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Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial

BACKGROUND: The prognosis of patients bearing high grade glioma remains dismal. Epidermal Growth Factor Receptor (EGFR) is well validated as a primary contributor of glioma initiation and progression. Nimotuzumab is a humanized monoclonal antibody that recognizes the EGFR extracellular domain and re...

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Autores principales: Solomón, Maria Teresa, Selva, Julio César, Figueredo, Javier, Vaquer, José, Toledo, Carolina, Quintanal, Nelson, Salva, Silvia, Domíngez, Rafael, Alert, José, Marinello, Jorge Juan, Catalá, Mauricio, Griego, Martha González, Martell, Juan Antonio, Luaces, Patricia Lorenzo, Ballesteros, Javier, de-Castro, Niurys, Bach, Ferdinand, Crombet, Tania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691625/
https://www.ncbi.nlm.nih.gov/pubmed/23782513
http://dx.doi.org/10.1186/1471-2407-13-299
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author Solomón, Maria Teresa
Selva, Julio César
Figueredo, Javier
Vaquer, José
Toledo, Carolina
Quintanal, Nelson
Salva, Silvia
Domíngez, Rafael
Alert, José
Marinello, Jorge Juan
Catalá, Mauricio
Griego, Martha González
Martell, Juan Antonio
Luaces, Patricia Lorenzo
Ballesteros, Javier
de-Castro, Niurys
Bach, Ferdinand
Crombet, Tania
author_facet Solomón, Maria Teresa
Selva, Julio César
Figueredo, Javier
Vaquer, José
Toledo, Carolina
Quintanal, Nelson
Salva, Silvia
Domíngez, Rafael
Alert, José
Marinello, Jorge Juan
Catalá, Mauricio
Griego, Martha González
Martell, Juan Antonio
Luaces, Patricia Lorenzo
Ballesteros, Javier
de-Castro, Niurys
Bach, Ferdinand
Crombet, Tania
author_sort Solomón, Maria Teresa
collection PubMed
description BACKGROUND: The prognosis of patients bearing high grade glioma remains dismal. Epidermal Growth Factor Receptor (EGFR) is well validated as a primary contributor of glioma initiation and progression. Nimotuzumab is a humanized monoclonal antibody that recognizes the EGFR extracellular domain and reaches Central Nervous System tumors, in nonclinical and clinical setting. While it has similar activity when compared to other anti-EGFR antibodies, it does not induce skin toxicity or hypomagnesemia. METHODS: A randomized, double blind, multicentric clinical trial was conducted in high grade glioma patients (41 anaplastic astrocytoma and 29 glioblastoma multiforme) that received radiotherapy plus nimotuzumab or placebo. Treatment and placebo groups were well-balanced for the most important prognostic variables. Patients received 6 weekly doses of 200 mg nimotuzumab or placebo together with irradiation as induction therapy. Maintenance treatment was given for 1 year with subsequent doses administered every 3 weeks. The objectives of this study were to assess the comparative overall survival, progression free survival, response rate, immunogenicity and safety. RESULTS: The median cumulative dose was 3200 mg of nimotuzumab given over a median number of 16 doses. The combination of nimotuzumab and RT was well-tolerated. The most prevalent related adverse reactions included nausea, fever, tremors, anorexia and hepatic test alteration. No anti-idiotypic response was detected, confirming the antibody low immunogenicity. The mean and median survival time for subjects treated with nimotuzumab was 31.06 and 17.76 vs. 21.07 and 12.63 months for the control group. CONCLUSIONS: In this randomized trial, nimotuzumab showed an excellent safety profile and significant survival benefit in combination with irradiation. TRIAL REGISTRATION: Cuban National Register for clinical trials (No. 1745) (http://registroclinico.sld.cu/ensayos).
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spelling pubmed-36916252013-06-26 Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial Solomón, Maria Teresa Selva, Julio César Figueredo, Javier Vaquer, José Toledo, Carolina Quintanal, Nelson Salva, Silvia Domíngez, Rafael Alert, José Marinello, Jorge Juan Catalá, Mauricio Griego, Martha González Martell, Juan Antonio Luaces, Patricia Lorenzo Ballesteros, Javier de-Castro, Niurys Bach, Ferdinand Crombet, Tania BMC Cancer Research Article BACKGROUND: The prognosis of patients bearing high grade glioma remains dismal. Epidermal Growth Factor Receptor (EGFR) is well validated as a primary contributor of glioma initiation and progression. Nimotuzumab is a humanized monoclonal antibody that recognizes the EGFR extracellular domain and reaches Central Nervous System tumors, in nonclinical and clinical setting. While it has similar activity when compared to other anti-EGFR antibodies, it does not induce skin toxicity or hypomagnesemia. METHODS: A randomized, double blind, multicentric clinical trial was conducted in high grade glioma patients (41 anaplastic astrocytoma and 29 glioblastoma multiforme) that received radiotherapy plus nimotuzumab or placebo. Treatment and placebo groups were well-balanced for the most important prognostic variables. Patients received 6 weekly doses of 200 mg nimotuzumab or placebo together with irradiation as induction therapy. Maintenance treatment was given for 1 year with subsequent doses administered every 3 weeks. The objectives of this study were to assess the comparative overall survival, progression free survival, response rate, immunogenicity and safety. RESULTS: The median cumulative dose was 3200 mg of nimotuzumab given over a median number of 16 doses. The combination of nimotuzumab and RT was well-tolerated. The most prevalent related adverse reactions included nausea, fever, tremors, anorexia and hepatic test alteration. No anti-idiotypic response was detected, confirming the antibody low immunogenicity. The mean and median survival time for subjects treated with nimotuzumab was 31.06 and 17.76 vs. 21.07 and 12.63 months for the control group. CONCLUSIONS: In this randomized trial, nimotuzumab showed an excellent safety profile and significant survival benefit in combination with irradiation. TRIAL REGISTRATION: Cuban National Register for clinical trials (No. 1745) (http://registroclinico.sld.cu/ensayos). BioMed Central 2013-06-19 /pmc/articles/PMC3691625/ /pubmed/23782513 http://dx.doi.org/10.1186/1471-2407-13-299 Text en Copyright © 2013 Solomón et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Solomón, Maria Teresa
Selva, Julio César
Figueredo, Javier
Vaquer, José
Toledo, Carolina
Quintanal, Nelson
Salva, Silvia
Domíngez, Rafael
Alert, José
Marinello, Jorge Juan
Catalá, Mauricio
Griego, Martha González
Martell, Juan Antonio
Luaces, Patricia Lorenzo
Ballesteros, Javier
de-Castro, Niurys
Bach, Ferdinand
Crombet, Tania
Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title_full Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title_fullStr Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title_full_unstemmed Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title_short Radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
title_sort radiotherapy plus nimotuzumab or placebo in the treatment of high grade glioma patients: results from a randomized, double blind trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691625/
https://www.ncbi.nlm.nih.gov/pubmed/23782513
http://dx.doi.org/10.1186/1471-2407-13-299
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