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Apparent diffusion coefficient changes predict survival after intra-arterial bevacizumab treatment in recurrent glioblastoma

Purpose Superselective intra-arterial cerebral infusion (SIACI) of bevacizumab (BV) has emerged as a novel therapy in the treatment of recurrent glioblastoma (GB). This study assessed the use of apparent diffusion coefficient (ADC) in predicting length of survival after SIACI BV and overall survival...

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Published in:Neuroradiology 2017-05, Vol.59 (5), p.499-505
Main Authors: Galla, Naveen, Chiang, Gloria, Chakraborty, Shamik, Singh, Ranjodh, John Tsiouris, A., Boockvar, John, Kovanlikaya, Ilhami
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container_end_page 505
container_issue 5
container_start_page 499
container_title Neuroradiology
container_volume 59
creator Galla, Naveen
Chiang, Gloria
Chakraborty, Shamik
Singh, Ranjodh
John Tsiouris, A.
Boockvar, John
Kovanlikaya, Ilhami
description Purpose Superselective intra-arterial cerebral infusion (SIACI) of bevacizumab (BV) has emerged as a novel therapy in the treatment of recurrent glioblastoma (GB). This study assessed the use of apparent diffusion coefficient (ADC) in predicting length of survival after SIACI BV and overall survival in patients with recurrent GB. Methods Sixty-five patients from a cohort enrolled in a phase I/II trial of SIACI BV for treatment of recurrent GB were retrospectively included in this analysis. MR imaging with a diffusion-weighted (DWI) sequence was performed before and after treatment. ROIs were manually delineated on ADC maps corresponding to the enhancing and non-enhancing portions of the tumor. Cox and logistic regression analyses were performed to determine which ADC values best predicted survival. Results The change in minimum ADC in the enhancing portion of the tumor after SIACI BV therapy was associated with an increased risk of death (hazard ratio = 2.0, 95% confidence interval(CI) [1.04–3.79], p  = 0.038), adjusting for age, tumor size, BV dose, and prior IV BV treatments. Similarly, the change in ADC after SIACI BV therapy was associated with greater likelihood of surviving less than 1 year after therapy (odds ratio = 7.0, 95% CI [1.08–45.7], p  = 0.04). Having previously received IV BV was associated with increased risk of death (OR 18, 95% CI [1.8–180.0], p  = 0.014). Conclusion In patients with recurrent GB treated with SIACI BV, the change in ADC value after treatment is predictive of overall survival.
doi_str_mv 10.1007/s00234-017-1820-4
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This study assessed the use of apparent diffusion coefficient (ADC) in predicting length of survival after SIACI BV and overall survival in patients with recurrent GB. Methods Sixty-five patients from a cohort enrolled in a phase I/II trial of SIACI BV for treatment of recurrent GB were retrospectively included in this analysis. MR imaging with a diffusion-weighted (DWI) sequence was performed before and after treatment. ROIs were manually delineated on ADC maps corresponding to the enhancing and non-enhancing portions of the tumor. Cox and logistic regression analyses were performed to determine which ADC values best predicted survival. Results The change in minimum ADC in the enhancing portion of the tumor after SIACI BV therapy was associated with an increased risk of death (hazard ratio = 2.0, 95% confidence interval(CI) [1.04–3.79], p  = 0.038), adjusting for age, tumor size, BV dose, and prior IV BV treatments. Similarly, the change in ADC after SIACI BV therapy was associated with greater likelihood of surviving less than 1 year after therapy (odds ratio = 7.0, 95% CI [1.08–45.7], p  = 0.04). Having previously received IV BV was associated with increased risk of death (OR 18, 95% CI [1.8–180.0], p  = 0.014). Conclusion In patients with recurrent GB treated with SIACI BV, the change in ADC value after treatment is predictive of overall survival.</description><identifier>ISSN: 0028-3940</identifier><identifier>EISSN: 1432-1920</identifier><identifier>DOI: 10.1007/s00234-017-1820-4</identifier><identifier>PMID: 28343250</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Angiogenesis Inhibitors - administration &amp; dosage ; Angiogenesis Inhibitors - therapeutic use ; Bevacizumab - administration &amp; dosage ; Bevacizumab - therapeutic use ; Brain cancer ; Brain Neoplasms - diagnostic imaging ; Brain Neoplasms - drug therapy ; Brain Neoplasms - pathology ; Chemotherapy ; Clinical outcomes ; Contrast Media ; Diagnostic Neuroradiology ; Diffusion Magnetic Resonance Imaging - methods ; Female ; Glioblastoma - diagnostic imaging ; Glioblastoma - drug therapy ; Glioblastoma - pathology ; Humans ; Imaging ; Infusions, Intra-Arterial ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neoplasm Recurrence, Local - diagnostic imaging ; Neoplasm Recurrence, Local - drug therapy ; Neoplasm Recurrence, Local - pathology ; Neurology ; Neuroradiology ; Neurosciences ; Neurosurgery ; Prognosis ; Radiology ; Retrospective Studies ; Survival analysis ; Survival Rate</subject><ispartof>Neuroradiology, 2017-05, Vol.59 (5), p.499-505</ispartof><rights>Springer-Verlag Berlin Heidelberg 2017</rights><rights>Neuroradiology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-f8fb76eabcb73bb6bd14592a86e9b3b1aac917c625559f6b8e9184899f99bc7c3</citedby><cites>FETCH-LOGICAL-c372t-f8fb76eabcb73bb6bd14592a86e9b3b1aac917c625559f6b8e9184899f99bc7c3</cites><orcidid>0000-0002-9341-3079</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28343250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Galla, Naveen</creatorcontrib><creatorcontrib>Chiang, Gloria</creatorcontrib><creatorcontrib>Chakraborty, Shamik</creatorcontrib><creatorcontrib>Singh, Ranjodh</creatorcontrib><creatorcontrib>John Tsiouris, A.