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: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
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
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PET with F-FDG is the standard modality in nuclear medicine for imaging multiple myeloma (MM). However, viable MM as detected by MRI or PET with other metabolic tracers, including C-methionine, may be missed-for example, because of low hexokinase 2 (HK2) expression of tumor cells. The aim of this study was to further investigate potential reasons for PET false negativity. A cohort of 15 mainly pretreated patients with relapsed or refractory biopsy-proven, serologically active MM who underwent both F-FDG and C-methionine PET/CT was retrospectively analyzed. In 9 of the 15 patients, F-FDG PET was negative in the presence of viable disease. In the remaining 6 patients, both F-FDG and C-methionine PET/CT revealed the same number of MM lesions. At immunohistochemistry, F-FDG-negative myeloma did not exhibit significant differences in HK2 or glucose-6-phosphatase expression from F-FDG-positive disease ( = 0.57 and = 0.44, respectively). Beyond HK2 expression, F-FDG negativity in (mainly pretreated) MM patients seems to be associated with additional causes not yet known.
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http://dx.doi.org/10.2967/jnumed.118.217539 | DOI Listing |