Esophagogastric Cancer Surgery: Comparison
Please note this is a comparison between Version 2 by Rita Xu and Version 3 by Rita Xu.

Esophagogastric cancer is among the most common malignancies worldwide. Surgery with or without neoadjuvant therapy is the only potentially curative treatment option. Although esophagogastric resections remain associated with major surgical trauma and significant postoperative morbidity. Prehabilitation has emerged as a novel strategy to improve clinical outcomes by optimizing physical and psychological status before major surgery through exercise and nutritional and psychological interventions.

  • esophageal cancer
  • gastric cancer
  • esophagectomy
  • gastrectomy

1. Introduction

Esophagogastric cancer (esophageal and gastric cancer; EGC) is among the most common malignancies worldwide, with over 1.6 million new cases and 1.2 million deaths annually [1][2][3]. Surgery is the main and only curative treatment option [4][5]. However, gastric and esophageal resections remain associated with high postoperative morbidity and mortality rates [4][5][6]. Current evidence indicates the benefits of neoadjuvant chemo(radio)therapy [7][8][9]. Preoperative cytotoxic treatment improves oncological outcomes, but impairs patients’ physical and nutritional status, promotes sarcopenia, and decreases physiological reserve, thus further increasing the surgery-related risk [4][10][11][12]. Consequently, there is a need for novel strategies to improve EGC surgery outcomes.
Recently, prehabilitation has emerged as a way to prepare a patient for major surgery. As it is a relatively new concept in surgical oncology, definitions of prehabilitation still vary. They consistently state that it is a pre-emptive preparation of a patient to reduce risks and enhance recovery after a stressful event. Prehabilitation has significantly reduced postoperative morbidity in some high-risk patients undergoing major abdominal surgery [13]. Additionally, it reduces systemic inflammation [14], attenuates chemotherapy-induced toxicity [15], modulates several host- and tumor-related pathways during standard chemotherapy [15], and may even promote tumor regression following neoadjuvant therapy [16]. Current studies on prehabilitation are very heterogenous in a perioperative care pathway and measured outcomes. Moreover, some studies show controversial results, as prehabilitation has no benefit in frail patients undergoing minimally invasive colorectal cancer surgery [17]. Therefore, the role of prehabilitation in modern EGC surgery remains unclear.

2. The Current Concept of Prehabilitation in Esophagogastric Cancer Surgery

Current definitions of prehabilitation vary but consistently state that it is a pre-emptive preparation of a patient to reduce risks and enhance recovery after a stressful event. EGC surgery is an ideal example of a stressor because of extensive surgical trauma, physiological consequences of previous cytotoxic treatments, and psychological distress. These factors interact with the burden of cancer, which includes impaired nutritional and physiological reserves due to cachexia, malnutrition, and sarcopenia. The preoperative period constitutes a unique opportunity to prepare the patient for these challenges because most are highly motivated to change behavior for perioperative benefits [18]. Contemporary prehabilitation programs may include one (unimodal) or several (multimodal) interventions aiming to correct modifiable risk factors, promote a patient’s physical activity, optimize nutritional status, and intervene in psychological wellbeing. There is no consensus on the optimal design of a prehabilitation program; thus, different approaches have been investigated (Table 1).
Table 1. Characteristics of studies investigating prehabilitation for esophagogastric cancer surgery.
Author; Year Design Description and Number of Participants; (n) Measured Outcomes N–O Score Jadad Score
Allen et al. [19]; 2021 RCT Esophagogastric cancer patients scheduled for surgery after neoadjuvant chemotherapy;

