Loading…

5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas

Introduction Photodynamic therapy (PDT) is a two-step treatment involving the administration of a photosensitive agent followed by its activation at a specific light wavelength for targeting of tumor cells. Materials/Methods A comprehensive review of the literature was performed to analyze the indic...

Full description

Saved in:
Bibliographic Details
Published in:Journal of neuro-oncology 2019-02, Vol.141 (3), p.595-607
Main Authors: Mahmoudi, K., Garvey, K. L., Bouras, A., Cramer, G., Stepp, H., Jesu Raj, J. G., Bozec, D., Busch, T. M., Hadjipanayis, C. G.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163
cites cdi_FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163
container_end_page 607
container_issue 3
container_start_page 595
container_title Journal of neuro-oncology
container_volume 141
creator Mahmoudi, K.
Garvey, K. L.
Bouras, A.
Cramer, G.
Stepp, H.
Jesu Raj, J. G.
Bozec, D.
Busch, T. M.
Hadjipanayis, C. G.
description Introduction Photodynamic therapy (PDT) is a two-step treatment involving the administration of a photosensitive agent followed by its activation at a specific light wavelength for targeting of tumor cells. Materials/Methods A comprehensive review of the literature was performed to analyze the indications for PDT, mechanisms of action, use of different photosensitizers, the immunomodulatory effects of PDT, and both preclinical and clinical studies for use in high-grade gliomas (HGGs). Results PDT has been approved by the United States Food and Drug Administration (FDA) for the treatment of premalignant and malignant diseases, such as actinic keratoses, Barrett’s esophagus, esophageal cancers, and endobronchial non-small cell lung cancers, as well as for the treatment of choroidal neovascularization. In neuro-oncology, clinical trials are currently underway to demonstrate PDT efficacy against a number of malignancies that include HGGs and other brain tumors. Both photosensitizers and photosensitizing precursors have been used for PDT. 5-aminolevulinic acid (5-ALA), an intermediate in the heme synthesis pathway, is a photosensitizing precursor with FDA approval for PDT of actinic keratosis and as an intraoperative imaging agent for fluorescence-guided visualization of malignant tissue during glioma surgery. New trials are underway to utilize 5-ALA as a therapeutic agent for PDT of the intraoperative resection cavity and interstitial PDT for inoperable HGGs. Conclusion PDT remains a promising therapeutic approach that requires further study in HGGs. Use of 5-ALA PDT permits selective tumor targeting due to the intracellular metabolism of 5-ALA. The immunomodulatory effects of PDT further strengthen its use for treatment of HGGs and requires a better understanding. The combination of PDT with adjuvant therapies for HGGs will need to be studied in randomized, controlled studies.
doi_str_mv 10.1007/s11060-019-03103-4
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6538286</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2168404984</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163</originalsourceid><addsrcrecordid>eNp9kU1r3DAQhkVoSDZJ_0APxdBLL0pHX5Z0KZTQpIVAISSQm9DKsq1gW1vJDuy_jzabph-HnjTwPvNqZl6E3hE4JwDyUyYEasBANAZGgGF-gFZESIYlk-wNWgGpJRaa3x-jk5wfAIBLRo7QMYNaaEHpCt0IbMcwxcE_LkOYgqusC0216eMcm-1UNFfNvU92s63amHZ1NSdv59FPcxXbqg9dj7tkG191Q4ijzWfosLVD9m9f3lN0d_n19uIbvv5x9f3iyzV2XPIZK6U8E9CCaF1DPKdO67WrrWSt5IQ6EGsqhGqEb2RDrRa6XlPgnHiqWEtqdoo-7303y3r0jSsDJTuYTQqjTVsTbTB_K1PoTRcfTS2Yompn8PHFIMWfi8-zGUN2fhjs5OOSDSVSl0Myqgv64R_0IS5pKusVqlYcuFa8UHRPuRRzTr59HYaA2UVm9pGZEpl5jszsmt7_ucZry6-MCsD2QC7S1Pn0--__2D4BuxCh7Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2168404984</pqid></control><display><type>article</type><title>5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas</title><source>Springer Nature</source><creator>Mahmoudi, K. ; Garvey, K. L. ; Bouras, A. ; Cramer, G. ; Stepp, H. ; Jesu Raj, J. G. ; Bozec, D. ; Busch, T. M. ; Hadjipanayis, C. G.</creator><creatorcontrib>Mahmoudi, K. ; Garvey, K. L. ; Bouras, A. ; Cramer, G. ; Stepp, H. ; Jesu Raj, J. G. ; Bozec, D. ; Busch, T. M. ; Hadjipanayis, C. G.