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快速变化时代慢性淋巴细胞白血病的个体化治疗策略

Tailored Treatment Strategies for Chronic Lymphocytic Leukemia in a Rapidly Changing Era.

作者信息

Brander Danielle, Islam Prioty, Barrientos Jacqueline C

机构信息

1 Duke University Health System, Duke Cancer Institute, Durham, NC.

2 Northwell Health Cancer Institute, Zucker School of Medicine at Hofstra/Northwell, Feinstein Institute for Medical Research, CLL Research and Treatment Program, New Hyde Park, NY.

出版信息

Am Soc Clin Oncol Educ Book. 2019 Jan;39:487-498. doi: 10.1200/EDBK_238735. Epub 2019 May 17.

DOI:10.1200/EDBK_238735
PMID:31099686
Abstract

The treatment landscape for chronic lymphocytic leukemia (CLL) is rapidly evolving, with multiple agents recently approved. They include a glycoengineered monoclonal antibody (obinutuzumab), B-cell receptor signaling inhibitors (ibrutinib, idelalisib, and duvelisib), and the BCL-2 inhibitor (venetoclax). These compounds are dramatically changing the natural course of the disease. Nonetheless, despite improved survival rates, particularly in higher-risk disease (older adults, patients with unmutated del(11q), and del(17p)/ mutated), there is still room for progress. Given the panoply of highly effective therapies commercially available, it is important to define a tailored treatment strategy for this heterogeneous condition that considers balance of treatment efficacy versus toxicity or tolerance. This article summarizes the most promising clinical advances by reviewing the data from recent clinical trials and discussing meaningful clinical endpoints, including the role of minimal residual disease assessment. The recent development of therapies targeting dysregulated pathways is revolutionary and may ultimately lead us to not only achieve prolonged remission durations but also envision the possibility of a functional cure for a larger population of patients.

摘要

慢性淋巴细胞白血病(CLL)的治疗格局正在迅速演变,最近有多种药物获批。这些药物包括一种糖基工程单克隆抗体(奥妥珠单抗)、B细胞受体信号抑制剂(伊布替尼、idelalisib和度维利塞)以及BCL-2抑制剂(维奈克拉)。这些化合物正在极大地改变该疾病的自然病程。尽管如此,尽管生存率有所提高,尤其是在高危疾病(老年患者、未突变的del(11q)患者以及del(17p)/突变患者)中,但仍有进步空间。鉴于有大量高效的商业可用疗法,为这种异质性疾病确定一种量身定制的治疗策略很重要,该策略要考虑治疗效果与毒性或耐受性之间的平衡。本文通过回顾近期临床试验的数据并讨论有意义的临床终点,包括微小残留病评估的作用,总结了最有前景的临床进展。针对失调通路的疗法的最新进展具有革命性,最终可能不仅使我们实现更长的缓解期,还能设想为更多患者实现功能性治愈的可能性。

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