Evidence map›Paper›PMID 24521695›Full record

Trial reportCancer biology & therapy2014

Nimotuzumab in combination with radiotherapy in high grade glioma patients: a single institution experience.

Maria Teresa Solomon, Nederlay Miranda, Eugenia Jorrín, Ivonne Chon, Jorge Juan Marinello, José Alert, Patricia Lorenzo-Luaces, Tania Crombet

Open access · bronzeAbstract readClinical Trial, Phase IIClinical Trial, Phase IIIClinical Trial, Phase IV
In one paragraph

Trial report in Cancer biology & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
2.7field-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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
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  6. Review
  7. Therapeutic Options in Neuro-Oncology.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. New Immunotherapeutic Approaches for Glioblastoma.Journal of immunology research · 2021
    Review
  12. A Review of Monoclonal Antibody-Based Treatments in Non-small Cell Lung Cancer.Advances in experimental medicine and biology · 2021
    Review
  13. Article
  14. Review
  15. Reported outcomes of children with newly diagnosed high-grade gliomas treated with nimotuzumab and irinotecan.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017
    Article
  16. Review
  17. Review
  18. Article
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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

8 authors at 3 institutions in 3 countries.

Maria Teresa SolomonCalixto García Hospital; Havana, Cuba.
Nederlay MirandaCalixto García Hospital; Havana, Cuba.
Eugenia JorrínCalixto García Hospital; Havana, Cuba.
Ivonne ChonNational Institute of Oncology and Radiobiology; Havana, Cuba.
Jorge Juan MarinelloNational Institute of Oncology and Radiobiology; Havana, Cuba.
José AlertNational Institute of Oncology and Radiobiology; Havana, Cuba.
Patricia Lorenzo-LuacesCenter of Molecular Immunology; Havana, Cuba.
Tania CrombetCenter of Molecular Immunology; Havana, Cuba.
Hospital Oncológico Docente "Conrado Benítez García" · CUInstituto de Oncología y Radiobiología · CUCenter of Molecular Immunology (Cuba) · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nimotuzumab, a humanized antibody targeting epidermal growth factor receptor, has potent anti-proliferative, anti-angiogenic, and pro-apoptotic effects in vitro and in vivo. It also reduces the number of radio-resistant CD133(+) glioma stem cells. The antibody has been extensively evaluated in patients with advanced head and neck, glioma, lung, esophageal, pancreatic, and gastric cancer. In this single institution experience, 35 patients with anaplastic astrocytoma (AA) or glioblastoma multiforme (GBM) were treated with irradiation and 200 mg doses of nimotuzumab. The first 6 doses were administered weekly, together with radiotherapy, and then treatment continued every 21 days until 1 year. The median number of doses was 12, and the median cumulative dose was thus 2400 mg of nimotuzumab. The most frequent treatment-related toxicities were increase in liver function tests, fever, nausea, anorexia, asthenia, dizziness, and tremors. These adverse reactions were classified as mild and moderate. The median survival time was 12.4 mo or 27.0 mo for patients with GBM or AA patients, respectively, who received curative-intent radiotherapy in combination with the antibody. The survival time of a matched population treated at the same hospital with irradiation alone was decreased (median 8.0 and 12.2 mo for GBM and AA patients, respectively) compared with that of the patients who received nimotuzumab and curative-intent radiotherapy. We have thus confirmed that nimotuzumab is a very well-tolerated drug, lacking cumulative toxicity after maintenance doses. This study, in a poor prognosis population, validates the previous data of survival gain after combining nimotuzumab and radiotherapy, in newly diagnosed high-grade glioma patients.

Indexed as

AdultAgedAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAstrocytomaBrain NeoplasmsCombined Modality TherapyDisease-Free SurvivalFemaleGlioblastomaHumansMaleMiddle AgedNeoplasm GradingYoung AdultAntibodies, Monoclonal, HumanizedAntineoplastic Agentsnimotuzumabanaplastic astrocytomaglioblastoma multiformehigh grade gliomamonoclonal antibodynimotuzumabradiotherapy

Identifiers

PMID24521695
PMCPMC4026072
OpenAlexW1988726305

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.