</creatorcontrib><description>Introduction Photodynamic therapy (PDT) is a two-step treatment involving the administration of a photosensitive agent followed by its activation at a specific light wavelength for targeting of tumor cells. Materials/Methods A comprehensive review of the literature was performed to analyze the indications for PDT, mechanisms of action, use of different photosensitizers, the immunomodulatory effects of PDT, and both preclinical and clinical studies for use in high-grade gliomas (HGGs). Results PDT has been approved by the United States Food and Drug Administration (FDA) for the treatment of premalignant and malignant diseases, such as actinic keratoses, Barrett’s esophagus, esophageal cancers, and endobronchial non-small cell lung cancers, as well as for the treatment of choroidal neovascularization. In neuro-oncology, clinical trials are currently underway to demonstrate PDT efficacy against a number of malignancies that include HGGs and other brain tumors. Both photosensitizers and photosensitizing precursors have been used for PDT. 5-aminolevulinic acid (5-ALA), an intermediate in the heme synthesis pathway, is a photosensitizing precursor with FDA approval for PDT of actinic keratosis and as an intraoperative imaging agent for fluorescence-guided visualization of malignant tissue during glioma surgery. New trials are underway to utilize 5-ALA as a therapeutic agent for PDT of the intraoperative resection cavity and interstitial PDT for inoperable HGGs. Conclusion PDT remains a promising therapeutic approach that requires further study in HGGs. Use of 5-ALA PDT permits selective tumor targeting due to the intracellular metabolism of 5-ALA. The immunomodulatory effects of PDT further strengthen its use for treatment of HGGs and requires a better understanding. The combination of PDT with adjuvant therapies for HGGs will need to be studied in randomized, controlled studies.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-019-03103-4</identifier><identifier>PMID: 30659522</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aminolevulinic acid ; Aminolevulinic Acid - therapeutic use ; Animals ; Brain cancer ; Brain Neoplasms - complications ; Brain Neoplasms - drug therapy ; Brain tumors ; Clinical trials ; Clinical Trials as Topic ; Esophagus ; FDA approval ; Glioma ; Glioma - complications ; Glioma - drug therapy ; Heme ; Humans ; Immunomodulation ; Keratosis ; Literature reviews ; Medicine ; Medicine &amp; Public Health ; Neuroimaging ; Neurology ; Oncology ; Photochemotherapy ; Photodynamic therapy ; Photosensitization ; Photosensitizing Agents - therapeutic use ; Surgery ; Topic Review ; Treatment Outcome ; Tumor cells ; Vascularization</subject><ispartof>Journal of neuro-oncology, 2019-02, Vol.141 (3), p.595-607</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Journal of Neuro-Oncology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163</citedby><cites>FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163</cites><orcidid>0000-0001-8615-6644</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30659522$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mahmoudi, K.</creatorcontrib><creatorcontrib>Garvey, K. L.</creatorcontrib><creatorcontrib>Bouras, A.</creatorcontrib><creatorcontrib>Cramer, G.</creatorcontrib><creatorcontrib>Stepp, H.</creatorcontrib><creatorcontrib>Jesu Raj, J. G.</creatorcontrib><creatorcontrib>Bozec, D.</creatorcontrib><creatorcontrib>Busch, T. M.</creatorcontrib><creatorcontrib>Hadjipanayis, C. G.</creatorcontrib><title>5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><addtitle>J Neurooncol</addtitle><description>Introduction Photodynamic therapy (PDT) is a two-step treatment involving the administration of a photosensitive agent followed by its activation at a specific light wavelength for targeting of tumor cells. Materials/Methods A comprehensive review of the literature was performed to analyze the indications for PDT, mechanisms of action, use of different photosensitizers, the immunomodulatory effects of PDT, and both preclinical and clinical studies for use in high-grade gliomas (HGGs). Results PDT has been approved by the United States Food and Drug Administration (FDA) for the treatment of premalignant and malignant diseases, such as actinic keratoses, Barrett’s esophagus, esophageal cancers, and endobronchial non-small cell lung cancers, as well as for the treatment of choroidal neovascularization. In neuro-oncology, clinical trials are currently underway to demonstrate PDT efficacy against a number of malignancies that include HGGs and other brain tumors. Both photosensitizers and photosensitizing