Barlogie Bart, Tricot Guido, Haessler Jeff, van Rhee Frits, Cottler-Fox Michele, Anaissie Elias, Waldron James, Pineda-Roman Mauricio, Thertulien Raymond, Zangari Maurizio, Hollmig Klaus, Mohiuddin Abid, Alsayed Yazan, Hoering Antje, Crowley John, Sawyer Jeffrey
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, 4301 W Markham, Little Rock, AR 72205, USA.
Blood. 2008 Jan 1;111(1):94-100. doi: 10.1182/blood-2007-06-097444. Epub 2007 Sep 25.
Myelodysplastic syndrome (MDS) is a well-recognized complication of chemotherapy for multiple myeloma (MM). Serial bone marrow metaphase examinations were performed for MM restaging in 3,077 patients undergoing high-dose therapy (HDT). MDS-associated cytogenetic abnormalities (MDS-CAs) were observed in 105 of 2,418 patients in whom cytogenetic data were available after HDT. MDS-CAs occurred transiently in 72 patients and on 3 successive occasions (persistent MDS-CAs) in 33 patients, for 10-year estimates of 4% and 2%, respectively; only 21 patients developed overt clinical MDS and 5, acute myeloblastic leukemia (AML). MDS-CA development was linked to lower CD34 yield at collection, longer time interval from MM diagnosis to HDT, older age, and lower platelet recovery after HDT; persistent MDS-CAs were predicted by CD34 yield of less than 3 x 10(6)/kg and need for more than 2 apheresis procedures. Applying a tertile frequency distribution over time to all 105 patients with MDS-CAs, its detection early after HDT was associated with longer time interval from diagnosis and low pre-HDT platelet count (likely resulting from pre-HDT damage), whereas late-onset MDS-CAs were noted among patients treated with Total Therapy 2 and Total Therapy 3 that applied post-HDT consolidation chemotherapy (suggesting possible post-HDT damage). While the risk of MDS-CAs was low and clinical MDS occurred infrequently, monitoring after post-HDT consolidation chemotherapy appears warranted.
骨髓增生异常综合征(MDS)是多发性骨髓瘤(MM)化疗公认的并发症。对3077例接受大剂量治疗(HDT)的患者进行了连续骨髓中期检查以重新分期MM。在2418例HDT后有细胞遗传学数据的患者中,105例观察到与MDS相关的细胞遗传学异常(MDS-CAs)。MDS-CAs在72例患者中短暂出现,在33例患者中连续3次出现(持续性MDS-CAs),10年估计发生率分别为4%和2%;仅21例患者发展为明显的临床MDS,5例发展为急性髓细胞白血病(AML)。MDS-CA的发生与采集时较低的CD34产量、从MM诊断到HDT的较长时间间隔、年龄较大以及HDT后较低的血小板恢复有关;持续性MDS-CAs可通过CD34产量低于3×10⁶/kg以及需要超过2次单采程序来预测。对所有105例有MDS-CAs的患者按时间进行三分位数频率分布分析,HDT后早期检测到MDS-CAs与从诊断开始的较长时间间隔和HDT前较低的血小板计数(可能由HDT前损伤导致)相关,而在接受HDT后巩固化疗的Total Therapy 2和Total Therapy 3治疗的患者中注意到迟发性MDS-CAs(提示可能存在HDT后损伤)。虽然MDS-CAs的风险较低且临床MDS很少发生,但HDT后巩固化疗后的监测似乎是必要的。