肿瘤细胞治疗研究
英文原题:Treatment of Older Adults with Newly Diagnosed Philadelphia Chromosome-Negative Acute Lymphoblastic Leukemia.
Treatment of Older Adults with Newly Diagnosed Philadelphia Chromosome-Negative Acute Lymphoblastic Leukemia.
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大约一半新诊断的急性淋巴细胞白血病(ALL)病例发生在成人中,但由于不良疾病生物学特征的频繁存在以及常规化疗耐受性有限,成人的治疗失败率和治疗相关死亡率显著更高。概要:在此,我们讨论近期临床试验的数据,这些试验研究了费城染色体阴性ALL老年患者初始治疗的新方法。这些试验探索了将新型药物纳入治疗方案,包括抗CD22抗体-药物偶联物inotuzumab、CD19-CD3双特异性T细胞衔接器blinatumomab以及BCL2抑制剂venetoclax,部分研究减弱或省略了化疗。我们还讨论了异基因干细胞移植巩固治疗在该人群中的作用,并强调了前线CD19定向CAR-T 细胞疗法巩固治疗B-ALL的可能性。最后,我们讨论了对老年成人ALL遗传多样性的进一步理解,包括TP53突变ALL、伴髓系基因突变ALL以及治疗相关ALL的发生。关键信息:总体而言,我们强调了Ph阴性ALL老年患者的进展,患者更频繁地达到可测量残留病阴性的完全缓解,但在改善治疗安全性以及治疗反应的深度和持久性方面仍有大量工作要做。
BACKGROUND: Approximately half of newly diagnosed cases of acute lymphoblastic leukemia (ALL) occur in adults, but adults experience significantly higher rates of treatment failure and treatment-related mortality due to frequent presence of adverse disease biology and limited tolerability of conventional chemotherapy. SUMMARY: Here, we discuss recent data from clinical trials investigating new approaches for initial treatment of Philadelphia chromosome-negative ALL in older adults. These trials investigate the incorporation of novel agents including the anti-CD22 antibody-drug conjugate inotuzumab, the CD19-CD3 bi-specific T-cell engager blinatumomab, and the BCL2 inhibitor venetoclax into treatment regimens, with some studies attenuating or omitting chemotherapy. We also discuss the role of allogeneic stem cell transplantation consolidation for this population and highlight the possibility of frontline CD19-directed chimeric antigen receptor T-cell therapy consolidation approaches for B-ALL. Finally, we discuss improved understanding of the genetic diversity of ALL in older adults including occurrence of ALL with TP53 mutation, ALL with myeloid gene mutations, and therapy-related ALL. KEY MESSAGE: Overall, we highlight progress for older adults with Ph-negative ALL with patients more frequently achieving a measurable residual disease-negative complete remission, but significant work remains to improve the safety of treatment as well as the depth and durability of treatment response.
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