Second and Third Look Laparoscopy in pT4 Colon Cancer Patients for Early Detection of Peritoneal Metastases

Colorectal Cancer Clinical Trial

— COLOPEC-II  

Official title:

Second and Third Look Laparoscopy in pT4 Colon Cancer Patients for Early Detection of Peritoneal Metastases; the COLOPEC-II Randomized Multicentre Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03413254
• Other study ID #: NL61507.018.17
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: March 1, 2018
• Est. completion date: October 1, 2028

Study information

• Verified date: February 2024
• Source: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The COLOPEC II multicentre randomized trial will investigate the role of second and third look laparoscopy to detect metachronous peritoneal metastases at a clinically occult stage during the follow-up of pT4 colon cancer patients. It is expected that detection of PM at a clinically occult stage will translate into survival benefit, due to higher percentage of patients eligible for curative intent treatment with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).

Description:

Problem description Approximately 20-30% of patients with pT4 colon cancer develop peritoneal metastases (PM). The only proven curative option for macroscopic PM is cytoreductive surgery (CRS) followed by hyperthermic intraperitoneal chemotherapy (HIPEC), but the efficacy and morbidity highly depend on the extent of peritoneal involvement. Unfortunately, due to restricted accuracy of imaging modalities and the absence of early symptoms, PM are often detected at a stage in which only about 20-25% of patients are eligible for CRS+HIPEC, and even these patients appear to have a relatively high peritoneal cancer index (PCI). New diagnostic strategies are urgently required to detect PM at an early stage, resulting in a higher percentage of patients eligible for CRS+HIPEC, which will translate into better survival because of the uniformly reported direct association between PCI and survival. Proposed solution Preliminary findings of the COLOPEC trial (NCT02231086) revealed that PM were already detected at intentionally adjuvant HIPEC within 2 months after resection of the primary tumour in 10% of patients with pT4 colon cancer. Based on these findings and literature, second look diagnostic laparoscopy (DLS) to detect PM when the disease is still potentially curable by CRS+HIPEC may be considered as an essential component of early follow-up of pT4 colon cancer. This needs confirmation in a larger patient cohort before implementing this in practice. Furthermore, metachronous PM develop later on (>12 months) in an additional 15-20% of the patients. These patients will be missed by a second look DLS and might therefore benefit from a third look DLS later on, which will be investigated in the COLOPEC II trial. Objective The primary aim of this study is to determine the added value of third look DLS after a negative second look DLS in pT4 colon cancer patients to detect PM at a clinically occult stage. Study design This is a randomized multicentre trial in which eligible patients will have routine CT-abdomen at 6 months postoperative (+3 months for those still treated with adjuvant chemotherapy), followed by second look DLS within 1 month after CT if no PM or other metastases not amenable for local treatment are detected. Patients without PM found during second look DLS will subsequently be randomized between routine follow-up including CT-abdomen at 18 months in the control arm, or an experimental arm with a third look DLS provided that PM or incurable metastases are absent at the 18 months CT-abdomen. The primary endpoint of the study is the proportion of PM detected after negative second look DLS. The primary endpoint will be determined at 20 months. Study population Patients aged 18-80 years who underwent intentionally curative resection of pT4a,bN0-2M0 colon cancer or rectosigmoid cancer above the peritoneal reflection, either with or without adjuvant systemic chemotherapy, who are fit enough and surgically accessible to undergo second look DLS between 6-10 months postoperatively and subsequent treatment of PM if detected. Intervention DLS will be performed in patients not already diagnosed with PM and without other metastases that impede curative intent treatment. Access to the abdominal cavity is obtained under general anaesthesia by open introduction away from areas of expected adhesions, followed by adhesiolysis if necessary. Complete staging of the intra-abdominal cavity is performed, with biopsy of any lesion suspicious of PM, and determining the PCI for those patients with suspected PM. Expected outcome It is hypothesized that in patients who had a negative second look DLS, PM become clinically apparent in 5% until 20 months postoperatively with routine follow-up. A third look DLS following a negative CT-abdomen at 18 months postoperative is expected to detect an additional 10% of PM. It is expected that detection of PM at a clinically occult stage will translate into survival benefit, based on the observation that survival rates after CRS+HIPEC are higher if the PCI is lower.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 389
• Est. completion date: October 1, 2028
• Est. primary completion date: March 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Curative intent resection of pT4a,bN0-2M0 colon cancer or rectosigmoid cancer above the peritoneal reflection, with or without adjuvant systemic therapy;
• Age between 18 and 80 years;
• Written informed consent.

Exclusion Criteria:

• Histological subtype other than (mucinous) adenocarcinoma or signet-ring cell carcinoma;
• Clinical condition that does not allow for second look surgery or subsequent treatment of PM if detected;
• Second look surgery thought not to be technically possible (i.e. because of extensive abdominal surgery / re-interventions).

