Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT06076811 |
| Other study ID # |
DANISH.MRD |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
August 1, 2023 |
| Est. completion date |
July 30, 2030 |
Study information
| Verified date |
October 2023 |
| Source |
University of Aarhus |
| Contact |
Claus L Andersen, PhD |
| Phone |
+45 7845 5319 |
| Email |
cla[@]clin.au.dk |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
Approximately two-thirds of all colorectal cancer patients undergo surgery with the aim of
curing them. However, despite the surgery, 20-25% of them experience relapse. It is possible
to reduce the risk of relapse with chemotherapy, but as chemotherapy is associated with
significant side effects, it is only given to patients at high risk of relapse. Currently,
the risk is assessed based on an examination of the removed tumor tissue.
In a previous research project, blood samples were taken after patients' surgery and examined
for the presence of circulating tumor DNA (ctDNA). When cancer cells in solid tumors die,
they release DNA, which can be detected in the blood. DNA in the blood has a half-life of
less than 2 hours, so if ctDNA is found in a blood sample taken, e.g., 14 days after surgery,
the patient most likely still has cancer cells in their body.
The results show that if a patient has ctDNA in their blood after surgery, the risk of
relapse is high. The presence of ctDNA in the blood has the potential to be a better
indicator of the risk of future relapse than the tumor examination used today. Therefore,
ctDNA analysis has the potential to become a marker that will be used in the future clinical
setting for monitoring colorectal cancer.
The overall objective of this study is to confirm that ctDNA found in a blood sample after
intended curative treatment for CRC is a marker of residual disease and risk of recurrence
and is applicable in clinical practice.
Description:
Colorectal cancer (CRC) is the third most common cancer worldwide. Approximately 75% of
patients initially present with potentially curable disease, but despite curatively intended
treatment up to 25 % of them experience a relapse of the disease. Upon diagnosis, survival of
CRC can be improved by offering adjuvant chemotherapy to patients with a high risk of
recurrence, or by early detection of recurrence enabling early intervention which improves
patient survival significantly. To achieve this, it is essential to have sensitive and
specific tools for correctly identifying patients with a high risk of recurrence and the need
for adjuvant therapy, and for early detection of recurrence facilitating early intervention.
Non-invasive analysis of circulating tumor DNA (ctDNA) is an emerging tool that has this
potential.
Objectives
The overall objective of the study is to confirm that ctDNA detected after intended curative
treatment for CRC is a marker of residual disease and risk of recurrence and is applicable in
clinical practice.
Primary objectives
P1: To determine the prognostic value of a patient's ctDNA status and compare it with other
known prognostic factors. Specifically, the aim is to determine the association between
3-year disease-free survival (DFS) and ctDNA detection status immediately after 1)
curative-intended surgery and 2) adjuvant chemotherapy.
P2: To identify a cohort of UICC stage III CRC patients with planned adjuvant chemotherapy.
These patients will be offered enrollment in the DANISH.MRD part II (Secondary objective 1
(S1)), and will further be included in a European collaboration named GUIDE.MR-01-CRC, funded
by the European Union via the Innovative Health Initiative.
Secondary objectives
S1: To technically assess, compare, and rank commercial ctDNA diagnostics and evaluate their
performance after intended-curative CRC treatment (postoperatively and post adjuvant
chemotherapy) to identify the best-performing method at each time point.
S2: To assess the effect of standard-of-care adjuvant chemotherapy on the level of ctDNA.
Especially, for patients with ctDNA detected after surgery, the aim is to measure and compare
the ctDNA levels in plasma samples drawn before and after adjuvant chemotherapy. Further, the
change in ctDNA level will be correlated to the oncological outcomes (time to clinical
recurrence, disease-free survival, and overall survival).
S3: To investigate if time to Molecular recurrence determined using serial ctDNA analyses in
longitudinally collected plasma samples is shorter than time to Clinical recurrence using
standard-of-care radiological imaging.
S4: To investigate the correlation between ctDNA analysis results and findings on CT scans.
ctDNA analysis will be restricted to blood sampling times that coincide with standard-of-care
CT scans (at 12 and 36 months postoperatively). If ctDNA analysis can predict the outcome of
the CT scan, the potential is that ctDNA analysis in the future can guide when to perform CT
scans.
S5: To investigate the prognostic power of ctDNA at the time point of indeterminate CT scans.
S6: To investigate, if molecular characterization of CRC cancers can stratify patients and
predict i.e., treatment response, growth patterns, cancer aggressiveness, clinical outcomes,
and whether the tumor sheds ctDNA into the circulation.
Investigational plan
The DANISH.MRD study is logistically divided into two parts, and patients are offered
participation in each part separately. The parts are called "DANISH.MRD part I - Surgery",
and "DANISH.MRD part II - Surveillance".
In DANISH.MRD part I blood samples are collected before and after surgery. For patients
receiving neoadjuvant therapy, a blood sample will also be collected before initiation of
this treatment.
In DANISH.MRD part II blood samples are collected immediately after adjuvant chemotherapy and
during standard-of-care surveillance.
Patients included in DANISH.MRD part I will help address Primary objective 1 (P1). The subset
of the part I patients that are also included in DANISH.MRD part II will help to address the
Secondary objectives S1-S6.
Both Part I and Part II DANISH.MRD patients receive standard follow-up care, which includes
scheduled visits for up to 5 years following their surgery.
Sample collection for DANISH.MRD part I - Surgery (Objectives P1-2, S1-S5)
- Blood sampling preoperatively and after surgery (between days 20-30, but before
initiation of adjuvant chemotherapy)
- Sampling of tissue from the resected specimen
Sample collection in DANISH.MRD part II - Surveillance (objectives S1-S5)
- Blood sampling post-adjuvant chemotherapy (ACT): postACT (14-30 days after the end of
ACT), and at months 8, 12, 16, 20, 24, 30 and 36 postoperatively.
