenge of recovery post-oesophagectomy is well-documented. Consistent with previous reports, in this cohort weight loss remained significant at 6-months [13] and symptom burden was considerable in early post-operative recovery. While HGS, a reliable indicator of whole-body muscle strength and nutritional status [51], remained stable over the study period, we have previously reported significant deficits in grip strength with loss of lean body mass during neo-adjuvant therapy [14]. Furthermore, sarcopenia remains prevalent in survivorship with 35% of patients sarcopenic at 1-year post-oesophagectomy [13]. This complex interplay between nutritional insufficiency and physical deterioration makes survivorship rehabilitation particularly challenging. We recently designed, implemented and evaluated the Rehabilitation Strategies Following Oesophagogastric Cancer (ReStOre) programme, a rehabilitation programme for oesophagogastric survivorship comprising exercise training, individualised dietary counselling and multidisciplinary education, with a strong focus on self-management [52–54], leading to clinically important improvements in cardiopulmonary fitness [52], inflammatory status [53], and multiple domains of HR-QOL [54]. The ReStOre programme, the first exemplar in oesophagogastric cancer rehabilitation, included participants up to 5-years post-surgery, however rehabilitative measures implemented earlier in survivorship, particularly within the first 6-months, are likely to have greatest effect [32] and address the issues identified by this work. Consistent with established clinical rehabilitation models, cancer rehabilitation commencing from diagnosis and continuing through the treatment trajectory, may have a key role in attenuating the impact of multiple attritional oncologic treatments, optimising patient condition for surgical intervention and supporting patients through recovery and into survivorship [8, 31].
This work has some limitations which are acknowledged. Firstly, participant retention was challenging with 69% of those initially recruited (n = 52) available for evaluation at 6-months (n = 36). This is an inevitable challenge of prospective data collection in a cohort undergoing complex surgical and medical interventions. Reasons for attrition are reported and were largely attributed to disease progression and protracted postoperative morbidity. Importantly, those included in the final analyses had comparable baseline characteristics to those lost to follow-up. Nonetheless, the final study cohort represent those who are recovering relatively well at 6 months post-surgery and therefore generalisability is limited. The sample size is comparable to other published work in this field [17, 30, 50]. The use of objective measures of physical functioning is a considerable strength of this work. By employing these methods, multiple measurable and modifiable targets for physical rehabilitation were identified which were well-aligned with patient-reported survivorship issues.
These results add to the growing evidence that improvements in oncological outcomes in oesophageal cancer have led to a newly emergent cohort of cancer survivors with considerable physical and nutritional concerns. Importantly, results identify deficits in both perceived role functioning and measured activity participation in recovery, suggesting that patients experience considerable challenges adjusting to the ‘new normal’ in survivorship. Multidisciplinary rehabilitation with a strong focus on self-management and overcoming barriers to habitual activity participation is warranted.
We would like to acknowledge the assistance and support of the Wellcome Trust/HRB Clinical Research Facility at St James’ Hospital in providing a dedicated environment for the conduct of high quality clinical research activities. We thank Sinead King, Upper Gastrointestinal Database Manager, St James’s Hospital for her assistance with data collection. We also wish to thank the study participants for kindly agreeing to take time to participate.
Study design and concept was developed by EMG, SLD, JOS, JVR and JH. EMG, AEB, SLD, LON, JG and GF completed data collection and management. Participant recruitment and medical oversight was provided by JAE and JVR. EMG and AEB conducted statistical analysis. EMG prepared the manuscript for publication. All authors read and approved the final manuscript.
This project was funded through a grant awarded by the Health Research Board, Ireland (POR HRA-POR-2014-535). The Health Research Board had no role in the design of the study, in the collection, analysis, and interpretation of data or in writing the manuscript.
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethical approval was obtained from the SJH–Tallaght Hospital Joint Research Ethics Committee (Reference number 2014–11 Chairman’s Action (2)). Participants provided written informed consent.
Not applicable.
The authors declare that they have no competing interests.
E. M. Guinan, Phone: +353-1-896-4125, Email: emguinan@tcd.ie
A. E. Bennett, Email: abennet@tcd.ie
S. L. Doyle, Email: doyles4@tcd.ie
L. O’Neill, Email: oneilll8@tcd.ie
J. Gannon, Email: gannonj1@tcd.ie
G. Foley, Email: foleyg4@tcd.ie
J. A. Elliott, Email: jelliott@tcd.ie
J. O’Sullivan, Email: osullij4@tcd.ie
J. V. Reynolds, Email: reynoldsjv@stjames.ie
J. Hussey, Email: jmhussey@tcd.ie
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.