Ohno R, Tomonaga M, Kobayashi T, Kanamaru A, Shirakawa S, Masaoka T, Omine M, Oh H, Nomura T, Sakai Y
Department of Medicine, Nagoya University Branch Hospital, Japan.
N Engl J Med. 1990 Sep 27;323(13):871-7. doi: 10.1056/NEJM199009273231304.
Background. Although colony-stimulating factors have been shown to accelerate recovery from severe neutropenia after intensive chemotherapy or bone marrow transplantation, their use in acute leukemia has been controversial because in vitro they stimulate leukemic colonies as well as normal granulocyte colonies. Methods. We conducted a prospective, randomized, controlled study to determine the safety and efficacy of recombinant human granulocyte colony-stimulating factor (CSF) after a standard course of intensive therapy in 108 patients with relapsed or refractory acute leukemia (67 with acute myelogenous leukemia, 30 with acute lymphocytic leukemia, 9 in blast crisis from chronic myelogenous leukemia, and 2 with acute leukemia arising from myelodysplastic syndromes). Treatment with granulocyte CSF (200 micrograms per square meter of body-surface area per day in a 30-minute infusion) was begun two days after the end of the chemotherapy and continued until the neutrophil count rose above 1500 per cubic millimeter. Results. Treatment with granulocyte CSF accelerated the recovery of neutrophils significantly (P less than 0.01), shortening it by about a week, but it had no effect on platelet recovery. Although the incidence of febrile episodes was almost the same, documented infections were significantly less frequent in the group treated with granulocyte CSF (P = 0.028). There was no evidence that granulocyte CSF accelerated the regrowth of leukemic cells. Fifty percent of 48 patients in the CSF group who could be evaluated and 36 percent of 50 controls had complete remission. The rate of relapse was almost the same in the two groups. Conclusions. It appears that recombinant human granulocyte CSF is safe in acute leukemia, accelerating neutrophil recovery and thereby reducing the incidence of documented infection without affecting the regrowth of leukemic cells. It should be used with caution, however, pending further confirmation of these early results.
背景。尽管集落刺激因子已被证明可加速强化化疗或骨髓移植后严重中性粒细胞减少症的恢复,但其在急性白血病中的应用一直存在争议,因为在体外它们既能刺激白血病细胞集落,也能刺激正常粒细胞集落。方法。我们进行了一项前瞻性、随机、对照研究,以确定重组人粒细胞集落刺激因子(CSF)在108例复发或难治性急性白血病患者(67例急性髓性白血病、30例急性淋巴细胞白血病、9例慢性髓性白血病急变期、2例骨髓增生异常综合征所致急性白血病)接受标准疗程强化治疗后的安全性和疗效。化疗结束两天后开始用粒细胞集落刺激因子治疗(每天每平方米体表面积200微克,静脉输注30分钟),持续至中性粒细胞计数升至每立方毫米1500以上。结果。粒细胞集落刺激因子治疗显著加速了中性粒细胞的恢复(P<0.01),使其缩短约一周,但对血小板恢复无影响。尽管发热发作的发生率几乎相同,但粒细胞集落刺激因子治疗组确诊感染的频率显著较低(P = 0.028)。没有证据表明粒细胞集落刺激因子加速了白血病细胞的再生长。集落刺激因子组48例可评估患者中有50%达到完全缓解,对照组50例中有36%达到完全缓解。两组的复发率几乎相同。结论。重组人粒细胞集落刺激因子在急性白血病中似乎是安全的,可加速中性粒细胞恢复,从而降低确诊感染的发生率,且不影响白血病细胞的再生长。然而,在这些早期结果得到进一步证实时,应谨慎使用。