Suppr超能文献

高危慢性淋巴细胞白血病先前接受靶向治疗后的异基因造血细胞移植。

Allogeneic hematopoietic cell transplantation after prior targeted therapy for high-risk chronic lymphocytic leukemia.

作者信息

Kim Haesook T, Shaughnessy Conner J, Rai Sharmila C, Reynolds Carol, Ho Vincent T, Cutler Corey, Koreth John, Gooptu Mahasweta, Romee Rizwan, Nikiforow Sarah, Armand Philippe, Alyea Edwin P, Antin Joseph H, Wu Catherine J, Soiffer Robert J, Ritz Jerome, Brown Jennifer R

机构信息

Department of Data Sciences, Dana-Farber Cancer Institute, Harvard School of Public Health, Boston, MA; and.

Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

出版信息

Blood Adv. 2020 Sep 8;4(17):4113-4123. doi: 10.1182/bloodadvances.2020002184.

Abstract

Allogeneic hematopoietic cell transplantation (alloHCT) can cure previously treated high-risk chronic lymphocytic leukemia (CLL) patients if they are suitable for transplant through the graft-versus-leukemia effect. However, since the emergence of targeted therapies, the role of alloHCT for high-risk CLL is less clear. To address this question, we evaluated 108 high-risk CLL patients who underwent alloHCT from 2010 to 2018. Thirty patients from the period of 2013 to 2018 received targeted therapy prior to alloHCT. The median age for the targeted therapy cohort was 60 years (range, 30-71 years), and 20% and 73% had complete and partial remission, respectively: 76% had del(17p), 46.2% had 5 or more cytogenetic abnormalities, and 78.9% were IGHV unmutated. The median number of prior therapies was 4 (range, 1-9). With a median follow-up time of 36 months (range, 10-72 months), the 3-year overall (OS) and progression-free survival (PFS) were 87% and 69%, respectively. The 3-year cumulative incidence of nonrelapse mortality and relapse was 7% and 24%, respectively. For the control cohort of 78 patients who underwent alloHCT from 2010 to 2014 and received only chemoimmunotherapy prior to transplant, the 3-year OS and PFS were 69% and 58%, respectively. Patients treated with targeted therapy prior to alloHCT had a significantly higher number of circulating T and B cells and a lower ratio of CD4 regulatory T cells to CD4 conventional T cells early after transplant. In summary, despite multiple high-risk features, the clinical outcome of CLL patients who receive targeted therapy prior to transplant is excellent and alloHCT should be offered while the disease is under control.

摘要

异基因造血细胞移植(alloHCT)可治愈先前接受过治疗的高危慢性淋巴细胞白血病(CLL)患者,前提是他们通过移植物抗白血病效应适合移植。然而,自靶向治疗出现以来,alloHCT在高危CLL中的作用尚不清楚。为了解决这个问题,我们评估了2010年至2018年接受alloHCT的108例高危CLL患者。2013年至2018年期间的30例患者在alloHCT之前接受了靶向治疗。靶向治疗队列的中位年龄为60岁(范围30 - 71岁),分别有20%和73%达到完全缓解和部分缓解:76%有del(17p),46.2%有5种或更多细胞遗传学异常,78.9%的免疫球蛋白重链可变区(IGHV)未发生突变。先前治疗的中位次数为4次(范围1 - 9次)。中位随访时间为36个月(范围10 - 72个月),3年总生存率(OS)和无进展生存率(PFS)分别为87%和69%。3年非复发死亡率和复发的累积发生率分别为7%和24%。对于2010年至2014年接受alloHCT且移植前仅接受化疗免疫治疗的78例患者的对照组,3年OS和PFS分别为69%和58%。移植后早期,在alloHCT之前接受靶向治疗的患者循环T细胞和B细胞数量明显更多,而CD4调节性T细胞与CD4常规T细胞的比例更低。总之,尽管存在多种高危特征,但移植前接受靶向治疗的CLL患者临床结局良好,应在疾病得到控制时提供alloHCT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a562/7479951/1f1d96d747c0/advancesADV2020002184absf1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验