Low Cross-Reactivity Between Cisplatin and Other Platinum Salts.


Journal

The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220

Informations de publication

Date de publication:
Historique:
received: 16 05 2017
revised: 20 01 2019
accepted: 28 01 2019
pubmed: 19 2 2019
medline: 25 9 2020
entrez: 19 2 2019
Statut: ppublish

Résumé

Hypersensitivity reactions to platinum salts (PS) (cisplatin [CI], carboplatin [CA], and oxaliplatin [OX]) can be severe and their incidence is increasing due to their widespread use in cancer treatment. To determine the rate of cross-reactivity between PS and whether CI can be administered without prior allergy testing in patients with a history of CA or OX hypersensitivity. From September 2002 to April 2016, patients with suspected immediate PS hypersensitivity were tested and cross-reactivity between the 3 PS was evaluated. We then studied patients who were given CI without desensitization after immediate hypersensitivity to other PS. A total of 155 patients were included. Skin tests were positive in 97 patients (OX: 51, CA: 43, and CI: 3). Cross-reactivity to CA in OX-allergic patients was 45% (23 of 51) (95% confidence interval [CI]: 36% to 66%) and cross-reactivity to OX in CA-allergic patients was 37% (16 of 43) (95% CI: 23% to 53%). In contrast, cross-reactivity to CI was 0% (0 of 51) (95% CI: 0% to 7%) in OX-allergic patients and 7% (3 of 43) (95% CI: 2% to 17%) in CA-allergic patients. All these 3 patients had previously been exposed to CI in previous courses of chemotherapy. CI was initiated in 24 patients with proven hypersensitivity to CA or OX and had no hypersensitivity reactions. Initiating CI in patients with proven immediate hypersensitivity to CA or OX appeared to be safe in our study.

Sections du résumé

BACKGROUND
Hypersensitivity reactions to platinum salts (PS) (cisplatin [CI], carboplatin [CA], and oxaliplatin [OX]) can be severe and their incidence is increasing due to their widespread use in cancer treatment.
OBJECTIVE
To determine the rate of cross-reactivity between PS and whether CI can be administered without prior allergy testing in patients with a history of CA or OX hypersensitivity.
METHODS
From September 2002 to April 2016, patients with suspected immediate PS hypersensitivity were tested and cross-reactivity between the 3 PS was evaluated. We then studied patients who were given CI without desensitization after immediate hypersensitivity to other PS.
RESULTS
A total of 155 patients were included. Skin tests were positive in 97 patients (OX: 51, CA: 43, and CI: 3). Cross-reactivity to CA in OX-allergic patients was 45% (23 of 51) (95% confidence interval [CI]: 36% to 66%) and cross-reactivity to OX in CA-allergic patients was 37% (16 of 43) (95% CI: 23% to 53%). In contrast, cross-reactivity to CI was 0% (0 of 51) (95% CI: 0% to 7%) in OX-allergic patients and 7% (3 of 43) (95% CI: 2% to 17%) in CA-allergic patients. All these 3 patients had previously been exposed to CI in previous courses of chemotherapy. CI was initiated in 24 patients with proven hypersensitivity to CA or OX and had no hypersensitivity reactions.
CONCLUSION
Initiating CI in patients with proven immediate hypersensitivity to CA or OX appeared to be safe in our study.

Identifiants

pubmed: 30776524
pii: S2213-2198(19)30167-9
doi: 10.1016/j.jaip.2019.01.057
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Platinum Compounds 0
Salts 0
Oxaliplatin 04ZR38536J
Carboplatin BG3F62OND5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1894-1900

Informations de copyright

Copyright © 2019 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Justine Pasteur (J)

Dermatology Department, Dijon University Hospital, Dijon, France. Electronic address: justine.pasteur@chu-dijon.fr.

Laure Favier (L)

Oncology Department, Centre Georges-François Leclerc, Dijon, France.

Corinne Pernot (C)

Pharmacy Department, Dijon University Hospital, Dijon, France.

Mathieu Guerriaud (M)

Centre de Recherche sur le Droit International des Marchés et des Investissements (CREDIMI), University of Burgundy, Dijon, France.

Charlotte Bernigaud (C)

Dermatology Department, Dijon University Hospital, Dijon, France.

Côme Lepage (C)

Gastroenterology Department, Dijon University Hospital, Dijon, France.

Jean-Louis Jouve (JL)

Gastroenterology Department, Dijon University Hospital, Dijon, France.

Nicolas Isambert (N)

Oncology Department, Centre Georges-François Leclerc, Dijon, France.

Evelyne Collet (E)

Dermatology Department, Dijon University Hospital, Dijon, France.

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Classifications MeSH