Evidence map›Paper›PMID 27444431›Full record

ArticleJournal of neuro-oncology2016

Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma.

Myra E van Linde, Johannes C van der Mijn, Thang V Pham, Jaco C Knol, Laurine E Wedekind, Koos E Hovinga, Esther Sanchez Aliaga, Jan Buter, Connie R Jimenez, Jaap C Reijneveld and 1 more

Open access · hybridAbstract 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 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. The Role of Fetuin-A in Tumor Cell Growth, Prognosis, and Dissemination.International journal of molecular sciences · 2024
    Review
  3. Review
  4. Article
  5. Article
  6. Glioblastoma: Is There Any Blood Biomarker with True Clinical Relevance?International journal of molecular sciences · 2020
    Review
  7. Review
  8. Review
  9. Review
  10. Article
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

11 authors at 1 institution in 1 country.

Myra E van LindeDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Johannes C van der MijnDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Thang V PhamDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Jaco C KnolDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Laurine E WedekindDepartment of Neurosurgery, Neuro-oncology Research Group, VU University Medical Center, Amsterdam, The Netherlands.
Koos E HovingaDepartment of Neurosurgery, VU University Medical Center, Amsterdam, The Netherlands.
Esther Sanchez AliagaDepartment of Radiology, VU University Medical Center, Amsterdam, The Netherlands.
Jan ButerDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Connie R JimenezDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Jaap C ReijneveldDepartment of Neurology, VU University Medical Center, Amsterdam, The Netherlands.
Henk M W VerheulDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands. h.verheul@vumc.nl.
Amsterdam UMC Location VUmc · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surgery followed by chemoradiation and adjuvant chemotherapy is standard of care for patients with a glioblastoma (GBM). Due to its limited benefit, an upfront method to predict dismal outcome would prevent unnecessary toxic treatment. We searched for a predictive blood derived biomarker in a cohort of 55 patients with GBM. Increasing age (HR 1.03, 95 % CI 1.01-1.06), and postoperative tumor residue (HR 1.07, 95 % CI 1.02-1.15) were independently associated with unfavourable progression free survival (PFS) in these patients. Corticosteroid use before start of chemoradiaton was strongly predictive for outcome (HR 3.26, 95 % CI 1.67-6.39) with a mean PFS and OS in patients using corticosteroids of 7.3 and 14.6 months, versus 16.1 and 21.6 months in patients not using corticosteroids (p = 0.0005, p < 0.0067 respectively). Despite earlier reports, blood concentrations of YKL-40, Fetuin-a and haptoglobin were not predictive for response. In addition, serum peptide profiles, determined by MALDI-TOF mass spectroscopy, were not predictive as well. In conclusion, further biomarker discovery studies are needed to predict treatment outcome for patients with GBM in the near future.

Indexed as

AdolescentAdrenal Cortex HormonesAdultAgedalpha-2-HS-GlycoproteinBlood PlateletsBrain NeoplasmsChemoradiotherapyChitinase-3-Like Protein 1Cohort StudiesDisease-Free SurvivalFemaleGlioblastomaHaptoglobinsHumansMaleAdrenal Cortex Hormonesalpha-2-HS-GlycoproteinCHI3L1 protein, humanChitinase-3-Like Protein 1HaptoglobinsBiomarkerFirst-line treatmentGlioblastoma multiformeProteomics

Identifiers

PMID27444431
PMCPMC4992035
OpenAlexW2483372440

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.