Schmiegelow K, Pulczynska M K
Department of Pediatrics, University Hospitals, Copenhagen, Denmark.
Am J Pediatr Hematol Oncol. 1990 Winter;12(4):462-7. doi: 10.1097/00043426-199024000-00010.
In a retrospective population-based study of 122 children with non-B-cell acute lymphoblastic leukemia (ALL), we analyzed the relation between risk of relapse and the degree of leukopenia achieved during oral methotrexate (MTX) and 6-mercaptopurine (6MP) maintenance chemotherapy (MT). After a median follow-up of 62 months for patients still in remission, 43 patients had relapsed (including 28 bone marrow relapses). Patients with a mean white blood cell count during MT (mWBCMT) of less than or equal to 3.5 x 10(9)/L had a significantly lower risk of hematological relapse (p = 0.007) as well as of any relapse (p = 0.02) compared to patients with higher mWBCMT. The clinical advantage of leukopenia could be demonstrated for all risk groups and was not explained by differences in year of diagnosis, gender, age, and white blood cell count at diagnosis, or the prescribed dose of MTX and 6MP. Although prospective studies are needed to establish the benefit of upward dose adjustments to achieve leukopenia, these results indicate a clinical advantage of keeping WBCs low during MT.
在一项基于人群的回顾性研究中,我们纳入了122例非B细胞急性淋巴细胞白血病(ALL)患儿,分析了口服甲氨蝶呤(MTX)和6-巯基嘌呤(6MP)维持化疗(MT)期间达到的白细胞减少程度与复发风险之间的关系。在对仍处于缓解期的患者进行了62个月的中位随访后,43例患者复发(包括28例骨髓复发)。与平均白细胞计数(mWBCMT)较高的患者相比,MT期间mWBCMT小于或等于3.5×10⁹/L的患者血液学复发风险显著降低(p = 0.007),任何复发风险也显著降低(p = 0.02)。白细胞减少的临床优势在所有风险组中均得到证实,且不能用诊断年份、性别、年龄、诊断时白细胞计数或MTX和6MP的规定剂量差异来解释。尽管需要进行前瞻性研究来确定上调剂量以实现白细胞减少的益处,但这些结果表明在MT期间保持白细胞低水平具有临床优势。