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Adjuvant HIPEC in High Risk Colon Cancer

Adjuvant Hyperthermic Intraperitoneal Chemotherapy in Patients With Colon Cancer at High Risk of Peritoneal Carcinomatosis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02231086
Acronym
COLOPEC
Enrollment
204
Registered
2014-09-04
Start date
2015-03-31
Completion date
2019-06-01
Last updated
2021-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms, Peritoneal Neoplasms

Keywords

Chemotherapy, Adjuvant, Laparoscopy, Peritoneal Lavage, HIPEC

Brief summary

This study aims to determine the oncological effectiveness of adjuvant HIPEC, using intraperitoneal oxaliplatin with concomitant i.v. 5-FU/LV, following a curative resection of a T4 or intra-abdominally perforated Colon cancer in preventing the development of peritoneal carcinomatosis in addition to the standard adjuvant systemic treatment. Hypothesis: The hypothesis is that adjuvant HIPEC preceding routine adjuvant systemic therapy using i.p. oxaliplatin with concomitant i.v. 5-FU/LV following a curative resection of a T4 or intra-abdominally perforated colon cancer reduces the development of peritoneal carcinomatosis in comparison to standard adjuvant systemic treatment alone.

Detailed description

Background: The peritoneum is the second most common site of recurrence in patients with colon cancer. Early detection of peritoneal carcinomatosis (PC) by imaging is difficult and adjuvant systemic treatment does not seem to affect peritoneal dissemination in contrast to haematogenous dissemination in the liver or lungs. Of all patients eventually presenting with clinically apparent PC, only a quarter have potentially curable disease. The curative option is cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CR/HIPEC), but the effectiveness depends highly on the extent of disease and is associated with a considerable complication rate. These clinical problems underline the need for effective adjuvant intraperitoneal therapy in high risk colon cancer patients in order to prevent the development of PC with treatment at a subclinical stage. Study design: This will be a multicentre study in which 176 eligible patients will be randomized to adjuvant HIPEC followed by adjuvant systemic chemotherapy in the experimental arm, or the standard adjuvant systemic chemotherapy alone in the control arm. Adjuvant HIPEC will be performed preferably simultaneously or within 10 days after resection of the primary tumour, either by laparoscopy or open approach, similar to the technique used for resection of the primary tumour. If adjuvant HIPEC cannot be performed within 10 days (i.e. complicated postoperative course), the procedure will be delayed until 5 to 8 weeks postoperatively. Subsequently, patients will receive routine adjuvant chemotherapy (CAPOX) within 3 weeks from HIPEC. Diagnostic laparoscopy will be performed routinely after 18 months postoperatively in both arms of the study in patients without evidence of disease based on routine follow-up using CT imaging and CEA. If peritoneal carcinomatosis is found during staging laparoscopy, CR/ HIPEC will be performed in patients with a maximum of 5 involved regions and without evidence of systemic disease. Study population: Patients who underwent intentionally curative resection for a T4N0-2M0 or intra-abdominally perforated colon cancer. Intervention: Adjuvant HIPEC procedure: access to the abdominal cavity by laparoscopy or laparotomy under general anaesthesia, adhesiolysis if necessary, complete staging of the intra-abdominal cavity, positioning of in- and outflow catheters, perfusion with a minimum of 2l isotonic dialysis fluid at a flow rate of 1-2l/min and an inflow temperature of 42-43˚C. Before the beginning of HIPEC, 5-fluorouracil 400 mg/m2 and leucovorin 20 mg/m2 will be administered intravenously to potentiate oxaliplatin activity. Oxaliplatin (460 mg/m2) is added to the perfusate after attaining at least 42 degrees inflow temperature with a total of 30 minutes perfusion time. Outcomes: Primary endpoint is peritoneal recurrence-free survival at 18 months. Secondary endpoints are number of participants with adverse events as a measure of safety and tolerability, incidence of PC at end of follow-up with or without concomitant liver/lung metastases, percentage of false negative CT at 18 months (second look laparoscopy/laparotomy as gold standard), disease-free survival, overall survival, quality of life and costs.

Interventions

PROCEDUREAdjuvant HIPEC (open/laparoscopic)

Adjuvant HIPEC procedure: access to the abdominal cavity by laparoscopy or laparotomy under general anaesthesia, adhesiolysis if necessary, complete staging of the intra-abdominal cavity, positioning of in- and outflow catheters, perfusion with a minimum of 2l isotonic dialysis fluid at a flow rate of 1-2l/min and an inflow temperature of 42-43˚C. Before the beginning of HIPEC, 5-fluorouracil 400 mg/m2 and leucovorin 20 mg/m2 will be administered intravenously to potentiate oxaliplatin activity. Oxaliplatin (460 mg/m2) is added to the perfusate after attaining at least 42 degrees inflow temperature with a total of 30 minutes perfusion time.

