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造血干细胞移植在费城染色体样急性淋巴细胞白血病中不断演变的作用:从高危标准治疗到精准策略

英文原题:The Evolving Role of Hematopoietic Stem Cell Transplantation in Philadelphia-like Acute Lymphoblastic Leukemia: From High-Risk Standard to Precision Strategies.

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The Evolving Role of Hematopoietic Stem Cell Transplantation in Philadelphia-like Acute Lymphoblastic Leukemia: From High-Risk Standard to Precision Strategies.

PubMed 2025/10/05(内容时间) Cancers (Basel) Q2 · IF 4.8(JCR 2025)

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研究概要

HSCT 仍是特定 Ph-like ALL 患者的重要治疗选择,尤其是那些分子风险特征差或 MRD 持续阳性的患者。

中文摘要

费城样急性淋巴细胞白血病(Ph-like ALL)是B细胞急性淋巴细胞白血病的一种高危亚型,其基因表达谱与BCR::ABL1阳性白血病相似,但缺乏BCR::ABL1融合基因。该病常伴有激酶活化相关改变,如CRLF2重排、JAK-STAT通路突变及ABL类融合。Ph-like ALL患者接受常规化疗后通常预后不佳,凸显了加强治疗和靶向治疗的必要性。

本综述总结造血干细胞移植(HSCT)治疗Ph-like ALL的现有证据。研究者分析了回顾性队列研究、登记数据和正在开展的临床试验,重点考察移植适应证、分子风险分层、可测量残留病(MRD)状态、移植时机及移植后策略。

回顾性数据提示,对于具有高危分子病变或诱导治疗结束时MRD阳性的患者,在首次完全缓解(CR1)时进行HSCT可能改善生存。然而,缺乏针对Ph-like ALL的前瞻性数据,限制了明确结论的形成。移植后复发仍是挑战;酪氨酸激酶抑制剂或JAK抑制剂作为移植后维持治疗等新策略正在探索中。嵌合抗原受体(CAR)T细胞等新兴免疫疗法可能改变治疗格局,并有望影响移植适应证。

对于经筛选的Ph-like ALL患者,尤其是分子风险特征不良或MRD持续阳性的患者,HSCT仍是重要治疗选择。但仍需进一步开展前瞻性研究,评估CR1期移植的适应证,以及将移植与靶向和免疫治疗策略结合的潜力。基于基因组分析和MRD评估制定个体化治疗方案,对改善这一高危亚型患者的结局至关重要。

展开英文摘要原文

Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL) is a high-risk subtype of B-cell ALL characterized by a gene expression profile similar to BCR::ABL1-positive leukemia, but lacking the BCR::ABL1 fusion gene. It is frequently associated with kinase-activating alterations, such as CRLF2 rearrangements, JAK-STAT pathway mutations, and ABL-class fusions. Patients with Ph-like ALL typically experience poor outcomes with conventional chemotherapy, underscoring the need for intensified and targeted therapeutic approaches.

This review summarizes current evidence regarding the role of hematopoietic stem cell transplantation (HSCT) in patients with Ph-like ALL. We analyzed retrospective cohort studies, registry data, and ongoing clinical trials, focusing on transplant indications, molecular risk stratification, measurable residual disease (MRD) status, timing of transplant, and post-transplant strategies.

Retrospective data suggest that HSCT in first complete remission (CR1) may improve survival in patients with high-risk molecular lesions or MRD positivity at the end of induction. However, the lack of prospective data specific to Ph-like ALL limits definitive conclusions. Post-transplant relapse remains a challenge, and novel strategies, including the use of tyrosine kinase inhibitors or JAK inhibitors as post-HSCT maintenance therapy, are being explored. Emerging immunotherapies, such as chimeric antigen receptor (CAR) T cells, may reshape the therapeutic landscape and potentially alter the indications for transplantation.

HSCT remains a crucial therapeutic option for selected patients with Ph-like ALL, particularly those with poor molecular risk features or persistent MRD. However, further prospective studies are needed to evaluate the indication for HSCT in CR1 and the potential integration of transplantation with targeted and immunotherapeutic strategies. Personalized treatment approaches based on genomic profiling and MRD assessment are essential to improve outcomes in this high-risk subset.

论文信息

作者
Molica M、Simio C、De Fazio L、Alati C、Rossi M、Martino M
第一作者单位
Department of Hematology-Oncology, Azienda Universitaria Ospedaliera Renato Dulbecco, 88100 Catanzaro, Italy.Italy
通讯作者单位
Hematology and Stem Cell Transplantation and Cellular Rerapies Unit (CTMO), Department of Hemato-Oncology and Radiotherapy, Grande Ospedale Metropolitano "Bianchi-Melacrino-Morelli", Presidio Morelli, 89128 Reggio Calabria, Italy.Italy
文献类型
综述
期刊
Cancers2025 Oct 5
原文标识
PubMed 41097763 · DOI 10.3390/cancers17193237