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| Name | Class |
|---|---|
| Zhongshan People's Hospital, Guangdong, China | OTHER |
| Affiliated Hospital of Guangdong Medical University | OTHER |
| Jieyang People's Hospital | OTHER |
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This multicenter retrospective study evaluated consecutive patients with large HCC and PVTT who received lenvatinib plus DEB-TACE with/without FOLFOX-HAIC between July 2019 and June 2021. Tumor response, time to progression (TTP), overall survival (OS), and treatment-related adverse events (TRAEs) were compared between the two groups.
Consecutive patients with large HCC and PVTT treated with lenvatinib plus drug-eluting bead transarterial chemoembolization (DEB-TACE) and hepatic arterial infusion chemotherapy (HAIC) with oxaliplatin, fluorouracil and leucovorin (Len+DEB-TACE+HAIC) or lenvatinib plus DEB-TACE (Len+DEB-TACE) from July 2019 to June 2021 were screened. Tumor response was evaluated according to modified Response Evaluation Criteria in Solid Tumors (mRECIST). Clinical outcomes, including tumor response, TTP, OS, and TRAEs were compared between the two groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Len+DEB-TACE+HAIC | Patients were treated with Len+DEB-TACE+HAIC. |
| |
| Len+DEB-TACE | Patients were treated with Len+DEB-TACE. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Len+DEB-TACE+HAIC | Procedure | Patients received TACE with drug-eluting beads and FOLFOX-HAIC. DEB-TACE and/or HAIC was repeated for viable tumors demonstrated by follow-up imaging in patients without worsening liver function or contraindications. Lenvatinib was orally administered at a dose of 12 mg/day (bodyweight 60 kg) or 8mg/day (bodyweight <60 kg). It was initiated within 7 days after the first DEB-TACE or DEB-TACE+HAIC and continued until unacceptable toxicity or disease progression occurred. |
| Measure | Description | Time Frame |
|---|---|---|
| Time to progression (TTP) | defined as the time from treatment initiation to the first occurrence of disease progression. | 3.5 years |
| Measure | Description | Time Frame |
|---|---|---|
| objective response rate (ORR) | defined as the percentage of patients with complete or partial response | 3.5 years |
| Disease control rate (DCR) | defined as the percentage of patients with complete or partial response, or stable disease |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with large HCC and PVTT.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Second Affiliated Hospital of Guangzhou Medical University | Guangzhou | Guangdong | 510260 | China |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 38869974 | Derived | Cai M, Liang L, Zhang J, Chen N, Huang W, Guo Y, Hong X, Lin L, Liu Y, Dan C, Deng H, Liu X, Zhou J, Chen Y, Chen H, Zhu K. Lenvatinib plus drug-eluting bead transarterial chemoembolization with/without hepatic arterial infusion chemotherapy for hepatocellular carcinoma larger than 7 cm with major portal vein tumor thrombosis: a multicenter retrospective cohort study. Int J Surg. 2024 Dec 1;110(12):7860-7870. doi: 10.1097/JS9.0000000000001819. |
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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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| Huizhou Municipal Central Hospital |
| OTHER |
| Guangzhou Development District Hospital | UNKNOWN |
| Affiliated Hospital of Nanjing University of Chinese Medicine | OTHER |
| First People's Hospital of Foshan | OTHER |
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| Len+DEB-TACE | Procedure | Patients received TACE with drug-eluting beads. DEB-TACE was repeated for viable tumors demonstrated by follow-up imaging in patients without worsening liver function or contraindications. Lenvatinib was orally administered at a dose of 12 mg/day (bodyweight 60 kg) or 8mg/day (bodyweight <60 kg). It was initiated within 7 days after the first DEB-TACE or DEB-TACE+HAIC and continued until unacceptable toxicity or disease progression occurred. |
|
| 3.5 years |
| overall survival | defined as the time from treatment initiation until death from any reason. | 3.5 years |
| treatment-related adverse events (TRAEs) | assessed based on Common Terminology Criteria for Adverse Events version 5.0 | 3.5 years |
| D009369 | Neoplasms |
| D008113 | Liver Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D004066 | Digestive System Diseases |
| D008107 | Liver Diseases |