Lee Chyh-Woei, Matulonis Ursula A, Castells Mariana C
Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA 02115, USA.
Gynecol Oncol. 2005 Nov;99(2):393-9. doi: 10.1016/j.ygyno.2005.06.028. Epub 2005 Jul 27.
Hypersensitivity reactions (HR) to chemotherapy often prompt permanent discontinuation and deprive the patient of the most active regimen. We investigated the safety and effectiveness of a rapid desensitization protocol used in inpatient and outpatient settings for patients with HR to various chemotherapy and related agents.
A 3-solution, 12-step protocol delivered doubling drug doses by step, infusing the target dose over 5.8 h for inpatient and 3.8 h for outpatient administration.
57 consecutive patients who had moderate to severe HR to chemotherapy were evaluated for desensitization. All 57 patients successfully completed 255 courses of desensitization (127 to carboplatin, 114 to paclitaxel, and 14 to four other agents) where 16 patients received 51 courses in the outpatient setting (34 to carboplatin and 17 to paclitaxel). 225 courses (88.2%) were completed without any HR. 18 patients had breakthrough symptoms (BS) over 30 courses (11.8%) that were less severe than their initial HR. After management of breakthrough symptoms, these patients finished all 30 courses and tolerated subsequent desensitizations on a modified protocol. 21 of 26 patients (81%) with HR to carboplatin had positive skin tests to carboplatin. Cancer response to chemotherapy administered by desensitization was within the expected range after 1-3 years of follow-up.
The rapid desensitization protocol was safe and effective in both the inpatient and outpatient settings and allowed appropriate patients with moderate to severe HR to continue chemotherapy. This study warrants the incorporation of the protocol into standard clinical practice.
化疗引起的超敏反应(HR)常常促使化疗永久中断,使患者无法接受最有效的治疗方案。我们调查了一种快速脱敏方案在住院和门诊环境中用于对各种化疗药物及相关制剂发生HR的患者的安全性和有效性。
一种三溶液、十二步骤的方案,逐步给予加倍的药物剂量,住院患者在5.8小时内输注目标剂量,门诊患者在3.8小时内输注目标剂量。
对57例对化疗有中度至重度HR的连续患者进行了脱敏评估。所有57例患者成功完成了255个脱敏疗程(127个针对卡铂,114个针对紫杉醇,14个针对其他四种药物),其中16例患者在门诊接受了51个疗程(34个针对卡铂,17个针对紫杉醇)。225个疗程(88.2%)完成时未发生任何HR。18例患者在30个疗程中出现了突破症状(BS)(11.8%),其严重程度低于初始HR。在对突破症状进行处理后,这些患者完成了所有30个疗程,并按照改良方案耐受了后续脱敏。26例对卡铂有HR的患者中有21例(81%)对卡铂皮肤试验呈阳性。脱敏后给予的化疗在随访1至3年后的癌症反应在预期范围内。
快速脱敏方案在住院和门诊环境中均安全有效,使有中度至重度HR的合适患者能够继续化疗。本研究值得将该方案纳入标准临床实践。