Prevention and Treatment of Complications of Endovascular Methods in Patients With Malignant Liver Tumors

NCT ID: NCT04764409

Last Updated: 2021-02-21

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 500 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-01-12
• Study Completion Date: 2023-12-12

Brief Summary

In the structure of malignant liver lesions, two main groups are distinguished - primary liver cancer and metastatic liver damage. The five-year survival rate of patients with malignant liver tumors does not exceed 6%. The main and radical method of treatment today is liver resection. However, surgical treatment is possible only in 10-25% of patients. At the same time, recurrence of malignant tumors is observed in 60-80% of cases within five years after surgery, and the number of candidates for repeated liver resection does not exceed 10%. The high toxicity of systemic chemotherapy limits its use in this group of patients. In this connection, minimally invasive and at the same time effective methods of local treatment of malignant liver tumors have been introduced into clinical practice. These methods include: hepatic artery chemoinfusion, chemoembolization and oil chemoembolization.

Currently, a large world experience has already been accumulated in the application of the above methods of treatment. However, any, even minimally invasive, surgical manipulation can be associated with the development of complications of varying severity. If complications arise, there is a risk of interruption of palliative care, which entails a significant reduction in life expectancy. According to domestic and foreign literature, the occurrence of complications after intra-arterial chemoembolization occurs in 0.4-10% of patients, and after intra-arterial chemoinfusion - in 5-30% of patients. In the overwhelming majority of scientific works, the description of the complications that have arisen is reduced to listing the latter. Currently, in the Russian and foreign scientific literature there is no systematization of complications, there is no single clinical classification, algorithms for the prevention and treatment of complications arising after local intravascular methods of treatment of patients with malignant liver tumors.

The study and systematization of complications arising after intra-arterial chemoembolization and chemoinfusion of the hepatic artery in patients with malignant liver tumors will make it possible to create prevention and treatment algorithms. Thus, it will help prevent interruption of palliative care and increase the life expectancy of this cohort of patients.

Conditions

Hepatic Cancer; Metastatic Cancer; Chemotherapy Effect

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Group 1

This group includes patients who underwent chemoembolization of hepatic arteria

Chemoembolization

Intervention Type: PROCEDURE

Transarterial Chemoembolization (TACE)

Group 2

This group includes patients who underwent chemoinfusion of hepatic arteria

Chemoinfusion

Intervention Type: PROCEDURE

Transarterial Infusion (TAI)

Interventions

Chemoembolization

Transarterial Chemoembolization (TACE)

Intervention Type: PROCEDURE

Chemoinfusion

Transarterial Infusion (TAI)

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Aged over 18 years old;

2. Histologically confirmed diagnosis of liver cancer or metastatic liver disease;

3. Patients who have not received systemic antitumor therapy within the last 6 months

Exclusion Criteria

1. Metachronous (within 3 years) or synchronous other oncological disease with the exception of healed carcinoma in situ;

2. The volume of liver damage according to computed tomography is more than 60%;

3. Increase in the level of transaminases by more than 2 times;

4. The level of bilirubin is more than 50 μmol / l;

5. Heart failure stage II B-III, Functional Class III-IV;

6. The presence of uncorrected coagulopathy;

7. Renal failure stage III-IV;

8. Ascites 2-3 degrees;

9. The general condition of the patient is below 60% on the Karnofsky index and above 2 points on the Eastern Cooperative Oncology Group (ECOG) scale;

10. Liver damage - more than 7 points on the Child-Pugh scale;

11. Damage to the central nervous system;

12. Anemia of severe severity;

13. Pregnancy;

14. Active autoimmune disease;

15. Presence of HIV infection, active forms of tuberculosis;

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Central Clinical Hospital RZD-Medicine, Russian Federation

OTHER

Sponsor Role: lead

Responsible Party

Stukalova Oksana Yuryevna

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Central Clinical Hospital RZD-Medicine, Russian Federation

Moscow, Moscow's Oblast, Russia

Site Status: RECRUITING

Countries

Russia

Central Contacts

Oksana Stukalova, Postgraduate

Role: CONTACT

docstukalova@mail.ru

+79852138906

Facility Contacts

Oksana Stukalova, postgraduate

Role: primary

docstukalova@mail.ru

+79852138906

Roman Ishenko, Professor

Role: backup

ishenkorv@rambler.ru

+79260878506

Other Identifiers

CCHRZD00001

Identifier Type: -

Identifier Source: org_study_id