Benz G, Gmür J, Gubler J
Departement für Innere Medizin, Medizinische Klinik A, Universitätsspital Zürich.
Schweiz Med Wochenschr. 1994 Feb 5;124(5):186-92.
Neutropenic typhlitis (NPT) was observed in 4 of 5 adult patients with acute leukemia treated with etoposide (VP16; 100 mg/m2/d for 6 days) and high-dose cytosine-arabinoside (HD ARAC, 2 g/m2 twice daily for 6 days) in a period of 11 months. One additional patient developed NPT after combination therapy with amsacrine (mAMSA, 120 mg/m2/d for 5 days) and etoposide (80 mg/m2/d for 5 days) during the same period. These 5 cases of NPT meant a drastic rise in the incidence of NPT at our institution, where a careful retrospective review of the charts of the 128 adult patients with leukemia treated during the preceding 5 years revealed only one case of NPT. Nonsurgical treatment led to recovery in all cases. No recurrence of NPT was observed during 3 further courses of aplasia with the use of selective (2 patients) or complete (1 patient) bowel decontamination. Etoposide may potentiate the gastrointestinal toxicity of high-dose cytosine-arabinoside with a higher incidence of NPT.
在11个月的时间里,5例接受依托泊苷(VP16;100mg/m²/天,共6天)和大剂量阿糖胞苷(HD ARAC,2g/m²,每日2次,共6天)治疗的成年急性白血病患者中有4例出现了中性粒细胞减少性盲肠炎(NPT)。同期,另有1例患者在接受安吖啶(mAMSA,120mg/m²/天,共5天)和依托泊苷(80mg/m²/天,共5天)联合治疗后发生了NPT。这5例NPT意味着我们机构NPT的发病率急剧上升,在此之前,对前5年治疗的128例成年白血病患者的病历进行仔细回顾性审查时仅发现1例NPT。所有病例均采用非手术治疗后康复。在使用选择性(2例患者)或完全(1例患者)肠道去污进行的3个再生障碍疗程中,未观察到NPT复发。依托泊苷可能会增强大剂量阿糖胞苷的胃肠道毒性,导致NPT的发生率更高。