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NCT06449937Recruiting

Local Liver Treatment for Multi-organ Colorectal Cancer Metastases

Analysis of the Efficacy of Local Liver Treatment for Multi-organ Colorectal Cancer Metastases: A Prospective, Multicenter, Non-randomized Concurrent Controlled Study

Source: ClinicalTrials.gov · Last updated 10 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study was to investigate the effect of only local radical treatment of liver metastases combined with systematic treatment in the treatment of patients with multiple organ metastases of colorectal cancer, whether it can benefit the prognosis and explore the risk factors related to the prognosis.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
130 (estimated)
First submitted
4 Jun 2024
Start date
Jul 2024
Primary completion date
Jul 2028
Lead sponsor
Anhui Provincial Hospital
NCT number
NCT06449937

What you commit to

  • Study type: Interventional
  • Planned participants: 130
  • From Jul 2024 to the primary completion date, Jul 2028
  • 6 sites 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

  • According to the investigator's judgment, patients with concomitant diseases that seriously endanger patient safety or affect patient completion of the study.

Other illness

  • History of hepatic encephalopathy or liver transplantation.
  • History of other malignant tumors (except thyroid cancer and carcinoma in situ) can be included in the study if the individual has remained disease-free for at least 5 years.
  • Patients with acute cardiovascular and cerebrovascular diseases such as acute cerebral infarction and acute coronary syndrome within 1 month, and the cardiovascular clinical symptoms or diseases were not well controlled.
  • Uncontrollable hypertension, blood pressure \> 160 / 95 mmHg after treatment, history of hypertensive crisis or hypertensive encephalopathy.
  • Uncontrollable infection \> grade 2 (NCI-CTC version 5.0).
  • Patients with respiratory insufficiency : PaO2 \< 60 mmHg at rest , with or without PaCO2 \> 50 mmHg.
  • Patients with a large amount of ascites (ultrasound examination showed an echoless area around the liver and spleen, pelvic cavity, and intestinal loops, and the mesentery and intestinal canal were seen floating in the echoless area ) or malignant ascites (cancer cells were found in ascites or ascites CEA was higher than peripheral blood).
  • Long-term unhealed wounds or fractures, major surgery or severe traumatic injury, fracture or ulcer occurred within 4 weeks.
  • Patients with a history of mental drug abuse and who could not quit or had mental disorders.

Lab values

  • NYHA class 3-4 or left ventricular ejection fraction (LVEF) \< 50 % by echocardiography.
  • Coagulation dysfunction ( INR \> 1.5 or APTT \> 1.5\*ULN ), with bleeding tendency.

Other

  • Patients with only liver metastasis confirmed by CT or MRI.
  • Evidence of brain metastases.
  • Pregnant or breast-feeding women.
  • According to the investigator's judgment, patients who are not suitable for inclusion.

Who the study is looking for

  • Male or female, 18-80 years of age.
  • Patients volunteered to join the study and signed informed consent, with good compliance and follow-up.
  • Primary colorectal tumors can be radically resected or resected and histopathologically diagnosed as colorectal cancer.
  • Patients with synchronous or metachronous diagnosis of liver metastasis and extrahepatic metastasis by computed tomography (CT) or magnetic resonance imaging (MRI).Extrahepatic metastases are stable and controllable as determined by Multi-disciplinary Treatment (MDT).
  • Patients receive only first- or second-line systemic therapy.
  • Radical local treatment can be performed after MDT evaluation, and the indications at least meet the following one:
    • Hepatectomy: liver metastases can be completely (R0) removed and required to retain sufficient functional liver tissue;
    • Ablation therapy: The maximum diameter of liver metastases\<3 cm, and the maximum number of ablation ≤ 5.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  • Life expectancy of at least 3 months.
  • Child-Pugh score ≤ 7.
  • Laboratory routine examination (blood routine, liver and kidney function, coagulation function, etc.) no significant abnormalities:
    • Absolute neutrophil count (ANC) ≥ 1.5×10\^9/l;
    • Platelet count (PLT) ≥ 100\*10\^9/l;
    • Hemoglobin ≥ 9g/dl;
    • TBIL\<1.5 times the upper limit of normal (ULN);
    • ALT and AST\< 5\*ULN;
    • Serum creatinine ≤ 1.5 \* ULN or Creatinine clearance\> 50 ml/min;
    • Albumin \> 30 g/l.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

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

SiteCityCountrySite status
The First People's Hospital of Chu Zhou
Coordinator of this site? Confirm its status
ChuzhouChinaRecruiting
Fuyang Cancer Hospital
Coordinator of this site? Confirm its status
FuyangChinaRecruiting
Anhui Province Hospital
Coordinator of this site? Confirm its status
HefeiChinaRecruiting
Ma'anshan People's Hospital
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Ma’anshanChinaRecruiting
The Second People's Hospital of WuHu
Coordinator of this site? Confirm its status
WuhuChinaRecruiting
The First Affiliated Hospital of Wannan Medical College
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WuhuChinaRecruiting

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