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无铂间期能否预测对卡铂过敏反应的发生率或严重程度?来自妇女和婴儿医院的经验。

Does the platinum-free interval predict the incidence or severity of hypersensitivity reactions to carboplatin? The experience from Women and Infants' Hospital.

作者信息

Schwartz Joanna R, Bandera Christina, Bradley AnnMarie, Brard Laurent, Legare Robert, Granai C O, Dizon Don S

机构信息

Women and Infants' Hospital of Rhode Island, Program in Women's Oncology, 101 Dudley Street, Providence, RI 02905, USA.

出版信息

Gynecol Oncol. 2007 Apr;105(1):81-3. doi: 10.1016/j.ygyno.2006.10.047. Epub 2006 Dec 8.

Abstract

OBJECTIVES

Carboplatin (C) is a standard treatment for gynecologic cancers, but its use in recurrence is associated with an increased risk of hypersensitivity reactions (HSR) in those previously treated with C. However, there is no way to predict those at risk for a C-HSR. We sought to evaluate whether the platinum-free interval (PFI) was predictive of incidence and severity of HSRs.

METHODS

Patients treated with C between 1/99 and 12/2005 were identified through our chemotherapy database. Records were reviewed in those receiving multiple C regimens or with C HSR. Severity was defined as mild or severe based on symptoms.

RESULTS

126 patients were identified who had multiple C regimens. 63 (50%) experienced C HSRs of which 36 (29%) were severe. The incidence of C HSR was 25.8% for PFI < 12 months and 56.5% if > or = 12 months (p=0.0023). The incidence of a severe C HSR significantly increased with time as well: 6.5% PFI < 12 months, 23.9% PFI 12-24 months and 47% PFI > or = 24 months (p=0.0091). Of those receiving a 3rd regimen of C, 8/8 had a HSR and these were severe in seven (88%). Of note, 60 patients received > 8 (range 9-19) cycles with the first C regimen, and none of the patients reacted after cycle 8.

CONCLUSIONS

A duration of greater than 12 months between C regimens is associated with an increased risk of both any--and severe--HSR. Our data also suggests that upfront treatment with C beyond eight cycles is not associated with an increased risk of HSR.

摘要

目的

卡铂(C)是妇科癌症的标准治疗药物,但在复发情况下使用时,对于先前接受过卡铂治疗的患者,其超敏反应(HSR)风险会增加。然而,目前尚无方法预测哪些患者有发生卡铂超敏反应的风险。我们试图评估无铂间期(PFI)是否可预测超敏反应的发生率和严重程度。

方法

通过我们的化疗数据库识别出1999年1月至2005年12月期间接受卡铂治疗的患者。对接受多种卡铂治疗方案或发生卡铂超敏反应的患者的记录进行审查。根据症状将严重程度定义为轻度或重度。

结果

确定了126例接受多种卡铂治疗方案的患者。63例(50%)发生了卡铂超敏反应,其中36例(29%)为重度。无铂间期小于12个月时,卡铂超敏反应的发生率为25.8%,无铂间期大于或等于12个月时,发生率为56.5%(p = 0.0023)。重度卡铂超敏反应的发生率也随时间显著增加:无铂间期小于12个月时为6.5%,12至24个月时为23.9%,大于或等于24个月时为47%(p = 0.0091)。在接受第三次卡铂治疗方案的患者中,8例中有8例发生超敏反应,其中7例(88%)为重度。值得注意的是,60例患者在第一个卡铂治疗方案中接受了超过8个周期(9至19个周期)的治疗,且在第8个周期后没有患者出现反应。

结论

卡铂治疗方案之间的间隔时间超过12个月会增加发生任何超敏反应和重度超敏反应的风险。我们的数据还表明,卡铂初始治疗超过8个周期与超敏反应风险增加无关。

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