Evidence map›Paper›PMID 35612598›Full record

ArticleStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2022

Monocentric evaluation of Ki-67 labeling index in combination with a modified RPA score as a prognostic factor for survival in IDH-wildtype glioblastoma patients treated with radiochemotherapy.

R Dumke, C Dumke, F Eberle, Ch Nimsky, U Keber, R Engenhart-Cabillic, S Lautenschläger

Open access · hybridAbstract read
In one paragraph

Article in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Sarcopenia is associated with chemoradiotherapy discontinuation and reduced progression-free survival in glioblastoma patients.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2024
    Article
  7. A Synopsis of Biomarkers in Glioblastoma: Past and Present.Current issues in molecular biology · 2024
    Review
  8. Association ofCancers · 2023
    Article
  9. Observational
  10. Article
  11. Article
  12. 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 1 institution in 1 country.

R DumkeDepartment of Radiation Oncology, Marburg University Hospital, Marburg, Hessen, Germany. rieke.dumke@t-online.de.ORCID http://orcid.org/0000-0002-7840-9055
C DumkeDepartment of Radiation Oncology, Marburg University Hospital, Marburg, Hessen, Germany.ORCID http://orcid.org/0000-0001-6233-2113
F EberleDepartment of Radiation Oncology, Marburg University Hospital, Marburg, Hessen, Germany.ORCID http://orcid.org/0000-0002-1473-6065
Ch NimskyDepartment of Neurosurgery, Marburg University Hospital, Marburg, Hessen, Germany.ORCID http://orcid.org/0000-0002-8216-9410
U KeberInstitute of Neuropathology, Marburg University Hospital, Marburg, Hessen, Germany.
R Engenhart-CabillicDepartment of Radiation Oncology, Marburg University Hospital, Marburg, Hessen, Germany.
S LautenschlägerDepartment of Radiation Oncology, Marburg University Hospital, Marburg, Hessen, Germany.
Philipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe prognosis for glioblastoma patients remains dismal despite intensive research on better treatment options. Molecular and immunohistochemical markers are increasingly being investigated as understanding of their role in disease progression grows. O(6)-methylguanine-DNA methyltransferase (MGMT) promoter methylation has been shown to have prognostic and therapeutic relevance for glioblastoma patients. Other markers implicated in tumor formation and/or malignancy are p53, Alpha thalassemia/mental retardation syndrome X-linked (ATRX), Epidermal Growth Factor Receptor splice variant III (EGFRvIII), and Ki-67, with loss of nuclear ATRX expression and lower Ki-67 index being associated with prolonged survival. For p53 and EGFRvIII the data are contradictory. Our aim was to investigate the markers mentioned above regarding progression-free (PFS) and overall survival (OS) to evaluate their viability as independent prognostic markers for our patient collective.

methodsIn this retrospective study, we collected data on patients undergoing radiotherapy due to isocitrate dehydrogenase (IDH) wildtype glioblastoma at a single university hospital between 2014 and 2020.

resultsOur findings confirm Ki-67 labeling index ≤ 20% as an independent prognostic factor for prolonged PFS as well as MGMT promoter methylation for both prolonged PFS and OS, in consideration of age and Eastern Cooperative Oncology Group (ECOG) status, chemotherapy treatment, and total radiation dose for PFS as well as additionally sex, resection status, and receipt of treatment for progression or recurrence for OS. Additionally, Ki-67 labeling index ≤ 20% showed a significant correlation with prolonged OS in univariate analysis. Modification of the recursive partitioning analysis (RPA) score to include Ki-67 labeling index resulted in a classification with the possible ability to distinguish long-term-survivors from patients with unfavorable prognosis.

conclusionMGMT promoter methylation and Ki-67 labeling index were independent predictors of survival in our collective. We see further studies pooling patient collectives to reach larger patient numbers concerning Ki-67 labeling index as being warranted.

Indexed as

Brain NeoplasmsGlioblastomaChemoradiotherapyDNA MethylationDNA Modification MethylasesDNA Repair EnzymesErbB ReceptorsHumansIsocitrate DehydrogenaseKi-67 AntigenO(6)-Methylguanine-DNA MethyltransferasePrognosisRetrospective StudiesTumor Suppressor Protein p53DNA Modification MethylasesDNA Repair EnzymesErbB ReceptorsIsocitrate DehydrogenaseKi-67 AntigenO(6)-Methylguanine-DNA MethyltransferaseTumor Suppressor Protein p53ATRXEGFRMGMTp53Recurrence

Identifiers

PMID35612598
PMCPMC9515058
OpenAlexW4281493369

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.