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Robotic-assisted Esophagectomy vs. Video-Assisted Thoracoscopic Esophagectomy(REVATE) Trial

Primary Purpose

Esophageal Squamous Cell Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Robot esophagectomy (RE)
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Squamous Cell Carcinoma focused on measuring Robotic esophagectomy, Video-assisted thoracoscopic esophagectomy, Recurrent laryngeal nerve lymh node, Esophageal squamous cell carcinoma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  1. Age between 18~80
  2. Histologically proven primary intrathoracic esophageal squamous cell carcinoma and will undergo McKeown MIE and bilateral RLN LND.
  3. Patients should have a performance status 0, 1 or 2 according to the European Clinical Oncology Group.
  4. Surgical resectable(cT1~4a, N0~3, M0)
  5. Written informed consent

Exclusion criteria are

  1. Previous major thoracic surgery rendering minimal invasive approach unfeasible
  2. prognosis determining malignancy other than esophageal cancer, inability to undergo curative resection and/or follow-up
  3. inability to provide oral or written informed consent.
  4. pre-existed vocal cord dysfunction will also be excluded.

Sites / Locations

  • Chang Gung memorial hospital-LinkouRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Robot Esophagectomy (RE)

Video-assisted thoracoscopic esophagectomy (VATE)

Arm Description

Patients in the RE group will receive robotic-assisted esophagectomy with standard total two-field lymphadenectomy.

Patients in the VATE group will receive thoracoscopic esophagectomy with standard total two-field lymphadenectomy.

Outcomes

Primary Outcome Measures

Rate of unsuccessful LND along the left RLN
Regardless of the presence of hoarseness, vocal cord function will be assessed by an experienced otolaryngologist using a nexile laryngoscope within one week of surgery. RLN palsy will be classified according to the following variables: site (unilateral versus bilateral); duration (temporary [i.e., recovering within 6 months] versus permanent [i.e. not recovering within 6 months]); and type of treatment required (type I: no therapy required; type II: injury requiring an elective surgical procedure; type III: injury requiring an urgent surgical procedure)

Secondary Outcome Measures

The number of nodes removed along the right and left RLN
number of lymph node removed
Post esophagectomy pneumonia rate
Post esophagectomy pneumonia is defined according to the Revised Uniform Pneumonia Score which includes temperature[°C](Range ≥ 36.1 and ≤ 38.4 =0, ≤ 36.0 and ≥ 38.5=1); leukocyte count [×1000/uL](≥ 4.0 and ≤ 11.0=0, <4.0 or >11.0=1); and pulmonary radiography(Range No infiltrate=0, Diffused or patchy infiltrate=1, Well-circumscribed infiltrate=2). A sum score of 2 points or higher, of which at least 1 point is assigned because of infiltrative findings on pulmonary radiography, indicates the presence of pneumonia.
Rate of major postoperative complication
Complication grade: modified Clavien-Dindo classification (MCDC) grade 2-4 Major complications (MCDC grade 2-4) Including: myocardial infarction, anastomotic leakage (clinical or radiologic diagnosis), anastomotic stenosis, chylothorax (chylous leakage, presence of chylous in chest tubes or indication start medium chain triglycerides containing tube feeding, gastric tube necrosis (proven by gastroscopy), pulmonary embolus, deep vein thrombosis. Minor complications (MCDC grade 1) Including: wound infections, pleural effusions, delayed gastric emptying
In hospital, 30 day and 90 day mortality
Death occurred during the same hospitalization , within 30 and 90 days after surgery
R0 resection rate
Microscopically negative proximal/distal and circumferential margin
Operation time(thoracic phase)
thoracic phase operation time(minutes)
Operation time(abdominal)
abdominal phase operation time(minutes)
Total operation time
total surgical time (expressed in minutes)
Unexpected events and complications occurring during surgery
massive hemorrhage, perforation of other organs
Blood loss during surgery
blood loss during surgery (expressed in mL per phase)
Rate of thoracotomy conversion
Number of patients requiring conversion to thoracotomy and related reasons
Length of mechanical ventilator use after surgery
expressed in minutes
Length of intensive care unit stay after surgery
expressed in hours
Length of postoperative hospital stay
expressed in days , calculated from the date of surgery to date of discharge
Re-intubation rate
Need for re-intubation after extubation
Re-entry ICU rate
Need to transfer back from ward to ICU after surgery
Overall survival rate
From date of surgery until the date of death from any cause
Disease free survival rate
From date of surgery until the date of first documented recurrence
Hospital Anxiety and Depression Scale (HADS)
The HADS aims to measure symptoms of anxiety and depression and consists of 14 items,seven items for the anxiety subscale and seven for the depression subscale. The questionnaire responses were analysed in the light of the results of this estimation of the severity of both anxiety and of depression. This enabled a reduction of the number of items in the questionnaire to just seven reflecting anxiety and seven reflecting depression.(Of the seven depression items five reflected aspects of reduction in pleasure response). Each item had been answered by the patient on a four point (0-3) response category so the possible scores ranged from 0 to 21 for anxiety and 0 to 21 for depression. a score of 0 to 7 for either subscale could be regarded as being in the normal range, a score of 11 or higher indicating probable presence ('caseness') of the mood disorder and a score of 8 to 10 being just suggestive of the presence of the respective state.
European Organisation for Research and Treatment of Cancer(EORTC) QLQ-C30 , QLQ-OES18
The EORTC QLQ-C30 incorporates a range of QOL issues in five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea/vomiting), a global health/QOL scale, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). The EORTC QLQ-OES18 contains four symptom scales (dysphagia, eating disorders, reflux, and pain) and six single items (difficulty swallowing saliva, choking, dry mouth, taste disorder, cough, and speech-related issues). Each question has four response choices ranging from 1 (not at all) to 4 (very much), except for the global QOL scale, which has seven response options ranging from 1 (very poor) to 7 (excellent). All questionnaire responses are linearly transformed to scores from 0 to 100.

