Department of Hematology, Copernicus Memorial Hospital, Łódź, Poland.
Department of Hematology, Institute of Hematology and Transfusion Medicine, Warszawa, Poland.
Adv Clin Exp Med. 2019 Aug;28(8):1051-1057. doi: 10.17219/acem/99911.
Development of a novel class of drugs, the B-cell receptor-signaling inhibitors, including ibrutinib, has been a major achievement in the therapy of refractory or relapsed chronic lymphocytic leukemia (CLL). However, the CLL patients who have discontinued the ibrutinib treatment in clinical trials have been reported to have poor prognosis.
In this retrospective study by the Polish Adult Leukemia Group (PALG), we analyzed the reasons for ibrutinib cessation and outcomes after discontinuing ibrutinib in refractory or relapsed CLL patients treated in a compassionate use program in Poland.
Polish CLL patients were included if they discontinued ibrutinib for any reason. The clinical data on the course of ibrutinib treatment was collected anonymously using electronic Case Report Forms (CRFs). The causes of discontinuation of ibrutinib as reported by the treating physicians were analyzed.
Thirty-seven patients who discontinued ibrutinib were identified. The median duration of ibrutinib treatment in this group was 4.4 months (range: 0.2-25.2). The main reason for discontinuing ibrutinib was adverse events (n = 20, 54%), while 14 (38%) patients discontinued therapy due to disease progression and 3 (8%) due to other causes. The most common treatment complications that led to ibrutinib cessation were severe respiratory tract infections (9 patients, 24%). In the group discontinuing ibrutinib for progressive disease, 11 patients progressed with untransformed CLL, while in 3 patients, a rare type of Richter transformation to Hodgkin's lymphoma was diagnosed. Twenty-nine patients (78%) died during the follow-up period, and median overall survival (OS) reached 2.0 months (95% CI = 0.8-5.5 months). Importantly, no significant survival difference was detected between patients who discontinued ibrutinib due to disease progression and due to adverse events.
The results of this analysis indicate that ibrutinib discontinuation in relapsed or refractory CLL is associated with poor prognosis regardless of the reason for ibrutinib cessation.
新型药物 B 细胞受体信号抑制剂的开发,包括伊布替尼,是治疗难治性或复发性慢性淋巴细胞白血病(CLL)的重大成就。然而,临床试验中已报道停止伊布替尼治疗的 CLL 患者预后不良。
在波兰成人白血病组(PALG)的这项回顾性研究中,我们分析了波兰同情用药项目中难治性或复发性 CLL 患者因任何原因停止伊布替尼治疗以及停止伊布替尼治疗后的结局。
如果患者因任何原因停止伊布替尼治疗,即纳入波兰 CLL 患者。使用电子病例报告表(CRF)匿名收集伊布替尼治疗过程中的临床数据。分析治疗医生报告的停止伊布替尼的原因。
确定了 37 例停止伊布替尼的患者。该组伊布替尼治疗的中位持续时间为 4.4 个月(范围:0.2-25.2)。停止伊布替尼的主要原因是不良事件(n=20,54%),14 例(38%)患者因疾病进展而停止治疗,3 例(8%)因其他原因而停止治疗。导致伊布替尼停药的最常见治疗并发症是严重呼吸道感染(9 例,24%)。在因疾病进展而停止伊布替尼治疗的患者中,11 例进展为未转化的 CLL,而 3 例诊断为罕见的Richter 转化为霍奇金淋巴瘤。在随访期间,29 例(78%)患者死亡,中位总生存期(OS)达到 2.0 个月(95%CI=0.8-5.5 个月)。重要的是,未发现因疾病进展和因不良事件而停止伊布替尼治疗的患者之间存在显著的生存差异。
该分析结果表明,无论停止伊布替尼的原因如何,复发或难治性 CLL 患者停止伊布替尼治疗与预后不良相关。