Literature DB >> 30417211

Nimotuzumab-containing regimen for pediatric diffuse intrinsic pontine gliomas: a retrospective multicenter study and review of the literature.

Rejin Kebudi1,2, Fatma Betul Cakir3,4, Sema Buyukkapu Bay2, Omer Gorgun1,2, Pelin Altınok5, Ayça Iribas2, Fulya Yaman Agaoglu2, Emin Darendeliler2.   

Abstract

PURPOSE: Nimotuzumab is an IgG1 antibody that targets epidermal growth factor receptor (EGFR). Overexpression of EGFR is detected in some pediatric brain tumors including diffuse intrinsic pontine gliomas (DIPG)s.
METHODS: Since May 2010, nimotuzumab, combined with carboplatin or vinorelbine or Temozolomide (TMZ), was administered during progressive disease (PD) after the use of the institutional protocol consisting of radiotherapy (RT) + TMZ and adjuvant TMZ. After May 2012, children with newly diagnosed disease received TMZ during RT, and nimotuzumab and TMZ after RT. Nimotuzumab was given as 150 mg/m2/dose once a week for 12 weeks, and then every other week with TMZ until PD. PD patients were switched to nimotuzumab + vinorelbine combination until death.
RESULTS: Nimotuzumab was used in 24 children with DIPG (seven in the PD group, 17 in the newly diagnosed patient group). In the PD group, median survival time was 12 months (7-42 months); 1-year and 2-year overall survival (OS) rates were 42.9 ± 18% and 14.3 ± 13%, respectively. The median survival in this group, after the initiation of nimotuzumab was 6 months (3-8 months). In the newly diagnosed patient group, median survival time was 11 months (3-35 months) and median progression free survival was 4 months (1-21 months). The 1-year OS in this group was 35.3 ± 11% and 2 year OS was 11.8 ± 7%. Nimotuzumab ± chemotherapy was well tolerated with no major adverse effect.
CONCLUSION: Nimotuzumab-containing regimens are feasible and tolerable; it might be that some patients either with newly diagnosed DIPG or with progressive disease may benefit modestly from nimotuzumab-containing combinations.

Entities:  

Keywords:  Anti-epidermal growth factor receptor antibody; Child; Diffuse pontine glioma; Treatment

Mesh:

Substances:

Year:  2018        PMID: 30417211     DOI: 10.1007/s00381-018-4001-9

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  2 in total

1.  Nimotuzumab as Additional Therapy for GLIOMA in Pediatric and Adolescent: A Systematic Review.

Authors:  Muhammad A Parenrengi; Wihasto Suryaningtyas; Asra Al Fauzi; Abdul Hafid Bajamal; Kurnia Kusumastuti; Budi Utomo; Ahmad Muslim Hidayat Thamrin; Bagus Sulistiono
Journal:  Cancer Control       Date:  2022 Jan-Dec       Impact factor: 3.302

2.  Targeted therapy for pediatric diffuse intrinsic pontine glioma: a single-center experience.

Authors:  Giada Del Baldo; Andrea Carai; Rachid Abbas; Antonella Cacchione; Mara Vinci; Valentina Di Ruscio; Giovanna Stefania Colafati; Sabrina Rossi; Francesca Diomedi Camassei; Nicola Maestro; Sara Temelso; Giulia Pericoli; Emmanuel De Billy; Isabella Giovannoni; Alessia Carboni; Martina Rinelli; Emanuele Agolini; Alan Mackay; Chris Jones; Silvia Chiesa; Mario Balducci; Franco Locatelli; Angela Mastronuzzi
Journal:  Ther Adv Med Oncol       Date:  2022-09-06       Impact factor: 5.485

  2 in total

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