Evidence map›Paper›PMID 27393350›Full record

ArticleJournal of neuro-oncology2016

The effects of sequential treatments on hippocampal volumes in malignant glioma patients.

Shantell C Nolen, Brian Lee, Shruti Shantharam, Hon J Yu, Lydia Su, John Billimek, Daniela A Bota

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
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  5. Observational
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  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Shantell C NolenDepartment of Neurology, UC Irvine Medical Center, 200 S. Manchester Avenue, Suite 206, Orange, CA, 92868, USA.
Brian LeeDepartment of Neurology, UC Irvine Medical Center, 200 S. Manchester Avenue, Suite 206, Orange, CA, 92868, USA.
Shruti ShantharamDepartment of Neurology, UC Irvine Medical Center, 200 S. Manchester Avenue, Suite 206, Orange, CA, 92868, USA.
Hon J YuDepartment of Radiology, UC Irvine Medical Center, Orange, USA.
Lydia SuDepartment of Radiology, UC Irvine Medical Center, Orange, USA.
John BillimekHealth Policy Research Institute, Orange, USA.
Daniela A BotaDepartment of Neurology, UC Irvine Medical Center, 200 S. Manchester Avenue, Suite 206, Orange, CA, 92868, USA. dbota@uci.edu.
University of California, Irvine Medical Center · USNeurological Surgery · USUniversity of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Joel E Milam · 1994 to 2026
$57.9M
Mechanisms of Chemotherapy Induced Cognitive DefectsK08NS072234 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI BOTA, DANIELA ANNENELIE · 2011 to 2015
$866k
NCI NIH HHS P30 CA062203NINDS NIH HHS K08 NS072234
6 · The paper itself

Abstract

Malignant gliomas (MG) are very aggressive tumors. In an effort to improve the outcome, the patients receive multi-modal therapies such as surgery, radiation and chemotherapy (temozolomide followed in many cases by bevacizumab). The survivors are affected by multiple learning and memory deficits. Greater deterioration over time in hippocampal specific cognitive tasks was shown in patients receiving bevacizumab in addition to radiation and temozolomide for a longer period of time (RTOG 0825). The rate of hippocampal atrophy in patients treated with radiation and temozolomide followed by bevacizumab is not yet determined, and is the goal of the present study. We used the serial MRIs obtained as parts of standard clinical care in patients with MG. Measurements were done using the Medical Image Processing, Analysis and Visualization (MIPAV) software. The hippocampus in the contralateral hemisphere was manually traced and measured, to avoid morphological structure changes induced by the tumor, radiation fields or surgical markers. We determined a longitudinal progression of hippocampal atrophy-with the maximum volume loss (33.26 %) for the patients that were on treatment for 5 years. There was no detectable hippocampal atrophy during the chemo-radiation followed by adjuvant temozolomide. A significant decrease in the absolute hippocampus volume was noted after 6 months of continuous bevacizumab treatment (p < 0.05). The hippocampal volume loss progressed over the next 3 years, and was higher than the one previously reported in Alzheimer disease patients. The hippocampal volume loss is minimal during the 1 month after diagnosis, when the patients receive chemo-radiation and adjuvant temozolomide. However, prolonged treatment including bevacizumab is associated with a significant rate of hippocampal volume loss.

Indexed as

Treatment OutcomeAdultAgedAntineoplastic AgentsAtrophyBevacizumabBrain NeoplasmsDacarbazineFemaleGliomaHippocampusHumansImage Processing, Computer-AssistedLongitudinal StudiesMagnetic Resonance ImagingMaleAntineoplastic AgentsBevacizumabDacarbazineTemozolomideBevacizumabHippocampusMalignant gliomaRadiationTemozolomide

Identifiers

PMID27393350
PMCPMC5097045
OpenAlexW2467935652

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.