Gehr Family Center for Leukemia Research, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA, USA.
Curr Treat Options Oncol. 2021 Jun 7;22(7):63. doi: 10.1007/s11864-021-00860-1.
Acute lymphoblastic leukemia (ALL) in adults is associated with poor outcomes as compared to children when treated with chemotherapy, leading to a considerably inferior cure rate. Historically, consolidation with allogeneic hematopoietic cell transplant (alloHCT) was routinely recommended for eligible adults with ALL in first complete remission (CR1) if a donor was available, since randomized studies showed superiority over continuing chemotherapy. With the increasing use of pediatric-inspired frontline regimens in young adults with ALL and the availability of novel salvage agents for relapsed/refractory B-cell ALL that have high potential in inducing a second CR, the role of early alloHCT in the treatment paradigm for ALL needs to be reevaluated, and the decision should be individualized for each patient. Simultaneously, alloHCT has evolved considerably lately, and historical randomized studies that have proven the benefit of alloHCT in adults with ALL in CR1 did not included the increasing use of reduced intensity conditioning and haploidentical transplants, and therefore, data may not entirely apply. Nowadays, detectable minimal residual disease (MRD) is the most prognostic determinant of ALL outcome and should be a major consideration in the decision to perform alloHcT in CR1. Nonetheless, other biological and clinical factors remain relevant and can support the complex decision-making. Such factors include high-risk leukemia genetics, the type of administered chemotherapy regimen and the ability of the patient to tolerate all key components of the regimen, and the availability of effective salvage therapies that allow alloHCT to be performed in CR2 in case of relapse after chemotherapy.
与儿童相比,成人急性淋巴细胞白血病(ALL)在接受化疗治疗时预后较差,导致治愈率明显较低。在历史上,如果有供体,在首次完全缓解(CR1)时,适合 ALL 的成人患者通常建议巩固异基因造血细胞移植(alloHCT),因为随机研究显示其优于继续化疗。随着在 ALL 年轻成人中越来越多地使用基于儿科的一线方案以及新型挽救性药物在复发/难治性 B 细胞 ALL 中的应用,这些药物在诱导第二次完全缓解方面具有很高的潜力,alloHCT 在 ALL 治疗模式中的作用需要重新评估,并且应根据每个患者的具体情况进行个体化决策。同时,alloHCT 最近也有了很大的发展,并且在 CR1 中已经证明了 alloHCT 对 ALL 成人有益的历史随机研究并未包括减少强度预处理和半相合移植的日益使用,因此,数据可能不完全适用。如今,可检测的微小残留病(MRD)是 ALL 预后的最主要决定因素,并且应该是决定在 CR1 中进行 alloHcT 的主要考虑因素。尽管如此,其他生物学和临床因素仍然相关,并可以支持复杂的决策制定。这些因素包括高风险白血病遗传学、所给予的化疗方案类型以及患者耐受方案所有关键成分的能力,以及在化疗后复发时可进行 alloHCT 的有效挽救性治疗的可用性。