Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New combo attack on liver tumors shows promise for Tough-to-Treat cancer

NCT ID NCT06071052

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This phase 2 trial tested a three-part treatment for people with colorectal cancer that spread to the liver and stopped responding to standard treatments. The approach combines two minimally invasive procedures (TACE and HAIC) with the targeted drug regorafenib. The goal was to see if this combination could shrink tumors and improve survival in 21 patients.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
regorafenib
What this could lead to
If this works, it could offer a new treatment option for people with colorectal cancer that has spread to the liver and hasn't responded to standard therapies.
What could go wrong
This is a small, early-phase study with only 21 participants, so results may not apply to everyone. The combination also carries risks like liver damage or side effects from the drugs and procedures.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

21 people

The number who actually took part.

Started

Dec 2023

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Patients aged 18-75 years old, gender unlimited; 2. Patients with liver metastasis of colorectal cancer by pathological histology or clinical diagnosis (refer to the Guidelines for the Diagnosis and Comprehensive Treatment of Liver metastasis of Colorectal Cancer, 2016 Edition), those who were mainly exposed to liver metastasis with large tumor load and suffered from no clear extrahepatic metastasis; 3. Patients with a liver area tumor no more than 5 tumor nodules, and a nodule size no more than10cm; 4. Patients subject to the failure of previous chemotherapy regimen containing irinotecan or oxaliplatin after at least six cycles of systemic chemotherapy; they cannot undergo surgery or refuse surgery; 5. Patients with liver tumor who did not receive interventional treatment (TACE, ablation, iodine particle treatment, etc.) within one year; 6. Patients with an expected survival period longer than 3 months; 7. Patients with favorable liver function (7 points for Child-Pugh A or B); 8. Patients with a physical fitness ECOG no more than one point; 9. Patients who understood and signed the Informed Consent Form. Exclusion Criteria: 1. Patients with distant metastases except the liver; 2. Patients subject to the treatment of TACE, ablation or iodine particles within one year; 3. Patients with obvious artero / venous fistula and cancer plugs in the main portal vein; 4. Patients who had suffered from or were currently developing other malignant tumors (except for the cured basal or squamous cell skin carcinoma or cervical carcinoma in situ); 5. Patients whose white blood cells were less than 3,000 cell / mm3, or platelet count less than 50,000 / mm3; 6. Patients subject to renal insufficiency (creatinine\> 2 mg/L); 7. Patients whose AST and / or ALT was / were more than 5 times the upper limit of normal; 8. Patients with poor coagulation function, an INR larger than 1.5, or currently subject to anticoagulant therapy or known hemorrhagic disease; 9. Patients with a history of major disease with heart, kidney, bone marrow, or lung, and central nervous system involvement; 10. Patients requiring antibiotic treatment due to recent infections; 11. Patients subject to comorbidities or social environment that could prevent them from following the study plan or even endanger their safety.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Colorectal cancer with liver metastasis are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • the first affiliated hospital, Sun-Yat sen university

    Guangzhou, Guangdong, 510000, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.