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Carboplatin-, oxaliplatin-, and cisplatin-specific IgE: cross-reactivity and value in the diagnosis of carboplatin and oxaliplatin allergy.
Caiado, Joana; Venemalm, Lennart; Pereira-Santos, Maria Conceição; Costa, Luis; Barbosa, Manuel Pereira; Castells, Mariana.
  • Caiado J; Immunoallergology Department, North Lisbon Hospital Center, Santa Maria Hospital, Lisbon, Portugal. Electronic address: joanacaiado@hotmail.com.
  • Venemalm L; Research & Development Allergy, Thermo Fisher Scientific, Uppsala, Sweden.
  • Pereira-Santos MC; Laboratory of Clinical Immunology, Instituto de Medicina Molecular/ Lisbon Medical School, Lisbon, Portugal.
  • Costa L; Oncology Department, North Lisbon Hospital Center, Santa Maria Hospital, Lisbon, Portugal.
  • Barbosa MP; Immunoallergology Department, North Lisbon Hospital Center, Santa Maria Hospital, Lisbon, Portugal.
  • Castells M; Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, Mass.
J Allergy Clin Immunol Pract ; 1(5): 494-500, 2013.
Article en En | MEDLINE | ID: mdl-24565621
BACKGROUND: The diagnosis of hypersensitivity reactions (HSR) to platins is based on the characterization of the reaction and the results of skin testing. Platins can be irritants when used in skin testing; therefore, in vitro testing may offer an alternative diagnostic tool. OBJECTIVE: To evaluate sensitivity and specificity of platin specific IgE (sIgE) in patients with HSRs and in controls. METHODS: Twenty-four patients with immediate HSR to platins were included (carboplatin, 12; oxaliplatin, 12): 19 women and 5 men (mean age, 61 years). The control group included 17 patients exposed to platin and with no HSR. Skin testing was performed on 22 patients. Carboplatin sIgE and oxaliplatin sIgE were measured in 24 patients and 17 controls; carboplatin sIgE was measured in 21 patients. RESULTS: Skin test results were positive in 22 patients (carboplatin, 12/12; oxaliplatin, 10/12). Seven of 12 patients sensitive to carboplatin (59%) had positive carboplatin sIgE, 2 also had positive cisplatin sIgE, and all had negative oxaliplatin sIgE; 9 of 12 patients sensitive to oxaliplatin (75%) had positive sIgE to oxaliplatin, 8 of 12 (67%) also had positive carboplatin and cisplatin sIgE, to which they had not been exposed. All 5 carboplatin controls had negative sIgE; 3 oxaliplatin controls (25%) had positive carboplatin sIgE, and 2 had positive oxaliplatin sIgE. CONCLUSION: Carboplatin sIgE is very specific but less sensitive. In contrast, oxaliplatin sIgE had higher sensitivity but lower specificity. Analysis of our data suggests that oxaliplatin exposure was more immunogenic. This could be clinically relevant because patients sensitized to carboplatin may be able to tolerate oxaliplatin, but patients sensitized to oxaliplatin may be at risk when exposed to carboplatin and cisplatin.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos Organoplatinos / Inmunoglobulina E / Carboplatino / Cisplatino / Hipersensibilidad a las Drogas / Antineoplásicos Tipo de estudio: Diagnostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2013 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos Organoplatinos / Inmunoglobulina E / Carboplatino / Cisplatino / Hipersensibilidad a las Drogas / Antineoplásicos Tipo de estudio: Diagnostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2013 Tipo del documento: Article