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Colon CancerSENTRYNCT06652672

Sentinel Node and Organ-sparing Surgery in Stage I Colon Carcinoma

A study testing Organ-sparing surgery in people with Colon Cancer and Colon Adenocarcinoma, run by Meander Medical Center at 1 site in Netherlands.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this study is to reduce the need for colectomy and its' associated morbidity and mortality in patients with pT1-2 colon carcinoma after endoscopic resection and an estimated lymph node metastasis (LNM) risk of >15%, or with macroscopically suspected T1 tumors, by performing an endoscopic-assisted… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Organ-sparing surgery
Could I receive a placebo?
No, everyone receives an active treatment
How many people
341 participants
Where
1 siteNetherlands
Study dates
12 Dec 2024to 12 Dec 2032
Phase
Interventional
Are there results?
Not yet: the study is under way

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Oral and written informed consent (IC)
  • Aged 18 years and older
  • Fit for both organ-sparing surgery and colectomy
  • Pathologically confirmed T1-2 adenocarcinoma of the colon following R0, R1, or Rx endoscopic resection with an estimated LNM risk >15% (Table 5.2.2. in module 5.2 of the Dutch CRC guideline); or a lesion macroscopically suspected to be (deep-invasive) T1 colon cancer, measuring <40 mm, for which wedge resection is considered the most suitable local resection technique as recommended by the MDT
  • The resection scar after local excision is expected to be clearly recognized at endoscopy, either by a tattoo or by detecting a scar in the colorectal segment where no other polypectomies were performed
  • Lesion located >25cm from the anus based on endoscopic measurement, or above sigmoid take-off

Who cannot join

  • Patients who opt for active follow-up instead of surgery following shared decision-making
  • Distant metastasis
  • Lynch syndrome
  • Another active malignancy requiring palliative treatment at the time of colon cancer diagnosis
  • Previous colorectal cancer within the last 5 years
  • Tumours that comprised >50% of the colon circumference before resection
Show all 13Show fewer
  • Tumours involving the ileocaecal valve
  • Pregnancy, lactation or a planned pregnancy during the course of the study
  • Known allergy to any of the compounds used for SLN identification (ICG, Iodine or Sodium iodide)
  • Previous colonic surgery (excluding appendectomy)
  • Contra-indication for laparoscopic or robotic surgery
  • Severe kidney- or liver failure
  • Hyperthyroidism or an autonomously functioning thyroid adenoma

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Bart CT van de Laar contact

+31338507137

bct.vande.laar@meandermc.nl

Netherlands1 site, 1 recruiting
  • Meander Medisch Centrum

    Amersfoort

    Bart CT van de Laar, MD, +31338507137, bct.vande.laar@meandermc.nl

    Recruiting

Other trials in Netherlands

About this study

Official title: Sentinel Node and Organ-sparing Surgery in Stage I Colon Carcinoma (SENTRY Trial)

The aim of this study is to reduce the need for colectomy and its' associated morbidity and mortality in patients with pT1-2 colon carcinoma after endoscopic resection and an estimated lymph node metastasis (LNM) risk of >15%, or with macroscopically suspected T1 tumors, by performing an endoscopic-assisted laparoscopic/robotic wedge resection of the tumor or scar, along with sentinel node (SLN) biopsy using indocyanine green (ICG). This intervention will be compared to the standard-of-care segmental resection using a partially randomized patient preference design. The primary outcome is the 3-year recurrence rate.

Read the detailed description

Colorectal cancer is the third most common type of cancer in the Netherlands and the second leading cause of cancer-related deaths. An increased incidence of T1-2 tumors has been observed following the introduction of population screening programs, leading to more frequent endoscopic excisions. The risk of LNM in T1-2 colon cancers is relatively low. However, local excision does not allow assessment of lymph node status. Moreover, the diagnostic accuracy of computed tomography (CT) and other preoperative imaging modalities for detecting LNM remains limited.

Segmental colonic resections are associated with substantial morbidity. Based on large population-based datasets, 33% of patients experience at least one complication, including anastomotic leakage, with a postoperative mortality rate of 1.5-3.1%. Morbidity is known to substantially impact quality of life and contribute to a high economic burden. Additionally, major symptoms of low anterior resection syndrome (LARS) are present in 21% of patients after segmental resection, with reported effects on quality of life comparable to those experienced by patients who undergo rectal cancer resection and develop LARS.

