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  4. Changes in Posttreatment Spleen Volume Associated with Immunotherapy Outcomes for Advanced Hepatocellular Carcinoma.
 
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Changes in Posttreatment Spleen Volume Associated with Immunotherapy Outcomes for Advanced Hepatocellular Carcinoma.

Journal
Journal of hepatocellular carcinoma
Journal Volume
11
Start Page
1015
End Page
1029
ISSN
2253-5969
Date Issued
2024
Author(s)
BANG-BIN CHEN  
PO-CHIN LIANG  
TIFFANY TING-FANG SHIH  
TSUNG-HAO LIU  
YING-CHUN SHEN  
LI-CHUN LU  
ZHONG-ZHE LIN  
CHIUN HSU  
CHIH-HUNG HSU  
ANN-LII CHENG  
YU-YUN SHAO  
DOI
10.2147/JHC.S462470
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/719687
Abstract
We investigated whether spleen volume (SV) changes were associated with treatment outcomes in advanced hepatocellular carcinoma (HCC) patients who received immunotherapy or first-line sorafenib.
Patients with advanced HCC who underwent immunotherapy or first-line sorafenib at our institute were retrospectively analyzed. CT was used to measure SV before and within 3 months of treatment initiation. Tumor assessment followed Response Evaluation Criteria in Solid Tumors version 1.1. The association between SV change and tumor response or progression-free survival (PFS) was analyzed. The inverse probability of treatment weighting (IPTW) was used to adjust for differences in baseline characteristics.
The immunotherapy group comprised 143 patients (124 men, mean age, 59.8 years ± 11.2 [standard deviation]), while the sorafenib group had 57 (47 men, mean age, 59.6 years ± 9.9). SV increased in 108 (75.5%) immunotherapy and 21 (36.8%) sorafenib patients. In the immunotherapy group, patients with increased SV were more likely than those with decreased SV to have a higher disease control rate (76.9% vs 57.1%, = 0.024) and durable clinical benefit (52.8% vs 25.7%, = 0.005). It was also associated with extended PFS in the immunotherapy group in both the univariate ( = 0.028) and multivariate ( = 0.014) analysis. By contrast, in the sorafenib group, an increased in SV was not associated with treatment response but was presumably associated with reduced PFS ( = 0.072) in the multivariate analysis. After IPTW adjustment, the increase in SV remained a significant predictor for DCB and PFS in the immunotherapy group.
Most patients exhibited an increase in SV after the initiation of immunotherapy, which may be used to predict response and prognosis. However, this association was not observed in patients who received sorafenib.
The study provides significant evidence that an increase in spleen volume is associated with better treatment outcomes in advanced hepatocellular carcinoma patients undergoing immunotherapy. These findings offer oncologists a new potential biomarker for optimizing treatment strategies. Specifically, increased spleen volume could be used to predict higher rates of disease control and durable clinical benefits, allowing for more personalized care.
Subjects
hepatocellular carcinoma
immunotherapy
response
sorafenib
survival
SDGs

[SDGs]SDG3

Type
journal article

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