Full Information

First Posted
October 11, 2018
Last Updated
June 28, 2021
Sponsor
Chang Gung Memorial Hospital
Collaborators
Shanghai Chest Hospital, Tianjin Medical University Cancer Institute and Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03713749
Brief Title
Robotic-assisted Esophagectomy vs. Video-Assisted Thoracoscopic Esophagectomy(REVATE) Trial
Official Title
Robotic-assisted Esophagectomy vs. Video-Assisted Thoracoscopic Esophagectomy(REVATE) : a Multicenter Open-label Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 22, 2018 (Actual)
Primary Completion Date
April 22, 2022 (Anticipated)
Study Completion Date
December 22, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital
Collaborators
Shanghai Chest Hospital, Tianjin Medical University Cancer Institute and Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The investigators will assess the adequacy of nodal dissection along the recurrent laryngeal nerve performed with robot-assisted versus video-assisted thoracoscopic esophagectomy in patients with esophageal squamous cell carcinoma through a prospective multicentre randomized study design.
Detailed Description
Radical lymph node dissection (LND) along the recurrent laryngeal nerve (RLN) is surgically demanding and can be associated with substantial postoperative morbidity. The question as to whether robot-assisted esophagectomy (RE) might be superior to video-assisted thoracoscopic esophagectomy (VATE) for performing LND along the RLN in patients with esophageal squamous cell carcinoma (ESCC) remains open. The investigators will conduct a multicenter, open-label, randomized controlled trial (termed REVATE) enrolling patients with ESCC scheduled to undergo LND along the RLN. Patients will be randomly assigned to either RE or VATE. The primary outcome measure will be the rate of unsuccessful LND along the left RLN, which will be defined as 1) failure to remove lymph nodes along the left RLN or 2) occurrence of left RLN palsy following LND. Secondary outcomes will include the number of successfully removed RLN nodes, postoperative recovery, length of hospital stay, 30- and 90-day mortality, quality of life, and oncological outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Squamous Cell Carcinoma
Keywords
Robotic esophagectomy, Video-assisted thoracoscopic esophagectomy, Recurrent laryngeal nerve lymh node, Esophageal squamous cell carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
212 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robot Esophagectomy (RE)
Arm Type
Experimental
Arm Description
Patients in the RE group will receive robotic-assisted esophagectomy with standard total two-field lymphadenectomy.
Arm Title
Video-assisted thoracoscopic esophagectomy (VATE)
Arm Type
No Intervention
Arm Description
Patients in the VATE group will receive thoracoscopic esophagectomy with standard total two-field lymphadenectomy.
Intervention Type
Device
Intervention Name(s)
Robot esophagectomy (RE)
Intervention Description
Patients in RE group will receive Robotic-assisted surgery in thoracic phase.
Primary Outcome Measure Information:
Title
Rate of unsuccessful LND along the left RLN
Description
Regardless of the presence of hoarseness, vocal cord function will be assessed by an experienced otolaryngologist using a nexile laryngoscope within one week of surgery. RLN palsy will be classified according to the following variables: site (unilateral versus bilateral); duration (temporary [i.e., recovering within 6 months] versus permanent [i.e. not recovering within 6 months]); and type of treatment required (type I: no therapy required; type II: injury requiring an elective surgical procedure; type III: injury requiring an urgent surgical procedure)