To minimize unnecessary completion surgery, histopathological risk stratification is applied. In the Netherlands, histopathological risk factors for the presence of LNM in pT1-2 colon cancer are poor (high-grade) differentiation, lymphovascular invasion, high-grade tumor budding (Bd 2-3), and Haggitt level 4. The risk of LNM varies depending on the number of risk factors, pT stage, polyp morphology, and margin status. Completion segmental resection is omitted for pT1-2 tumors with a predicted LNM risk below 15%. Management is guided by risk stratification: for a 5-15% risk, active follow-up is preferred; for a 15-25% risk, active follow-up may be considered as an alternative to completion segmental resection through shared decision-making; and for a >25% risk, segmental resection is the preferred treatment. However, the vast majority of patients with a >15% risk of LNM who undergo surgery experience potential harm but no benefit, as they ultimately do not have LNM. Additionally, suspected T1 tumors are sometimes difficult or impossible to resect endoscopically. In such cases, wedge resection or segmental resection is the standard of care. Depending on T stage and other histopathological risk factors identified after wedge resection, a subsequent segmental resection may still be required. By adding SLN biopsy to the procedure, we aim to avoid the need for segmental resection after wedge resection.

The investigators hypothesize that, in patients who have undergone R0/R1/Rx endoscopic resection of T1-2 colon cancer and have a >15% risk of LNM, or in those with macroscopically suspected T1 tumors, an SLN biopsy combined with wedge resection of the residual tumor or scar can safely spare the majority of patients with negative SLNs from undergoing segmental resection. In our systematic review and meta-analysis, we found a pooled accuracy of 98% and a sensitivity of 80% for SLN detection in T1-2 colon cancer. The investigators use endoscopic submucosal injection of ICG at the tumor site, which carries a low risk of intra-abdominal spillage that could hinder SLN identification.

The SLN biopsy will be combined with an endoscopy-assisted wedge resection of the tumor or scar following endoscopic resection. During the endoscopy-assisted wedge resection, the surgeon first identifies and mobilizes the colon to facilitate the wedge resection. A gastroenterologist then performs a colonoscopy to visualize the scar from the previously resected tumor. With intraluminal endoscopic visualization, the surgeon places a suture to provide traction and position the linear stapler. The gastroenterologist confirms complete inclusion of the scar and ensures lumen patency before the stapler is fired. Endoscopy-assisted limited wedge resection is associated with low complication rates and is performed at lower cost compared to laparoscopic segmental resection. Because no anastomosis is created, the risk of anastomotic leakage is eliminated. This approach could reduce morbidity, mortality, hospital stay, and stoma rates. Although staple line failure and leakage are theoretical risks, such complications have not been reported in previous cases.

Patients with a positive SLN (macro- or micrometastasis) or T3-4 tumors are offered segmental resection. Node-positive patients are recommended to undergo adjuvant chemotherapy if performance status allows. SLN-negative patients do not undergo further surgery and are managed with an intensive follow-up strategy. Assuming 80% sensitivity and a 20% prevalence of lymph node metastasis, the risk of retained positive nodes after SLN biopsy is approximately 4%. Additionally, tumor deposits (TDs) could potentially be missed when patients are treated with SLN biopsy and wedge resection. However, only 0.45% of patients with stage I disease are TD-positive. The investigators consider the absolute risks of missed lymph node metastases and TDs acceptable, given the reduced perioperative morbidity and mortality associated with segmental resection.

The SENTRY trial will be the first to offer organ-sparing surgery combined with an SLN biopsy for patients with selected early-stage colon cancer. This organ-sparing approach is anticipated to improve postoperative mortality, morbidity, hospital stay, quality of life, and costs compared to standard segmental resection, without compromising oncologic outcomes. This multicenter, partially randomized, patient-preference trial will compare the organ-sparing approach with standard-of-care segmental resection to assess oncologic safety.

Being tested
Organ-sparing surgery, Standard of care segmental resection
Keywords
Colon cancer, Fluorescence, Sentinel lymph node, Indocyanine green (ICG), Organ sparing surgery, Organ preserving surgery, Local resection
Medical subject headings
Colonic Neoplasms

What participants receive

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

  • Organ-sparing surgeryProcedure or surgery

    Endoscopy-assisted laparoscopic/robotic wedge resection and sentinel lymph node biopsy using submucosal injection of ICG.

  • Standard of care segmental resectionProcedure or surgery

    Standard of care segmental resection of the affected part of the colon including removal of regional lymph nodes.

