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滤泡性淋巴瘤的精准医学:聚焦于预测性生物标志物。

Precision medicine in follicular lymphoma: Focus on predictive biomarkers.

机构信息

Department of Hematology, ICO-Hospital Germans Trias i Pujol, Institut de Recerca Josep Carreras, Universitat Autònoma de Barcelona, Badalona, Spain.

出版信息

Hematol Oncol. 2020 Dec;38(5):625-639. doi: 10.1002/hon.2781. Epub 2020 Aug 24.

Abstract

Current care for patients with follicular lymphoma (FL) offers most of them long-term survival. Improving it further will require careful patient selection. This review focuses on predictive biomarkers (ie, those whose outcome correlations depend on the treatment strategy) in FL, because awareness of what patient subsets benefit most or least from each therapy will help in this task. The first part of this review aims to summarize what biomarkers are predictive in FL, the magnitude of the effect and the quality of the evidence. We find predictive biomarkers in the setting of (a) indication of active treatment, (b) front-line induction (use of anthracyline-based regimens, CHOP vs bendamustine, addition of rituximab), (c) post-(front-line)induction (rituximab maintenance, radioimmunotherapy), and (d) relapse (hematopoietic stem cell transplant) and targeted agents. The second part of this review discusses the challenges of precision medicine in FL, including (a) cost, (b) clinical relevance considerations, and (c) difficulties over the broad implementation of biomarkers. We then provide our view on what biomarkers may become used in the next few years. We conclude by underscoring the importance of assessing the potential predictiveness of available biomarkers to improve patient care but also that there is a long road ahead before reaching their broad implementation due to remaining scientific, technological, and economic hurdles.

摘要

目前滤泡性淋巴瘤(FL)患者的治疗方法为大多数患者提供了长期生存。进一步提高疗效需要仔细选择患者。这篇综述重点关注 FL 中的预测性生物标志物(即那些其结果相关性取决于治疗策略的标志物),因为了解哪些患者亚组从每种治疗中获益最多或最少将有助于完成这项任务。本综述的第一部分旨在总结 FL 中哪些生物标志物具有预测性、影响程度和证据质量。我们发现了在以下情况下具有预测性的生物标志物:(a)需要积极治疗的指征,(b)一线诱导(使用蒽环类药物方案、CHOP 与苯达莫司汀、添加利妥昔单抗),(c)一线后诱导(利妥昔单抗维持、放射免疫治疗),以及(d)复发(造血干细胞移植)和靶向药物。本综述的第二部分讨论了 FL 中精准医学的挑战,包括(a)成本,(b)临床相关性考虑,以及(c)广泛实施生物标志物的困难。然后,我们提出了我们对未来几年可能使用哪些生物标志物的看法。最后,我们强调了评估现有生物标志物的潜在预测性以改善患者护理的重要性,但由于仍存在科学、技术和经济障碍,要实现广泛应用还有很长的路要走。

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