A PHP Error was encountered

Severity: Warning

Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests

Filename: helpers/my_audit_helper.php

Line Number: 197

Backtrace:

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML

File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global

File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword

File: /var/www/html/index.php
Line: 317
Function: require_once

Donafenib lenvatinib combined with transarterial chemoembolization as initial therapy for unresectable hepatocellular carcinoma: a retrospective real-world study. | LitMetric

Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Background: The combination of tyrosine kinase inhibitors (TKIs) with transarterial chemoembolization (TACE) holds promise for unresectable hepatocellular carcinoma (HCC). This study aimed to directly compare the efficacy and safety of donafenib (Dona)-TACE lenvatinib (LEN)-TACE as first-line therapies.

Methods: In this retrospective study, 93 unresectable HCC patients (49 Dona-TACE, 44 LEN-TACE; 93% hepatitis B virus-infected) treated between October 2020 and May 2023 were analyzed. Patients received TACE (conventional or drug-eluting beads) combined with Dona (200 mg twice daily) or LEN (8-12 mg/day). Outcomes included overall survival (OS), progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and adverse events (AEs). Survival analyses employed Kaplan-Meier and log-rank tests.

Results: Median OS (mOS) was 14.00 months (Dona-TACE) 19.00 months (LEN-TACE) [hazard ratio (HR) =1.25; 95% confidence interval (CI): 0.78-1.99; P=0.330]. Median PFS was 7.37 5.77 months (HR =0.785; 95% CI: 0.46-1.33; P=0.354), with no significant differences. ORR (55.10% 61.36%, P=0.541) and DCR (75.51% 81.82%, P=0.460) were comparable. Dona-TACE showed significantly lower overall AE rates (any grade: 85.71% 100.00%, P=0.013; grade ≥3: 22.45% 45.45%, P=0.027), including reduced hypertension (2.04% 36.36%, P<0.001), diarrhea (6.12% 25.00%, P=0.011), and vomiting (0.00% 40.91%, P<0.001).

Conclusions: Dona-TACE and LEN-TACE demonstrated comparable efficacy in unresectable HCC, but Dona-TACE exhibited a superior safety profile, suggesting its potential as a preferable option for patients with higher comorbidity risks. Further prospective studies are warranted to validate these findings.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12332680PMC
http://dx.doi.org/10.21037/qims-2025-364DOI Listing

Publication Analysis

Top Keywords

transarterial chemoembolization
8
unresectable hepatocellular
8
hepatocellular carcinoma
8
donafenib lenvatinib
4
lenvatinib combined
4
combined transarterial
4
chemoembolization initial
4
initial therapy
4
therapy unresectable
4
carcinoma retrospective
4

Similar Publications