Oyekunle A A, Kröger N, Zabelina T, Ayuk F, Schieder H, Renges H, Fehse N, Waschke O, Fehse B, Kabisch H, Zander A R
Department of Bone Marrow Transplantation, University-Hospital Hamburg-Eppendorf, Hamburg, Germany.
Bone Marrow Transplant. 2006 Jan;37(1):45-50. doi: 10.1038/sj.bmt.1705207.
We examined retrospectively 44 patients with refractory acute leukemia (acute myeloid leukemia (AML)/acute lymphoblastic leukemia=25/19) who underwent allogeneic transplantation at our center between 11/1990 and 04/2004. The median leukemic blasts was 25% and age 28 years (range, 3-56). Twenty-one patients had untreated relapse, 13 failed reinduction, eight in partial remission and two aplastic. Conditioning was myeloablative using cyclophosphamide, busulfan, total-body irradiation and etoposide (Bu/Cy/VP, n=22; TBI/Cy/VP, n=17; others, n=5) followed by marrow or peripheral blood transplant (n=23/21) from unrelated or related donors (n=28/16). All patients had graft-versus-host disease (GVHD) prophylaxis with cyclosporin and methotrexate. One patient experienced late graft failure. Severe acute-GVHD and chronic-GVHD appeared in eight and 14 patients, respectively. Thirteen patients (30%) remain alive after a median of 25.3 months (range, 2.4-134.1); with 31 deaths, mostly from relapse (n=15) and infections (n=12). Overall survival (OS) and progression-free survival (PFS) at 5 years was 28 and 26%, respectively. OS and PFS were significantly better with blasts < or =20% and time to transplant < or =1 year while transplant-related mortality was less with the use of TBI. We conclude that patients with refractory leukemia can benefit from allogeneic BMT, especially with < or =20% marrow blast.
我们回顾性研究了1990年11月至2004年4月间在本中心接受异基因移植的44例难治性急性白血病患者(急性髓细胞白血病/急性淋巴细胞白血病=25/19)。白血病原始细胞中位数为25%,年龄28岁(范围3 - 56岁)。21例患者为未治疗的复发,13例再诱导失败,8例处于部分缓解期,2例为再生障碍性贫血。预处理采用环磷酰胺、白消安、全身照射和依托泊苷进行清髓(白消安/环磷酰胺/依托泊苷,n = 22;全身照射/环磷酰胺/依托泊苷,n = 17;其他,n = 5),随后接受来自无关或相关供者的骨髓或外周血移植(n = 23/21)(无关供者/相关供者=28/16)。所有患者均接受环孢素和甲氨蝶呤预防移植物抗宿主病(GVHD)。1例患者发生晚期移植物失败。分别有8例和14例患者出现严重急性GVHD和慢性GVHD。13例患者(30%)在中位时间25.3个月(范围2.4 - 134.1个月)后仍存活;31例死亡,主要死于复发(n = 15)和感染(n = 12)。5年总生存率(OS)和无进展生存率(PFS)分别为28%和26%。原始细胞≤20%且移植时间≤1年时,OS和PFS显著更好,而使用全身照射时移植相关死亡率更低。我们得出结论,难治性白血病患者可从异基因骨髓移植中获益,尤其是骨髓原始细胞≤20%的患者。