(n = 54)
Primary outcome:
  • Change in AT by CPET.
Secondary outcomes:
  • Change in peak VO2 by CPET;
  • Sarcopenia measured by computed tomography;
  • HGS;
  • Health-related quality of life by EORTC QLQ-C30 questionnaire, Beck Anxiety Inventory, and Beck Depression score;
  • Full adherence to the planned neoadjuvant chemotherapy and its toxicity;
  • Weekly step count;
  • Postoperative morbidity;
  • 30-day hospital readmission rate;
  • 3-year mortality rate.
N/A 3
Minnella et al. [20]; 2018 RCT Esophagogastric cancer patients scheduled for surgery ± neoadjuvant treatment; (n = 68) Primary outcome:
  • Change in functional capacity over time by 6MWD.
Secondary outcomes:
  • Postoperative morbidity at 30 days;
  • Length of hospital stay;
  • 30-day hospital visits;
  • 30-day readmission rates;
  • 30-day death rates;
  • Full adherence to the planned neoadjuvant chemotherapy;
  • Compliance with prehabilitation program.
N/A 3
Valkenet et al. [21]; 2018 RCT Esophageal cancer patients scheduled for surgery ± neoadjuvant treatment; (n = 270) Primary outcome:
  • Postoperative pneumonia rate.
Secondary outcomes:
  • Respiratory muscle function: maximum inspiratory pressure and inspiratory muscle endurance;
  • Pulmonary function: expiratory volume in 1 s and FVC;
  • Postoperative complication rate;
  • Duration of mechanical bowel ventilation;
  • Length of hospital stay;
  • Quality of life by EuroQol-5D and SF-12 questionnaires;
  • Physical activity by SQUASH questionnaire;
  • Fatigue by MFI-20 questionnaire.
N/A 3
van Adrichem et al. [22]; 2014 RCT Esophageal cancer patients scheduled for surgery ± neoadjuvant CRT; (n = 45) Primary outcome:
  • Postoperative pulmonary complications rate.
Secondary outcomes:
  • Length of stay;
24], 4 pilot studies [23][27][28][29], 2 non-randomized control trials [25][26], and 1 matched-pair analysis [30]. Despite the fact that all studies focused on prehabilitation for EGC surgery, they are heterogeneous in applied interventions and measured outcomes. Table 2 and Table 3 show the structure of prehabilitation programs and their impact on clinical outcomes.
Table 2. Structure of interventions in prehabilitation programs for esophagogastric cancer surgery.
Author; Year Prehabilitation Group Control Group
Type of Prehabilitation (Unimodal vs. Multimodal) Timing of Prehabilitation Interventions Used for Prehabilitation
Allen et al. [
CRT: chemoradiotherapy; N/A: not applicable.
Table 3. Outcomes of included studies evaluating prehabilitation for esophagogastric cancer surgery.
Author; Year Prehabilitation Impact on Physical Status Prehabilitation Impact on Postoperative Outcomes Other Effects of Prehabilitation
19]; 2021 Multimodal Prehabilitation was initiated for 15 preoperative weeks.
  • Exercise intervention: supervised aerobic, resistance, and flexibility training twice a week and home-based exercise training three times per week;
  • Nutritional intervention: needs-based nutritional interventions with frequent, tailored dietetic input from specialist dieticians, increasing calorie and protein intake where appropriate depending on assessments and physical activity levels;
  • Psychological intervention: six sessions of medical coaching, which included discussion of health status, strength recognition, resilience profiling and development, social and support systems, emotional management, and goal setting.
  • Standard of care
Allen et al. [19]; 2021 Prehabilitation attenuated peak VO2 decrease and skeletal muscle loss following neoadjuvant therapy. Additionally, HGS was better retained in the prehabilitation group, and patients in this group were more physically active by higher weekly step count. Prehabilitation had no impact on the

number and severity of complications, length of hospital stay, 30-day readmission rates, and 3-year cancer-related mortality.
Prehabilitation improved QoL by global health status after 2 cycles of neoadjuvant chemotherapy and at 2 weeks, 6 weeks, and 6 months postoperatively. Additionally, prehabilitation resulted in better BAI and DBI II scores preoperatively and 6 weeks and 6 months postoperatively.