precursors have been used for PDT. 5-aminolevulinic acid (5-ALA), an intermediate in the heme synthesis pathway, is a photosensitizing precursor with FDA approval for PDT of actinic keratosis and as an intraoperative imaging agent for fluorescence-guided visualization of malignant tissue during glioma surgery. New trials are underway to utilize 5-ALA as a therapeutic agent for PDT of the intraoperative resection cavity and interstitial PDT for inoperable HGGs. Conclusion PDT remains a promising therapeutic approach that requires further study in HGGs. Use of 5-ALA PDT permits selective tumor targeting due to the intracellular metabolism of 5-ALA. The immunomodulatory effects of PDT further strengthen its use for treatment of HGGs and requires a better understanding. The combination of PDT with adjuvant therapies for HGGs will need to be studied in randomized, controlled studies.</description><subject>Aminolevulinic acid</subject><subject>Aminolevulinic Acid - therapeutic use</subject><subject>Animals</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - complications</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain tumors</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic</subject><subject>Esophagus</subject><subject>FDA approval</subject><subject>Glioma</subject><subject>Glioma - complications</subject><subject>Glioma - drug therapy</subject><subject>Heme</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Keratosis</subject><subject>Literature reviews</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Oncology</subject><subject>Photochemotherapy</subject><subject>Photodynamic therapy</subject><subject>Photosensitization</subject><subject>Photosensitizing Agents - therapeutic use</subject><subject>Surgery</subject><subject>Topic Review</subject><subject>Treatment Outcome</subject><subject>Tumor cells</subject><subject>Vascularization</subject><issn>0167-594X</issn><issn>1573-7373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kU1r3DAQhkVoSDZJ_0APxdBLL0pHX5Z0KZTQpIVAISSQm9DKsq1gW1vJDuy_jzabph-HnjTwPvNqZl6E3hE4JwDyUyYEasBANAZGgGF-gFZESIYlk-wNWgGpJRaa3x-jk5wfAIBLRo7QMYNaaEHpCt0IbMcwxcE_LkOYgqusC0216eMcm-1UNFfNvU92s63amHZ1NSdv59FPcxXbqg9dj7tkG191Q4ijzWfosLVD9m9f3lN0d_n19uIbvv5x9f3iyzV2XPIZK6U8E9CCaF1DPKdO67WrrWSt5IQ6EGsqhGqEb2RDrRa6XlPgnHiqWEtqdoo-7303y3r0jSsDJTuYTQqjTVsTbTB_K1PoTRcfTS2Yompn8PHFIMWfi8-zGUN2fhjs5OOSDSVSl0Myqgv64R_0IS5pKusVqlYcuFa8UHRPuRRzTr59HYaA2UVm9pGZEpl5jszsmt7_ucZry6-MCsD2QC7S1Pn0--__2D4BuxCh7Q</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Mahmoudi, K.</creator><creator>Garvey, K. L.</creator><creator>Bouras, A.</creator><creator>Cramer, G.</creator><creator>Stepp, H.</creator><creator>Jesu Raj, J. G.</creator><creator>Bozec, D.</creator><creator>Busch, T. M.</creator><creator>Hadjipanayis, C. G.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8615-6644</orcidid></search><sort><creationdate>20190201</creationdate><title>5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas</title><author>Mahmoudi, K. ; Garvey, K. L. ; Bouras, A. ; Cramer, G. ; Stepp, H. ; Jesu Raj, J. G. ; Bozec, D. ; Busch, T. M. ; Hadjipanayis, C. G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aminolevulinic acid</topic><topic>Aminolevulinic Acid - therapeutic use</topic><topic>Animals</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - complications</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain tumors</topic><topic>Clinical trials</topic><topic>Clinical Trials as Topic</topic><topic>Esophagus</topic><topic>FDA approval</topic><topic>Glioma</topic><topic>Glioma - complications</topic><topic>Glioma - drug therapy</topic><topic>Heme</topic><topic>Humans</topic><topic>Immunomodulation</topic><topic>Keratosis</topic><topic>Literature reviews</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Oncology</topic><topic>Photochemotherapy</topic><topic>Photodynamic therapy</topic><topic>Photosensitization</topic><topic>Photosensitizing Agents - therapeutic use</topic><topic>Surgery</topic><topic>Topic Review</topic><topic>Treatment Outcome</topic><topic>Tumor cells</topic><topic>Vascularization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahmoudi, K.</creatorcontrib><creatorcontrib>Garvey, K. L.</creatorcontrib><creatorcontrib>Bouras, A.</creatorcontrib><creatorcontrib>Cramer, G.</creatorcontrib><creatorcontrib>Stepp, H.</creatorcontrib><creatorcontrib>Jesu Raj, J. G.</creatorcontrib><creatorcontrib>Bozec, D.