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毛细胞白血病患者的回顾性评估:一项长期单中心数据分析

Retrospective Evaluation of Hairy Cell Leukemia Patients: Analysis of a Long-Term Single Center Data.

作者信息

Biglari Mohammad, Kamranzadeh Foumani Hosein, Bagherian Maryam, Chahardouli Bahram, Ghavamzadeh Ardeshir

机构信息

Hematology, Oncology and Stem Cell Transplantation Research Center, Research Institute for Oncology, Hematology and Cell Therapy, Tehran University of Medical Sciences, Tehran, Iran.

Cancer & Cell Therapy Research Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Int J Hematol Oncol Stem Cell Res. 2022 Oct 1;16(4):209-216. doi: 10.18502/ijhoscr.v16i4.10878.

Abstract

Hairy cell leukemia (HCL) is a distinct lymphoproliferative disorder with unique circulating lymphocyte morphology. It is now regarded as an indolent disease yet treatable with purine analogs. We are going to present a complete long-term clinical and prognostic report of our HCL patients as a large cohort in Iran. All patients diagnosed with HCL, according to the World Health Organization (WHO) criteria, were enrolled in this study. They were referred to our academic center between 1995 and 2020. Treatment with a daily cladribine regimen was initiated as indicated and patients were followed. Survival data and clinical outcomes of patients were calculated. A total of 50 patients were studied (76% male). The median time to treatment was 4.8 months and complete remission was achieved in 92% of patients. Nine patients (18%) experienced relapse with a median time to relapse of 47 months. After a median follow-up of 51 months, the median OS was not reached and after 234 months, the overall survival rate was 86%. Survival was worse in patients with non-classic HCL (vHCL) compared to classic HCL. Our long-term follow-up data confirmed the favorable outcomes of Iranian HCL patients with cladribine and provide a useful viewpoint of the disease.

摘要

毛细胞白血病(HCL)是一种具有独特循环淋巴细胞形态的独特淋巴增殖性疾病。它现在被视为一种惰性疾病,但可用嘌呤类似物治疗。我们将作为伊朗的一个大型队列,呈现我们的HCL患者完整的长期临床和预后报告。根据世界卫生组织(WHO)标准确诊为HCL的所有患者均纳入本研究。他们在1995年至2020年期间被转诊至我们的学术中心。根据指示开始每日使用克拉屈滨方案进行治疗,并对患者进行随访。计算患者的生存数据和临床结局。共研究了50例患者(76%为男性)。治疗的中位时间为4.8个月,92%的患者实现了完全缓解。9例患者(18%)复发,复发的中位时间为47个月。中位随访51个月后,未达到中位总生存期,234个月后,总生存率为86%。与经典HCL相比,非经典HCL(vHCL)患者的生存率更差。我们的长期随访数据证实了伊朗HCL患者使用克拉屈滨的良好结局,并提供了关于该疾病的有用观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe6f/9985807/588df178e280/IJHOSCR-16-209-g001.jpg

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