Evidence map›Paper›PMID 41697315›Full record

ArticleAbdominal radiology (New York)2026

Baseline CT imaging features combined with clinical indicators predict prognosis in unresectable HCC treated with HAIC plus targeted therapy and immunotherapy.

Haiqin Deng, Liu Liu, Ziyu Liu, Yi Li, Caihong Li, Xue Mo, Yin Zhou, Yun Mao

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Article in Abdominal radiology (New York), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Haiqin Dengdepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Liu Liudepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Ziyu Liudepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yi Lidepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Caihong Lidepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xue Modepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yin Zhoudepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China. zyin1988@126.com.
Yun Maodepartment of radiology, First Affiliated Hospital of Chongqing Medical University, Chongqing, China. maoyun1979@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the prognostic value of baseline contrast-enhanced CT features imaging combined with clinical indicators in patients with unresectable hepatocellular carcinoma (uHCC) treated with hepatic arterial infusion chemotherapy plus targeted therapy and immunotherapy (HAIC-TI).

methodsPatients with uHCC who received at least two cycles of HAIC-TI were retrospectively analyzed. Inclusion required pre-treatment contrast-enhanced CT and modified Response Evaluation Criteria in Solid Tumors (mRECIST) assessments after two HAIC-TI cycles. Patients were classified into progressive disease (PD) group and non-PD group (complete response [CR], partial response [PR], or stable disease [SD]) to identify predictors of early progression. Baseline predictors of early progression were identified using binary logistic regression analysis. For survival analysis, the patients were reclassified into the responder group (CR or PR) and the non-responder group (SD or PD). Overall survival (OS) was estimated using the Kaplan-Meier method and compared by log-rank test. Prognostic factors for OS were identified using Cox regression.

resultsA total of 132 patients were included in this study. The objective response rate (ORR) was 47.7% and disease control rate (DCR) was 86.4% based on mRECIST criteria. The median progression free survival (PFS) was significantly prolonged in the responder group compared to the non-responder group (29.6 months vs. 8.0 months, p < 0.001). Correspondingly, the median OS was longer in the responder group (not reached) than in the non-responder group (10.5 months) (p < 0.001). Non-peripheral washout on baseline CT was associated with a lower risk of early progression (odds ratio = 0.280, p = 0.027). Multivariate analysis identified satellite nodules (hazard ratio [HR] = 2.419, p = 0.002), prolonged prothrombin time(HR = 1.930, p = 0.009), Child-Pugh class B (HR = 2.346, p = 0.009), and unfavorable early treatment response (HR = 2.478, p < 0.001) as independent predictors of shorter OS, while more HAIC-TI cycles (HR = 0.505, p = 0.010) were associated with longer OS. Further subgroup analysis revealed that the number of HAIC sessions was not statistically significant in the responder group (p = 0.27), nor in non-responder group (p = 0.34).

conclusionsFor patients with non-peripheral washout pattern in the delayed phase on imaging, the HAIC-TI treatment represents a feasible therapeutic strategy. It is noteworthy that early treatment responders showed significantly superior survival prognosis, whereas non-responders did not attain meaningful survival advantages despite receiving additional HAIC treatment cycles.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularImmunotherapyLiver NeoplasmsTomography, X-Ray ComputedAgedContrast MediaFemaleHumansInfusions, Intra-ArterialMaleMiddle AgedPrognosisRetrospective StudiesContrast MediaHepatic arterial infusion chemotherapyHepatocellular carcinomaImaging featuresPrognosis

Identifiers

PMID41697315
PMCPMC13388655

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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.