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青少年及年轻成人慢性淋巴细胞白血病患者的临床和分子特征及治疗模式。

Clinical and molecular characteristics and treatment patterns of adolescent and young adult patients with chronic lymphocytic leukaemia.

机构信息

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Clinical Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Br J Haematol. 2021 Jul;194(1):61-68. doi: 10.1111/bjh.17498. Epub 2021 May 10.

DOI:10.1111/bjh.17498
PMID:33973230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9284944/
Abstract

Chronic lymphocytic leukaemia (CLL) rarely presents in adolescent and young adult (AYA) patients (patients aged 15-39 years). Disease characteristics and outcomes of AYA patients with CLL are not well understood, particularly in the era of novel oral targeted therapies. We analysed outcomes of 227 AYA patients with CLL diagnosed in the last two decades and evaluated at our institution. Median time to first treatment (TTFT) was 2·2 years, and five- and 10-year overall survival (OS) were 90% and 78%, respectively. Pre-treatment elevated beta 2-microglobulin, advanced Rai stage, del(11q) or del(17p) by FISH, unmutated IGHV and CD38 positivity were associated with both shorter TTFT and OS. Within the subgroup of patients who received oral targeted therapy at any time, del(11q) or del(17p) and complex karyotype were associated with shorter OS. First-line treatment choice was significantly associated with time to second treatment (P < 0·001). Patients harbouring del(11q) or del(17p) experienced shorter time to Richter transformation and were more likely to undergo an allogeneic stem cell transplant. There was a significant association between age and both OS and time to Richter transformation. Our study is the first analysis of AYA patients with CLL with a large number of patients treated with oral targeted therapies.

摘要

慢性淋巴细胞白血病(CLL)在青少年和年轻成人(AYA)患者(年龄 15-39 岁)中很少见。AYA 患者 CLL 的疾病特征和结局尚不清楚,特别是在新型口服靶向治疗时代。我们分析了在过去二十年中在我们机构诊断并接受评估的 227 例 AYA CLL 患者的结局。首次治疗的中位时间(TTFT)为 2.2 年,5 年和 10 年总生存率(OS)分别为 90%和 78%。治疗前β2-微球蛋白升高、晚期 Rai 分期、FISH 检测到 del(11q)或 del(17p)缺失、IGHV 未突变和 CD38 阳性与 TTFT 和 OS 均较短相关。在任何时候接受口服靶向治疗的患者亚组中,del(11q)或 del(17p)缺失和复杂核型与较短的 OS 相关。一线治疗选择与第二次治疗的时间显著相关(P<0.001)。携带 del(11q)或 del(17p)的患者经历更短的 Richter 转化时间,并且更有可能接受异基因干细胞移植。年龄与 OS 和 Richter 转化时间均有显著相关性。我们的研究是对接受口服靶向治疗的大量 AYA CLL 患者的首次分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/7207bf8379d1/nihms-1703741-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/a90cb9421b20/nihms-1703741-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/c9bf104b4968/nihms-1703741-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/7207bf8379d1/nihms-1703741-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/a90cb9421b20/nihms-1703741-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/c9bf104b4968/nihms-1703741-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2391/9284944/7207bf8379d1/nihms-1703741-f0003.jpg

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