A higher proportion of patients in the prehabilitation group received neoadjuvant chemotherapy at full dose.
Minnella et al. [17]; 2018 Multimodal Prehabilitation was initiated before the initial surgery or at the time of neoadjuvant therapy.
  • Exercise intervention: individualized, home-based exercise training program including aerobic and strengthening exercise;
  • Nutritional intervention: metabolic requirement was adjusted to meet the increased nutritional demand. Food-based dietary advice was given, and a whey protein supplement was prescribed to guarantee a daily protein intake.
  • Standard of care
Minnella et al. [17]; 2018
Prehabilitation improved functional capacity before and after surgery by increasing 6MWD. Prehabilitation had no impact on the number and severity of complications, length of hospital stay, emergency department visits, and readmission rates. N/A Valkenet et al. [31]; 2018 Unimodal Prehabilitation was initiated for 2 weeks or longer. When neoadjuvant therapy was administered, prehabilitation started afterward.
Valkenet et al. [31]; 2018Prehabilitation resulted in a higher increase in inspiratory muscle strength and endurance.
  • Exercise intervention: inspiratory muscle training.
Prehabilitation did not affect postoperative pneumonia and other postoperative complication rates.
  • Standard of care
Prehabilitation did not affect the quality of life, fatigue, and physical activity levels.
  • Stay in ICU;
  • Number of reintubations;
van Adrichem et al. [32]; 2014
  • Maximal inspiratory pressure before and after training;
  • Lung functions (FVC, FEV1, FEV1/FVC, and PIF);
  • Feasibility by the number of IMT-related adverse events, compliance to training, and a self-estimated load of participation.
Unimodal
N/A 3
Prehabilitation was initiated for 3 weeks. When neoadjuvant therapy was administered, prehabilitation started afterward.
  • Exercise intervention: high-intensity inspiratory muscle training.
van Adrichem et al. [32]; 2014
  • Exercise intervention: endurance inspiratory muscle training
The increase in maximal inspiratory pressure was similar between the groups which received preoperative inspiratory muscle training.
The incidence of postoperative pulmonary complications, length of stay, and the number of reintubations were lower in the high-intensity inspiratory muscle training group. N/A Xu et al. [23]; 2015 Pilot study (RCT) Xu et al. [22]Esophageal cancer patients scheduled for neoadjuvant CRT and surgery; (n = 59) ; 2015Primary outcomes:
  • Functional walking capacity by 6MWD and strength by HGS;
Multimodal
  • Nutritional status by BW and fat-free lean mass by bioelectrical impedance.
Prehabilitation was initiated for 4–5 weeks during the neoadjuvant chemoradiotherapy.
Secondary outcome:
  • Exercise intervention: nurse-supervised walking;
  • Nutritional intervention: nutritional advice.
  • Treatment tolerance by interruptions in chemotherapy or radiotherapy; unplanned hospital admission; grade > 2 neutropenia; fever > 38.5 °C; intravenous nutritional support and wheelchair use.
N/A 3
  • Standard of care
Xu et al. [22]; 2015 Prehabilitation ameliorated decline in 6MWD and hand-grip strength. N/A Prehabilitation ameliorated weight and lean muscle mass loss.

