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免疫调节药物和主动免疫疗法治疗慢性淋巴细胞白血病。

Immunomodulatory drugs and active immunotherapy for chronic lymphocytic leukemia.

机构信息

Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL 33612, USA.

出版信息

Cancer Control. 2012 Jan;19(1):54-67. doi: 10.1177/107327481201900106.

Abstract

BACKGROUND

The last decade witnessed the emergence of several therapeutic options for patients with chronic lymphocytic leukemia (CLL) for first-line and relapsed settings. The vast majority of patients with relapsed or refractory CLL carry poor prognostic features, which are strong predictors of shorter overall survival and resistance to first-line treatment, particularly fludarabine-based regimens.

METHODS

This article highlights the current role of immunomodulatory drugs (IMiDs) and active immunotherapy as treatment options for this select group. The rationale of using IMiDs is discussed from the perspective of lenalidomide as a novel active agent. Relevant clinical trials using IMiDs alone or in combinations are discussed. New immunotherapeutic experimental approaches are also described.

RESULTS

As a single agent, lenalidomide offers an overall response rate of 32% to 47% in patients with relapsed/refractory disease. Recent studies have shown promising activity as a single agent in treatment-naive patients. The combination of lenalidomide with immunotherapy (rituximab and ofatumumab) has also shown clinical responses. Encouraging preclinical and early clinical data have been observed with different immunotherapeutic approaches.

CONCLUSIONS

The use of IMiDs alone or in combination with immunotherapy represents a treatment option for relapsed/refractory or treatment-naive patients. Mature data and further studies are needed to validate overall and progression-free survival. The toxicity profile of lenalidomide might limit its use and delay further studies. Immunotherapy offers another potential alternative, but further understanding of the immunogenicity of CLL cells and the mechanisms of tumor fl are reaction is needed to improve the outcomes in this field.

摘要

背景

在过去的十年中,出现了几种治疗慢性淋巴细胞白血病(CLL)患者的一线和复发治疗选择。绝大多数复发或难治性 CLL 患者具有不良预后特征,这些特征是总体生存时间较短和对一线治疗(尤其是基于氟达拉滨的方案)耐药的强烈预测因素。

方法

本文重点介绍了免疫调节药物(IMiDs)和主动免疫疗法作为这一特定人群治疗选择的当前作用。从来那度胺作为新型活性药物的角度讨论了使用 IMiDs 的原理。讨论了单独使用 IMiDs 或联合使用的相关临床试验。还描述了新的免疫治疗实验方法。

结果

来那度胺作为单一药物,在复发/难治性疾病患者中的总体缓解率为 32%至 47%。最近的研究表明,来那度胺在未经治疗的患者中作为单一药物具有良好的活性。来那度胺与免疫疗法(利妥昔单抗和奥法妥珠单抗)联合使用也显示出临床反应。不同免疫治疗方法的临床前和早期临床数据令人鼓舞。

结论

来那度胺单独使用或与免疫疗法联合使用是复发/难治性或初治患者的治疗选择。需要成熟的数据和进一步的研究来验证总体生存率和无进展生存率。来那度胺的毒性谱可能会限制其使用并延迟进一步的研究。免疫疗法提供了另一种潜在的选择,但需要进一步了解 CLL 细胞的免疫原性和肿瘤反应机制,以改善该领域的结果。

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