老年人新诊断费城染色体阴性急性淋巴细胞白血病的治疗。

IF 1.7 4区 医学 Q3 HEMATOLOGY
Lourdes M Mendez, Daniel J DeAngelo, Marlise R Luskin
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引用次数: 0

摘要

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的频繁存在和常规化疗的有限耐受性,成人的治疗失败率和治疗相关死亡率明显更高。在这里,我们讨论了近期临床试验的数据,研究了老年人费城染色体阴性ALL初始治疗的新方法。这些试验研究了将抗cd22抗体-药物结合物inotuzumab、CD19-CD3双特异性t细胞结合物blinatumomab和BCL2抑制剂venetoclax等新型药物纳入治疗方案,其中一些研究减轻或省略了化疗。我们还讨论了同种异体干细胞移植巩固在这一人群中的作用,并强调了一线cd19定向CAR-T巩固治疗B-ALL的可能性。最后,我们讨论了对老年人ALL遗传多样性的进一步了解,包括ALL伴TP53突变、ALL伴髓系基因突变和治疗相关ALL的发生。总的来说,我们强调了老年ph阴性ALL患者的进展,患者更频繁地实现可测量残余疾病阴性完全缓解,但仍有重要的工作要做,以提高治疗的安全性以及治疗反应的深度和持久性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of Older Adults with Newly Diagnosed Philadelphia Chromosome-Negative Acute Lymphoblastic Leukemia.

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. 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 front-line CD19-directed CAR-T 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. 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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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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