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Gastric CancerNCT03049345

Gastric Cancer Sentinel Lymph Node Mapping

A study testing Sentinel Lymph Node Sampling, Radioactive Tracers and Methylene Blue 20 MG/ML in people with Gastric Cancer and Sentinel Lymph Node, run by McGill University Health Centre/Research Institute of the McGill University Health Centre at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Gastric cancer has an incidence in North America of over 24,000 new cases annually, of which approximately 15% are diagnosed at an early stage. Standard of care for early gastric cancer (EGC) treatment has historically included anatomical resection with regional lymphadenectomy. Read more about this study

Who is it for?
Any age
What is being tested?
Sentinel Lymph Node Sampling, Radioactive Tracers and Methylene Blue 20 MG/ML
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteCanada
Study dates
1 Jul 2016to 30 Sep 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • All patients who are deemed healthy enough to withstand laparoscopic or open anatomic gastrectomy with extended regional (D2) lymphadenectomy will be eligible. Patients much have biopsy-proven, single lesion, <4cm gastric adenocarcinoma, of stage cT1/T2/T3 N0 M0.

Who cannot join

  • Not able to withstand anatomical gastric resection with D2 lymphadenectomy, patient refusal, N+ve disease on pre-op work up, disease progression before surgery

Trial locations and contacts

1 site in 1 country.

Canada1 site, 1 recruiting
  • Montreal General Hospital

    Montreal, Quebec, H3G1A4

    Carmen L Mueller, MD MEd, 5146776465, carmen.mueller@mcgill.ca

    Carmen L Mueller, MD MEd

    Recruiting

Other trials in Canada

About this study

Official title: Gastric Cancer Sentinel Lymph Node Sampling: Refining Patient Selection for Organ Sparing Resection of Early Gastric Cancer in a North American Context

Gastric cancer has an incidence in North America of over 24,000 new cases annually, of which approximately 15% are diagnosed at an early stage. Standard of care for early gastric cancer (EGC) treatment has historically included anatomical resection with regional lymphadenectomy. However, with the recent emergence of organ-sparing techniques, select patients with a very low risk of lymph node metastases are able to avoid anatomical resection and its inherent short and long term consequences. Despite this advance, EGC patients with high risk features continue to require anatomical resection to achieve adequate lymph node staging, despite the fact that 75-95% of these patients ultimately are found to have node negative disease. Due to the inadequacy of standard imaging modalities to reliably detect nodal metastases in EGC patients, sentinel lymph node sampling for gastric cancer was developed using principals similar to those used broadly for breast and melanoma patients. Early reports from Asia suggest this technique has very high success rates, accuracy and sensitivity, however it has never been verified in a North American context. This study aims to test SLN sampling for North American gastric cancer patients at a high volume regional treatment centre, with an aim to expand the application of organ sparing resection to EGC patients.

This project aims to determine the sensitivity and accuracy of sentinel lymph node sampling for early gastric cancer patients at a high volume, North American, tertiary care centre.

Read the detailed description

Gastric cancer incidence in North America is 7.4/100,000 population, with 24,590 new cases diagnosed annually in the United States1. Of these, approximately 15% are detected at the early gastric cancer stage with no spread to regional lymph nodes2. Recent advances in gastric cancer detection, such as endoscopic use of narrow band imaging and magnification endoscopy, can help improve the detection rate of early lesions3-5. Gastric cancers detected at an early stage have an excellent prognosis, with reported long term overall survival rates of 71-92%6-9 due to the low rate of peritoneal and distant metastatic spread which frequently occur in patients with more advanced lesions. However, the mainstay of treatment even for early gastric cancers (EGC) remains anatomical resection with regional lymphadenectomy. While oncologically sound, anatomical resection is often associated with complications and unpleasant short and long-term side effects, including post-operative weight loss, dumping syndrome, vitamin deficiencies, anastomotic complications, delayed gastric emptying, and bile reflux, among others. Given the long life expectancy of patients after resection of EGC, curative resection with organ preservation to improve post-operative quality of life should be a treatment goal.

Recently, organ-sparing techniques have emerged which allow select early gastric cancers to be treated without anatomical resection. These techniques, including endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD), allow for curative resection of highly-selected lesions with complete organ preservation. The shortcoming of all organ sparing resection techniques presently is that lymphadenectomy is not performed, leading some patients to perhaps be under-staged and therefore under-treated.

