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伊布替尼治疗后疾病进展的慢性淋巴细胞白血病患者的临床结局。

Clinical outcomes in patients with chronic lymphocytic leukemia with disease progression on ibrutinib.

机构信息

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.

出版信息

Blood Cancer J. 2022 Sep 1;12(9):124. doi: 10.1038/s41408-022-00721-6.

Abstract

Patients with chronic lymphocytic leukemia (CLL) with disease progression on ibrutinib have worse outcomes compared to patients stopping ibrutinib due to toxicity. A better understanding of expected outcomes in these patients is necessary to establish a benchmark for evaluating novel agents currently available and in development. We evaluated outcomes of 144 patients with CLL treated at Mayo Clinic with 2018 iwCLL disease progression on ibrutinib. The median overall survival (OS) for the entire cohort was 25.5 months; it was 29.8 months and 8.3 months among patients with CLL progression (n = 104) and Richter transformation (n = 38), respectively. Longer OS was observed among patients with CLL progression who had received ibrutinib in the frontline compared to relapsed/refractory setting (not reached versus 28.5 months; p = 0.04), but was similar amongst patients treated with 1, 2, or ≥3 prior lines (18.5, 30.9, and 26.0 months, respectively, p = 0.24). Among patients with CLL disease progression on ibrutinib, OS was significantly longer when next-line treatment was chimeric antigen receptor T-cell therapy (median not reached) or venetoclax-based treatment (median 29.8 months) compared to other approved treatments, such as chemoimmunotherapy, phosphoinositide 3'-kinase inhibitors, and anti-CD20 monoclonal antibodies (9.1 months; p = 0.03). These findings suggest an unmet need for this growing patient population.

摘要

患有慢性淋巴细胞白血病 (CLL) 的患者在伊布替尼治疗后疾病进展的情况下,与因毒性而停止伊布替尼治疗的患者相比,预后更差。为了确定目前可及和正在开发的新型药物的评估基准,需要更好地了解这些患者的预期结果。我们评估了在梅奥诊所接受治疗的 144 例患有 CLL 的患者,这些患者在 2018 年因伊布替尼而出现 iwCLL 疾病进展。整个队列的中位总生存期(OS)为 25.5 个月;在 CLL 进展(n=104)和 Richter 转化(n=38)患者中,分别为 29.8 个月和 8.3 个月。与复发/难治性患者相比,在一线治疗中接受伊布替尼治疗的 CLL 进展患者的 OS 更长(未达到与 28.5 个月;p=0.04),但在接受 1、2 或≥3 线治疗的患者中,OS 相似(分别为 18.5、30.9 和 26.0 个月,p=0.24)。在伊布替尼治疗后 CLL 进展的患者中,与其他批准的治疗方法(如化疗免疫治疗、磷脂酰肌醇 3-激酶抑制剂和抗 CD20 单克隆抗体)相比,当二线治疗是嵌合抗原受体 T 细胞治疗(中位未达到)或 venetoclax 为基础的治疗时(中位 29.8 个月),OS 明显更长(9.1 个月;p=0.03)。这些发现表明,对于这一不断增长的患者群体,存在未满足的需求。

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