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限时联合治疗方案在慢性淋巴细胞白血病中的应用:实现药物假期的有前途策略。

Time-limited, Combined Regimen in Chronic Lymphocytic Leukemia: A Promising Strategy to Achieve a Drug Holiday.

机构信息

Pukou CLL Center, Pukou Division of Jiangsu Province Hospital, Nanjing, 211800, China.

Department of Hematology, the First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, 210029, China.

出版信息

Curr Med Sci. 2021 Jun;41(3):431-442. doi: 10.1007/s11596-021-2385-3. Epub 2021 Jun 28.

DOI:10.1007/s11596-021-2385-3
PMID:34181208
Abstract

Chemoimmunotherapy (CIT) is defined as standard first line treatment for chronic lymphocytic leukemia (CLL) patients while patients with unfavorable biological characteristics such as unmutated immunoglobulin heavy chain (UM-IGHV) and TP53 aberration failed to benefit from it. The emergency of the small molecular targeted agents including Bruton's tyrosine kinase (BTK) inhibitor (BTKi) leads to a brand-new era, from a CIT to a chemo-free era in CLL. However, the treatment of target agents is not enough to attain a deep remission and high rate of complete remission (CR), especially in patients with high risks. The long duration brought about problems, such as cost, drug resistance and toxicity. To benefit CLL in progression free survival (PFS) and long-term remission, exploration of time-limited therapies, mainly with BTKi plus CIT and BCL2i based combination therapy has become a mainstream in clinical trials. The time-limited combination therapy shed light on the promising potentiality to attain sustainable deep remission and partly overcame the risk factors, although long term follow-up is required to consolidate the conclusion. In this review, we intend to introduce key results of clinical trials with combination therapy, discuss the achievements and limitations and put forward future direction for clinical trial design in this field.

摘要

化疗免疫治疗(CIT)被定义为慢性淋巴细胞白血病(CLL)患者的标准一线治疗,而具有不利生物学特征的患者,如未突变的免疫球蛋白重链(UM-IGHV)和 TP53 异常,未能从中受益。小分子靶向药物的出现,包括布鲁顿酪氨酸激酶(BTK)抑制剂(BTKi),开创了一个全新的时代,CLL 从 CIT 到无化疗时代。然而,靶向药物的治疗还不足以达到深度缓解和高完全缓解(CR)率,尤其是在高风险患者中。治疗时间长带来了成本、耐药性和毒性等问题。为了使 CLL 在无进展生存期(PFS)和长期缓解中获益,探索限时治疗,主要是 BTKi 联合 CIT 和 BCL2i 的联合治疗,已成为临床试验的主流。限时联合治疗为实现可持续深度缓解提供了有希望的潜力,并在一定程度上克服了风险因素,尽管需要长期随访来巩固结论。在这篇综述中,我们旨在介绍联合治疗临床试验的关键结果,讨论其成就和局限性,并为该领域临床试验设计提出未来方向。

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本文引用的文献

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Chemotherapy-free frontline therapy for CLL: is it worth it?CLL 一线治疗无化疗:值得吗?
Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):24-32. doi: 10.1182/hematology.2020000085.
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A fixed-duration, measurable residual disease-guided approach in CLL: follow-up data from the phase 2 ICLL-07 FILO trial.CLL 中采用固定时间、可衡量的残留病灶指导治疗方法:来自 2 期 ICLL-07 FILO 试验的随访数据。
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Prediction of Outcome in Patients With Chronic Lymphocytic Leukemia Treated With Ibrutinib: Development and Validation of a Four-Factor Prognostic Model.
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伊布替尼治疗的慢性淋巴细胞白血病患者预后的预测:建立并验证一个四因素预后模型。
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Venetoclax Plus Rituximab in Relapsed Chronic Lymphocytic Leukemia: 4-Year Results and Evaluation of Impact of Genomic Complexity and Gene Mutations From the MURANO Phase III Study.维奈托克联合利妥昔单抗治疗复发慢性淋巴细胞白血病:III 期 MURANO 研究的 4 年结果和基因组复杂性及基因突变影响评估。
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Prognostic value of high-sensitivity measurable residual disease assessment after front-line chemoimmunotherapy in chronic lymphocytic leukemia.一线化学免疫治疗后高灵敏度可测量残留病评估在慢性淋巴细胞白血病中的预后价值
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