According to the Japanese Gastric Cancer Treatment Guidelines10, early lesions are deemed appropriate for organ-sparing endoscopic resection if they meet the following criteria: confined to the mucosa (T1a), tumour size <2cm, no ulceration, and well-differentiated tumour grade. Together, tumours with these features have a very low risk of lymph node metastases (<1%). Long-term outcomes of ESD are highly favorable, with local recurrence and overall survival rates comparable to anatomical resection7,8. For tumours that do not meet the above criteria however, risk of lymph node involvement is drastically increased, with submucosal invasion, ulceration, tumour size >3cm, poorly differentiated tumour type, and lymphovascular invasion conferring a risk of lymphatic metastases of 4-26%11. For this reason, current best practices recommend EGCs with high risk features continue to undergo anatomical resection with regional lymphadenectomy. However 75-95% of such patients will ultimately have no regional metastases on final pathological analysis, suggesting they could have been spared anatomical resection if only their lymph node basins had been definitively staged prior to surgery.

Presently, several imaging modalities are available to characterize lymph node stage for gastric cancer, including endoscopic ultrasound (EUS), computed tomography (CT) and positron emission tomography (PET). Unfortunately, the sensitivity of these modalities is woefully inadequate to accurately predict microscopic lymph node metastases, and therefore they cannot be reliably used to differentiate high risk EGCs that require anatomical resection and lymphadenectomy from those amenable to organ-sparing resection12-15.

To address this gap in the ability to accurately detect nodal metastases in early gastric cancer, sentinel lymph node (SNL) sampling was pioneered in Asia and has undergone refinement and study there since the early 2000s. A recent multi-institutional study of 397 patients conducted across 12 centres in Japan reported rates of SLN detection of 97.5% and accuracy of SLN stage when compared to post-resection stage of 99%16. These numbers rival those reported for SLN biopsy of breast and melanoma cancers in large randomized controlled trials17,18. Indeed, for these tumour types, SLN biopsy is now the standard of care globally for staging clinically node-negative patients due to its diagnostic superiority over other staging modalities. Following the success of SLN sampling in gastric cancer, select Asian institutions are now applying this technique to diverting sentinel node-negative (SLN -ve) T1 and T2 gastric cancer patients away from anatomical resection with extensive lymphadenectomy and towards organ-sparing endoscopic or wedge resection.

The Upper GI Oncology Program at the McGill University Health Centre sees approximately 80 gastric cancer patients per year, in whom SLN sampling has the potential to inform resection decisions ~25-30%. Currently, the program performs 15-20 ESDs annually for both early esophageal and gastric lesions, and approximately 30-40 anatomical resections are performed in node-negative gastric and esophageal cancer patients per year. Implementation of the gastric SNL sampling technique would enable expansion of the ESD program to offer organ-sparing curative resections to EGC patients who presently can only be offered anatomical resection.

The purpose of this study is to determine the utility and feasibility of SLN sampling for gastric cancer in a North American context.

Being tested
Sentinel Lymph Node Sampling, Radioactive Tracers, Methylene Blue 20 MG/ML
Medical subject headings
Stomach Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Sentinel Lymph Node SamplingProcedure or surgery

    The day before surgery, 2mL of endoscopically-placed technetium 99m sulfur colloid solution will be injected submucosally at 4 points around the tumour. At the time of surgery, 2cc of 1% isosulfan blue dye will be similarly injected. Laparoscopically, the gastrocolic ligament will be opened to expose all gastric lymph node drainage basins. Using visual inspection and a laparoscopic gamma probe, blue nodes and those emitting 10x greater than background activity will be considered sentinel nodes and extracted. Sentinel lymph nodes and resected specimens will be analyzed by permanent section.

  • Radioactive TracersDrug

    see above

  • Methylene Blue 20 MG/MLDrug

    see above

Study groups in NCT03049345
Study groupRoleWhat they receive
Sentinel Node Sampling ArmExperimentalThe day before surgery, 2mL of endoscopically-placed technetium 99m sulfur colloid solution will be injected submucosally at 4 points around the tumour. At the time of surgery, 2cc of 1% isosulfan blue dye will be similarly injected. Laparoscopically, the gastrocolic ligament will be opened to expose all gastric lymph node drainage basins. Using visual inspection and a laparoscopic gamma probe, blue nodes and those emitting 10x greater than background activity will be considered sentinel nodes and extracted. Patients will then under regular gastric cancer resection with D2 lymphadenectomy as per routine in our institution.
Receives: Procedure: Sentinel Lymph Node Sampling; Drug: Radioactive Tracers; Drug: Methylene Blue 20 MG/ML

