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"Phase III Randomized Trial Comparing D2 vs D3 Lymphadenectomy With Gastric Cancer Following Neoadjuvant Chemotherapy

Primary Purpose

Gastric Cancer

Status
Recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
D3 Lymphadenectomy
Sponsored by
Tata Memorial Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring D2 versus D3 Lymphadenectomy

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ECOG performance status of 0 - 1 in patients deemed fit to undergo surgery at the pre-anaesthetic check
  • Histologically proven gastric adenocarcinoma
  • No evidence of distant metastases, or locally advanced inoperable disease, as evaluated by computed tomography, chest radiography, ultrasonography, and / or laparotomy
  • Patient able to provide valid informed consent
  • Patient completed at least 1 cycle of neoadjuvant chemotherapy

Exclusion Criteria:

  • Presence of any 1 of the following:
  • Previous or concomitant other cancer
  • Primary Oesophageal involvement extending to the stomach
  • Distant hepatic / extrahepatic disease discovered on laparotomy
  • Gross local disease in the porta precluding a curative resection
  • Patient did not consent for the trial

Sites / Locations

  • Dr Shailesh Vinayak ShrikhandeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

D2 Lymphadenectomy

D3 Lymphadenectomy

Arm Description

Intervention D3 Lymphadenectomy

Comparator D2 Lymphadenectomy

Outcomes

Primary Outcome Measures

primary endpoint:Overall Survival
overall survival will be calculated from randomization to death.

Secondary Outcome Measures

Disease-free survival
Disease-free survival will be calculated from definitive resection to the first event (i.e., local recurrence, distant recurrence, or death from any cause

Full Information

First Posted
July 31, 2013
Last Updated
April 26, 2022
Sponsor
Tata Memorial Centre
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1. Study Identification