Additionally, patients in the prehabilitation group had a significantly lower need for intravenous nutritional support and wheelchair use.
Yamana et al. [24]; 2015 RCT Yamana et al. [18]; 2015Esophageal cancer patients scheduled for surgery ± neoadjuvant treatment; (n = 63) Primary outcome:
Unimodal
  • Postoperative pulmonary complication rate.
Secondary outcomes:
  • Respiratory function by FVC, FEV1, FEV1%, and PEF.
N/A 3
Yamana et al. Prehabilitation was initiated for ≥7 days before the surgery. [18]; 2015
  • Exercise intervention: respiratory muscle training; muscle strengthening exercises for the lower limbs and abdominal muscles; biking on an ergometer.
Prehabilitation did not affect respiratory function representing parameters (FVC, FEV1, FEV1%, and PEF).
  • Standard of care
Prehabilitation ameliorated the severity of postoperative complications (by lower Clavien–Dindo score) and postoperative pneumonia (by lower Utrecht Pneumonia Scoring System score). N/A Christensen et al. [25]; 2018 Christensen et al. Non-randomized control trial [23]; 2018Patients with GOJ adenocarcinoma scheduled for neoadjuvant treatment and surgery; (n = 50) Unimodal
Christensen et al. Prehabilitation was initiated at the time of neoadjuvant treatment. [23]; 2018Primary outcome:
  • Frequency of serious adverse events (defined as events that prevented surgery).
Secondary outcomes:
  • Neoadjuvant treatment tolerability;
Prehabilitation resulted in improved fitness and muscle strength.
  • Exercise intervention: supervised high-intensity aerobic and resistance exercise.
Prehabilitation did not affect the postoperative complication rate.
  • Postoperative complication rate;
  • Postoperative hospital stay;
  • Patient-reported tolerability to neoadjuvant treatment by FACT-E questionnaire;
  • Response to treatment by infiltration of the resection margin and immunoscore, tumor regression grade by Mandard, and pathological tumor stage (pTNM).
8 N/A
  • Standard of care
Prehabilitation resulted in improved quality of life by FACT-E score.
Dettling et al. [26]; 2013 Non-randomized controlled trial Patients scheduled for esophagectomy ± neoadjuvant treatment; (
n = 83) Dettling et al. [24]; 2013 Unimodal Prehabilitation was initiated for 2 weeks or longer.Primary outcomes:
Dettling et al. [24]
  • Feasibility by the occurrence of adverse effects, patients’ satisfaction;
  • Exercise intervention: inspiratory muscle training.
  • Initial effectiveness by pre-operative improvement in respiratory function.
Secondary outcomes:
  • Postoperative pneumonia rate;
  • Length of hospital stay;
  • Duration of mechanical ventilation;
  • Reintubation rate;
  • Length of stay in the ICU;
  • Postoperative morbidity rate.
8 N/A
; 2013
  • Standard of care
Argudo et al. [27]; 2020 Pilot study (prospective interventional study) Esophagogastric cancer patients scheduled for neoadjuvant treatment and surgery; (n
Prehabilitation increased inspiratory muscle strength and endurance. Prehabilitation did not affect postoperative pneumonia and other complication rates. N/A = 40) Argudo et al. [19]; 2020
Argudo et al. [19]; 2020
  • Feasibility by TELOS components;
  • Tolerability;
  • Exercise capacity by cardiopulmonary exercise testing;
  • Pulmonary and muscle function;
  • Peripheral muscle function;
  • Health-related quality of life by EORTC QLQ-C30 questionnaire.
Multimodal Prehabilitation was initiated after neoadjuvant chemotherapy for 5 weeks. 6
  • Exercise intervention: high-intensity interval training on the ergometric bicycle; respiratory muscle training using a respiratory muscle trainer.
N/A
  • Nutritional intervention: individualized nutritional therapy based on nutritional status and ability to fulfill caloric-protein requirements.
  • N/A
Prehabilitation improved exercise capacity in terms of VO2 peak and workload and distance improvement in the 6MWD and inspiratory and expiratory muscle strength. N/A Prehabilitation resulted in the improvement of some domains of health-related quality of life (social and role functions). Piraux et al. [28]; 2020
Piraux et al. [Pilot study (prospective interventional study) 20]; 2020Esophagogastric cancer

Unimodalpatients scheduled for surgery ± neoadjuvant treatment; (n = 23) Prehabilitation was initiated for 2–4 weeks before the surgery.Primary outcome
  • Feasibility (recruitment, retention and attendance rates, adverse events, and patient satisfaction).
Secondary outcomes
  • Functional exercise capacity by 6MWD;
  • Exercise intervention: aerobic, resistance, and respiratory muscle training using an online tele-prehabilitation platform.
  • CRF by FACIT-F scale;
  • Quality of life by FACT-G questionnaire;
  • Anxiety and depression by HADS questionnaire.
Piraux et al. 6
N/A
  • N/A
[20 Yamamoto et al. [29]; 2016 Pilot study (prospective interventional study) Gastric cancer patients

aged ≥ 65 years with a diagnosis of sarcopenia scheduled for gastrectomy;

(n = 22)
  • Sarcopenia parameters (handgrip strength, gait speed, and skeletal muscle mass index).
Yamamoto et al. [21]; 2016
  • Nutritional intake (total number of calories and protein daily intake);
Multimodal
  • Body composition (body mass, fat mass, lean body mass);
6 N/A
]; 2020 N/A N/A Prehabilitation improved fatigue, quality of life, physical well-being, emotional well-being, and anxiety. Prehabilitation was initiated for 3 weeks, although the actual duration differed depending on the surgery date.
Yamamoto et al. [21]; 2016
  • Exercise intervention: handgrip training, walking, and resistance training;
  • Nutritional intervention: nutritional advice and 2.4 g daily oral supplementation with leucine metabolite b-hydroxy-b-methylbutyrate (HMB).
  • N/A
Prehabilitation significantly increased handgrip strength. N/A Prehabilitation improved nutritional uptake by increasing calorie and protein intake. Cho et al. [30]; 2014
Cho et al. Matched pair analysis [25]; 2014Patients with clinical stage I gastric cancer and metabolic syndrome scheduled for gastrectomy;

