De Witte T, Zwaan F, Hermans J, Vernant J, Kolb H, Vossen J, Lönnqvist B, Beelen D, Ferrant A, Gmür J
University Hospital Nijmegen, The Netherlands.
Br J Haematol. 1990 Feb;74(2):151-5. doi: 10.1111/j.1365-2141.1990.tb02558.x.
This retrospective survey of the EBMT Leukaemia Working Party describes 78 patients with myelodysplasia (MDS) or secondary acute myelogenous leukaemia (sAML) who received an allogeneic bone marrow transplant (BMT). The status of underlying disease at the time of transplantation was prognostic for the 2-year disease-free survival. Thirty-four patients received intensive chemotherapy prior to the conditioning for BMT. The 2-year disease-free survival was 60% for the 16 patients transplanted in complete remission. The results were significantly less favourable for those with more advanced disease who only partially responded to prior intensive chemotherapy (2-year disease-free survival: 18%) while none of those who either relapsed or were resistant to chemotherapy survived BMT for 2 years. Forty-four patients had not received any prior intensive chemotherapy. The disease-free survival at 2 years after BMT was 58 +/- 19% when a patient was transplanted for refractory anaemia (RA(S], 74 +/- 14% for refractory anaemia with excess of blasts (RAEB), 50 +/- 16% for RAEB in transformation (RAEBt), and 18 +/- 11% for secondary AML. Allogeneic BMT can therefore be considered as curative treatment for patients with MDS. Patients with sAML who have a histocompatible donor should be given chemotherapy intensive enough to induce complete remission. If this is achieved these individuals have a prognosis comparable to those with de novo AML in first remission after BMT.
欧洲血液与骨髓移植协会(EBMT)白血病工作组的这项回顾性调查描述了78例接受异基因骨髓移植(BMT)的骨髓增生异常综合征(MDS)或继发性急性髓系白血病(sAML)患者。移植时潜在疾病的状态对2年无病生存率具有预后意义。34例患者在进行BMT预处理前接受了强化化疗。16例在完全缓解状态下接受移植的患者2年无病生存率为60%。对于疾病进展更严重且对先前强化化疗仅部分缓解的患者,结果明显较差(2年无病生存率:18%),而那些复发或对化疗耐药的患者无一例BMT后存活2年。44例患者未接受任何先前的强化化疗。BMT后2年,难治性贫血(RA[S])患者的无病生存率为58±19%,难治性贫血伴原始细胞增多(RAEB)患者为74±14%,转化中的RAEB(RAEBt)患者为50±16%,继发性AML患者为18±11%。因此,异基因BMT可被视为MDS患者的治愈性治疗方法。有组织相容性供者的sAML患者应接受足够强度的化疗以诱导完全缓解。如果实现了完全缓解,这些个体的预后与BMT后首次缓解的初发AML患者相当。