Hematology, Department of Translational and Precision Medicine, 'Sapienza' University, Roma, Italy.
Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
Hematol Oncol. 2024 Mar;42(2):e3255. doi: 10.1002/hon.3255.
Zanubrutinib has been approved for treating patients with different lymphoproliferative disorders and now represents a significant breakthrough in treating relapsed/refractory and previously untreated patients with chronic lymphocytic leukemia (CLL). Because few systematic studies or comparative randomized clinical trials have been conducted, optimal use of zanubrutinib in approved indications may be challenging. This article presents the results of a group discussion among an ad hoc constituted panel of experts to identify and address unmet clinical needs (UCNs) in using zanubrutinib in patients with CLL. Key UCNs were selected according to the criterion of clinical relevance using the Delphi process. Panel members reviewed the results of first-line and upstream controlled trials in which the efficacy and toxicity profile of zanubrutinib and other BTK inhibitors were investigated in patients with CLL. Based on a critical discussion of data, the panel produced recommendations for using zanubrutinib and proposals for new studies to increase the evidence for the optimal treatment of patients with CLL. The recommendations given by the panel are intended for use not only by expert centers but, above all, by less experienced hematologists as well as general practitioners.
泽布替尼已获批用于治疗多种淋巴增殖性疾病,代表着治疗复发/难治性及初治慢性淋巴细胞白血病(CLL)患者的重大突破。由于缺乏系统研究或对照随机临床试验,在获批适应证范围内优化泽布替尼的使用可能颇具挑战。本文呈现了专家组专题讨论的结果,旨在识别并解决 CLL 患者使用泽布替尼的未满足临床需求(UCN)。采用德尔菲法,根据临床相关性标准选择关键 UCN。专家组回顾了泽布替尼及其他 BTK 抑制剂在 CLL 患者中开展的一线及上游对照试验的结果,评估了其疗效和毒性特征。在对数据进行批判性讨论的基础上,专家组提出了使用泽布替尼的建议,并提出了新的研究建议,以增加 CLL 患者最佳治疗的证据。专家组的建议不仅旨在供专家中心使用,而且更重要的是供经验相对较少的血液科医生以及全科医生使用。