Narimatsu Hiroto, Iino Masaki, Ichihashi Takuji, Yokozawa Toshiya, Hayakawa Masaya, Kiyoi Hitoshi, Takeo Takaaki, Sawamoto Akiyo, Iida Hiroatsu, Tsuzuki Motohiro, Yanada Masamitsu, Naoe Tomoki, Suzuki Ritsuro, Sugiura Isamu
Department of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.
Int J Hematol. 2008 Sep;88(2):154-158. doi: 10.1007/s12185-008-0108-1. Epub 2008 Jun 17.
To examine the prognostic significance of minimal residual disease (MRD) in t(8;21) acute myeloid leukemia (AML), 96 bone marrow samples from 26 Japanese patients in complete remission (CR) were analyzed regarding the RUNX1/MTG8 transcript using real-time reverse transcriptase polymerase chain reaction assay. All patients were treated with intensive chemotherapy. The median copy number of the RUNX1/MTG8 transcript, measured after each treatment course decreased over time. However, an increase in the MRD level was documented in three patients after the second consolidation, and all of them subsequently relapsed. The relapse-free survival (RFS) did not differ between the patients whose MRD levels were below or above 1,000 copies/microg after the first consolidation, with respective 2-year rates of 62 and 86% (P = 0.21). With respect to the MRD level after induction therapy, our data also failed to show any favorable effect of a lower MRD on RFS. Although these findings need to be confirmed with a larger number of patients, our data indicate that the MRD level at a given time during the early course in CR does not predict the outcome in Japanese patients.
为研究微小残留病(MRD)在t(8;21)急性髓系白血病(AML)中的预后意义,我们采用实时逆转录聚合酶链反应分析法,对26例处于完全缓解(CR)期的日本患者的96份骨髓样本进行了RUNX1/MTG8转录本分析。所有患者均接受了强化化疗。每个疗程后测得的RUNX1/MTG8转录本的中位拷贝数随时间下降。然而,3例患者在第二次巩固治疗后出现MRD水平升高,随后均复发。首次巩固治疗后MRD水平低于或高于1000拷贝/μg的患者,其无复发生存期(RFS)无差异,2年发生率分别为62%和86%(P = 0.21)。关于诱导治疗后的MRD水平,我们的数据也未能显示较低的MRD对RFS有任何有利影响。尽管这些发现需要更多患者来证实,但我们的数据表明,CR期早期特定时间的MRD水平并不能预测日本患者的预后。