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
The rat prostatic adenocarcinoma Nb-Pr-A.I.-3, an androgen-insensitive tumor, was evaluated with the following treatments: cyclophosphamide, cis-platinum, adriamycin, and the following combination therapies: cyclophosphamide and cis-platinum; adriamycin and cis-platinum; adriamycin, cis-platinum, and cyclophosphamide. Successful therapeutic combinations included cyclophosphamide alone (P Less Than 0.001) and the triple-drug combination (P Less Than 0.001). Significance was based on the final tumor volume at the termination of the experiment. Cyclophosphamide treatment alone was the only therapeutic regimen that resulted in complete tumor regression (16%) (2/12). Cyclophosphamide therapy also resulted in the lowest number of animals with metastasis (25%). On the basis of this study, the authors rate this animal model as a suitable one for trials of various chemotherapeutic combinations as well as for determining combination or single agents useful in preducing tumor regression and a decreased number of metastasis.
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Source |
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http://dx.doi.org/10.1007/BF00258474 | DOI Listing |
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