Time Frame
Till 6 months postoperatively
Secondary Outcome Measure Information:
Title
The number of nodes removed along the right and left RLN
Description
number of lymph node removed
Time Frame
The pathological analysis will be finished within 2 weeks.
Title
Post esophagectomy pneumonia rate
Description
Post esophagectomy pneumonia is defined according to the Revised Uniform Pneumonia Score which includes temperature[°C](Range ≥ 36.1 and ≤ 38.4 =0, ≤ 36.0 and ≥ 38.5=1); leukocyte count [×1000/uL](≥ 4.0 and ≤ 11.0=0, <4.0 or >11.0=1); and pulmonary radiography(Range No infiltrate=0, Diffused or patchy infiltrate=1, Well-circumscribed infiltrate=2). A sum score of 2 points or higher, of which at least 1 point is assigned because of infiltrative findings on pulmonary radiography, indicates the presence of pneumonia.
Time Frame
Duration of hospital stay, an expected average of 2~3 weeks
Title
Rate of major postoperative complication
Description
Complication grade: modified Clavien-Dindo classification (MCDC) grade 2-4 Major complications (MCDC grade 2-4) Including: myocardial infarction, anastomotic leakage (clinical or radiologic diagnosis), anastomotic stenosis, chylothorax (chylous leakage, presence of chylous in chest tubes or indication start medium chain triglycerides containing tube feeding, gastric tube necrosis (proven by gastroscopy), pulmonary embolus, deep vein thrombosis. Minor complications (MCDC grade 1) Including: wound infections, pleural effusions, delayed gastric emptying
Time Frame
Duration of hospital stay, an expected average of 2~3 weeks
Title
In hospital, 30 day and 90 day mortality
Description
Death occurred during the same hospitalization , within 30 and 90 days after surgery
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks and within 30 days or 90 days
Title
R0 resection rate
Description
Microscopically negative proximal/distal and circumferential margin
Time Frame
The pathological analysis will be finished within 2 weeks.
Title
Operation time(thoracic phase)
Description
thoracic phase operation time(minutes)
Time Frame
Day of surgery
Title
Operation time(abdominal)
Description
abdominal phase operation time(minutes)
Time Frame
Day of surgery
Title
Total operation time
Description
total surgical time (expressed in minutes)
Time Frame
Day of surgery
Title
Unexpected events and complications occurring during surgery
Description
massive hemorrhage, perforation of other organs
Time Frame
Day of surgery, up to 24 hours after surgery.
Title
Blood loss during surgery
Description
blood loss during surgery (expressed in mL per phase)
Time Frame
Day of surgery, up to 24 hours after surgery.
Title
Rate of thoracotomy conversion
Description
Number of patients requiring conversion to thoracotomy and related reasons
Time Frame
Day of surgery, up to 24 hours after surgery.
Title
Length of mechanical ventilator use after surgery
Description
expressed in minutes
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2~3 weeks
Title
Length of intensive care unit stay after surgery
Description
expressed in hours
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2~3 weeks
Title
Length of postoperative hospital stay
Description
expressed in days , calculated from the date of surgery to date of discharge
