CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Breaching the Blood-Brain Barrier: Evolving Strategies for Central Nervous System Disease in Adult Acute Lymphoblastic Leukemia.
Breaching the Blood-Brain Barrier: Evolving Strategies for Central Nervous System Disease in Adult Acute Lymphoblastic Leukemia.
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成人急性淋巴细胞白血病(ALL)的中枢神经系统(CNS)受累仍是治疗失败和长期生存的关键决定因素。本综述为成人ALL中CNS疾病的诊断、风险分层、预防和治疗提供了全面的、基于证据的框架,重点关注免疫治疗为基础和减少化疗的方案所带来的不断演变的挑战,并介绍了我们机构针对CNS导向治疗的方法。
现代CNS预防策略将鞘内化疗与可穿透CNS的全身性药物相结合,已显著降低CNS复发率,但诊断和治疗方面的局限性依然存在。blinatumomab和inotuzumab ozogamicin等免疫疗法的日益广泛应用改善了全身性疾病控制,而在此背景下CNS复发越来越受到关注,尤其是在经过大量既往治疗的患者中。这一模式可能反映了多种因素,包括CNS穿透有限、疾病控制改善后使先前亚临床CNS受累得以显现,以及复发/难治性疾病的高危生物学特征。相比之下,靶向CD19的CAR-T 细胞疗法已在CNS疾病中显示出有意义的活性,而针对白血病 trafficking 通路和IL-15信号传导的研究性策略在临床前研究中提供了额外的希望。随着成人ALL治疗向减少化疗的方案转变,关于CNS腔内疾病控制的新担忧已经出现。持久缓解将需要将严格的鞘内预防、风险适应性的全身治疗以及能够穿透CNS微环境的新型药物整合到每一个治疗方案中。
PURPOSE OF REVIEW: Central nervous system (CNS) involvement in adult acute lymphoblastic leukemia (ALL) remains a critical determinant of treatment failure and long-term survival. This review provides a comprehensive, evidence-based framework for the diagnosis, risk stratification, prophylaxis, and treatment of CNS disease in adult ALL, with emphasis on the evolving challenges introduced by immunotherapy-based and chemotherapy-sparing regimens and presents our institutional approach to CNS-directed therapy. RECENT FINDINGS: Modern CNS prophylaxis combining intrathecal chemotherapy with CNS-penetrating systemic agents has dramatically reduced CNS relapse rates, yet diagnostic and therapeutic limitations persist. The increasing use of immunotherapies, such as blinatumomab and inotuzumab ozogamicin, has improved systemic disease control, while CNS relapse is increasingly recognized in this context, particularly among heavily pretreated patients.
This pattern likely reflects multiple factors, including limited CNS penetration, improved disease control that unmasks previously subclinical CNS involvement, and the high-risk biology of relapsed/refractory disease. In contrast, CD19-directed CAR T-cell therapies have demonstrated meaningful activity in CNS disease, while investigational strategies targeting leukemic trafficking pathways and IL-15 signaling offer additional preclinical promise.
As adult ALL treatment has shifted toward chemotherapy-sparing regimens, new concerns have emerged regarding disease control within the CNS compartment. Durable remission will require integration of rigorous intrathecal prophylaxis, risk-adapted systemic therapy, and novel agents capable of penetrating the CNS microenvironment into every treatment algorithm.
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