Evidence map›Paper›PMID 26935578›Full record

Trial reportJournal of neuro-oncology2016

Cilengitide with metronomic temozolomide, procarbazine, and standard radiotherapy in patients with glioblastoma and unmethylated MGMT gene promoter in ExCentric, an open-label phase II trial.

Mustafa Khasraw, Adrian Lee, Sally McCowatt, Zoltan Kerestes, Marc E Buyse, Michael Back, Ganessan Kichenadasse, Stephen Ackland, Helen Wheeler

Abstract readClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report 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 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Anti-epidermal growth factor receptor therapy for glioblastoma in adults.The Cochrane database of systematic reviews · 2020
    Pooled it
  3. Article
  4. TGF-β signaling in health, disease, and therapeutics.Signal transduction and targeted therapy · 2024
    Review
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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

9 authors at 4 institutions in 2 countries.

Mustafa KhasrawNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia. mustafa.khasraw@sydney.edu.au.
Adrian LeeNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia.
Sally McCowattNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia.
Zoltan KerestesNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia.
Marc E BuyseInternational Drug Development Institute (IDDI), Louvain-la-Neuve, Belgium.
Michael BackNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia.
Ganessan KichenadasseInternational Drug Development Institute (IDDI), Louvain-la-Neuve, Belgium.
Stephen AcklandCalvary Mater Newcastle Hospital, Newcastle, Australia.
Helen WheelerNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, Australia.
Royal North Shore Hospital · AUInternational Drug Development Institute (Belgium) · BEUniversity of Sydney · AUCalvary Mater Newcastle Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Newly diagnosed glioblastoma multiforme with unmethylated MGMT promoter has a poor prognosis, with a median survival of 12 months. This phase II study investigated the efficacy and safety of combining the selective integrin inhibitor cilengitide with a combination of metronomic temozolomide and procarbazine for these patients. Eligible patients (newly diagnosed, histologically confirmed supratentorial glioblastoma with unmethylated MGMT promoter) were entered into this multicentre study. Cilengitide (2000 mg IV twice weekly) was commenced 1 week prior to radiotherapy combined with daily temozolomide (60 mg/m(2)) and procarbazine (50 or 100 mg) and, after 4 weeks' break, followed by six adjuvant cycles of temozolomide (50-60 mg/m(2)) and procarbazine (50 or 100 mg) on days 1-20, every 28 days. Cilengitide was continued for up to 12 months or until disease progression or unacceptable toxicity. The primary endpoint for efficacy was a 12-month overall survival rate of 65 %. Twenty-nine patients completed study treatment. Sixteen patients survived for 12 months or more, an overall survival rate of 55 %. The median overall survival was 14.5 months (95 % CI 11.1-19.6) and the median progression-free survival was 7.4 months (95 % CI 6.1-8). Cilengitide combined with metronomic temozolomide and procarbazine in MGMT-promoter unmethylated glioblastoma did not improve survival compared with historical data and does not warrant further investigation.

Indexed as

AdultAgedAntineoplastic AgentsCentral Nervous System NeoplasmsChemoradiotherapyDacarbazineDisease-Free SurvivalDisease ProgressionDNA MethylationDNA Modification MethylasesDNA Repair EnzymesDrug Therapy, CombinationFemaleGlioblastomaHumansKaplan-Meier EstimateAntineoplastic AgentsCilengitideDacarbazineDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanProcarbazineSnake VenomsTemozolomideTumor Suppressor ProteinsCilengitideGlioblastomaProcarbazineRadiotherapyTemozolomide

Identifiers

PMID26935578
OpenAlexW2289944541

What OpenQuestion holds

Textmetadata
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.