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慢性淋巴细胞白血病一线治疗进展:德国慢性淋巴细胞白血病研究小组(GCLLSG)关于管理和一线治疗的现行建议。

Advances in first-line treatment of chronic lymphocytic leukemia: current recommendations on management and first-line treatment by the German CLL Study Group (GCLLSG).

机构信息

Department I of Internal Medicine, Center of Integrated Oncology Cologne-Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.

CECAD - Cologne Cluster of Excellence in Cellular Stress Responses in Aging-associated Diseases, University of Cologne, Cologne, Germany.

出版信息

Eur J Haematol. 2016 Jan;96(1):9-18. doi: 10.1111/ejh.12678. Epub 2015 Nov 6.


DOI:10.1111/ejh.12678
PMID:26332019
Abstract

The management of patients with CLL is undergoing significant changes; during the last decade, the outcome of first-line therapies has been markedly improved with the addition of anti-CD20 antibodies to chemotherapy. Today, chemoimmunotherapy for physically fit patients ≤ 65 years should consist of fludarabine, cyclophosphamide, and rituximab (FCR). The combination of bendamustine and rituximab (BR) should be considered in physically fit patients > 65 years and in patients with a higher risk of infections. Patients with reduced fitness and/or relevant comorbidity should receive chlorambucil with a CD20 antibody, preferably obinutuzumab. Regardless of their fitness, patients with CLL carrying genetic aberrations such as del(17p) and/or TP53 mutation poorly respond to chemoimmunotherapy and therefore require different therapeutic approaches. An increasing understanding of the disease biology has led to the development of targeted drugs for the treatment of CLL, such as the BTK inhibitor ibrutinib and PI3K inhibitor idelalisib. These agents have shown efficacy in high-risk and relapsed/refractory patients and are currently being evaluated in clinical trials for first-line therapy. It is anticipated that these compounds and further other novel agents will profoundly change the therapy of CLL.

摘要

慢性淋巴细胞白血病(CLL)患者的管理正在发生重大变化;在过去十年中,通过在化疗中添加抗 CD20 抗体,一线治疗的疗效得到了显著改善。如今,对于身体状况良好的≤65 岁患者,化疗免疫疗法应包括氟达拉滨、环磷酰胺和利妥昔单抗(FCR)。对于身体状况良好的>65 岁患者和有更高感染风险的患者,应考虑采用苯达莫司汀和利妥昔单抗(BR)联合治疗。对于体能下降和/或存在相关合并症的患者,应接受氯苯丁酸与 CD20 抗体联合治疗,最好是奥滨尤妥珠单抗。无论其体能状况如何,携带 del(17p)和/或 TP53 突变等遗传异常的 CLL 患者对化疗免疫疗法反应不佳,因此需要采用不同的治疗方法。对疾病生物学的深入了解导致了用于治疗 CLL 的靶向药物的发展,例如 BTK 抑制剂伊布替尼和 PI3K 抑制剂idelalisib。这些药物在高危和复发/难治性患者中显示出疗效,目前正在临床试验中评估一线治疗的效果。预计这些化合物和其他新型药物将极大地改变 CLL 的治疗方法。

相似文献

[1]
Advances in first-line treatment of chronic lymphocytic leukemia: current recommendations on management and first-line treatment by the German CLL Study Group (GCLLSG).

Eur J Haematol. 2015-11-6

[2]
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Am J Hematol. 2015-5

[3]
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[4]
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[5]
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[6]
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[7]
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Haematologica. 2018-11-22

[8]
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[9]
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Hematology Am Soc Hematol Educ Program. 2018-11-30

[10]
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Expert Rev Anticancer Ther. 2010-10

引用本文的文献

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[2]
DAP Kinase-Related Apoptosis-Inducing Protein Kinase 2 (DRAK2) Is a Key Regulator and Molecular Marker in Chronic Lymphocytic Leukemia.

Int J Mol Sci. 2020-10-16

[3]
Early treatment with FCR versus watch and wait in patients with stage Binet A high-risk chronic lymphocytic leukemia (CLL): a randomized phase 3 trial.

Leukemia. 2020-2-18

[4]
Immunoregulatory effects of Lurbinectedin in chronic lymphocytic leukemia.

Cancer Immunol Immunother. 2020-2-13

[5]
Resistance to complement activation, cell membrane hypersialylation and relapses in chronic lymphocytic leukemia patients treated with rituximab and chemotherapy.

Oncotarget. 2018-8-3

[6]
Two mouse models reveal an actionable PARP1 dependence in aggressive chronic lymphocytic leukemia.

Nat Commun. 2017-7-28

[7]
New Pharmacotherapies in Chronic Lymphocytic Leukemia.

P T. 2017-2

[8]
Renal insufficiency is an independent prognostic factor in patients with chronic lymphocytic leukemia.

Haematologica. 2017-1

[9]
Challenges in the Role of Gammaglobulin Replacement Therapy and Vaccination Strategies for Hematological Malignancy.

Front Immunol. 2016-8-22

[10]
The Phospholipase Cγ2 Mutants R665W and L845F Identified in Ibrutinib-resistant Chronic Lymphocytic Leukemia Patients Are Hypersensitive to the Rho GTPase Rac2 Protein.

J Biol Chem. 2016-10-14

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