(n = 72)
Primary outcome: N/A
  • Postoperative complications rate.
Secondary outcomes:
  • The operative time;
Prehabilitation decreased hospital stay and the number of severe postoperative complications (anastomotic leakage, pancreatic fistula, intra-abdominal abscess, and other severe abdominal complications).
  • Intraoperative blood loss;
  • Hospital stay;
  • Visceral fat and body weight.
7 N/A
 
RCT: randomized controlled trial; CRT: chemoradiotherapy; N/A: not applicable; GOJ: gastroesophageal junction; AT: anaerobic threshold; CPET: cardiopulmonary exercise testing; 6MWD: six minute walking distance; HGS: hand-grip strength; BW: body weight; FVC: forced vital capacity; FEV1: forced expiratory volume in the first second; FEV1%: forced expiratory volume in the first second predicted; PEF: peak expiratory flow. Among them, there are 5 randomized control trials (RCTs) [19][20][21][22][
Cho et al.
[
25
]
; 2014
Unimodal
Prehabilitation was initiated for 4 weeks.
  • Exercise intervention: aerobic exercise, resistance training, and stretching.
  • Standard of care
Prehabilitation significantly decreased BMI, bodyweight, abdominal circumference, and visceral fat.

References

  1. Arnold, M.; Sierra, M.S.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Patterns and Trends in Colorectal Cancer Incidence and Mortality. Gut 2017, 66, 683–691.
  2. Huang, F.-L.; Yu, S.-J. Esophageal Cancer: Risk Factors, Genetic Association, and Treatment. Asian J. Surg. 2018, 41, 210–215.
  3. Karimi, P.; Islami, F.; Anandasabapathy, S.; Freedman, N.D.; Kamangar, F. Gastric Cancer: Descriptive Epidemiology, Risk Factors, Screening, and Prevention. Cancer Epidemiol. Biomark. Prev. 2014, 23, 700–713.
  4. Bausys, A.; Luksta, M.; Kuliavas, J.; Anglickiene, G.; Maneikiene, V.; Gedvilaite, L.; Celutkiene, J.; Jamontaite, I.; Cirtautas, A.; Lenickiene, S.; et al. Personalized Trimodal Prehabilitation for Gastrectomy. Medicine 2020, 99, e20687.
  5. Stratilatovas, E.; Baušys, A.; Baušys, R.; Sangaila, E. Mortality after Gastrectomy: A 10 Year Single Institution Experience. Acta Chir. Belg. 2015, 115, 123–130.
  6. Griffin, S.M.; Jones, R.; Kamarajah, S.K.; Navidi, M.; Wahed, S.; Immanuel, A.; Hayes, N.; Phillips, A.W. Evolution of Esophagectomy for Cancer Over 30 Years: Changes in Presentation, Management and Outcomes. Ann. Surg. Oncol. 2020, 28, 3011–3022.
  7. Bausys, A.; Senina, V.; Luksta, M.; Anglickiene, G.; Molnikaite, G.; Bausys, B.; Rybakovas, A.; Baltruskeviciene, E.; Laurinavicius, A.; Poskus, T.; et al. Histologic Lymph Nodes Regression after Preoperative Chemotherapy as Prognostic Factor in Non-Metastatic Advanced Gastric Adenocarcinoma. J. Cancer 2021, 12, 1669–1677.
  8. Bausys, A.; Ümarik, T.; Luksta, M.; Reinsoo, A.; Rackauskas, R.; Anglickiene, G.; Kryzauskas, M.; Tõnismäe, K.; Senina, V.; Seinin, D.; et al. Impact of the Interval Between Neoadjuvant Chemotherapy and Gastrectomy on Short- and Long-Term Outcomes for Patients with Advanced Gastric Cancer. Ann. Surg. Oncol. 2021, 28, 4444–4455.
  9. Bolger, J.C.; Loughney, L.; Tully, R.; Cunningham, M.; Keogh, S.; McCaffrey, N.; Hickey, W.; Robb, W.B. Perioperative Prehabilitation and Rehabilitation in Esophagogastric Malignancies: A Systematic Review. Dis. Esophagus 2019, 32, doz058.