Unique Protocol Identification Number
NCT02139605
Brief Title
"Phase III Randomized Trial Comparing D2 vs D3 Lymphadenectomy With Gastric Cancer Following Neoadjuvant Chemotherapy
Official Title
Phase III Randomized Controlled Trial Comparing D2 Versus D3 Lymphadenectomy on Outcomes of Non-metastatic, Resectable, But Locally Advanced, Gastric Cancer Following Neoadjuvant (Perioperative) Chemotherapy (ELANCe Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Recruiting
Study Start Date
July 5, 2013 (Actual)
Primary Completion Date
July 2025 (Anticipated)
Study Completion Date
July 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tata Memorial Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Stomach cancer is the second most common cause of cancer-related deaths in India. Curative surgery offers the only chance of improving survival in this cancer. In patients whose cancer has not spread to other parts of the body (beyond the stomach and lymph nodes around it), removal of stomach (gastrectomy) with lymph nodes around the stomach and along the major vessels supplying blood to the stomach (D2 lymphadenectomy) is regarded as current standard of care at Tata Memorial Centre. However, the extent of lymphadenectomy is controversial. Some studies have suggested that removing more lymph nodes, even around the major vessels of the abdomen (aorta and inferior vena cava) may not only help to accurately determine the disease spread, but may also confer an additional survival benefit. Removing more lymph nodes around the major vessels may increase the risk of morbidity to the patient. In the last 5-6 years, stomach cancer specialists around the world have resorted to giving half the cycles of chemotherapy to the patient before the surgery (neoadjuvant chemotherapy), and the other half after the surgery in what is called 'perioperative chemotherapy'. This has been shown to lead to more patients surviving to 5 years, than before. The investigators feel that perioperative chemotherapy with D2 lymphadenectomy may constitute the best care for our patients with stomach cancer such that no further removal of lymph nodes beyond is required. However, the investigators have no evidence in literature to support this hypothesis. The investigators have thus designed this trial based on which we propose that there exists no difference between a D2 lymphadenectomy and a D3 lymphadenectomy following neoadjuvant chemotherapy for non-metastatic, locally advanced but resectable gastric cancer. The data will enable the development of clear management guidelines for lymph node dissection in stomach cancer.
Detailed Description
The only data comparing D2 and D3 comes from a multi-institutional, non-randomised study which reported that D3 lymphadenectomy conferred a survival advantage over D2 in tumours that were 50-100mm in diameter, with or without lymph nodal disease. Of the three published randomised controlled trials(RCT) comparing D2 versus D2+paraaortic nodal dissection (PAND), two of the studies in which the long-term results are available, were carried out in Japan. In both these studies, the patients were not offered chemotherapy until after they developed a recurrence. Another reason is the benefit on survival, albeit modest, in patients undergoing D3 lymphadenectomy that has been noted in the study by Wu et al. Another important reason for comparing D2 versus D2+PAND, lies in the fact that none of the aforementioned RCTs have been performed after the 1998 revision in the definition of lymph node stations by the Japanese Gastric cancer association. Hence, none of these results can be considered representative of the current classifications. Duly considering the possible higher morbidity that has been shown with a complete para aortic lymph node dissection, the investigators propose to study a more extensive lymphadenectomy than D2 but without increasing the risk of morbidity in the patient. D2 lymphadenectomy has been performed at Tata Memorial Centre (TMC), since 2002 with morbidity and mortality rates comparable to world literature It is the standard form of lymphadenectomy in TMC. Hence, the trial will be performed by surgeons experienced in the technique. D3 is performed in some centres in Japan, Italy and Taiwan (where the only randomized controlled trial demonstrated a survival benefit of D3 over D1). Both the procedures are well established and regarded as standards in different parts of the world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
D2 versus D3 Lymphadenectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Gastrectomy with D2 or D3 lymphadenectomy
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
D2 Lymphadenectomy
Arm Type
Active Comparator
Arm Description
Intervention D3 Lymphadenectomy
Arm Title
D3 Lymphadenectomy
Arm Type
Experimental
Arm Description
Comparator D2 Lymphadenectomy
Intervention Type
Procedure
Intervention Name(s)
D3 Lymphadenectomy
Intervention Description
D3 Lymphadenectomy involves surgical removal of lymph nodes from echelon or compartments 1 to 3 in gastric cancer patients
Primary Outcome Measure Information:
Title
primary endpoint:Overall Survival
Description
overall survival will be calculated from randomization to death.
Time Frame
5 year
Secondary Outcome Measure Information:
Title
Disease-free survival
Description
Disease-free survival will be calculated from definitive resection to the first event (i.e., local recurrence, distant recurrence, or death from any cause
Time Frame
2 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ECOG performance status of 0 - 1 in patients deemed fit to undergo surgery at the pre-anaesthetic check Histologically proven gastric adenocarcinoma No evidence of distant metastases, or locally advanced inoperable disease, as evaluated by computed tomography, chest radiography, ultrasonography, and / or laparotomy Patient able to provide valid informed consent Patient completed at least 1 cycle of neoadjuvant chemotherapy Exclusion Criteria: Presence of any 1 of the following: Previous or concomitant other cancer Primary Oesophageal involvement extending to the stomach Distant hepatic / extrahepatic disease discovered on laparotomy Gross local disease in the porta precluding a curative resection Patient did not consent for the trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Shailesh V Shrikhande, MBBS MS MD
Phone
+91 222417 7000
Ext
7173
Email
shailushrikhande@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Ashwin Luis Desouza, MBBS MS
Phone
+91 222417 7000
Ext
6329
Email
ashwindesouza@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Shailesh V Shrikhande, MBBS MS MD
Organizational Affiliation
Tata Memorial Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr Shailesh Vinayak Shrikhande
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr Shailesh v Shrikhande, MBBS MS MD
Phone
+91 22 2417 7000
Ext
7173
Email
shailushrikhande@hotmail.com
First Name & Middle Initial & Last Name & Degree
Dr Bhawna Sirohi, MBBS DCH
Phone
+91 22 2417 7000
Ext
6755
Email
bhawna.Sirohi13@gmail.com
First Name & Middle Initial & Last Name & Degree
Dr Shailesh V Shrikhande, MBBS MS MD
First Name & Middle Initial & Last Name & Degree
Dr.Ashwin L Desouza, MBBS MS
First Name & Middle Initial & Last Name & Degree
Dr Mukta Ramadwar, MBBS MD MRC
First Name & Middle Initial & Last Name & Degree
Dr Mahesh Goel, MBBS MS
First Name & Middle Initial & Last Name & Degree
Dr Shaesta Mehta, MBBS DNB MD
First Name & Middle Initial & Last Name & Degree
Dr Nitin shetty S Shetty, MBBS MD DNB
First Name & Middle Initial & Last Name & Degree
Dr Supreeta Arya, MD DNB DMRD
First Name & Middle Initial & Last Name & Degree
Dr Keadar Deodhar, MBBS MD MRC
First Name & Middle Initial & Last Name & Degree
Dr Munita Bal, MBBS MD DNB
First Name & Middle Initial & Last Name & Degree
Dr.Shraddha Patkar, MBBS MS
First Name & Middle Initial & Last Name & Degree
Dr.Abhishek Mitra, MBBS MS

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
data of patient kept confidential

Learn more about this trial

"Phase III Randomized Trial Comparing D2 vs D3 Lymphadenectomy With Gastric Cancer Following Neoadjuvant Chemotherapy

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