Broome C B, Schiff R I, Friedman H S
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710, USA.
Med Pediatr Oncol. 1996 Feb;26(2):105-10. doi: 10.1002/(SICI)1096-911X(199602)26:2<105::AID-MPO7>3.0.CO;2-P.
Carboplatin is the drug of choice for the treatment of nonresectable astrocytomas in children, but patients who are intolerant may require cranial irradiation which is associated with significant morbidity. Hypersensitivity reactions, including urticaria, bronchospasm, and hypotension, have been reported in 1% to 30% of patients treated with carboplatin. Although a few patients have attempted to continue therapy following pretreatment with antihistamines and corticosteroids, most have had recurrent severe reactions and have discontinued therapy. Two children with a history of severe systemic reactions to carboplatin were pretreated with 1 to 2 mg/kg of oral prednisolone the night before and the morning of their infusion. The initial desensitization was carried out in the intensive care unit (ICU) using doses of 1, 2.5, 5, 10, 25, and 50 mg of carboplatin infused at 1 mg/min every 15 minutes. This was well-tolerated and the remainder of the dose was infused at the standard rate of 200 mg/hr. One patient continued to receive infusions in the clinic without any difficulty. The other patient tolerated a second infusion, but during his third he experienced a systemic reaction that required discontinuation of the infusion and treatment with diphenhydramine. Desensitization was repeated in the ICU with pretreatment with prednisolone, diphenhydramine, and ranitidine, starting with 0.1 mg of carboplatin, and increasing more slowly than in the first protocol. This was well-tolerated, and subsequent infusions have been administered beginning with 1 mg doses without adverse effects. Both boys continued therapy with carboplatin; their astrocytomas are stable and they are clinically well. The use of the desensitization protocol enabled them to avoid cranial irradiation and improved their chances for normal neurologic development.
卡铂是治疗儿童不可切除星形细胞瘤的首选药物,但不耐受的患者可能需要进行颅脑照射,而这会带来显著的发病率。据报道,接受卡铂治疗的患者中有1%至30%出现过过敏反应,包括荨麻疹、支气管痉挛和低血压。尽管有少数患者在使用抗组胺药和皮质类固醇进行预处理后试图继续治疗,但大多数患者出现了反复的严重反应并停止了治疗。两名有卡铂严重全身反应史的儿童在输注前一晚和当天早晨口服1至2 mg/kg的泼尼松龙进行预处理。初始脱敏在重症监护病房(ICU)进行,使用卡铂剂量为1、2.5、5、10、25和50 mg,以1 mg/min的速度每隔15分钟输注一次。这一过程耐受性良好,其余剂量以200 mg/hr的标准速度输注。一名患者在门诊继续接受输注,没有任何困难。另一名患者耐受了第二次输注,但在第三次输注时出现了全身反应,需要停止输注并用苯海拉明治疗。在ICU重复进行脱敏,使用泼尼松龙、苯海拉明和雷尼替丁进行预处理,从0.1 mg卡铂开始,增加速度比第一个方案更慢。这一过程耐受性良好,随后的输注从1 mg剂量开始,没有不良反应。两名男孩都继续使用卡铂治疗;他们的星形细胞瘤病情稳定,临床状况良好。脱敏方案的使用使他们避免了颅脑照射,并提高了正常神经发育的机会。