Imamura Masahiro, Shigematsu Akio
Department of Hematology, Sapporo Hokuyu Hospital, Higashi-Sapporo 6-6-5-1, 003-0006 Shiroishi-ku, Sapporo Japan.
Exp Hematol Oncol. 2015 Jul 16;4:20. doi: 10.1186/s40164-015-0015-0. eCollection 2015.
The outcomes of adult acute lymphoblastic leukemia (ALL) patients with chemotherapy or autologous hematopoietic stem cell transplantation (HSCT) are unsatisfactory. Therefore, allogeneic (allo) HSCT has been applied to those patients in first complete remission (CR1), and has shown a long-term survival rate of approximately 50 %. In terms of myeloablative conditioning (MAC) regimen, higher dose of cyclophosphamide (CY) and total body irradiation (TBI) (the standard CY + TBI) has been generally applied to allo HSCT. Other MAC regimens such as busulfan-based or etoposide-based regimens have also been used. Among those, medium-dose etoposide (ETP) in addition to the standard CY + TBI conditioning regimen appears to be promising for allo HSCT in adult ALL when transplanted in ALL patients aged under 50 years in CR1 and also in CR2, showing an excellent outcome without increasing relapse or transplant-related mortality (TRM) rates. By contrast, reduced-intensity conditioning (RIC) regimens have also been applied to adult ALL patients and favorable outcomes have been obtained; however, relapse and TRM rates remain high. Therefore, an allo HSCT conditioning regimen which deserves further study for adult ALL patients aged under 50 years in CR1 and CR2 appears to be medium-dose ETP + CY + TBI and RIC is suitable for patients aged over 50 years or for younger patients with comorbid conditions. On the contrary, new therapeutic strategies for adult ALL patients are increasingly utilized with better outcomes; namely, various tyrosine kinase inhibitors for Philadelphia chromosome (Ph)-positive ALL, human leukocyte antigen-haploidentical HSCT, and pediatric-inspired regimens for Ph-negative ALL. Therefore, the optimal treatment modality should be selected considering patient's age, Ph-positivity, donor availability, risk classification, efficacy, and safety.
采用化疗或自体造血干细胞移植(HSCT)治疗的成人急性淋巴细胞白血病(ALL)患者的预后并不理想。因此,异基因(allo)HSCT已应用于那些首次完全缓解(CR1)的患者,并显示出约50%的长期生存率。就清髓性预处理(MAC)方案而言,较高剂量的环磷酰胺(CY)和全身照射(TBI)(标准的CY + TBI)已普遍应用于allo HSCT。其他MAC方案,如基于白消安或依托泊苷的方案也已被使用。其中,除标准的CY + TBI预处理方案外,中等剂量的依托泊苷(ETP)对于年龄在50岁以下处于CR1期和CR2期的成人ALL患者进行allo HSCT似乎很有前景,在不增加复发率或移植相关死亡率(TRM)的情况下显示出良好的结果。相比之下,减低强度预处理(RIC)方案也已应用于成人ALL患者并获得了良好的结果;然而,复发率和TRM仍然很高。因此,对于年龄在50岁以下处于CR1期和CR2期的成人ALL患者,一种值得进一步研究的allo HSCT预处理方案似乎是中等剂量ETP + CY + TBI,而RIC适用于年龄超过50岁的患者或有合并症的年轻患者。相反,成人ALL患者的新治疗策略越来越多地被采用并取得了更好的结果;即,用于费城染色体(Ph)阳性ALL的各种酪氨酸激酶抑制剂、人类白细胞抗原半相合HSCT以及用于Ph阴性ALL的儿童启发式方案。因此,应根据患者的年龄、Ph阳性状态、供体可用性、风险分类、疗效和安全性来选择最佳治疗方式。