Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
single-center clinical trial studies have verified the safety and effectiveness of transcatheter arterial chemoembolization (TACE) combined with lenvatinib in preventing postoperative recurrence of microvascular invasion (MVI) positive HCC patients. Explore a new clinical first-line treatment plan for patients with liver cancer microvascular invasion after surgery.
Focusing on the current status of clinical treatment of microvascular invasion (MVI) positive postoperative hepatocellular carcinoma (HCC) , single-center clinical trial studies have verified the safety and effectiveness of transcatheter arterial chemoembolization (TACE) combined with lenvatinib in preventing postoperative recurrence of MVI-positive HCC patients. Explore a new clinical first-line treatment plan for patients with liver cancer microvascular invasion after surgery.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| control group | Active Comparator | patients receive transcatheter arterial chemoembolization (TACE) only. |
|
| Intervention group | Experimental | patients receive transcatheter arterial chemoembolization (TACE) and lenvatinib 8mg per day. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lenvatinib | Drug | Lenvatinib is taken orally. |
| |
| TACE |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of adverse events | To evaluate the safety of TACE combined with lenvatinib treatment in preventing postoperative recurrence in patients with MVI-positive HCC | Up to 8 weeks |
| Changes in tumor volume | To evaluate the effectiveness of TACE combined with lenvatinib treatment in preventing postoperative recurrence in patients with MVI-positive HCC | Up to 8 weeks |
| Recurrence-free survival (RFS) evaluation | To evaluate the recurrence-free survival of patients with MVI-positive HCC after TACE combined with lenvatinib treatment | Through study completion, an average of 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Disease recurrence time evaluation | To evaluate the tumor recurrence time of patients with MVI-positive HCC after TACE combined with lenvatinib treatment | Through study completion, an average of 1 year |
| Overall survival ( OS) evaluation |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Weilin Wang | Contact | +8657187783820 | wam@zju.edu.cn | |
| Yuan Ding | Contact | +8618858101960 | dingyuan@zju.edu |
| Name | Affiliation | Role |
|---|---|---|
| Zhongquan Sun | Second Affiliated Hospital, School of Medicine, Zhejiang University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Weilin Wang | Recruiting | Hangzhou | None Selected | 310009 | China |
Not provided
| ID | Term |
|---|---|
| D006528 | Carcinoma, Hepatocellular |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
Not provided
Not provided
| ID | Term |
|---|---|
| C531958 | lenvatinib |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Procedure |
TACE treatment once. |
|
|
Overall survival time as assessed by IRC
| Through study completion, an average of 1 year |
| The Second Affiliated Hospital, Zhejiang University School of Medicine | Recruiting | Hangzhou | Zhejiang | 310009 | China |
|
| D009369 | Neoplasms |
| D008113 | Liver Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D004066 | Digestive System Diseases |
| D008107 | Liver Diseases |