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2~3 weeks
Title
Re-intubation rate
Description
Need for re-intubation after extubation
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2~3 weeks
Title
Re-entry ICU rate
Description
Need to transfer back from ward to ICU after surgery
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2~3 weeks
Title
Overall survival rate
Description
From date of surgery until the date of death from any cause
Time Frame
Assessed 24/36/60 months after surgery
Title
Disease free survival rate
Description
From date of surgery until the date of first documented recurrence
Time Frame
Assessed up to 24/36/60 months after surgery
Title
Hospital Anxiety and Depression Scale (HADS)
Description
The HADS aims to measure symptoms of anxiety and depression and consists of 14 items,seven items for the anxiety subscale and seven for the depression subscale. The questionnaire responses were analysed in the light of the results of this estimation of the severity of both anxiety and of depression. This enabled a reduction of the number of items in the questionnaire to just seven reflecting anxiety and seven reflecting depression.(Of the seven depression items five reflected aspects of reduction in pleasure response). Each item had been answered by the patient on a four point (0-3) response category so the possible scores ranged from 0 to 21 for anxiety and 0 to 21 for depression. a score of 0 to 7 for either subscale could be regarded as being in the normal range, a score of 11 or higher indicating probable presence ('caseness') of the mood disorder and a score of 8 to 10 being just suggestive of the presence of the respective state.
Time Frame
pre-operative < 5 days and 4 weeks, 3/6 months and yearly up to 5 years post-operatively.
Title
European Organisation for Research and Treatment of Cancer(EORTC) QLQ-C30 , QLQ-OES18
Description
The EORTC QLQ-C30 incorporates a range of QOL issues in five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea/vomiting), a global health/QOL scale, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). The EORTC QLQ-OES18 contains four symptom scales (dysphagia, eating disorders, reflux, and pain) and six single items (difficulty swallowing saliva, choking, dry mouth, taste disorder, cough, and speech-related issues). Each question has four response choices ranging from 1 (not at all) to 4 (very much), except for the global QOL scale, which has seven response options ranging from 1 (very poor) to 7 (excellent). All questionnaire responses are linearly transformed to scores from 0 to 100.
Time Frame
pre-operative < 5 days and 4 weeks, 3/6 months and yearly up to 5 years post-operatively.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Age between 18~80 Histologically proven primary intrathoracic esophageal squamous cell carcinoma and will undergo McKeown MIE and bilateral RLN LND. Patients should have a performance status 0, 1 or 2 according to the European Clinical Oncology Group. Surgical resectable(cT1~4a, N0~3, M0) Written informed consent Exclusion criteria are Previous major thoracic surgery rendering minimal invasive approach unfeasible prognosis determining malignancy other than esophageal cancer, inability to undergo curative resection and/or follow-up inability to provide oral or written informed consent. pre-existed vocal cord dysfunction will also be excluded.
Facility Information:
Facility Name
Chang Gung memorial hospital-Linkou
