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NCT06208371RecruitingPhase 3

Localized Treatment Versus Palliative Chemotherapy in CRC Patients With 10 or More CRLM

The DECIDE-CRLM-10 Randomized Controlled Study: Comparison of Chemotherapy Combined With Localized Treatment for Liver Metastases Versus Palliative Chemotherapy Alone in Colorectal Patients With 10 or More Liver Metastases

Source: ClinicalTrials.gov · Last updated 30 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to investigate the effectiveness of localized interventions in improving the 5-year survival rate for colorectal cancer patients with ≥10 liver metastases. We aim to answer the following question: Can localized interventions, including surgery and/or ablation and/or stereotactic body radiotherapy (SBRT), enhance the 5-year survival rate compared to palliative chemotherapy alone in patients with ≥10 colorectal liver metastases (CRLM)? Participants in this study, who have achieved disease control through chemotherapy, will undergo either localized interventions (surgery and/or ablation and/or SBRT) or receive palliative chemotherapy alone. Researchers will compare the survival outcomes between these groups to determine the potential benefits of localized interventions for patients with ≥10 CRLM.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
117 (estimated)
First submitted
5 Jan 2024
Start date
15 Jan 2024
Primary completion date
30 Jun 2029
Lead sponsor
Sun Yat-sen University
NCT number
NCT06208371

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 117
  • From 15 Jan 2024 to the primary completion date, 30 Jun 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Definite presence of extrahepatic metastasis and/or primary tumor not amenable to curative surgical resection.
  • Clinically severe cardiovascular diseases such as cerebrovascular accident (within 6 months before enrollment), myocardial infarction (within 6 months before enrollment), uncontrolled hypertension despite appropriate medical treatment, unstable angina, congestive heart failure (NYHA 2-4), and arrhythmias requiring medication.
  • Any other diseases, metastatic lesions causing functional impairment, or suspicious findings in the physical examination indicating possible contraindications for the use of investigational drugs or placing the patient at a high risk of treatment-related complications.

Other illness

  • Bleeding tendencies or coagulation disorders.
  • Severe uncontrollable systemic complications such as infection or diabetes.
  • History or physical examination indicating central nervous system diseases (such as primary brain tumor, uncontrollable epilepsy, any brain metastasis, or history of stroke).
  • Diagnosis of other malignant tumors within the past 5 years (excluding basal cell carcinoma after radical surgery and/or cervical carcinoma in situ).

Other

  • Severe arterial embolism or ascites.
  • Hypertensive crisis or hypertensive encephalopathy.
  • Pregnant or lactating women.
  • Women of childbearing potential not using or refusing to use effective non-hormonal contraceptive methods (intrauterine devices, combined barrier contraceptive methods with spermicidal gel, or sterilization) or men with reproductive potential.
  • Inability or unwillingness to comply with the study protocol.

Who the study is looking for

  • Age ≥ 18 years.
  • Histologically confirmed colorectal adenocarcinoma.
  • Baseline imaging (CT, MRI, or PET/CT as necessary) or pathological confirmation of liver metastasis, with no extrahepatic metastasis (consideration for inclusion may be given to lesions with a diameter less than 10mm in the lungs or lymph nodes if metastasis is difficult to confirm or is suspected).
  • Disease control (PR or SD) achieved after a minimum of 8 cycles of systemic chemotherapy.
  • Evaluation by a centralized liver surgeon expert group to confirm presence of ≥10 liver metastases, which can be managed through surgery and/or ablation and/or SBRT to achieve NED. Non-resectability is defined as one or more of the following: ① Unable to undergo R0 resection; ② Predicted insufficient remaining liver volume after resection; ③ After resection, none of the three hepatic veins can be preserved, and the preservation of residual liver inflow and outflow and bile ducts cannot be guaranteed, and adjacent two liver segments cannot be preserved.
  • Curative surgery possible for the primary colorectal lesion.
  • Normal hematological, hepatic, and renal functions at baseline.
  • Child-Pugh grade A liver function.
  • ECOG performance status 0-1.
  • Tolerability to undergo further surgery and chemotherapy.
  • Life expectancy \> 3 months.
  • Signed written informed consent.
  • Willing and able to undergo follow-up until death, study completion, or study termination.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sun Yat-sen Cancer Center
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.