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卡铂皮肤试验:一种预测对卡铂化疗过敏反应的皮肤试验方案。

Carboplatin skin testing: a skin-testing protocol for predicting hypersensitivity to carboplatin chemotherapy.

作者信息

Zanotti K M, Rybicki L A, Kennedy A W, Belinson J L, Webster K D, Kulp B, Peterson G, Markman M

机构信息

Cleveland Clinic Foundation, Cleveland, OH 44012, USA.

出版信息

J Clin Oncol. 2001 Jun 15;19(12):3126-9. doi: 10.1200/JCO.2001.19.12.3126.

Abstract

PURPOSE

A high incidence of moderate to severe hypersensitivity reactions (HRs) is noted in patients who have been treated with multiple courses of carboplatin. Presently, there is no reliable way to predict which patients may be at risk for this potentially severe adverse reaction. We developed a skin-test protocol to identify patients at high risk for HR to carboplatin chemotherapy.

PATIENTS AND METHODS

Patients undergoing more than seven courses of carboplatin received a 0.02-mL intradermal injection of an undiluted aliquot of their planned carboplatin infusion 1 hour before each course of the agent. A positive skin test was prospectively defined as that resulting in a wheel of at least 5 mm with a surrounding flare. We recently reported a 27% incidence of HRs in patients receiving more than seven courses of carboplatin. These patients served as historical controls for the current study.

RESULTS

Forty-seven patients with recurrent ovarian or primary peritoneal carcinoma receiving carboplatin were skin tested. Thirteen of 47 patients (28%) manifested a positive skin test at a median of nine total courses of carboplatin (range, eight to 17 courses). This rate of skin-test positivity was not significantly different from the incidence of documented HR reported in a historical control group (P =.89), suggesting comparable populations. A negative skin test accurately predicted the absence of HR in 166 of 168 courses of chemotherapy. Only two of 47 patients (4%) experienced a HR after a negative skin test. Thus, administering carboplatin only to patients with a negative skin test may result in a significant reduction in HRs relative to historical controls (P =.002).

CONCLUSION

An easily performed skin test appears to predict patients in whom carboplatin may be safely administered. Treatment modifications based on the results of skin testing may reduce the incidence of HRs in patients receiving repeated courses of carboplatin.

摘要

目的

在接受多疗程卡铂治疗的患者中,观察到中度至重度过敏反应(HRs)的高发生率。目前,尚无可靠方法预测哪些患者可能面临这种潜在严重不良反应的风险。我们制定了一种皮肤试验方案,以识别卡铂化疗发生HRs的高危患者。

患者和方法

接受超过七个疗程卡铂治疗的患者,在每次用药前1小时,皮内注射0.02 mL未稀释的计划使用的卡铂输注液等分试样。前瞻性地将阳性皮肤试验定义为产生至少5 mm的风团并伴有周围红晕。我们最近报告了接受超过七个疗程卡铂治疗的患者中HRs发生率为27%。这些患者作为本研究的历史对照。

结果

47例接受卡铂治疗的复发性卵巢癌或原发性腹膜癌患者接受了皮肤试验。47例患者中有13例(28%)在卡铂总疗程中位数为9个疗程时(范围为8至17个疗程)出现阳性皮肤试验。该皮肤试验阳性率与历史对照组中记录的HR发生率无显著差异(P = 0.89),表明人群具有可比性。阴性皮肤试验在168个化疗疗程中的166个准确预测了无HRs。47例患者中只有2例(4%)在阴性皮肤试验后发生了HRs。因此,仅对皮肤试验阴性的患者给予卡铂,相对于历史对照,可能会显著降低HRs的发生率(P = 0.002)。

结论

一种易于实施的皮肤试验似乎可以预测哪些患者可以安全地使用卡铂。根据皮肤试验结果调整治疗方案,可能会降低接受重复疗程卡铂治疗患者的HRs发生率。

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