City
Taoyuan
ZIP/Postal Code
333
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yin-Kai Chao
Phone
+886-3-3281200
Ext
3633
Email
chaoyk@gmail.com
First Name & Middle Initial & Last Name & Degree
Yin Kai Chao, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22504922
Citation
Udagawa H, Ueno M, Shinohara H, Haruta S, Kaida S, Nakagawa M, Tsurumaru M. The importance of grouping of lymph node stations and rationale of three-field lymphoadenectomy for thoracic esophageal cancer. J Surg Oncol. 2012 Nov;106(6):742-7. doi: 10.1002/jso.23122. Epub 2012 Apr 13.
Results Reference
background
PubMed Identifier
16718401
Citation
Mizutani M, Murakami G, Nawata S, Hitrai I, Kimura W. Anatomy of right recurrent nerve node: why does early metastasis of esophageal cancer occur in it? Surg Radiol Anat. 2006 Aug;28(4):333-8. doi: 10.1007/s00276-006-0115-y. Epub 2006 May 23.
Results Reference
background
PubMed Identifier
26464155
Citation
Sato Y, Kosugi S, Aizawa N, Ishikawa T, Kano Y, Ichikawa H, Hanyu T, Hirashima K, Bamba T, Wakai T. Risk Factors and Clinical Outcomes of Recurrent Laryngeal Nerve Paralysis After Esophagectomy for Thoracic Esophageal Carcinoma. World J Surg. 2016 Jan;40(1):129-36. doi: 10.1007/s00268-015-3261-8.
Results Reference
background
PubMed Identifier
12715226
Citation
Fujita H, Sueyoshi S, Tanaka T, Fujii T, Toh U, Mine T, Sasahara H, Sudo T, Matono S, Yamana H, Shirouzu K. Optimal lymphadenectomy for squamous cell carcinoma in the thoracic esophagus: comparing the short- and long-term outcome among the four types of lymphadenectomy. World J Surg. 2003 May;27(5):571-9. doi: 10.1007/s00268-003-6913-z. Epub 2003 Apr 28.
Results Reference
background
PubMed Identifier
15780563
Citation
Gockel I, Kneist W, Keilmann A, Junginger T. Recurrent laryngeal nerve paralysis (RLNP) following esophagectomy for carcinoma. Eur J Surg Oncol. 2005 Apr;31(3):277-81. doi: 10.1016/j.ejso.2004.10.007.
Results Reference
background
PubMed Identifier
20884018
Citation
Berry MF, Atkins BZ, Tong BC, Harpole DH, D'Amico TA, Onaitis MW. A comprehensive evaluation for aspiration after esophagectomy reduces the incidence of postoperative pneumonia. J Thorac Cardiovasc Surg. 2010 Dec;140(6):1266-71. doi: 10.1016/j.jtcvs.2010.08.038. Epub 2010 Sep 29.
Results Reference
background
PubMed Identifier
10594510
Citation
Hulscher JB, van Sandick JW, Devriese PP, van Lanschot JJ, Obertop H. Vocal cord paralysis after subtotal oesophagectomy. Br J Surg. 1999 Dec;86(12):1583-7. doi: 10.1046/j.1365-2168.1999.01333.x.
Results Reference
background
PubMed Identifier
22668811
Citation
Luketich JD, Pennathur A, Awais O, Levy RM, Keeley S, Shende M, Christie NA, Weksler B, Landreneau RJ, Abbas G, Schuchert MJ, Nason KS. Outcomes after minimally invasive esophagectomy: review of over 1000 patients. Ann Surg. 2012 Jul;256(1):95-103. doi: 10.1097/SLA.0b013e3182590603.
Results Reference
background
PubMed Identifier
26196135
Citation
Zhou C, Zhang L, Wang H, Ma X, Shi B, Chen W, He J, Wang K, Liu P, Ren Y. Superiority of Minimally Invasive Oesophagectomy in Reducing In-Hospital Mortality of Patients with Resectable Oesophageal Cancer: A Meta-Analysis. PLoS One. 2015 Jul 21;10(7):e0132889. doi: 10.1371/journal.pone.0132889. eCollection 2015.
Results Reference
background
PubMed Identifier
22552194
Citation
