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作者用全反式维甲酸(ATRA)治疗55例急性早幼粒细胞白血病(APL),14例出现白细胞增多症,发生率为25.4%,其中外周血白细胞高限在20×10 ̄9/L~50×10 ̄9/L之间5例,单用ATRA治疗,4例获完全缓解(80%);白细胞高限大于50×10 ̄9/L9例,采用ATRA与三尖杉酯碱或羟基脲联合化疗,8例获完全缓解(88.9%)。另外,在9例白细胞高限大于50×10 ̄9/L的病例中,5例出现白细胞滞留综合征,经治疗后4例滞留症状消失。表明ATRA与化疗相结合,对ATRA治疗期间出现的白细胞增多症是一种有效的措施,可以减低早期死亡率。
The authors treated 55 cases of acute promyelocytic leukemia (APL) with all-trans retinoic acid (ATRA), and 14 cases had leukocytosis with an incidence of 25.4%, of which the high limit of peripheral blood leukocytes was 20 x 10 ~ 9 Five patients were between /L and 50×10 ̄9/L. After treatment with ATRA alone, complete remission (80%) was achieved in 4 patients; leukocyte high limit was greater than 50×10 ̄9/L9, and ATRA and harringtonine were used. Alkali or hydroxyurea combined with chemotherapy, 8 cases were completely relieved (88.9%). In addition, in 9 cases with a leukocyte high limit greater than 50×10 ̄ 9/L, 5 patients had leukocyte retention syndrome. After treatment, the retention symptoms disappeared in 4 patients. It was shown that combining ATRA with chemotherapy is an effective measure for the leukocytosis that occurs during ATRA treatment and can reduce early mortality.