Conversion Therapy Using TACE/HAIC With Anti-Angiogenic and Immunotherapy for Initially Unresectable Hepatocellular Carcinoma Achieving Complete Response or Resectability, Followed by Surgery or Continued Systemic Treatment: A Prospective Cohort Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Unresectable Hepatocellular Carcinom. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Clinical Outcomes of Initially Unresectable Hepatocellular Carcinoma Patients Receiving TACE/HAIC Plus Anti-Angiogenic Agents and Immune Checkpoint Inhibitors as Conversion Therapy, Achieving Complete Radiological Response or Resectability, Followed by Systemic Treatment or Surgical Resection: A Prospective Cohort Study
Overview
This is a prospective cohort study designed to evaluate the effectiveness and safety of two post-conversion treatment strategies for patients with initially unresectable hepatocellular carcinoma (uHCC). Participants first receive conversion therapy with transarterial chemoembolization (TACE) or hepatic arterial infusion chemotherapy (HAIC) combined with anti-angiogenic agents and immune checkpoint inhibitors (ICIs). After this therapy, patients who achieve complete radiological response (rCR) or meet resectability criteria will either undergo surgical resection or continue systemic therapy. The study aims to compare outcomes between these two strategies to help guide treatment decisions for advanced liver cancer.
Primary outcome measures
- Event-Free Survival (EFS) [Time frame: From initiation of post-conversion therapy to the first documented event (recurrence, progression, or death), up to 36 months]
Secondary outcome measures (4)
- 2-Year Event-Free Survival (EFS) Rate [Time frame: 2 years after initiation of post-conversion therapy]
- Overall Survival (OS) [Time frame: Up to 36 months after initiation of post-conversion therapy]
- Treatment Safety [Time frame: From initiation of post-conversion therapy through 30 days after last treatment or surgery, up to 36 months follow-up]
- Cost-Effectiveness of Post-Conversion Treatment Strategies [Time frame: Up to 36 months after initiation of post-conversion therapy]
Eligibility criteria
Inclusion criteria
- Signed written informed consent.
- Age 18-75 years.
- Hepatocellular carcinoma (HCC) confirmed by histology/cytology or diagnosed according to the AASLD criteria.
- Initially unresectable HCC (uHCC), defined according to the Chinese Guidelines for Diagnosis and Treatment of Primary Liver Cancer (2024 edition) and the Chinese Expert Consensus on Conversion and Perioperative Therapy for Primary Liver Cancer (2024 edition): HCC considered unsafe for curative resection due to inability to ensure both oncological completeness (R0 resection) and functional hepatic reserve (adequate future liver remnant with good vascular supply and biliary drainage to maintain postoperative liver function and minimize morbidity and mortality). Mainly includes CNLC stage Ib-IIIa or potentially resectable cases. Some stage Ia patients may also be considered uHCC if the tumor is adjacent to major intrahepatic vessels or involves the first/second hepatic hilum making R0 resection infeasible, or if severe cirrhosis increases risk of postoperative liver failure and complications; these can be considered after successful conversion and supportive treatment.
- No prior systemic therapy before conversion treatment.
- Conversion therapy regimen must include TACE or HAIC plus anti-angiogenic agents and immune checkpoint inhibitors (ICIs).
- Anti-angiogenic agents may include lenvatinib, sorafenib, apatinib, donafenib, anlotinib, bevacizumab.
- ICIs may include pembrolizumab, atezolizumab, nivolumab, sintilimab, tislelizumab, toripalimab, penpulimab, cadonilimab, KN-046.
- After conversion therapy, hepatic lesions achieve radiological complete response (rCR) by mRECIST criteria on contrast-enhanced CT or MRI, or are assessed to have reached resectability criteria (eligible for curative hepatectomy or downstaging enabling safe surgery).
- After achieving rCR or resectability, patients must have received either liver resection or continued systemic therapy with scheduled follow-up.
- Child-Pugh class A or B liver function.
- Eastern Cooperative Oncology Group performance status (ECOG PS) 0-1.
Exclusion criteria
- Presence of another primary malignancy in other organs.
- History of other malignancies.
- Recurrent HCC occurring <2 years after previous curative surgery or adjuvant therapy.
- Received treatments other than TACE or HAIC plus anti-angiogenic agents and ICIs during the conversion phase.
- Received treatments during postoperative or maintenance systemic therapy that differ from the initial conversion regimen.
- Severe organ dysfunction.
- Incomplete radiological assessment data after treatment.
- Child-Pugh class C liver function.
- Pregnant or breastfeeding women.
- Patients undergoing only functional future liver remnant (FLR) hypertrophy procedures (e.g., ALPPS or PVE) for insufficient FLR without other criteria for uHCC conversion.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07206511 · B2025-437R