Evidence map›Paper›PMID 22284691›Full record

ArticleInternational journal of radiation oncology, biology, physics2012

Glioblastoma treatment: bypassing the toxicity of platinum compounds by using liposomal formulation and increasing treatment efficiency with concomitant radiotherapy.

Gabriel Charest, Léon Sanche, David Fortin, David Mathieu, Benoit Paquette

Registry-linked trialAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03672721 (A Phase II Study in Relapsing Glioblastoma of Intraarterial Concurrent Chemoradiation Therapy Using IA Carboplatin), which is not on this map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 21% 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.

NCT03672721 phase1 / phase2recruitingnot on this mapstarted 2018, after this paper: background citation

A Phase II Study in Relapsing Glioblastoma of Intraarterial Concurrent Chemoradiation Therapy Using IA Carboplatin

TypeinterventionalSponsorUniversité de SherbrookeRan2018 to 2026Enrolled35ConditionsGlioblastoma Multiforme, RelapseArmsIA Carbo+ Radiation
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Review
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  8. The use of radiosensitizing agents in the therapy of glioblastoma multiforme-a comprehensive review.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2022
    Review
  9. Review
  10. Design, Synthesis, and Cytotoxicity Assessment of [Nanomaterials (Basel, Switzerland) · 2021
    Article
  11. Review
  12. Review
  13. Article
  14. IntratumoralEJNMMI research · 2019
    Article
  15. Review
  16. Article
  17. Nanotechnology for Cancer Therapy Based on Chemotherapy.Molecules (Basel, Switzerland) · 2018
    Review
  18. MicroRNA in Glioblastoma: An Overview.International journal of genomics · 2017
    Review
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Gabriel CharestCenter for Research in Radiotherapy, Department of Nuclear Medicine and Radiobiology, Université de Sherbrooke, Sherbrooke, Québec, Canada.
Léon Sanche
David Fortin
David Mathieu
Benoit Paquette
Université de Sherbrooke · CACentre Hospitalier Universitaire de Sherbrooke · CA

Funding

CIHR 81356-2CIHR MOP 81356
6 · The paper itself

Abstract

purposeTreatments of glioblastoma with cisplatin or oxaliplatin only marginally improve the overall survival of patients and cause important side effects. To prevent adverse effects, improve delivery, and optimize the tumor response to treatment in combination with radiotherapy, a potential approach consists of incorporating the platinum agent in a liposome. METHODS AND MATERIALS: In this study, cisplatin, oxaliplatin, carboplatin, Lipoplatin (the liposomal formulation of cisplatin), and Lipoxal (the liposomal formulation of oxaliplatin) were tested on F98 glioma orthotopically implanted in Fischer rats. The platinum compounds were administered by intracarotid infusion and were assessed for the ability to reduce toxicity, improve cancer cell uptake, and increase survival of animals when combined or not combined with radiotherapy.

resultsThe tumor uptake was 2.4-fold more important for Lipoxal than the liposome-free oxaliplatin. Lipoxal also improved the specificity of oxaliplatin as shown by a higher ratio of tumor to right hemisphere uptake. Surprisingly, Lipoplatin led to lower tumor uptake compared with cisplatin. However, Lipoplatin had the advantage of largely reducing the toxicity of cisplatin and allowed us to capitalize on the anticancer activity of this agent.

conclusionAmong the five platinum compounds tested, carboplatin showed the best increase in survival when combined with radiation for treatment of glioma implanted in Fischer rats.

Indexed as

AnimalsAntineoplastic AgentsBrain NeoplasmsCarboplatinCarotid ArteriesCisplatinCombined Modality TherapyGlioblastomaInfusions, Intra-ArterialLiposomesOrganoplatinum CompoundsOxaliplatinRadiosurgeryRatsRats, Inbred F344Antineoplastic AgentsCarboplatinCisplatinlipoplatinLiposomesOrganoplatinum CompoundsOxaliplatin

Identifiers

PMID22284691
PMCPMC3828172
OpenAlexW2139312833

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.