Biere SS, van Berge Henegouwen MI, Maas KW, Bonavina L, Rosman C, Garcia JR, Gisbertz SS, Klinkenbijl JH, Hollmann MW, de Lange ES, Bonjer HJ, van der Peet DL, Cuesta MA. Minimally invasive versus open oesophagectomy for patients with oesophageal cancer: a multicentre, open-label, randomised controlled trial. Lancet. 2012 May 19;379(9829):1887-92. doi: 10.1016/S0140-6736(12)60516-9. Epub 2012 May 1.
Results Reference
background
PubMed Identifier
20495981
Citation
Noshiro H, Iwasaki H, Kobayashi K, Uchiyama A, Miyasaka Y, Masatsugu T, Koike K, Miyazaki K. Lymphadenectomy along the left recurrent laryngeal nerve by a minimally invasive esophagectomy in the prone position for thoracic esophageal cancer. Surg Endosc. 2010 Dec;24(12):2965-73. doi: 10.1007/s00464-010-1072-4. Epub 2010 May 22.
Results Reference
background
PubMed Identifier
25716873
Citation
Park SY, Kim DJ, Yu WS, Jung HS. Robot-assisted thoracoscopic esophagectomy with extensive mediastinal lymphadenectomy: experience with 114 consecutive patients with intrathoracic esophageal cancer. Dis Esophagus. 2016 May;29(4):326-32. doi: 10.1111/dote.12335. Epub 2015 Feb 26.
Results Reference
background
PubMed Identifier
26023036
Citation
van der Sluis PC, Ruurda JP, Verhage RJ, van der Horst S, Haverkamp L, Siersema PD, Borel Rinkes IH, Ten Kate FJ, van Hillegersberg R. Oncologic Long-Term Results of Robot-Assisted Minimally Invasive Thoraco-Laparoscopic Esophagectomy with Two-Field Lymphadenectomy for Esophageal Cancer. Ann Surg Oncol. 2015 Dec;22 Suppl 3:S1350-6. doi: 10.1245/s10434-015-4544-x. Epub 2015 May 29.
Results Reference
background
PubMed Identifier
27568155
Citation
Cerfolio RJ, Wei B, Hawn MT, Minnich DJ. Robotic Esophagectomy for Cancer: Early Results and Lessons Learned. Semin Thorac Cardiovasc Surg. 2016 Spring;28(1):160-9. doi: 10.1053/j.semtcvs.2015.10.006. Epub 2015 Oct 30.
Results Reference
background
PubMed Identifier
22392356
Citation
Suda K, Ishida Y, Kawamura Y, Inaba K, Kanaya S, Teramukai S, Satoh S, Uyama I. Robot-assisted thoracoscopic lymphadenectomy along the left recurrent laryngeal nerve for esophageal squamous cell carcinoma in the prone position: technical report and short-term outcomes. World J Surg. 2012 Jul;36(7):1608-16. doi: 10.1007/s00268-012-1538-8.
Results Reference
background
PubMed Identifier
21899652
Citation
Weksler B, Sharma P, Moudgill N, Chojnacki KA, Rosato EL. Robot-assisted minimally invasive esophagectomy is equivalent to thoracoscopic minimally invasive esophagectomy. Dis Esophagus. 2012 Jul;25(5):403-9. doi: 10.1111/j.1442-2050.2011.01246.x. Epub 2011 Sep 7.
Results Reference
background
PubMed Identifier
28801820
Citation
Chao YK, Hsieh MJ, Liu YH, Liu HP. Lymph Node Evaluation in Robot-Assisted Versus Video-Assisted Thoracoscopic Esophagectomy for Esophageal Squamous Cell Carcinoma: A Propensity-Matched Analysis. World J Surg. 2018 Feb;42(2):590-598. doi: 10.1007/s00268-017-4179-0.
Results Reference
background
PubMed Identifier
25607756
Citation
Low DE, Alderson D, Cecconello I, Chang AC, Darling GE, D'Journo XB, Griffin SM, Holscher AH, Hofstetter WL, Jobe BA, Kitagawa Y, Kucharczuk JC, Law SY, Lerut TE, Maynard N, Pera M, Peters JH, Pramesh CS, Reynolds JV, Smithers BM, van Lanschot JJ. International Consensus on Standardization of Data Collection for Complications Associated With Esophagectomy: Esophagectomy Complications Consensus Group (ECCG). Ann Surg. 2015 Aug;262(2):286-94. doi: 10.1097/SLA.0000000000001098.
Results Reference
background
PubMed Identifier
19638912
Citation
