» Articles » PMID: 12798720

Relationship Between a History of Systemic Allergic Reactions and Risk of Subsequent Carboplatin Hypersensitivity

Overview
Journal Gynecol Oncol
Date 2003 Jun 12
PMID 12798720
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The establishment of clinical features identifying patients at a heightened risk for the development of carboplatin hypersensitivity may assist in the management of this important toxicity. Based on a previous report suggesting a history of "bee sting" allergy predicted for paclitaxel hypersensitivity, we attempted to determine if there was a relationship between a history of prior systemic allergic reactions and the subsequent development of carboplatin hypersensitivity.

Patients And Methods: The medical records of all women treated in the Gynecologic Cancer Program of the Cleveland Clinic from June 1995 to May 2002 who received >6 cycles of platinum-based chemotherapy were retrospectively reviewed for a history of prior systemic hypersensitivity (e.g., medications, environmental exposure). The incidence of "positive" allergic histories was then examined in relation to the subsequent risk of patients developing either a documented carboplatin hypersensitivity reaction or a "positive" carboplatin skin test.

Results: The analysis included 174 patients (91 undergoing "carboplatin skin testing") who received > 6 courses of carboplatin. Of 53 patients with no recorded history of systemic hypersensitivity treated prior to our routine use of carboplatin skin testing, 19% experienced an allergic reaction, in contrast to a 40% incidence of a documented carboplatin reaction in 30 patients with a recorded history of hypersensitivity to a medication or environmental exposure (P < 0.05). For the 55 patients with no history of systemic hypersensitivity who underwent carboplatin skin-testing, 27% had a positive test result, in comparison to a 36% positive test rate in women with a previous history of a systemic hypersensitivity reaction recorded in the medical record (P > 0.05).

Conclusion: This analysis suggests that patients with a prior history of systemic hypersensitivity to medications or environmental exposures may be at a heightened risk for experiencing allergic reactions to carboplatin.

Citing Articles

Delayed and immediate cutaneous adverse events during pembrolizumab combination chemotherapy against cervical cancer: Case series.

Adachi T, Matsui T, Okata-Karigane U, Takahashi C, Tahara U, Hyodo M J Dermatol. 2024; 52(1):132-137.

PMID: 39526614 PMC: 11700920. DOI: 10.1111/1346-8138.17521.


Advancing perspectives on the off-label use of anticancer drugs: an updated classification and exploration of categories.

Chen X, Ou S, Luo J, He Z, Jiang Q Front Pharmacol. 2024; 15:1374549.

PMID: 38898925 PMC: 11186405. DOI: 10.3389/fphar.2024.1374549.


Platinum desensitization therapy and its impact on the prognosis of ovary high-grade serous adenocarcinoma: a real world-data.

Li K, Yin R Front Immunol. 2024; 15:1346464.

PMID: 38312839 PMC: 10834667. DOI: 10.3389/fimmu.2024.1346464.


Cross-reactivity between halogenated platinum salts in an immediate-type respiratory hypersensitivity model.

Lehmann D, Williams W Inhal Toxicol. 2019; 30(11-12):472-481.

PMID: 30654668 PMC: 8404061. DOI: 10.1080/08958378.2018.1554015.


Analysis and treatment of 45 platinum-allergic gynecologic malignant tumors.

Ma X, Li X Int J Clin Oncol. 2018; 23(6):1160-1166.

PMID: 30078140 DOI: 10.1007/s10147-018-1326-z.