Literature DB >> 25818285

Ocular abnormalities in patients treated with a novel anti-GD2 monoclonal antibody, hu14.18K322A.

Brian C Tse1, Fariba Navid2, Catherine A Billups3, Thomas O'Donnell1, Mary E Hoehn4.   

Abstract

PURPOSE: To determine the incidence of and factors associated with the development of mydriasis and impaired accommodation in patients with refractory or recurrent neuroblastoma receiving the anti-GD2 antibody hu14.18K322A.
METHODS: The medical records of eligible patients with refractory or recurrent neuroblastoma who received escalating doses of hu14.18K322A, ranging from 2 to 70 mg/m(2)/dose for 4 consecutive days every 28 days, were retrospectively reviewed to identify ocular abnormalities arising during the treatment period.
RESULTS: A total of 38 patients (median age, 7 years; 23 males) were included. All patients underwent comprehensive eye examinations prior to each course of therapy. Mydriasis was seen in 13 patients (34%), and impaired accommodation was seen in 9 (24%), indicating a dose-related effect between hu14.18K322A and both mydriasis (P = 0.021) and impaired accommodation (P = 0.029). Age and sex were not associated with ocular abnormalities. Ocular symptoms resolved in the majority of patients after the drug was discontinued.
CONCLUSIONS: Side effects of mydriasis and impaired accommodation have a dose-dependent relationship with hu14.18K322A. These side effects do not warrant discontinuation of treatment, as they usually resolve after completion of therapy. Management of ocular side effects should focus on treating symptoms with manifest refraction, bifocals, or tinted spectacles.
Copyright © 2015 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25818285      PMCID: PMC4698825          DOI: 10.1016/j.jaapos.2014.11.005

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  11 in total

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Authors:  Alice L Yu; Andrew L Gilman; M Fevzi Ozkaynak; Wendy B London; Susan G Kreissman; Helen X Chen; Malcolm Smith; Barry Anderson; Judith G Villablanca; Katherine K Matthay; Hiro Shimada; Stephan A Grupp; Robert Seeger; C Patrick Reynolds; Allen Buxton; Ralph A Reisfeld; Steven D Gillies; Susan L Cohn; John M Maris; Paul M Sondel
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Review 2.  Anti-GD2 antibody therapy for GD2-expressing tumors.

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3.  A phase I study of neuroblastoma with the anti-ganglioside GD2 antibody 14.G2a.

Authors:  R Handgretinger; P Baader; R Dopfer; T Klingebiel; P Reuland; J Treuner; R A Reisfeld; D Niethammer
Journal:  Cancer Immunol Immunother       Date:  1992       Impact factor: 6.968

4.  Phase I trial of a novel anti-GD2 monoclonal antibody, Hu14.18K322A, designed to decrease toxicity in children with refractory or recurrent neuroblastoma.

Authors:  Fariba Navid; Paul M Sondel; Raymond Barfield; Barry L Shulkin; Robert A Kaufman; Jim A Allay; Jacek Gan; Paul Hutson; Songwon Seo; Kyungmann Kim; Jacob Goldberg; Jacquelyn A Hank; Catherine A Billups; Jianrong Wu; Wayne L Furman; Lisa M McGregor; Mario Otto; Stephen D Gillies; Rupert Handgretinger; Victor M Santana
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8.  Phase I trial of a human-mouse chimeric anti-disialoganglioside monoclonal antibody ch14.18 in patients with refractory neuroblastoma and osteosarcoma.

Authors:  A L Yu; M M Uttenreuther-Fischer; C S Huang; C C Tsui; S D Gillies; R A Reisfeld; F H Kung
Journal:  J Clin Oncol       Date:  1998-06       Impact factor: 44.544

9.  A phase I study of human/mouse chimeric antiganglioside GD2 antibody ch14.18 in patients with neuroblastoma.

Authors:  R Handgretinger; K Anderson; P Lang; R Dopfer; T Klingebiel; M Schrappe; P Reuland; S D Gillies; R A Reisfeld; D Neithammer
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10.  Gangliosides and allied glycosphingolipids in human peripheral nerve and spinal cord.

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Review 4.  Anti-GD2 Directed Immunotherapy for High-Risk and Metastatic Neuroblastoma.

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