Kiehl Michael G, Kraut Ludwig, Schwerdtfeger Rainer, Hertenstein Bernd, Remberger Mats, Kroeger Nicolaus, Stelljes Mathias, Bornhaeuser Martin, Martin Hans, Scheid Christoph, Ganser Arnold, Zander Axel R, Kienast Joachim, Ehninger Gerhard, Hoelzer Dieter, Diehl Volker, Fauser Axel A, Ringden Olle
Clinic for Bone Marrow Transplantation and Hematology/Oncology, Dr-Ottmar-Kohler-Strasse 2, 55743 Idar-Oberstein, Germany.
J Clin Oncol. 2004 Jul 15;22(14):2816-25. doi: 10.1200/JCO.2004.07.130.
The role of unrelated allogeneic stem-cell transplantation in acute lymphoblastic leukemia (ALL) patients is still not clear, and only limited data are available from the literature. We analyzed factors affecting clinical outcome of ALL patients receiving a related or unrelated stem-cell graft from matched donors.
The total study population was 264 adult patients receiving a myeloablative allogeneic stem-cell transplant for ALL at nine bone marrow transplantation centers between 1990 and 2002. Of these, 221 patients receiving a matched related or unrelated graft were analyzed. One hundred forty-eight patients received transplantation in complete remission; 62 patients were in relapse; and 11 patients were refractory to chemotherapy before transplant. Fifty percent of patients received bone marrow, and 50% received peripheral blood stem cell from a human leukocyte antigen-identical related (n = 103), or matched unrelated (n = 118) donor.
Disease-free survival (DFS) at 5 years was 28%, with 76 patients (34%) still alive (2.2 to 103 months post-transplantation), and 145 deceased (65 relapses, transplant-related mortality, 45%). We observed an advantage regarding DFS in favor of patients receiving transplantation during their first complete remission (CR) in comparison with patients receiving transplantation in or after second CR (P =.014) or who relapsed (P <.001). We observed a clear trend toward improved survival in favor of B-lineage ALL patients compared with T-lineage ALL patients (P =.052), and Philadelphia chromosome-positive patients had no poorer outcome than Philadelphia chromosome-negative patients. Total-body irradiation-based conditioning improved DFS in comparison with busulfan (P =.041).
Myeloablative matched related or matched unrelated allogeneic hematopoietic stem-cell transplantation in ALL patients should be performed in first CR.
无关供者异基因干细胞移植在急性淋巴细胞白血病(ALL)患者中的作用仍不明确,且文献中仅有有限的数据。我们分析了影响接受来自匹配供者的相关或无关干细胞移植的ALL患者临床结局的因素。
研究总人群为1990年至2002年间在9个骨髓移植中心接受清髓性异基因干细胞移植治疗ALL的264例成年患者。其中,对221例接受匹配的相关或无关移植物的患者进行了分析。148例患者在完全缓解期接受移植;62例患者处于复发期;11例患者在移植前对化疗耐药。50%的患者接受骨髓移植,50%的患者接受来自人类白细胞抗原相同的相关供者(n = 103)或匹配的无关供者(n = 118)的外周血干细胞移植。
5年无病生存率(DFS)为28%,76例患者(34%)仍存活(移植后2.2至103个月),145例患者死亡(65例复发,移植相关死亡率45%)。我们观察到,与在第二次完全缓解期或之后接受移植的患者(P = 0.014)或复发患者(P < 0.001)相比,在首次完全缓解期(CR)接受移植的患者在DFS方面具有优势。与T系ALL患者相比,我们观察到B系ALL患者有明显的生存改善趋势(P = 0.052),且费城染色体阳性患者的结局并不比费城染色体阴性患者差。与白消安相比,基于全身照射的预处理改善了DFS(P = 0.041)。
ALL患者应在首次完全缓解期进行清髓性匹配相关或匹配无关异基因造血干细胞移植。