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Not yet recruitingNCT07379489Updated Jan 30, 2026

Adjuvant Anti-PD-1 Therapy in Resected Hepatocellular Carcinoma

An observational study in HCC, Adjuvant Therapy and Recurrence, sponsored by Tongji Hospital. Not yet recruiting. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-01-30.

Sponsored by Tongji Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years to 75 Years
Sex
All
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Study summary

Early hepatocellular carcinoma (HCC) recurrence (driven by residual tumors) and late recurrence (driven by de novo tumors) exhibit distinct biological behaviors, suggesting differential therapeutic vulnerabilities. The beneficiaries of adjuvant PD-1 inhibitors (aPD-1) and their efficacy across these temporally divergent recurrence patterns remains unestablished.

Read the detailed description

Hepatocellular carcinoma (HCC), a leading cause of global cancer-related mortality, continues to rise in incidence and lethality despite advancements in early detection and surgical techniques. Curative liver resection, while the cornerstone of therapeutic management, is frequently undermined by postoperative recurrence, a phenomenon observed in up to 70% of patients within five years, with early (≤2 years) and late (>2 years) recurrences reflecting distinct biological origins. Early recurrences predominantly stem from residual micro-metastases of the primary tumor, strongly associated with aggressive histopathological features such as microvascular invasion (MVI), multifocality, and satellite nodules. In contrast, late recurrences often arise de novo from the cirrhotic liver microenvironment, driven by persistent viral activity or chronic hepatic inflammation rather than the index tumor's biological behavior. Despite decades of research, postoperative adjuvant strategies, including antiviral therapy, transarterial chemoembolization, and traditional agents like Huaier granules, have yielded inconsistent results or lack robust evidence for standardization. The emergence of immune checkpoint inhibitors (ICIs) has reignited hope, yet recent randomized controlled trials (RCT) underscore unresolved challenges. The IMbrave050 trial initially demonstrated reduced recurrence with adjuvant Atezolizumab-Bevacizumab (median follow-up of 17 months). However, with longer follow-up (35 months), results shifted to negative. Another RCT has shown promising outcomes for patients with MVI-positive HCC who received adjuvant therapy with Sintilimab. Nevertheless, the median follow-up was only 23 months, which does not provide adequate resolution of late recurrence. Similarly, a recent prospective cohort study reported positive results of adjuvant immunotherapy in high-risk patients. These studies, limited by follow-up durations insufficient to capture late-recurrence dynamics, leave critical questions unanswered: Do adjuvant ICIs durably suppress recurrence, or merely delay its onset? In addition, there is currently no gold standard for defining high recurrence risk. Common pathological factors include MVI and satellite nodules13, but the same patient may have multiple high-risk factors simultaneously. Machine learning (ML) is increasingly being used in the construction of predictive models, and its performance often exceeds that of models based on standard statistical methods and traditional staging systems14, 15. Therefore, there is great potential for using ML to integrate clinical and pathological characteristics and quantify these risk factors to accurately identify high-risk populations and guide postoperative management strategies.

In order to fill these research gaps, we constructed an ML model to predict the risk of HCC recurrence through previous studies, and found that high-risk groups were more likely to be the potential benefit population of HCC. Therefore, this study aimed to verify the value of ML model in guiding postoperative adjuvant PD-1 inhibitors.

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Conditions studied

  • HCC
  • Adjuvant Therapy
  • Recurrence
  • Immune Checkpoint Inhibitor

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03

In context

Recurrence

4,279 studies on the registry are indexed under Recurrence; 988 are open to participants now.

This study's planned enrollment of 300 is above the median of 200 across 702 observational studies indexed under Recurrence.

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Lead sponsor

Tongji Hospital is the lead sponsor of 373 studies on the registry; 204 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

The target population was patients with hepatocellular carcinoma who were undergoing curative surgery as initial treatment and who were receiving active surveillance or adjuvant PD-1 inhibitors postoperatively.

Inclusion criteria

  • Aged between 18 and 75;
  • achieved complete tumor resection;
  • histological verification of HCC;
  • liver function classified as Child-Pugh grade A or B;
  • No other serious systemic disease or organ dysfunction.

Exclusion criteria

Exclusion Criteria:

  • history of other malignancies or recurrent HCC;
  • extrahepatic metastasis;
  • prior treatments for HCC;
  • ongoing severe postoperative complications;
  • mixed or other types of liver cancer;
  • received other adjuvant therapy.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Patient registry
No

Groups and cohorts

  • Active surveillance cohort
  • Adjuvant PD-1 inhibitor cohort

    Drug: PD-1 Inhibitors

Interventions

  • DrugPD-1 Inhibitors

    Patients in the adjuvant cohort received at least one cycle of PD-1 inhibitors.

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What researchers measure

Primary outcomes

  1. Disease free survival

    Time frame: From date of surgery until the date of first documented recurrence or date of death from any cause, whichever came first, assessed up to 96months.

Secondary outcomes

  1. Overall survival

    Time frame: From date of enrollment until the date of death from any cause, assessed up to 96 months.

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07379489
Lead sponsor
Tongji Hospital
Responsible party
Wan-Guang Zhang (Professor, Tongji Hospital) — Principal investigator
First posted
Jan 30, 2026
Start date
Jan 31, 2026 (estimated)
Primary completion
Dec 31, 2029 (estimated)
Completion
Dec 31, 2031 (estimated)
Last update
Jan 30, 2026

Study contacts

Wanguang Zhang, PhD
Contact
wgzhang@tjh.tjmu.edu.cn
+8613886195965

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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