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

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
Sun Yat-sen Cancer Center
RECRUITING
Guangzhou
Contact Information
Primary
Yuhong Li, PhD
liyh@sysucc.org.cn
87342487
Time Frame
Start Date: 2024-01-15
Estimated Completion Date: 2029-06-30
Participants
Target number of participants: 117
Treatments
Experimental: Liver-localized treatment group
Participants in this group will undergo liver-localized interventions, which may include surgical resection and/or ablation therapy and/or SBRT, aiming to achieve NED.
Active_comparator: Palliative chemotherapy only group
Participants in this group will receive standard palliative chemotherapy. The focus is on managing symptoms and controlling the progression of the disease.
Related Therapeutic Areas
Sponsors
Leads: Sun Yat-sen University

This content was sourced from clinicaltrials.gov