Division of Hematology/Oncology, University of California, San Diego, CA.
Division of Blood and Marrow Transplantation, Moores Cancer Center, University of California, San Diego, CA.
Semin Hematol. 2020 Jul;57(3):122-129. doi: 10.1053/j.seminhematol.2020.09.001. Epub 2020 Sep 5.
Outcomes for older adults (defined here as ≥55-65 years old) with acute lymphoblastic leukemia (ALL) are poor, with long-term survival less than 20%. Pediatric chemotherapy regimens produce long-term cure rates of 80% to 90% in children and 60% to 70% in adolescents and young adults with Ph-negative ALL, however, tolerability of intensive chemotherapy becomes problematic with advanced age due to comorbidities and reduced tolerability of chemotherapy leading to high rates of treatment-related mortality. For older adults with Ph-positive ALL, BCR-ABL1-directed tyrosine kinase inhibitors in combination with corticosteroids or chemotherapy produce deep remissions with low treatment-related toxicity but optimal postremission therapy is not known. New therapeutic approaches for older adults with ALL involve integration of the novel targeted agents including monoclonal antibody-based therapy with blinatumomab and inotuzumab ozogamicin in the frontline. Ongoing studies will ideally define optimal combinations and sequencing of novel agents with or without chemotherapy, tyrosine kinase inhibitors, and/or corticosteroids to maximize efficacy while avoiding treatment-related death. Anti-CD19 chimeric antigen receptor modified T cells are a promising modality, with high rates of remission and minimal residual disease negativity achieved in early phase trials for adults with relapsed/refractory B-cell ALL but the tolerability of chimeric antigen receptor modified T cell therapies in older adults is yet to be well defined. Advances in minimal residual disease detection have helped to effectively stratify adults in complete response in terms of relapse risk and predicted relative benefit for allogeneic hematopoietic cell transplant. For older adults with ALL in complete response at high risk for relapse for whom myeloablative conditioning is predicted to result in excessive transplant-related mortality, reduced-intensity conditioning allogeneic hematopoietic cell transplant is a less toxic approach for providing a graft-versus-leukemia effect and long-term disease control.
对于患有急性淋巴细胞白血病(ALL)的老年人(这里定义为≥55-65 岁),其预后较差,长期生存率低于 20%。儿科化疗方案可使儿童中 Ph 阴性 ALL 的长期治愈率达到 80%至 90%,青少年和年轻成人中达到 60%至 70%,然而,由于合并症和化疗耐受性降低,高龄患者接受强化化疗的耐受性会出现问题,导致治疗相关死亡率较高。对于 Ph 阳性 ALL 的老年患者,BCR-ABL1 靶向酪氨酸激酶抑制剂联合皮质类固醇或化疗可产生深度缓解,治疗相关毒性低,但尚不清楚最佳缓解后治疗方法。对于 ALL 的老年患者,新的治疗方法涉及新型靶向药物的整合,包括单克隆抗体为基础的治疗药物与blinatumomab 和 inotuzumab ozogamicin 用于一线治疗。正在进行的研究理想情况下将确定新型药物的最佳组合和顺序,无论是否联合化疗、酪氨酸激酶抑制剂和/或皮质类固醇,以最大限度地提高疗效,同时避免治疗相关死亡。嵌合抗原受体修饰的 T 细胞是一种很有前途的治疗方法,在复发/难治性 B 细胞 ALL 成人的早期临床试验中,其缓解率和微小残留病阴性率很高,但嵌合抗原受体修饰的 T 细胞疗法在老年患者中的耐受性尚未得到很好的定义。微小残留病检测的进展有助于根据复发风险对完全缓解的成人进行有效分层,并预测异基因造血细胞移植的相对获益。对于完全缓解但复发风险高且预测清髓性预处理会导致移植相关死亡率过高的 ALL 老年患者,降低强度预处理异基因造血细胞移植是一种毒性较小的方法,可提供移植物抗白血病效应和长期疾病控制。