ArticleCancer immunology, immunotherapy : CII2025
Local therapy overcomes primary resistance to target-immunotherapy combination in unresectable hepatocellular carcinoma.
Article in Cancer immunology, immunotherapy : CII, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Advancing immune checkpoint inhibitor rechallenge: key insights into efficacy, safety, and personalized strategies in advanced solid tumors.Frontiers in oncology · 2026Pooled it
- Mechanisms of Immune Checkpoint Inhibitor Resistance in Hepatocellular Carcinoma and Strategies for Reversal.Cancers · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeTo evaluate the characteristics and management of primary (PR) and acquired resistance (AR) to immune checkpoint inhibitor (ICI) combination treatment in patients with unresectable hepatocellular carcinoma (uHCC). EXPERIMENTAL
designPatients with uHCC who received ICI combination therapy were retrospectively included. Baseline characteristics, pattern of progression, post-resistance management, and prognosis were recorded and analyzed according to resistance type. The primary endpoint was overall survival (OS).
resultsA hundred and eighty-eight out of 262 patients (71.8%) developed resistance, including 35.1% with PR and 36.6% with AR. All AR developed within 2 years. Patients with AR had better general conditions, smaller tumors, fewer vessel invasion and better prognosis (median OS [mOS]: 25.8 vs. 8.63 months) than those with PR. Patients with AR were less likely to have multiple lesions and sites exhibiting progression. Occurrence of new lesions led to a decrease in OS in patients with PR but an increase in those with AR. Patients with either PR or AR receiving post-resistance anti-tumor treatment showed improved OS, but patients with AR had significantly longer OS than those with PR. The combination of subsequent local therapy (mOS 25.6 vs. 10.0 months) and changes in the ICI regimen (mOS 27.5 vs. 13.4 months) led to improved OS among patients with PR.
conclusionsAR normally develops within 2 years after the beginning of treatment. Patients with AR have better characteristics in general, less invasive pattens of progression, and better prognosis compared to those with PR. Subsequent local therapy and changes in ICI treatment showed potential to overcome primary resistance.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.