Clinical Trials Logo

Clinical 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. 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03049345
Study type Interventional
Source McGill University Health Centre/Research Institute of the McGill University Health Centre
Contact
Status Recruiting
Phase N/A
Start date July 1, 2016
Completion date September 30, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT05551416 - The EpiGASTRIC/EDGAR Project: New Strategies for the Early Detection and Prevention of Gastric Cancer
Recruiting NCT05518929 - Hypoxia During Gastroenterological Endoscope Procedures Sedated With Ciprofol In Overweight Or Obesity Patients Phase 4
Recruiting NCT06006390 - CEA Targeting Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of CEA Positive Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT03219593 - Apatinib as the First-Line Therapy in Elderly Locally Advanced or Metastatic Gastric Cancer Phase 2
Recruiting NCT05489211 - Study of Dato-Dxd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03) Phase 2
Recruiting NCT05536102 - The Effectiveness and Safety of XELOX and Tislelizumab + PLD for Resectable Gastric Cancer (LidingStudy) Phase 2
Active, not recruiting NCT03170960 - Study of Cabozantinib in Combination With Atezolizumab to Subjects With Locally Advanced or Metastatic Solid Tumors Phase 1/Phase 2
Recruiting NCT06010862 - Clinical Study of CEA-targeted CAR-T Therapy for CEA-positive Advanced/Metastatic Malignant Solid Tumors Phase 1
Recruiting NCT05415098 - Study of Safety, Pharmacokinetic and Efficacy of APG-5918 in Advanced Solid Tumors or Lymphomas Phase 1
Active, not recruiting NCT04082364 - Combination Margetuximab, Retifanlimab, Tebotelimab, and Chemotherapy Phase 2/3 Trial in HER2+ Gastric/GEJ Cancer Phase 2/Phase 3
Withdrawn NCT03766607 - Trastuzumab Beyond Progression in HER2 Positive Metastatic Gastric Cancer Phase 2
Recruiting NCT04118114 - Phase II Study of PRL3-ZUMAB in Advanced Solid Tumors Phase 2
Completed NCT01924533 - Efficacy and Safety Study of Olaparib in Combination With Paclitaxel to Treat Advanced Gastric Cancer. Phase 3
Terminated NCT01641939 - A Study of Trastuzumab Emtansine Versus Taxane in Participants With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Advanced Gastric Cancer Phase 2/Phase 3
Recruiting NCT05107674 - A Study of NX-1607 in Adults With Advanced Malignancies Phase 1
Active, not recruiting NCT04908813 - Study of HLX22 in Combanition With Trastuzumab and Chemotherapy Versus Placebo in Combination With Trastuzumab and Chemotherapy for Treatment of Locally Advanced or Metastatic Gastric Cancer Phase 2
Active, not recruiting NCT04249739 - Pembrolizumab + Capecitabine/Oxaliplatin (CapeOx) -HER2 Nagative and Pembrolizumab + Trastuzumab + Cisplatin/Capecitabine HER2 Positive Phase 2
Recruiting NCT05514158 - To Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of Disitamab Vedotin Combined With RC98 in the Treatment of Subjects With HER2-expressing Locally Advanced or Metastatic Gastric Cancer (Including AEG) Phase 1
Recruiting NCT04931654 - A Study to Assess the Safety and Efficacy of AZD7789 in Participants With Advanced or Metastatic Solid Cancer Phase 1/Phase 2
Recruiting NCT03175224 - APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors Phase 2