Related Conditions & MeSH terms

• Colonic Neoplasms
• Colorectal Cancer
• Neoplasm Metastasis
• Peritoneal Metastases

Intervention

Other:
• Routine follow-up
Patients visit the outpatient clinic twice a year during the first two to three years and annually thereafter, until five years postoperative. CEA-levels are determined at 3, 6, 9, 12, 15, 18, 21, 24, 30, 36, 48 and 60 months after primary resection. Detection of liver metastases with ultrasound or CT is performed at 12, 24, 36, 48 and 60 months postoperative. At 6 and 18 months postoperative, a CT-scan is part of the study protocol, but ultrasound of the liver is allowed for other time intervals during follow-up. Colonoscopy is performed at 12 and 48 months postoperative.

Procedure:
• Second look DLS
Second look DLS is performed within one month from negative CT at 6-9 months (depending last date of adjuvant chemotherapy) and normal CEA. Laparoscopic access to the abdominal cavity is obtained under general anaesthesia, followed by adhesiolysis if necessary. Complete staging is performed, with biopsy of any lesion suspicious of PM, and determining the peritoneal cancer index (PCI) in case of PM. Conversion to laparotomy not allowed for better exposure, but only for intra-operative complications.
• Third look DLS
Third look DLS is performed within one month from negative CT at 18 months and normal CEA. Laparoscopic access to the abdominal cavity is obtained under general anaesthesia, followed by adhesiolysis if necessary. Complete staging is performed, with biopsy of any lesion suspicious of PM, and determining the peritoneal cancer index (PCI) in case of PM. Conversion to laparotomy not allowed for better exposure, but only for intra-operative complications.

Locations

Country	Name	City	State
Netherlands	Flevoziekenhuis	Almere
Netherlands	Amsterdam UMC, location AMC	Amsterdam
Netherlands	Amsterdam UMC, location VUmc	Amsterdam
Netherlands	Antoni van Leeuwenhoek	Amsterdam
Netherlands	OLVG	Amsterdam
Netherlands	Catharina hospital	Eindhoven
Netherlands	University Medical Center Groningen	Groningen
Netherlands	St. Antonius hospital	Nieuwegein
Netherlands	Radboudumc	Nijmegen
Netherlands	University Medical Center Utrecht	Utrecht

Sponsors (1)

Lead Sponsor	Collaborator
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of peritoneal metastases detected after a negative second look DLS	Peritoneal metastases that are detected using either routine follow-up or third look DLS according to randomization.	20 months
Secondary	Incidence of PM at second look DLS after curative treatment of primary tumour, depending on pathological pT4 stage, pathological nodal stage and histology	Occult peritoneal metastases not detected by routine CT scan 6-9 months after primary resection of pT4 colon cancer, that are detected at second look DLS performed at 6-10 months after the primary resection.	6-10 months
Secondary	Incidence of PM during first 20 months after curative resection of primary tumour, depending on pathological pT4 stage, pathological nodal stage and histology	This outcome measure tries to stratify pT4 colon cancer patients in clinically relevant subgroups based on their risk to develop PM.	20 months
Secondary	Incidence of PM in patients who did or did not undergo adjuvant chemotherapy	This outcome measure analysis a potential impact of adjuvant chemotherapy on the development of PM.	20 months
Secondary	Sensitivity, specificy, NPV and PPV of CT imaging to detect PM compared to DLS	Diagnostic accuracy of CT using DLS findings as gold standard.	20 months
Secondary	Proportion of detected PM eligible for curative intent CRS+HIPEC at different follow-up intervals	This outcome measures determines the clinical impact of PM detection, considering potentially curative intent treatment.	20 months
Secondary	30-day morbidity related to second/third look DLS	This outcome measure is important to determine the harm/benefit ratio of DLS.	From the second or third look DLS till 30 days postoperative
Secondary	Extent of adhesiolysis required at second/third look DLS assessed with the Zühlke score	The Zühlke score measures the severity of intraabdominal adhesions.; Filmy adhesions.; Stronger adhesions requiring some sharp dissection.; Dense vascularized adhesions requiring sharp dissection.; Extreme dense vascularized adhesions with high risk for organ damage during dissection.; A higher score indicates a worse outcome.	20 months
Secondary	5-year peritoneal recurrence free survival	This outcome measure determines whether third look DLS has any impact on the overall detection of PM.	5 years
Secondary	5-year disease-free survival	Important long-term oncological endpoint to determine the potential oncological benefit of third look DLS.	5 years
Secondary	5-year overall survival	Important long-term oncological endpoint to determine the potential oncological benefit of third look DLS.	5 years
Secondary	Quality of life assessed with the CRC-29 questionnaire	Assessing impact of invasive diagnostic procedures on QOL.	2 years
Secondary	Quality of life assessed with the EQ-5D-5L questionnaire	Assessing impact of invasive diagnostic procedures on QOL.	2 years