Zhao Yang, An Xin, Xiang Xiao-Juan, Feng Fen, Wang Feng-Hua, Wang Zhi-Qiang, Xu Rui-Hua, He You-Jian, Li Yu-Hong
State Key Laboratory of Oncology, South China, Guangzhou, Guangdong 510060, People's Republic of China.
Chin J Cancer. 2010 Jan;29(1):102-5. doi: 10.5732/cjc.009.10179.
Oxaliplatin is one of the effective drugs for the treatment of advanced colorectal cancer (CRC). Oxaliplatin-induced allergic reactions in European and American patients have been reported, but in China there are only a few case reports. This study investigated the incidence rate and characteristics of oxaliplatin-induced allergic reactions in Chinese patients with CRC.
Clinical data of 109 patients with advanced CRC receiving oxaliplatin plus capecitabine (the XELOX regimen) as first-line therapy were collected and analyzed retrospectively.
Of 109 patients, 13 (11.9%) patients had hypersensitivity. In 546 cycles, 23 (4.2%) cycles involved hypersensitivity. Grade-I,-II, and -III reactions were seen in 13 cycles, 8 cycles, and 2 cycles, respectively, and no grade-IV reaction was observed. Allergic reactions usually occurred at the median time during the fifth cycle (range, the 1st-8th cycle) of oxaliplatin-containing therapy, and the cumulative oxaliplatin dose was 1200 mg (range, 400-1600 mg). Symptoms associated with anaphylaxis appeared 5-360 min (median, 180 min) after oxaliplatin infusion, and were relieved after withdrawing the oxaliplatin infusion and treating with antiallergic drugs. A total of 8 patients continued to receive oxaliplatin therapy after prophylactic administration of antiallergic drugs, such as steroids, and 4 patients did not report persistent allergic reactions. Compared with men, oxaliplatin-induced allergic reactions were more commonly seen in women patients (P<0.05), while age, body surface area, performance status, tumor location, and pathologic type showed no significant difference.
Oxaliplatin-induced allergic reactions occurred in Chinese patients with CRC, and the incidence rate, occurrence time, degree of severity, and clinical outcome were consistent with literature published abroad.
奥沙利铂是治疗晚期结直肠癌(CRC)的有效药物之一。欧美患者中已报道过奥沙利铂引起的过敏反应,但在中国仅有少数病例报告。本研究调查了中国CRC患者中奥沙利铂引起的过敏反应的发生率及特征。
回顾性收集并分析109例接受奥沙利铂联合卡培他滨(XELOX方案)作为一线治疗的晚期CRC患者的临床资料。
109例患者中,13例(11.9%)出现过敏反应。在546个周期中,23个周期(4.2%)出现过敏反应。I级、II级和III级反应分别见于13个周期、8个周期和2个周期,未观察到IV级反应。过敏反应通常发生在含奥沙利铂治疗的第5个周期(范围为第1 - 8个周期)的中位时间,奥沙利铂累积剂量为1200 mg(范围为400 - 1600 mg)。过敏反应症状在奥沙利铂输注后5 - 360分钟(中位时间为180分钟)出现,在停止奥沙利铂输注并使用抗过敏药物治疗后缓解。共有8例患者在预防性使用类固醇等抗过敏药物后继续接受奥沙利铂治疗,4例患者未报告持续的过敏反应。与男性相比,奥沙利铂引起的过敏反应在女性患者中更常见(P<0.05),而年龄、体表面积、体能状态、肿瘤部位和病理类型无显著差异。
中国CRC患者中发生了奥沙利铂引起的过敏反应,其发生率、发生时间、严重程度及临床结局与国外发表的文献一致。