</creatorcontrib><creatorcontrib>Busch, T. M.</creatorcontrib><creatorcontrib>Hadjipanayis, C. G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neuro-oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahmoudi, K.</au><au>Garvey, K. L.</au><au>Bouras, A.</au><au>Cramer, G.</au><au>Stepp, H.</au><au>Jesu Raj, J. G.</au><au>Bozec, D.</au><au>Busch, T. M.</au><au>Hadjipanayis, C. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas</atitle><jtitle>Journal of neuro-oncology</jtitle><stitle>J Neurooncol</stitle><addtitle>J Neurooncol</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>141</volume><issue>3</issue><spage>595</spage><epage>607</epage><pages>595-607</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><abstract>Introduction Photodynamic therapy (PDT) is a two-step treatment involving the administration of a photosensitive agent followed by its activation at a specific light wavelength for targeting of tumor cells. Materials/Methods A comprehensive review of the literature was performed to analyze the indications for PDT, mechanisms of action, use of different photosensitizers, the immunomodulatory effects of PDT, and both preclinical and clinical studies for use in high-grade gliomas (HGGs). Results PDT has been approved by the United States Food and Drug Administration (FDA) for the treatment of premalignant and malignant diseases, such as actinic keratoses, Barrett’s esophagus, esophageal cancers, and endobronchial non-small cell lung cancers, as well as for the treatment of choroidal neovascularization. In neuro-oncology, clinical trials are currently underway to demonstrate PDT efficacy against a number of malignancies that include HGGs and other brain tumors. Both photosensitizers and photosensitizing precursors have been used for PDT. 5-aminolevulinic acid (5-ALA), an intermediate in the heme synthesis pathway, is a photosensitizing precursor with FDA approval for PDT of actinic keratosis and as an intraoperative imaging agent for fluorescence-guided visualization of malignant tissue during glioma surgery. New trials are underway to utilize 5-ALA as a therapeutic agent for PDT of the intraoperative resection cavity and interstitial PDT for inoperable HGGs. Conclusion PDT remains a promising therapeutic approach that requires further study in HGGs. Use of 5-ALA PDT permits selective tumor targeting due to the intracellular metabolism of 5-ALA. The immunomodulatory effects of PDT further strengthen its use for treatment of HGGs and requires a better understanding. The combination of PDT with adjuvant therapies for HGGs will need to be studied in randomized, controlled studies.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30659522</pmid><doi>10.1007/s11060-019-03103-4</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-8615-6644</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0167-594X
ispartof Journal of neuro-oncology, 2019-02, Vol.141 (3), p.595-607
issn 0167-594X
1573-7373
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6538286
source Springer Nature
subjects Aminolevulinic acid
Aminolevulinic Acid - therapeutic use
Animals
Brain cancer
Brain Neoplasms - complications
Brain Neoplasms - drug therapy
Brain tumors
Clinical trials
Clinical Trials as Topic
Esophagus
FDA approval
Glioma
Glioma - complications
Glioma - drug therapy
Heme
Humans
Immunomodulation
Keratosis
Literature reviews
Medicine
Medicine & Public Health
Neuroimaging
Neurology
Oncology
Photochemotherapy
Photodynamic therapy
Photosensitization
Photosensitizing Agents - therapeutic use
Surgery
Topic Review
Treatment Outcome
Tumor cells
Vascularization
title 5-aminolevulinic acid photodynamic therapy for the treatment of high-grade gliomas
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T23%3A40%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=5-aminolevulinic%20acid%20photodynamic%20therapy%20for%20the%20treatment%20of%20high-grade%20gliomas&rft.jtitle=Journal%20of%20neuro-oncology&rft.au=Mahmoudi,%20K.&rft.date=2019-02-01&rft.volume=141&rft.issue=3&rft.spage=595&rft.epage=607&rft.pages=595-607&rft.issn=0167-594X&rft.eissn=1573-7373&rft_id=info:doi/10.1007/s11060-019-03103-4&rft_dat=%3Cproquest_pubme%3E2168404984%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c474t-888e350f05fcd1e42c99bc6a73f7412c05b2558d5ed7d2a9596b20441e283f163%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2168404984&rft_id=info:pmid/30659522&rfr_iscdi=true