Colon cancer patients with a high risk of developing PC, but do not have (yet) proven macroscopic peritoneal metastasis, are standardly treated with adjuvant systemic chemotherapy. Standard adjuvant systemic chemotherapy consists in the Netherlands of a capecitabine and oxaliplatin (CAPOX) or 5-FU and oxaliplatin (FOLFOX) for a total of 6 months.

Presence or absence of peritoneal recurrence will be evaluated by laparoscopy in case of negative routine examination (CEA and CT thorax/abdomen) at 18 months postoperatively in both study arms.

Sponsors

ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
Dutch Health Care Insurance Board
CollaboratorOTHER
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age between 18 and 75 years * Intention to start routine adjuvant systemic therapy * adequate clinical condition to undergo simultaneous HIPEC or re- laparoscopy or re-laparotomy with HIPEC within either 10 days or between week 5-8 from --primary resection * written informed consent * white blood cell count of at least 3000/mm3, platelet count of at least 100.000/mm3 * no bleeding diathesis or coagulopathy * normal creatinine or creatinine clearance of at least 50 ml/min

Exclusion criteria

* postoperative complications that interfere with adjuvant HIPEC within 8 weeks (i.e. persisting intra-abdominal abscess, significant fascial dehiscence, enteric fistula) * no intention to start routine adjuvant systemic therapy * liver and/or lung metastases * pregnant or lactating women * unstable or uncompensated respiratory or cardiac disease * serious active infections * other concurrent chemotherapy * hypersensitivity to fluorouracil, folinic acid or another substance of leucovorin or oxaliplatin * stomatitis, ulceration in the mouth or gastrointestinal tract. * severe diarrhea * severe hepatic and / or renal dysfunction. * plasma bilirubin concentrations greater than 85 μmol/l. * pernicious anemia or other anaemias due to vitamin B12 deficiency. * peripheral sensory neuropathy with functional impairment.

Design outcomes

Primary

MeasureTime frameDescription
Peritoneal Recurrence Free Survival at 18 Months18 monthsPeritoneal recurrence-free survival at 18 months determined by CT and CEA. If CEA was normal and CT did not show any signs of peritoneal metastase at 18 months, a diagnostic laparoscopy was performed in those patients who consented to this intervention. Complete peritoneal staging was performed during laparoscopy, and biopsies were taken from suspicious lesions. If no peritoneal lesions were seen or biopsies were negative, this indicated that the patient was free from peritoneal recurrence.

Secondary

MeasureTime frameDescription
Hospital Stay for Simultaneous and Staged HIPEC, Either Open or Laparoscopic10 weeksHospital stay for simultaneous and staged HIPEC, either open or laparoscopic.
False-negative Rate of CT-scan for Peritoneal Metastases5 yearsThe presence or absence of peritoneal metastasis on CT-scan will be compared to the findings during diagnostic laparoscopy, histological biopsy or fine needle aspiration cytology.
Patterns of Dissemination (Peritoneal Plus or Minus Distant Metastases)5 yearsPatterns of dissemination (peritoneal plus or minus distant metastases).
Treatment Related Toxicity of Adjuvant HIPEC30 days after adjuvant HIPECToxicity directly related to adjuvant HIPEC included 30-day complication rate, re-intervention rate, and re-admission rate.
Overall Survival5 yearsOverall survival.
Quality of Life Questionnaire Survey 5- Year Follow-up5 yearsQuality of life questionnaire survey 5- year follow-up.
Disease-free Survival5 yearsDisease-free survival.