  10. Jack, S.; West, M.A.; Raw, D.; Marwood, S.; Ambler, G.; Cope, T.M.; Shrotri, M.; Sturgess, R.P.; Calverley, P.M.A.; Ottensmeier, C.H.; et al. The Effect of Neoadjuvant Chemotherapy on Physical Fitness and Survival in Patients Undergoing Oesophagogastric Cancer Surgery. Eur. J. Surg. Oncol. 2014, 40, 1313–1320.
  11. Sinclair, R.; Navidi, M.; Griffin, S.M.; Sumpter, K. The Impact of Neoadjuvant Chemotherapy on Cardiopulmonary Physical Fitness in Gastro-Oesophageal Adenocarcinoma. Ann. R. Coll. Surg. Engl. 2016, 98, 396–400.
  12. Sell, N.M.; Silver, J.K.; Rando, S.; Draviam, A.C.; Mina, D.S.; Qadan, M. Prehabilitation Telemedicine in Neoadjuvant Surgical Oncology Patients During the Novel COVID-19 Coronavirus Pandemic. Ann. Surg. 2020, 272, e81–e83.
  13. Barberan-Garcia, A.; Ubré, M.; Roca, J.; Lacy, A.M.; Burgos, F.; Risco, R.; Momblán, D.; Balust, J.; Blanco, I.; Martínez-Pallí, G. Personalised Prehabilitation in High-Risk Patients Undergoing Elective Major Abdominal Surgery: A Randomized Blinded Controlled Trial. Ann. Surg. 2018, 267, 50–56.
  14. Jones, L.W.; Eves, N.D.; Peddle, C.J.; Courneya, K.S.; Haykowsky, M.; Kumar, V.; Winton, T.W.; Reiman, T. Effects of Presurgical Exercise Training on Systemic Inflammatory Markers among Patients with Malignant Lung Lesions. Appl. Physiol. Nutr. Metab. 2009, 34, 197–202.
  15. Jones, L.W.; Fels, D.R.; West, M.; Allen, J.D.; Broadwater, G.; Barry, W.T.; Wilke, L.G.; Masko, E.; Douglas, P.S.; Dash, R.C.; et al. Modulation of Circulating Angiogenic Factors and Tumor Biology by Aerobic Training in Breast Cancer Patients Receiving Neoadjuvant Chemotherapy. Cancer Prev. Res. 2013, 6, 925–937.
  16. West, M.A.; Astin, R.; Moyses, H.E.; Cave, J.; White, D.; Levett, D.Z.H.; Bates, A.; Brown, G.; Grocott, M.P.W.; Jack, S. Exercise Prehabilitation May Lead to Augmented Tumor Regression Following Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal Cancer. Acta Oncol. 2019, 58, 588–595.
  17. Carli, F.; Bousquet-Dion, G.; Awasthi, R.; Elsherbini, N.; Liberman, S.; Boutros, M.; Stein, B.; Charlebois, P.; Ghitulescu, G.; Morin, N.; et al. Effect of Multimodal Prehabilitation vs Postoperative Rehabilitation on 30-Day Postoperative Complications for Frail Patients Undergoing Resection of Colorectal Cancer: A Randomized Clinical Trial. JAMA Surg. 2020, 155, 233–242.
  18. Durrand, J.; Singh, S.J.; Danjoux, G. Prehabilitation. Clin. Med. 2019, 19, 458–464.
  19. Allen, S.K.; Brown, V.; White, D.; King, D.; Hunt, J.; Wainwright, J.; Emery, A.; Hodge, E.; Kehinde, A.; Prabhu, P.; et al. Multimodal Prehabilitation During Neoadjuvant Therapy Prior to Esophagogastric Cancer Resection: Effect on Cardiopulmonary Exercise Test Performance, Muscle Mass and Quality of Life—A Pilot Randomized Clinical Trial. Ann. Surg. Oncol. 2021, 29, 1839–1850.
  20. Minnella, E.M.; Awasthi, R.; Loiselle, S.-E.; Agnihotram, R.V.; Ferri, L.E.; Carli, F. Effect of Exercise and Nutrition Prehabilitation on Functional Capacity in Esophagogastric Cancer Surgery: A Randomized Clinical Trial. JAMA Surg. 2018, 153, 1081–1089.
  21. Valkenet, K.; Trappenburg, J.C.A.; Ruurda, J.P.; Guinan, E.M.; Reynolds, J.V.; Nafteux, P.; Fontaine, M.; Rodrigo, H.E.; van der Peet, D.L.; Hania, S.W.; et al. Multicentre Randomized Clinical Trial of Inspiratory Muscle Training versus Usual Care before Surgery for Oesophageal Cancer. Br. J. Surg. 2018, 105, 502–511.
