No registrations found.
ID
Source
Brief title
Health condition
peritoneal metastases (PM), colorectal cancer (CRC), cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC), liquid biopsy, circulating tumor DNA (ctDNA)
Dutch: peritoneale metastasen (PM), colorectaal carcinoom (CRC), cytoreductie en hypertherme intraperitoneale chemotherapie (HIPEC), liquid biopsy, circulerend tumor DNA (ctDNA)
Sponsors and support
Afdeling Heelkunde
Boelelaan 1117
1081 HV, Amsterdam
Afdeling Heelkunde
Boelelaan 1117
1081 HV, Amsterdam
Intervention
Outcome measures
Primary outcome
Plasma levels of ctDNA preoperatively.
Secondary outcome
Plasma levels of ctDNA postoperatively.
Background summary
Rationale: Patient selection and follow-up after cytoreductive surgery and HIPEC (Hyperthermic IntraPEritoneal Chemotherapy) for peritoneal metastases (PM) of colorectal origin are hampered by limitations of diagnostic modalities. Conventional radiological imaging has a low sensitivity for detection of peritoneal metastases and is unable to detect the extensiveness of the disease. The HIPEC procedure is significantly more effective in early disease but unfortunately due to limitations of tests peritoneal metastases are often diagnosed in an advanced stage, limiting treatment options. Circulating tumour DNA (ctDNA) in plasma (also called: Liquid Biopsies) has shown promising preliminary results for diagnosis and follow-up of patients with colorectal cancer. The use of ctDNA could potentially improve detection of PM, improve patient selection for HIPEC and possibly detect recurrent disease during follow-up at an earlier stage. Currently the ctDNA tests have not been evaluated in patients with PM.
Objective: To evaluate feasibility of ctDNA detection in patients with PM undergoing cytoreductive surgery and HIPEC.
Study design: Prospective feasibility study
Study population: Patients with known PM and planned to undergo cytoreductive surgery and HIPEC for PM of colorectal origin.
Intervention (if applicable): Not applicable
Main study parameters/endpoints: Main study parameter is the presence of detectable mutated ctDNA in the patient’s plasma at time of diagnosis. Secondly the quantity is evaluated after cytoreductive therapy 2-4 weeks postoperatively to evaluate treatment effect.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
This study has no benefits for the patient. Also participation does not add any burden or risks, other than the minor complications related to venapunction. These include: hematoma or puncture related anxiety.
Study objective
Primary Objective:
- To evaluate the detection of circulating tumor DNA (ctDNA) in patients with peritoneal metastases (PM) of colorectal origin undergoing cytoreductive surgery and hyperthermic intraperitoneal chemohterapy (HIPEC) at time of diagnosis in a feasibility trial (N=20 patients).
Secondary Objective:
- To evaluate a potential decrease of levels of ctDNA decrease after cytoreductive surgery and HIPEC
Feasibility; The study is feasible if the following criteria are met
1. If in at least 70% of the patients ctDNA status correlates with mutational status of the tissue specimen preoperatively (qualitative)
2. If at least 50% of the patients with detectable mutated ctDNA show decreased levels of ctDNA after treatment (quantitative)
Study design
Plasma levels of ctDNA preoperatively: day of HIPEC surgery, prior to surgery.
Plasma levels of ctDNA postoperatively: 2-4 weeks after HIPEC surgery.
Intervention
This is an observational cohort study to assess the correlation between ctDNA and cytoreductive surgery. No interventions are performed.
Treatment and follow-up of patients will not be influenced by ctDNA results.
Two additional viles of blood (2*9mL Streck) are taken before (on the day of HIPEC surgery) and after cytoreductive surgery and HIPEC (2-4 weeks after HIPEC surgery).
Nina R Sluiter
De Boelelaan 1117
Amsterdam 1081 HV
The Netherlands
+31 (0)20 4445234
n.sluiter@vumc.nl
Nina R Sluiter
De Boelelaan 1117
Amsterdam 1081 HV
The Netherlands
+31 (0)20 4445234
n.sluiter@vumc.nl
Inclusion criteria
- Orally and written informed consent
- Age 18 years and older
- Elective cytoreductive surgery followed by HIPEC
- Peritoneal metastases only
- Regular preoperative work-up
Exclusion criteria
- Patients who are legally or mentally incapable or unable to give informed consent
- Patients younger than 18 years
- Presence of liver metastases on CT-scan/peroperatively
- Presence of pulmonary metastases on CT-scan/peroperatively
- Anxiety for vena puncture
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6960 |
NTR-old | NTR7148 |
CCMO | NL57226.029.16 |
OMON | NL-OMON43017 |