Kantarjian H M, Talpaz M, Keating M J, Estey E H, O'Brien S, Beran M, McCredie K B, Gutterman J, Freireich E J
Department of Hematology, M. D. Anderson Cancer Center, Houston, Texas 77030.
Cancer. 1991 Sep 15;68(6):1201-7. doi: 10.1002/1097-0142(19910915)68:6<1201::aid-cncr2820680604>3.0.co;2-1.
In a pilot study, 32 patients with Philadelphia chromosome-positive chronic myelogenous leukemia were treated with intensive chemotherapy induction followed by interferon-alpha (IFN-A) maintenance. Intensive chemotherapy consisted of three cycles of daunorubicin 120 mg/m2 on day 1, cytarabine 80 mg/m2 daily for 10 days, vincristine 2 mg on day 1, and prednisone 100 mg daily for 5 days (DOAP). Maintenance therapy with IFN-A at a doses of 3 x 10(6) to 5 x 10(6) units/m2 daily was adjusted according to counts and toxicity. The outcome of patients was compared with a matched historic population of 64 patients treated with IFN-A alone. Overall, 60% of patients had a cytogenetic response (partial or complete) with induction chemotherapy, but only eight (25%) had a sustained cytogenetic response with IFN-A maintenance. After a median follow-up of 67 months, the 6-year survival rate of the 32 patients was 58%, compared with 36% for the matched historic group (P = 0.084). The incidence of lymphoid blastic transformation in the two groups was 25% and 48%, respectively (P = 0.10) and durable cytogenetic responses, 25% and 19%, respectively (P = 0.48). In summary, the addition of intensive chemotherapy induction to IFN-A maintenance does not improve the survival rate, incidence of lymphoid blastic transformation, or incidence of durable cytogenetic response compared with the results achieved with IFN-A therapy alone.
在一项初步研究中,对32例费城染色体阳性的慢性粒细胞白血病患者进行了强化化疗诱导,随后采用α-干扰素(IFN-A)维持治疗。强化化疗包括三个周期,第1天给予柔红霉素120 mg/m²,阿糖胞苷80 mg/m²每日1次,共10天,第1天给予长春新碱2 mg,泼尼松100 mg每日1次,共5天(DOAP方案)。根据血细胞计数和毒性情况调整IFN-A维持治疗剂量,每日3×10⁶至5×10⁶单位/m²。将这些患者的治疗结果与64例仅接受IFN-A治疗的匹配历史对照人群进行比较。总体而言,60%的患者在诱导化疗后有细胞遗传学反应(部分或完全反应),但只有8例(25%)在IFN-A维持治疗后有持续的细胞遗传学反应。中位随访67个月后,32例患者的6年生存率为58%,而匹配的历史对照组为36%(P = 0.084)。两组中淋巴细胞母细胞转化的发生率分别为25%和48%(P = 0.10),持久细胞遗传学反应的发生率分别为25%和19%(P = 0.48)。总之,与单纯IFN-A治疗的结果相比,在IFN-A维持治疗基础上加用强化化疗诱导并不能提高生存率、淋巴细胞母细胞转化的发生率或持久细胞遗传学反应的发生率。