Hudson M M, Weinstein H J, Donaldson S S, Greenwald C, Kun L, Tarbell N J, Humphrey W A, Rupp C, Marina N M, Wilimas J
Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38101.
J Clin Oncol. 1993 Jun;11(6):1080-4. doi: 10.1200/JCO.1993.11.6.1080.
We report an unexpectedly high incidence of hypersensitivity to etoposide among 45 patients with newly diagnosed Hodgkin's disease treated with vinblastine, etoposide, prednisone, and doxorubicin (VEPA) plus radiation.
Twenty-three of 45 patients (51%) had one or more acute hypersensitivity reactions to etoposide administration. The 23 patients were 8 to 18 years of age (median, 15 years); 12 were males. Four patients had experienced prior allergic reactions to antibiotics or intravenous contrast media.
Hypersensitivity reactions followed the first or second dose of VEPA in most cases. The reactions occurred at a median time of 5 minutes (range, 3 to 120) from the start of the etoposide infusion. Fifteen patients reacted early (within 10 minutes), four midway through the infusion, and four after completion of the infusion. Signs and symptoms included flushing, respiratory problems, changes in blood pressure, and abdominal pain with or without nausea and vomiting. Respiratory problems included dyspnea, chest pain/tightness, bronchospasm, and cyanosis. Symptoms were alleviated by discontinuing the etoposide infusions and administering diphenhydramine and/or hydrocortisone; epinephrine was required to reverse bronchospasm in three cases. All 23 patients recovered without adverse sequelae and were rechallenged with etoposide. Fifteen patients tolerated subsequent etoposide infused at a slower rate, with antihistamine and/or corticosteroid premedication; five had recurrent hypersensitivity despite these measures. Three of these five developed similar symptoms when teniposide was substituted for etoposide. Three patients who had isolated episodes of hypotension on completion of the etoposide infusion successfully received subsequent infusions without premedication or change in infusion rate or concentration.
Despite this unexpectedly high incidence of hypersensitivity among Hodgkin's disease patients treated with etoposide, rechallenge with the drug was successful in 78% of cases.
我们报告了45例新诊断的霍奇金病患者在接受长春碱、依托泊苷、泼尼松和多柔比星(VEPA)联合放疗治疗时,对依托泊苷过敏的发生率意外地高。
45例患者中有23例(51%)在接受依托泊苷治疗时发生了一次或多次急性过敏反应。这23例患者年龄在8至18岁之间(中位数为15岁);其中12例为男性。4例患者既往曾对抗生素或静脉造影剂有过敏反应。
大多数情况下,过敏反应发生在首次或第二次使用VEPA后。反应发生的中位时间为依托泊苷输注开始后5分钟(范围为3至120分钟)。15例患者反应较早(在10分钟内),4例在输注中途出现反应,4例在输注结束后出现反应。体征和症状包括潮红、呼吸问题、血压变化以及伴有或不伴有恶心和呕吐的腹痛。呼吸问题包括呼吸困难、胸痛/胸闷、支气管痉挛和发绀。通过停止依托泊苷输注并给予苯海拉明和/或氢化可的松,症状得到缓解;3例患者需要使用肾上腺素来逆转支气管痉挛。所有23例患者均康复且无不良后遗症,并再次接受依托泊苷治疗。15例患者在使用抗组胺药和/或皮质类固醇进行预处理的情况下,以较慢的速度耐受了后续的依托泊苷输注;尽管采取了这些措施,仍有5例患者出现了复发性过敏反应。在这5例患者中,有3例在将替尼泊苷替代依托泊苷时出现了类似症状。3例在依托泊苷输注结束时出现孤立性低血压发作的患者,在没有预处理或改变输注速度或浓度的情况下,成功接受了后续输注。
尽管在接受依托泊苷治疗的霍奇金病患者中过敏发生率意外地高,但78%的病例再次使用该药物治疗成功。