Clavien PA, Barkun J, de Oliveira ML, Vauthey JN, Dindo D, Schulick RD, de Santibanes E, Pekolj J, Slankamenac K, Bassi C, Graf R, Vonlanthen R, Padbury R, Cameron JL, Makuuchi M. The Clavien-Dindo classification of surgical complications: five-year experience. Ann Surg. 2009 Aug;250(2):187-96. doi: 10.1097/SLA.0b013e3181b13ca2.
Results Reference
background
PubMed Identifier
23199187
Citation
van der Sluis PC, Ruurda JP, van der Horst S, Verhage RJ, Besselink MG, Prins MJ, Haverkamp L, Schippers C, Rinkes IH, Joore HC, Ten Kate FJ, Koffijberg H, Kroese CC, van Leeuwen MS, Lolkema MP, Reerink O, Schipper ME, Steenhagen E, Vleggaar FP, Voest EE, Siersema PD, van Hillegersberg R. Robot-assisted minimally invasive thoraco-laparoscopic esophagectomy versus open transthoracic esophagectomy for resectable esophageal cancer, a randomized controlled trial (ROBOT trial). Trials. 2012 Nov 30;13:230. doi: 10.1186/1745-6215-13-230.
Results Reference
background
PubMed Identifier
29380005
Citation
Li ZG, Zhang XB, Wen YW, Liu YH, Chao YK. Incidence and Predictors of Unsuspected Recurrent Laryngeal Nerve Lymph Node Metastases After Neoadjuvant Chemoradiotherapy in Patients with Esophageal Squamous Cell Carcinoma. World J Surg. 2018 Aug;42(8):2485-2492. doi: 10.1007/s00268-018-4516-y.
Results Reference
background
PubMed Identifier
29608683
Citation
Chiu CH, Wen YW, Chao YK. Lymph node dissection along the recurrent laryngeal nerves in patients with oesophageal cancer who had undergone chemoradiotherapy: is it safe? Eur J Cardiothorac Surg. 2018 Oct 1;54(4):657-663. doi: 10.1093/ejcts/ezy127.
Results Reference
background
PubMed Identifier
27810391
Citation
Rice TW, Ishwaran H, Ferguson MK, Blackstone EH, Goldstraw P. Cancer of the Esophagus and Esophagogastric Junction: An Eighth Edition Staging Primer. J Thorac Oncol. 2017 Jan;12(1):36-42. doi: 10.1016/j.jtho.2016.10.016. Epub 2016 Oct 31.
Results Reference
background
PubMed Identifier
28111535
Citation
Japan Esophageal Society. Japanese Classification of Esophageal Cancer, 11th Edition: part I. Esophagus. 2017;14(1):1-36. doi: 10.1007/s10388-016-0551-7. Epub 2016 Nov 10. No abstract available.
Results Reference
background
PubMed Identifier
26883435
Citation
Weijs TJ, Seesing MF, van Rossum PS, Koeter M, van der Sluis PC, Luyer MD, Ruurda JP, Nieuwenhuijzen GA, van Hillegersberg R. Internal and External Validation of a multivariable Model to Define Hospital-Acquired Pneumonia After Esophagectomy. J Gastrointest Surg. 2016 Apr;20(4):680-7. doi: 10.1007/s11605-016-3083-5. Epub 2016 Feb 16.
Results Reference
background
PubMed Identifier
26752982
Citation
Tachimori Y, Ozawa S, Numasaki H, Matsubara H, Shinoda M, Toh Y, Udagawa H, Fujishiro M, Oyama T, Uno T; Registration Committee for Esophageal Cancer of the Japan Esophageal Society. Efficacy of lymph node dissection by node zones according to tumor location for esophageal squamous cell carcinoma. Esophagus. 2016;13:1-7. doi: 10.1007/s10388-015-0515-3. Epub 2015 Nov 17.
Results Reference
background
PubMed Identifier
31182150
Citation
Chao YK, Li ZG, Wen YW, Kim DJ, Park SY, Chang YL, van der Sluis PC, Ruurda JP, van Hillegersberg R. Robotic-assisted Esophagectomy vs Video-Assisted Thoracoscopic Esophagectomy (REVATE): study protocol for a randomized controlled trial. Trials. 2019 Jun 10;20(1):346. doi: 10.1186/s13063-019-3441-1.
Results Reference
derived

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Robotic-assisted Esophagectomy vs. Video-Assisted Thoracoscopic Esophagectomy(REVATE) Trial

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