</creatorcontrib><creatorcontrib>Boockvar, John</creatorcontrib><creatorcontrib>Kovanlikaya, Ilhami</creatorcontrib><title>Apparent diffusion coefficient changes predict survival after intra-arterial bevacizumab treatment in recurrent glioblastoma</title><title>Neuroradiology</title><addtitle>Neuroradiology</addtitle><addtitle>Neuroradiology</addtitle><description>Purpose Superselective intra-arterial cerebral infusion (SIACI) of bevacizumab (BV) has emerged as a novel therapy in the treatment of recurrent glioblastoma (GB). This study assessed the use of apparent diffusion coefficient (ADC) in predicting length of survival after SIACI BV and overall survival in patients with recurrent GB. Methods Sixty-five patients from a cohort enrolled in a phase I/II trial of SIACI BV for treatment of recurrent GB were retrospectively included in this analysis. MR imaging with a diffusion-weighted (DWI) sequence was performed before and after treatment. ROIs were manually delineated on ADC maps corresponding to the enhancing and non-enhancing portions of the tumor. Cox and logistic regression analyses were performed to determine which ADC values best predicted survival. Results The change in minimum ADC in the enhancing portion of the tumor after SIACI BV therapy was associated with an increased risk of death (hazard ratio = 2.0, 95% confidence interval(CI) [1.04–3.79], p  = 0.038), adjusting for age, tumor size, BV dose, and prior IV BV treatments. Similarly, the change in ADC after SIACI BV therapy was associated with greater likelihood of surviving less than 1 year after therapy (odds ratio = 7.0, 95% CI [1.08–45.7], p  = 0.04). Having previously received IV BV was associated with increased risk of death (OR 18, 95% CI [1.8–180.0], p  = 0.014). Conclusion In patients with recurrent GB treated with SIACI BV, the change in ADC value after treatment is predictive of overall survival.</description><subject>Angiogenesis Inhibitors - administration &amp; dosage</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Bevacizumab - administration &amp; dosage</subject><subject>Bevacizumab - therapeutic use</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - diagnostic imaging</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - pathology</subject><subject>Chemotherapy</subject><subject>Clinical outcomes</subject><subject>Contrast Media</subject><subject>Diagnostic Neuroradiology</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Female</subject><subject>Glioblastoma - diagnostic imaging</subject><subject>Glioblastoma - drug therapy</subject><subject>Glioblastoma - pathology</subject><subject>Humans</subject><subject>Imaging</subject><subject>Infusions, Intra-Arterial</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; 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This study assessed the use of apparent diffusion coefficient (ADC) in predicting length of survival after SIACI BV and overall survival in patients with recurrent GB. Methods Sixty-five patients from a cohort enrolled in a phase I/II trial of SIACI BV for treatment of recurrent GB were retrospectively included in this analysis. MR imaging with a diffusion-weighted (DWI) sequence was performed before and after treatment. ROIs were manually delineated on ADC maps corresponding to the enhancing and non-enhancing portions of the tumor. Cox and logistic regression analyses were performed to determine which ADC values best predicted survival. Results The change in minimum ADC in the enhancing portion of the tumor after SIACI BV therapy was associated with an increased risk of death (hazard ratio = 2.0, 95% confidence interval(CI) [1.04–3.79], p  = 0.038), adjusting for age, tumor size, BV dose, and prior IV BV treatments. Similarly, the change in ADC after SIACI BV therapy was associated with greater likelihood of surviving less than 1 year after therapy (odds ratio = 7.0, 95% CI [1.08–45.7], p  = 0.04). Having previously received IV BV was associated with increased risk of death (OR 18, 95% CI [1.8–180.0], p  = 0.014). Conclusion In patients with recurrent GB treated with SIACI BV, the change in ADC value after treatment is predictive of overall survival.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28343250</pmid><doi>10.1007/s00234-017-1820-4</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9341-3079</orcidid></addata></record>
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subjects Angiogenesis Inhibitors - administration & dosage
Angiogenesis Inhibitors - therapeutic use
Bevacizumab - administration & dosage
Bevacizumab - therapeutic use
Brain cancer
Brain Neoplasms - diagnostic imaging
Brain Neoplasms - drug therapy
Brain Neoplasms - pathology
Chemotherapy
Clinical outcomes
Contrast Media
Diagnostic Neuroradiology
Diffusion Magnetic Resonance Imaging - methods
Female
Glioblastoma - diagnostic imaging
Glioblastoma - drug therapy
Glioblastoma - pathology
Humans
Imaging
Infusions, Intra-Arterial
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Recurrence, Local - diagnostic imaging
Neoplasm Recurrence, Local - drug therapy
Neoplasm Recurrence, Local - pathology
Neurology
Neuroradiology
Neurosciences
Neurosurgery
Prognosis
Radiology
Retrospective Studies
Survival analysis
Survival Rate
title Apparent diffusion coefficient changes predict survival after intra-arterial bevacizumab treatment in recurrent glioblastoma
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