Efficacy and Safety of Neoadjuvant Therapy in Patients With Resectable HCC Screened by a Multimodal Deep Learning Model.

PHASE4Not yet recruitingINTERVENTIONAL
Enrollment

312

Participants

Timeline

Start Date

May 1, 2024

Primary Completion Date

December 31, 2027

Study Completion Date

December 31, 2028

Conditions
HCC
Interventions
DRUG

HAIC + Tirelizumab +lenvatinib +liver resection

Patients in the neoadjuvant group received two cycles of neoadjuvant hepatic arterial infusion chemotherapy (HAIC, adoption of the FOFOLX6 program, Folinic acid+5-fluorouracil+Oxaliplatin, 21 days between second HAIC treatments with a window of ±3 days) + Tirelizumab (First treatment with Tirelizumab was started 0-1 days after HAIC, 200 mg IV, followed by a second treatment 21 days later)+ lenvatinib (Oral 8 mg or 12mg once a day depending body weight). Assessment of tumor status and surgical safety after receiving neoadjuvant therapy, and eligible patients then underwent surgical resection.

PROCEDURE

liver resection

Direct liver resection or laparoscopic liver resection depending on tumor status.

All Listed Sponsors
lead

Chen Xiaoping

OTHER

NCT06311916 - Efficacy and Safety of Neoadjuvant Therapy in Patients With Resectable HCC Screened by a Multimodal Deep Learning Model. | Biotech Hunter | Biotech Hunter