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of patients in whom sentinel lymph node status accurately predicts true nodal status after anatomical gastrectomy and complete pathological examination

    The % of patients in whom SLN status matched nodal status overall will be calculated

    Measured: 3-4 weeks after study completion

  2. Sensitivity of Sentinel Lymph Node Sampling Method

    # of patients with +ve SLN / # of patients with +ve lymph nodes in total

    Measured: 3-4 weeks after study completion

  3. Specificity of Sentinel Lymph Node Sampling Method

    # of patients with -ve SLNs / # of patients with -ve lymph nodes in total

    Measured: 3-4 weeks after study completion

Secondary outcomes (8)
  1. Adverse events due to SLN sampling technique

    Complications of SLN intervention (allergic reaction, intra-operative bleeding, conversion to open approach)

    Measured: at time of surgery

  2. Length of stay

    # of days patient stays in hospital after procedure

    Measured: 90 days from study completion

  3. R0 Resection rate

    # of patients who have complete measurable disease excision at time of surgery

    Measured: 3-4 weeks after study completion

  4. 3 year Disease free survival rate

    # of patients who are free of gastric cancer at 3 years out of all study patients

    Measured: 3 years after study completion

  5. conversion to open

    Number of patients who required a conversion to open technique after starting laparoscopically

    Measured: at time of surgery

  6. Patient mortality

    # of patients who die within 30 days of surgery or who die while in hospital

    Measured: 90 days after surgery

  7. 3 year overall survival rate

    number of patients who are still alive at 3 years out of all study patients

    Measured: 3 years after study completion

  8. Adverse surgical events

    # of patients who suffered any of the following surgical complications: urinary tract infection, pneumonia, ileus, anastomotic leak, reoperation within 30 days of surgery, readmission within 30 days of discharge, myocardial infarction, venous thromboembolism, bleeding requiring blood transfusion

    Measured: 30 days after study completion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Feb 2017
  2. Study start1 Jul 2016
  3. Primary completion30 Jun 2022 (estimated)
  4. Study completion30 Sep 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Model description
human subjects
Masking
None (open label)
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03049345
Sponsor's protocol ID
14-288-GEN
Status last verified
Sep 2019
First submitted
6 Feb 2017
Last updated
6 Sep 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kitagawa Y, Takeuchi H, Takagi Y, Natsugoe S, Terashima M, Murakami N, Fujimura T, Tsujimoto H, Hayashi H, Yoshimizu N, Takagane A, Mohri Y, Nabeshima K, Uenosono Y, Kinami S, Sakamoto J, Morita S, Aikou T, Miwa K, Kitajima M. Sentinel node mapping for gastric cancer: a prospective multicenter trial in Japan. J Clin Oncol. 2013 Oct 10;31(29):3704-10. doi: 10.1200/JCO.2013.50.3789. Epub 2013 Sep 9.

    PubMed 24019550
  • Gotoda T, Yanagisawa A, Sasako M, Ono H, Nakanishi Y, Shimoda T, Kato Y. Incidence of lymph node metastasis from early gastric cancer: estimation with a large number of cases at two large centers. Gastric Cancer. 2000 Dec;3(4):219-225. doi: 10.1007/pl00011720.

    PubMed 11984739
  • Mueller CL, Lisbona R, Sorial R, Siblini A, Ferri LE. Sentinel Lymph Node Sampling for Early Gastric Cancer-Preliminary Results of A North American Prospective Study. J Gastrointest Surg. 2019 Jun;23(6):1113-1121. doi: 10.1007/s11605-018-04098-5. Epub 2019 Mar 11.

    PubMed 30859424

Questions about this trial

What is this clinical trial studying?

A study testing Sentinel Lymph Node Sampling, Radioactive Tracers and Methylene Blue 20 MG/ML in people with Gastric Cancer and Sentinel Lymph Node, run by McGill University Health Centre/Research Institute of the McGill University Health Centre at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 6 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of patients in whom sentinel lymph node status accurately predicts true nodal status after anatomical gastrectomy and complete pathological examination (time frame: 3-4 weeks after study completion). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03049345, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Sep 2019.

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