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The investigators design a phase IIB clinical study to explore the efficacy and safety of Donafenib combined with Sintilimab and HAIC in neoadjuvant of resectable Hepatocellular Carcinoma.
This trial is a single-arm, non-randomized and single-center clinical study of Donafenib combined with Sintilimab and HAIC in Neoadjuvant of Resectable Hepatocellular CarcinomaIt will estimate that 30 patients who met the study criteria will be enrolled in Tianjin Medical University Cancer Institute and Hospital and neoadjuvant in Donafenib combined with Sintilimab and HAIC. The investigators will follow up and collect subjects' data monthly to evaluate the efficacy and safety of treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Donafenib combined with Sintilimab and HAIC | Experimental | Donafenib:200mg bid; Sintilimab:200mg Q3D; HAIC:Q3W. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Donafenib | Drug | 200 mg BID,oral administration will start before the first HAIC treatment . |
|
| Measure | Description | Time Frame |
|---|---|---|
| MPR(Major Pathological Response) | After neoadjuvant therapy, the proportion of residual tumor cells was less than 30%. | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| ORR(Objective Response Rate) | The rate of participants that achieve either a complete response (CR) or a partial response (PR). | 1 year |
| DCR(Disease Control Rate) | The percentage of cases with remission (PR + CR) and stable lesions (SD) after treatment was assessable. |
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Inclusion Criteria:
Voluntarily join the study and sign the informed consent;
Age 18 ~ 80 years old (including 80 years old), male and female;
Patients with hepatohcellular carcinoma diagnosed clinically or confirmed by histology / cytology according to the code for diagnosis and treatment of primary liver cancer (2022 Edition);
Hepatocellular carcinoma and technically resectable (CNLC stage Ⅱb to Ⅲa), estimated residual liver volume >30%, in patients with cirrhosis, the residual liver volume is >40%. And meets at least one of the following conditions:
At least one assessable lesion (mRECIST criteria),and did not receive radiotherapy or local treatmen;
ECOG 0 ~ 1;
Major organs are functioning normally. Hemoglobin ≥ 90 g / L; ANC ≥ 1.5 × 109/L; Platelet count ≥ 100 × 109/L; Albumin ≥ 28 g / L; Total bilirubin ≤ 3 × ULN; AST, ALT ≤ 5 × ULN; TSH ≤ ULN; INR or PT ≤ 1.5 × ULN, APTT ≤ ULN.
If HBsAg (+) and/or anti-HCV (+), antiviral therapy should be standard based on HBV DNA or HCV RNA test results;
Be able to cooperate to observe adverse events. -
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| WEI ZHANG, Doctor | Contact | 18622025401 | zhangweitjch@163.com |
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| ID | Term |
|---|---|
| D006528 | Carcinoma, Hepatocellular |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
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| ID | Term |
|---|---|
| C000710249 | donafenib |
| C000632826 | sintilimab |
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| Sintilimab | Drug | 200 mg Q3W,Intravenous infusion will perform before HAIC treatment. |
|
| HAIC | Other | HAIC,Q3W. The total number of HAIC treatments was determined by the investigator based on patient needs. Dose: Oxaliplatin 85 mg / m2 for 2h, Calcium folinate 400 mg / m2 for 2h, 5-FU 400 mg / m2 for 10min, followed by 5-FU 1200 mg / m2 for 23 hours). |
|
| 3 year |
| RFS(Recurrence-free Survival) | The time experienced from the enrollment date until tumor recurrence or death from any cause, if the subject died before the disease recurred. Survival subjects whose tumor recurrence was not confirmed by the database deadline were deleted according to the date of the last imaging tumor assessment. The date of tumor recurrence was the date of the first imaging confirmation of tumor recurrence. | 1 year |
| OS(Overall Survival) | Overall survival is defined as time from the start of treatment until death due to any reason. R0 resection: The tumor was completely resected, and the submicroscopic margin was negative, that is, no tumor remained. | 3 year |
| pCR(Pathological Complete Response) | No residual tumor was found pathologically in patients with neoadjuvant therapy induced tumor regression. | 1 year |
| D009369 | Neoplasms |
| D008113 | Liver Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D004066 | Digestive System Diseases |
| D008107 | Liver Diseases |