Feldweg Anna M, Lee Chyh-Woei, Matulonis Ursula A, Castells Mariana
Division of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 1 Jimmy Fund Way, Smith Building Room 626D, Boston, MA 02115, USA.
Gynecol Oncol. 2005 Mar;96(3):824-9. doi: 10.1016/j.ygyno.2004.11.043.
Administration of paclitaxel is associated with hypersensitivity reactions (HSRs) in up to 9% of patients despite premedication. The purpose of this study was to evaluate the effectiveness of a standardized desensitization protocol in patients with HSRs to taxanes, based on our experience with carboplatin desensitization.
We analyzed seventeen consecutive patients with documented HSRs to taxanes who required continued treatment with a taxane agent. The patients were treated with either paclitaxel or docetaxel using the 6- to 7-h standard desensitization protocol.
Seventeen patients who previously had severe taxane HSRs successfully completed 77 planned cycles of desensitization to paclitaxel or docetaxel, 72 of which were without reactions. Four patients developed HSRs during the desensitization protocol that were much less severe than their original HSRs and tolerated the re-administration of infusions without further reactions. Of these four patients, the first had palmar erythema 8 h after her 1st desensitization. The second patient had mild abdominal pain during her 1st cycle, and the third patient developed mild chest burning during her 2nd and 4th cycles. These three patients also completed subsequent desensitization cycles without reactions. The fourth patient developed a delayed urticaria reaction and gastrointestinal symptoms 6 h after completing her 1st desensitization. She elected to be treated with an alternative chemotherapy and did not receive additional courses of desensitization.
The rapid standard desensitization protocol provides a safe and effective strategy for the re-administration of paclitaxel or docetaxel even after severe HSRs.
尽管进行了预处理,但高达9%的患者在使用紫杉醇时仍会出现过敏反应(HSR)。本研究的目的是根据我们对卡铂脱敏的经验,评估标准化脱敏方案对紫杉烷类药物过敏患者的有效性。
我们分析了17例连续记录有紫杉烷类药物过敏反应且需要继续使用紫杉烷类药物治疗的患者。使用6至7小时的标准脱敏方案对患者进行紫杉醇或多西他赛治疗。
17例先前有严重紫杉烷类药物过敏反应的患者成功完成了77个计划的紫杉醇或多西他赛脱敏周期,其中72个周期无反应。4例患者在脱敏方案期间出现过敏反应,其严重程度远低于最初的过敏反应,并且能够耐受再次输注而无进一步反应。在这4例患者中,第一例在第一次脱敏后8小时出现手掌红斑。第二例患者在第一个周期出现轻度腹痛,第三例患者在第二个和第四个周期出现轻度胸部烧灼感。这3例患者也完成了后续的脱敏周期且无反应。第四例患者在完成第一次脱敏后6小时出现迟发性荨麻疹反应和胃肠道症状。她选择接受替代化疗,未接受额外的脱敏疗程。
快速标准脱敏方案为即使在严重过敏反应后重新使用紫杉醇或多西他赛提供了一种安全有效的策略。