  22. van Adrichem, E.J.; Meulenbroek, R.L.; Plukker, J.T.M.; Groen, H.; van Weert, E. Comparison of Two Preoperative Inspiratory Muscle Training Programs to Prevent Pulmonary Complications in Patients Undergoing Esophagectomy: A Randomized Controlled Pilot Study. Ann. Surg. Oncol. 2014, 21, 2353–2360.
  23. Xu, Y.-J.; Cheng, J.C.-H.; Lee, J.-M.; Huang, P.-M.; Huang, G.-H.; Chen, C.C.-H. A Walk-and-Eat Intervention Improves Outcomes for Patients With Esophageal Cancer Undergoing Neoadjuvant Chemoradiotherapy. Oncologist 2015, 20, 1216–1222.
  24. Yamana, I.; Takeno, S.; Hashimoto, T.; Maki, K.; Shibata, R.; Shiwaku, H.; Shimaoka, H.; Shiota, E.; Yamashita, Y. Randomized Controlled Study to Evaluate the Efficacy of a Preoperative Respiratory Rehabilitation Program to Prevent Postoperative Pulmonary Complications after Esophagectomy. Dig. Surg. 2015, 32, 331–337.
  25. Christensen, J.F.; Simonsen, C.; Banck-Petersen, A.; Thorsen-Streit, S.; Herrstedt, A.; Djurhuus, S.S.; Egeland, C.; Mortensen, C.E.; Kofoed, S.C.; Kristensen, T.S.; et al. Safety and Feasibility of Preoperative Exercise Training during Neoadjuvant Treatment before Surgery for Adenocarcinoma of the Gastro-Oesophageal Junction. BJS Open 2019, 3, 74–84.
  26. Dettling, D.S.; van der Schaaf, M.; Blom, R.L.G.M.; Nollet, F.; Busch, O.R.C.; van Berge Henegouwen, M.I. Feasibility and Effectiveness of Pre-Operative Inspiratory Muscle Training in Patients Undergoing Oesophagectomy: A Pilot Study. Physiother. Res. Int 2013, 18, 16–26.
  27. Argudo, N.; Rodó-Pin, A.; Martínez-Llorens, J.; Marco, E.; Visa, L.; Messaggi-Sartor, M.; Balañá-Corberó, A.; Ramón, J.M.; Rodríguez-Chiaradía, D.A.; Grande, L.; et al. Feasibility, Tolerability, and Effects of Exercise-Based Prehabilitation after Neoadjuvant Therapy in Esophagogastric Cancer Patients Undergoing Surgery: An Interventional Pilot Study. Dis. Esophagus 2020, 34, doaa086.
  28. Piraux, E.; Caty, G.; Reychler, G.; Forget, P.; Deswysen, Y. Feasibility and Preliminary Effectiveness of a Tele-Prehabilitation Program in Esophagogastric Cancer Patients. J. Clin. Med. 2020, 9, 2176.
  29. Yamamoto, K.; Nagatsuma, Y.; Fukuda, Y.; Hirao, M.; Nishikawa, K.; Miyamoto, A.; Ikeda, M.; Nakamori, S.; Sekimoto, M.; Fujitani, K.; et al. Effectiveness of a Preoperative Exercise and Nutritional Support Program for Elderly Sarcopenic Patients with Gastric Cancer. Gastric Cancer 2017, 20, 913–918.
  30. Cho, H.; Yoshikawa, T.; Oba, M.S.; Hirabayashi, N.; Shirai, J.; Aoyama, T.; Hayashi, T.; Yamada, T.; Oba, K.; Morita, S.; et al. Matched Pair Analysis to Examine the Effects of a Planned Preoperative Exercise Program in Early Gastric Cancer Patients with Metabolic Syndrome to Reduce Operative Risk: The Adjuvant Exercise for General Elective Surgery (AEGES) Study Group. Ann. Surg. Oncol. 2014, 21, 2044–2050.
  31. Jadad, A.R.; Moore, R.A.; Carroll, D.; Jenkinson, C.; Reynolds, D.J.; Gavaghan, D.J.; McQuay, H.J. Assessing the Quality of Reports of Randomized Clinical Trials: Is Blinding Necessary? Control. Clin. Trials 1996, 17, 1–12.
  32. Ottawa Hospital Research Institute. Available online: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed on 20 February 2022).
More
ScholarVision Creations