Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
This prospective nonrandomized, multicenter clinical trial was performed to investigate the efficacy and safety of I-labeled metuximab in adjuvant treatment of unresectable hepatocellular carcinoma. Patients were assigned to treatment with transcatheter arterial chemoembolization (TACE) combined with I-metuximab or TACE alone. The primary outcome was overall tumor recurrence. The secondary outcomes were safety and overall survival. The median time to tumor recurrence was 6 mo in the TACE + I-metuximab group ( = 160) and 3 mo in the TACE group ( = 160) (hazard ratio, 0.55; 95% CI, 0.43-0.70; < 0.001). The median overall survival was 28 mo in the TACE + I-metuximab group and 19 mo in the TACE group (hazard ratio, 0.62; 95% CI, 0.47-0.82; = 0.001). TACE + I-metuximab showed a greater antirecurrence benefit, significantly improved the 5-y survival of patients with advanced hepatocellular carcinoma, and was well tolerated by patients.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973296 | PMC |
http://dx.doi.org/10.2967/jnumed.121.262136 | DOI Listing |
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