Callahan Megan B, Lachance Jason A, Stone Rebecca L, Kelsey Julie, Rice Laurel W, Jazaeri Amir A
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Am J Obstet Gynecol. 2007 Aug;197(2):199.e1-4; discussion 199.e4-5. doi: 10.1016/j.ajog.2007.04.044.
The purpose of this study was to evaluate the results of substituting cisplatin for carboplatin in women who experienced a carboplatin-associated hypersensitivity reaction while undergoing treatment for gynecologic cancers.
Using a comprehensive data repository, we identified all epithelial ovarian cancer and primary peritoneal cancer patients who experienced a documented significant hypersensitivity reaction to carboplatin and were subsequently treated with cisplatin at our institution from 1995 to the present. We also performed a review of published case reports of similar patient management.
We identified a total of 24 patients who met inclusion criteria. Eighteen patients (75%) tolerated cisplatin without any adverse events. Six patients (25%) eventually developed a reaction to cisplatin; none was life threatening, and only 1 required hospitalization. Twenty-three of the 24 patients (96%) tolerated at least 1 cycle of cisplatin. Of the 5 patients who initially tolerated cisplatin but eventually experienced a reaction, the mean number of cycles tolerated was 3.4.
The use of cisplatin without desensitization is a reasonable approach for continuing platinum-based chemotherapy in patients with a significant carboplatin hypersensitivity reaction. Patients should be advised of risks and closely monitored, given published case reports of anaphylaxis.
本研究旨在评估在接受妇科癌症治疗时发生卡铂相关过敏反应的女性中,用顺铂替代卡铂的效果。
利用一个综合数据库,我们确定了1995年至今在我们机构中所有经历过记录在案的对卡铂严重过敏反应且随后接受顺铂治疗的上皮性卵巢癌和原发性腹膜癌患者。我们还对已发表的类似患者管理的病例报告进行了回顾。
我们共确定了24名符合纳入标准的患者。18名患者(75%)耐受顺铂且无任何不良事件。6名患者(25%)最终出现了对顺铂的反应;均无生命危险,只有1名患者需要住院治疗。24名患者中有23名(96%)耐受至少1个周期的顺铂。在最初耐受顺铂但最终出现反应的5名患者中,耐受的平均周期数为3.4个。
对于有严重卡铂过敏反应的患者,不进行脱敏而使用顺铂是继续铂类化疗的一种合理方法。鉴于已发表的过敏反应病例报告,应告知患者风险并密切监测。