Study groups in NCT06652672
Study groupRoleWhat they receive
Organ-sparing surgeryExperimentalLocal resection with sentinel lymph node biopsy
Receives: Procedure: Organ-sparing surgery
Standard of care segmental resectionActive comparatorNot described
Receives: Procedure: Standard of care segmental resection

What is being measured

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

  1. 3-year recurrence rate

    Measured: 3 years postoperatively

  2. Successful sentinel lymph node biopsy

    Percentage of patients undergoing a successful sentinel lymph node biopsy with one or more sentinel lymph nodes detected

    Measured: Intraoperative

Secondary outcomes (19)
  1. 5-year recurrence rate

    Measured: 5 years postoperatively

  2. 3-year overall survival

    Measured: 3 years postoperatively

  3. 5-year overall survival

    Measured: 5 years after postoperatively

  4. 90-days complication rate

    Clavien-Dindo classification

    Measured: 90 days postoperatively

  5. 90-days postoperative mortality

    Measured: 90 days postoperatively

  6. Proportion of patients with preference for standard and experimental treatment, and without preference

    Measured: 1 day postoperatively

  7. Procedure time of organ-sparing surgery and segmental resection

    Measured: Directly after surgery, on the same day

  8. Successful wedge resections

    Percentage of patients undergoing a successful wedge resection

    Measured: Intraoperative

  9. Intraoperative complications

    Measured: Intraoperative

  10. Upstaging of sentinel lymph nodes due to ultrastaging

    If sentinel lymph nodes test negative after routine HE staining, ultrastaging is performed. During this process, the lymph nodes are sectioned at 200 µm intervals and examined at three levels using HE staining, as well as immunohistochemistry for cytokeratin AE1/AE3. Sentinel lymph nodes are considered upstaged if they are initially negative on HE staining but are positive during ultrastaging, either with macrometastases (>2 mm) or micrometastases (0.2-2 mm).

    Measured: During postoperative pathological examination, conducted within two weeks after surgery.

  11. Quality of life - EQ5D-5L

    EuroQoL 5-Dimension 5-Level. Range 1-5 per dimension. Higher means worse quality of life.

    Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively

  12. Quality of life - QLQ-CR29

    QLQ-CR29 questionnaire: Organisation for Research and Treatment of Cancer (EORTC) colorectal quality of life module QLQ-CR29. Range 0-100. Higher scores indicate higher levels of symptoms or less functioning.

    Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.

  13. Quality of life - QLQ-C30

    European Organization for Research and Treatment (EORTC) quality of life questionnaire (QLQ-C30): Range 0-100. A high score on each scale represents a high level in the examined topic, a high score on the global health status for instance represents a high quality of life and a high score in a symptom scale represents a high level of symptoms/problems.

    Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.

  14. Quality of life - Surv100

    Surv100 questionnaire: European Organization for Research and Treatment (EORTC) quality of life questionnaire survivorship (Surv100). 100 items on a 4- or 7-point Likert scale. A high score on each scale represents a high level in the examined topic, a high score on the global health status for instance represents a high quality of life and a high score in a symptom scale represents a high level of symptoms/problems.

    Measured: From enrollment to the end of study. Questionnaires will be sent 36, 48, and 60 months postoperatively

  15. Quality of life - LARS

    LARS questionnaire: Low Anterior Resection Syndrome (LARS) score. 0-20 points, no LARS; 21-29 points, minor LARS; 30-42 points, major LARS.

    Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively

  16. Quality of life - WAI

    WAI questionnaire: Work Ability Index. Range 7-49. The total WAI scores are categorized into 4 levels: poor (7-27), moderate (28-36), good (37-43), and excellent (44-49).

    Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively

  17. Quality of life - iMCQ

    iMTA Medical Consumption Questionnaire (iMCQ): The iMCQ includes questions related to frequently occurring contacts with health care providers.

    Measured: From enrollment to the end of study. Questionnaires will be sent 6, 12, 18, and 24 months postoperatively

  18. Costs associated with wedge resection and sentinel lymph node biopsy.

    Bottom-up micro costing will be applied.

    Measured: 5 years postoperatively

  19. Costs standard of care segmental resection

    Bottom-up micro costing will be applied.

    Measured: 5 years postoperatively

Timeline

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

  1. First posted22 Oct 2024
  2. Study start12 Dec 2024
  3. Primary completion12 Dec 2030 (estimated)
  4. Study completion12 Dec 2032 (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
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
Multi-center, prospective, non-inferior, partially randomized patient-preference trial
Masking
None (open label)
Enrolment
341 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06652672
Sponsor's protocol ID
NL84875.100.23
Other IDs
NL84875.100.23
Acronym
SENTRY
Status last verified
Nov 2025
First submitted
8 Oct 2024
Last updated
20 Nov 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Organ-sparing surgery in people with Colon Cancer and Colon Adenocarcinoma, run by Meander Medical Center at 1 site in Netherlands.

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 6 inclusion and 13 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: looking for participants now, as of the sponsor's last update on 20 Nov 2025. 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 Netherlands. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Bart CT van de Laar (+31338507137, bct.vande.laar@meandermc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

3-year recurrence rate (time frame: 3 years postoperatively). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 20 Nov 2025.

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