Countries

Netherlands

Participant flow

Participants by arm

ArmCount
Standard Adjuvant Systemic Chemotherapy
Standard adjuvant systemic chemotherapy according to the Dutch colon cancer guideline, using a capecitabine and oxaliplatin (CAPOX) or 5-FU and oxaliplatin (FOLFOX) schedule. Presence or absence of peritoneal recurrence will be evaluated by laparoscopy in case of negative routine examination (CEA and CT thorax/abdomen) at 18 months postoperatively. Standard adjuvant systemic chemotherapy: Colon cancer patients with a high risk of developing PC, but do not have (yet) proven macroscopic peritoneal metastasis, are standardly treated with adjuvant systemic chemotherapy. Standard adjuvant systemic chemotherapy consists in the Netherlands of a capecitabine and oxaliplatin (CAPOX) or 5-FU and oxaliplatin (FOLFOX) for a total of 6 months. Diagnostic laparoscopy: Presence or absence of peritoneal recurrence will be evaluated by laparoscopy in case of negative routine examination (CEA and CT thorax/abdomen) at 18 months postoperatively in both study arms.
102
Adjuvant HIPEC (Open/Laparoscopic)
Adjuvant HIPEC will be performed simultaneously with primary tumor resection, or as a staged procedure (\<10 days or 5-8 weeks postoperatively). The chemotherapy during oxaliplatin-HIPEC consists of an intravenous phase with leucovorin 20 mg/m2 (maximum 40 mg) and 5-fluorouracil 400 mg/m2 (maximum 800 mg) and an intraperitoneal phase with oxaliplatin 460 mg/m2 (maximal 920 mg). Standard adjuvant systemic chemotherapy according to the national guideline will be given within 3 weeks from HIPEC. Presence or absence of peritoneal recurrence will be evaluated by laparoscopy in case of negative routine examination (CEA and CT thorax/abdomen) at 18 months postoperatively. Adjuvant HIPEC (open/laparoscopic): Adjuvant HIPEC procedure: access to the abdominal cavity by laparoscopy or laparotomy under general anaesthesia, adhesiolysis if necessary, complete staging of the intra-abdominal cavity, positioning of in- and outflow catheters, perfusion with a minimum of 2l isotonic dialysis flui
100
Total202

Baseline characteristics

CharacteristicAdjuvant HIPEC (Open/Laparoscopic)TotalStandard Adjuvant Systemic Chemotherapy
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
33 Participants68 Participants35 Participants
Age, Categorical
Between 18 and 65 years
67 Participants134 Participants67 Participants
Age, Continuous61.5 years61 years61 years
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
Netherlands
100 Participants202 Participants102 Participants
Sex: Female, Male
Female
47 Participants97 Participants50 Participants
Sex: Female, Male
Male
53 Participants105 Participants52 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1020 / 100
other
Total, other adverse events
102 / 102100 / 100
serious
Total, serious adverse events
46 / 10295 / 100

Outcome results

Primary

Peritoneal Recurrence Free Survival at 18 Months

Peritoneal recurrence-free survival at 18 months determined by CT and CEA. If CEA was normal and CT did not show any signs of peritoneal metastase at 18 months, a diagnostic laparoscopy was performed in those patients who consented to this intervention. Complete peritoneal staging was performed during laparoscopy, and biopsies were taken from suspicious lesions. If no peritoneal lesions were seen or biopsies were negative, this indicated that the patient was free from peritoneal recurrence.

Time frame: 18 months

ArmMeasureValue (NUMBER)
Standard Adjuvant Systemic ChemotherapyPeritoneal Recurrence Free Survival at 18 Months79 participants
Adjuvant HIPEC (Open/Laparoscopic)Peritoneal Recurrence Free Survival at 18 Months80 participants
Secondary

Disease-free Survival

Disease-free survival.

Time frame: 5 years

Secondary

False-negative Rate of CT-scan for Peritoneal Metastases

The presence or absence of peritoneal metastasis on CT-scan will be compared to the findings during diagnostic laparoscopy, histological biopsy or fine needle aspiration cytology.

Time frame: 5 years

Secondary

Hospital Stay for Simultaneous and Staged HIPEC, Either Open or Laparoscopic

Hospital stay for simultaneous and staged HIPEC, either open or laparoscopic.

Time frame: 10 weeks

Secondary

Overall Survival

Overall survival.

Time frame: 5 years

Secondary

Patterns of Dissemination (Peritoneal Plus or Minus Distant Metastases)

Patterns of dissemination (peritoneal plus or minus distant metastases).

Time frame: 5 years

Secondary

Quality of Life Questionnaire Survey 5- Year Follow-up

Quality of life questionnaire survey 5- year follow-up.

Time frame: 5 years

Secondary

Treatment Related Toxicity of Adjuvant HIPEC

Toxicity directly related to adjuvant HIPEC included 30-day complication rate, re-intervention rate, and re-admission rate.

Time frame: 30 days after adjuvant HIPEC

Population: Only measured in experimental group

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Standard Adjuvant Systemic ChemotherapyTreatment Related Toxicity of Adjuvant HIPEC0 Participants
Adjuvant HIPEC (Open/Laparoscopic)Treatment Related Toxicity of Adjuvant HIPEC0 Participants

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026