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NCT Number: NCT05734300

The "SPARCOL" Study

Mortality following elective colorectal cancer surgery range between 2.5-6% and increase for the elderly and frail patient regardless of T-stage. Around 80% of the patients who present with a colon cancer and is in a condition where surgery is possible will be offered resection of the tumor. A part of the colon is always removed together with the lymph nodes in order to ensure that cancer cells are not left behind. The risk of lymph node metastasis is dependent on several histopathological characteristics of the tumor. The overall risk of lymph node metastases is less than 20 % in patients with early colon cancer. This indicates that the majority of patients with early colon cancer have no benefit of additional resection besides local tumor excision. The alternative to resecting a larger part of the bowel is to make more focused surgery only resecting a small part of the bowel part through a combination of laparoscopic and endoscopic techniques. This new organ sparing approach is called Combined Endoscopic Laparoscopic Surgery (CELS). The investigators aimed to examinate the hypothesis that organ preserving approach (CELS) provides superior quality of recovery in elderly frail patients with small colon cancers when compared with standard surgery in RCT.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Copenhagen University Hospital - Herlev, Copenhagen, Herlev, Denmark

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and Female participants providing written informed consent aged 75 years and older
  • PS score ≥1 and /or ASA score ≥3
  • Macroscopically or pathological colonic adenocarcinoma
  • Clinical TNM classification T1/T2 N0 M0
  • Eligible and suitable for CELS resection according to MDT
  • Tumor must be located in colon, and not involving the ileac valve or taking up more than 50% of the lumen in an air-distended bowel wall

Exclusion criteria

  • Unable to give informed consent
  • Histological high-risk features in biopsy material from tumor (mucin, signet cells, de- differentiation)
  • Suspected other malignancy than adenocarcinoma (e.g. neuroendocrine tumors)
  • Preoperative chemo/radiotherapy
  • Creation of stoma perioperative
  • Non-Danish speakers

Treatment and study plan

Combined Endoscopic Laparoscopic Surgery (CELS)

Procedure

The main surgical advantage in this procedure is the ability to view the colon intra- and extraluminal simultaneously. The laparoscopic approach enables manipulation and mobilization of the colon, while the endoscopic view secures that the resection is complete and not overlapping the ileac valve or creating stenosis.

Compared to the traditional oncological colon resection, the CELS resection is a minimally invasive procedure - organ sparing procedure leading to a reduced surgical stress response.

Standard resection

Procedure

In this study standard resection of the colon will be performed according to complete mesocolic excision (CME) principles.

Primary outcomes

  1. Change in patient-reported postoperative recovery - Quality of Recovery 15

    Time frame: Change in QoR-15 will be assessed repeatedly at baseline, 4-8 hours postoperatively (4-8H), postoperative day (POD) 1, POD 2, POD 3, POD 7, POD 10-14 and POD 30

    Validated to measure recovery after surgery and general anesthesia, and additionally validated for use in Danish language and culture. The scale is arbitrary and ranges from 0 to 150. Higher scores means better recovery. The established minimum clinically important difference in QoR-15 is 8.0, and the SD of QoR- 15 scores after major surgery is in the order of 16.

Secondary outcomes

  1. Change in exercise capacity and physical condition

    Time frame: Changes will be assessed repeatedly at baseline, Postoperative day 1, Postoperative day 2, Postoperative day 3 or at the time of hospital discharge, whatever comes first. Postoperative day 10-14 and 30 days postoperatively.

    The 30 Second Sit to Stand Test. A measurement that assesses functional lower extremity strength in older adults. Test result is the number of times the participant comes to a full standing position in 30 seconds. Higher number of stands within 30 seconds means better result.

  2. Change in exercise capacity and physical condition

    Time frame: Changes will be assessed repeatedly at baseline, Postoperative day 1, Postoperative day 2, Postoperative day 3 or at the time of hospital discharge, whatever comes first. Postoperative day 10-14 and 30 days postoperatively.

