Lee K-H, Lee J-H, Choi S-J, Lee J-H, Kim S, Seol M, Lee Y-S, Kim W-K, Seo E-J, Park C-J, Chi H-S, Lee J-S
Division of Oncology-Hematology, Department of Medicine, College of Medicine, University of Ulsan, Asan Medical Center, Seoul, Korea.
Bone Marrow Transplant. 2003 Oct;32(8):835-42. doi: 10.1038/sj.bmt.1704223.
A total of 118 consecutive adult patients with acute leukemia (78 AML, 36 ALL, and four acute mixed lineage leukemia) underwent allogeneic hematopoietic cell transplantation (HCT) after conditioning with BuCy (n=113) or a nonmyeloablative regimen of busulfan-fludarabine (n=5). After a median follow-up of 35.8 months (range, 6.4-91.0), 34 patients experienced at least one episode of leukemia relapse. Of 34 initial episodes, 14 (41%) occurred in extramedullary sites, with (n=8) or without (n=6) concomitant bone marrow involvement. The median time to relapse in the extramedullary sites was longer than that of relapse in bone marrow only (13.5 vs 6.1 months, P=0.046). Acute leukemia subtype and disease status at HCT showed an independent predictive value for overall relapse, as well as for extramedullary relapse with or without bone marrow involvement (Philadelphia chromosome positive acute leukemia vs low-risk AML, relative risk 22.68 (95% CI, 2.18-235.64); other than first CR vs first CR, relative risk 5.61 (95% CI, 1.80-17.51)), but not for bone marrow relapse. Our study suggests that there may be different pathogenetic mechanisms for bone marrow vs extramedullary relapse of acute leukemia after allogeneic HCT. The mode of relapse needs to be investigated in future reports of acute leukemia treated with allogeneic HCT.
共有118例连续的成年急性白血病患者(78例急性髓系白血病、36例急性淋巴细胞白血病和4例急性混合谱系白血病)在接受白消安-环磷酰胺(n = 113)或白消安-氟达拉滨非清髓方案(n = 5)预处理后接受了异基因造血细胞移植(HCT)。中位随访35.8个月(范围6.4 - 91.0个月)后,34例患者经历了至少一次白血病复发。在34次初始复发中,14例(41%)发生在髓外部位,伴有(n = 8)或不伴有(n = 6)骨髓受累。髓外部位复发的中位时间长于仅骨髓复发的时间(13.5个月对6.1个月,P = 0.046)。急性白血病亚型和HCT时的疾病状态对总体复发以及有无骨髓受累的髓外复发均显示出独立的预测价值(费城染色体阳性急性白血病与低危急性髓系白血病,相对危险度22.68(95%可信区间,2.18 - 235.