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:MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?
MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
在第一线治疗期间和挽救治疗之后评估微小残留病(MRD)是急性淋巴细胞白血病(ALL)标准管理的一部分。持续或复发的MRD是最相关的预后因素之一,并识别出一组对标准化疗耐药的患者。尽管继续第一线治疗,这些患者仍有很高的复发风险。虽然干细胞移植(SCT)是一种合适的策略,但高MRD患者即使在SCT后也表现出增加的复发率。大约四分之一的成人ALL患者出现MRD失败,定义为标准诱导和巩固治疗后MRD高于0.01%。用于治疗调整的最佳时间点和MRD水平仍有争议。为了根除MRD并由此提高治愈机会,正在使用与化疗相比具有不同作用机制的新靶向化合物。这些化合物包括单克隆抗体、CAR-T 细胞和分子靶向化合物。本文讨论了决策的关键因素、可用的化合物和后续治疗。
Evaluation of minimal residual disease (MRD) during first-line treatment and after salvage therapy is part of the standard management of acute lymphoblastic leukemia (ALL). Persistent or recurrent MRD is one of the most relevant prognostic factors and identifies a group of patients with resistance to standard chemotherapy. These patients have a high risk of relapse despite continued first-line therapy. Although stem cell transplantation (SCT) is an appropriate strategy, patients with high MRD show an increased relapse rate even after SCT.
Approximately one-quarter of adult ALL patients develop an MRD failure, defined as MRD above 0. 01% after standard induction and consolidation. The best time point and level of MRD for treatment modification are matters of debate.
In order to eradicate MRD and thereby improve chances for a cure, new targeted compounds with different mechanisms of action compared to chemotherapy are being utilized. These compounds include monoclonal antibodies, chimeric antigen receptor T cells, and molecular targeted compounds. Essential factors for decision-making, available compounds, and follow-up therapies are discussed.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。