    Six minutes' walk test is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.

  3. Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire - EORTC C30.

    Time frame: Changes will be assessed repeatedly at basline, 3 months, 6 months, 1 year follow-up

    EORTC C30, questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).

  4. Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire- EORTC CRC.

    Time frame: Changes will be assessed repeatedly at basline, 3 months, 6 months, 1 year follow-up

    EORTC CRC questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).

  5. Frailty questionnaire Geriatric 8 (G8)

    Time frame: Basline

    The G-8 Score is a screening tool containing 8 questions. The total G-8 score lies between 0 and 17. A higher score indicates a better health status.

  6. Duration of surgery

    Time frame: Intraoperative

    Duration of surgery in minutes

  7. Blood loss

    Time frame: Intraoperative

    Blood loss in ml

  8. Intraoperative complications

    Time frame: Intraoperative

    Descriptive registration of intraoperative complications;

  9. Conversion rate

    Time frame: Intraoperative

    Conversion rate (%) from laparoscopic surgery to open surgery

  10. Rate of complete resection margin

    Time frame: Postoperative day 14

    R0 (tumor-free margin >1 mm) corresponds to resection for cure or complete remission. R1 to microscopic residual tumor, R2 to macroscopic residual tumor.

  11. Assessment of histopathological risk factors

    Time frame: Postoperative day 14

    Assessment of histopathological risk factor defined as presence of at least one of the risk factors: Kikuchi level ≥sm2, vascular invasion, lymphatic invasion, poorly differentiated adenocarcinoma, and tumour budding BD2-3.

  12. Long-term oncological outcomes: Disease-free survival

    Time frame: During 3-year follow-up periode

    Time from surgery until the recurrence of disease or death

  13. Long-term oncological outcomes: Overall survival

    Time frame: During 3-year follow-up periode

    Overall survival was defined as the time elapsed from the date of surgery to the last day of follow-up or the date of death

  14. Long-term oncological outcomes: Recurrence

    Time frame: During 3-year follow-up periode

    Locoregional and/or distant recurrence after surgery defined as any histological, morphological, and clinical evidence of tumour growth during follow-up periode

  15. Clavien-Dindo classification

    Time frame: Within 90 days postoperative.

    Grading system used in surgery for grading adverse events (i.e. complications) which occur as a result of surgical procedures. Grade I to V, where V is death of the patient

  16. The Comprehensive Complication Index

    Time frame: Within 90 days postoperative.

    e Comprehensive Complication Index (CCI®) reflects the gravity of this overall complication burden on the patient on a scale from 0 (no complication) to 100 (death)

  17. Length of hospital stay

    Time frame: Within 90 days postoperative.

    Clinical metric that measures the length of time in days elapsed between a patient's hospital admittance and discharge.

  18. 90-day mortality

    Time frame: Within 90 days postoperative.

    Death within 90 days after surgery, as either an inpatient or outpatient

  19. Hospital readmissions

    Time frame: Within 90 days postoperative.

    Unplanned readmissions that happen within 3 days of discharge from the index (i.e., initial) admission

  20. Rate of secondary standard resection

    Time frame: Within 90 days postoperative.

    Rate in percent of performed secondary surgery after primary CELS resection

Study contacts

Contact information is provided by the study sponsor or research team.

Ilze Ose, MD

CONTACT

[email protected]

27293399 ext. 0045

Ismail Gögenur, Prof.

CONTACT

[email protected]

26336426 ext. 0045

Sponsors and collaborators

Lead sponsor

Zealand University Hospital

Other

Registry information

Official study title

Organ SPARring Surgery vs. Standard Resection for Early Stage COLon Cancer in Elderly Frail Patients

Important dates

Study start
2023
Primary completion
2025
Study completion
2027
First posted
Feb 17, 2023
Registry last updated
Jul 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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