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
98%
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Spatially fractionated (SFRT) and FLASH radiotherapy (RT) are alternative means of dose delivery that are expected to widen the therapeutic window of clinical RT. The biological mechanisms for the observed effects of normal tissue-sparing with maintained tumor control probability are unknown. First, we introduce the preclinical research technologies for SFRT and FLASH-RT with photon beams, which include carbon nanotubes and modifications of standard small animal irradiators. As a novel concept, we highlight the potential importance of line-focussed x-ray tubes. Following that, we review immunological anti-tumor responses observed in various animal models for both alternative irradiation modalities. While there is agreement that SFRT and FLASH modulate the tumor immune microenvironment, at present, it is not clear if the anti-tumor immunity generated is more beneficial than that resulting from conventional RT. Further preclinical research is required to determine which aspects of the SFRT-mediated or FLASH-mediated anti-tumor immune response could be exploited for the eventual benefit of cancer patients.
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Source |
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http://dx.doi.org/10.1097/PPO.0000000000000781 | DOI Listing |