Schmitt K, Zoubek A, Schwarz R, Tulzer G, Koller E, Krieger O, Lutz D, Gadner H
Children's Hospital, Vienna, Austria.
Med Pediatr Oncol. 1996 Apr;26(4):254-7. doi: 10.1002/(SICI)1096-911X(199604)26:4<254::AID-MPO6>3.0.CO;2-I.
We report on two girls, 3 and 13 years old, with acute promyelocytic leukemia (APL) who were successfully treated with all-trans retinoic acid (ATRA) 45 mg/m2/day. "Retinoic acid syndrome" was prevented with short-time treatment of high dose (4 x 1.5 g/m2) cytarabine. This regimen was well tolerated, although both children were critically ill. They achieved a complete remission confirmed by light microscopy, but reverse transcriptase polymerase chain reaction remained positive after ATRA, underlining the need of further chemotherapy.
我们报告了两名分别为3岁和13岁的急性早幼粒细胞白血病(APL)女童,她们接受了全反式维甲酸(ATRA)45 mg/m²/天的治疗并取得成功。通过短期高剂量(4×1.5 g/m²)阿糖胞苷治疗预防了“维甲酸综合征”。尽管两名患儿病情都很危急,但该治疗方案耐受性良好。她们通过光学显微镜检查证实达到完全缓解,但在接受ATRA治疗后逆转录酶聚合酶链反应仍为阳性,这突出表明需要进一步化疗。