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接受扩增 NK 细胞治疗的成人 T 细胞白血病/淋巴瘤患者的长期生存

英文原题:Long-Term Survival of Patients with Adult T-Cell Leukemia/Lymphoma Treated with Amplified Natural Killer Cell Therapy.

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Long-Term Survival of Patients with Adult T-Cell Leukemia/Lymphoma Treated with Amplified Natural Killer Cell Therapy.

PubMed 2024/09/19(内容时间) Reports (MDPI) Q3 · IF 0.5(JCR 2025)

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研究概要

ANK 疗法作为 ATL 的一线治疗具有巨大潜力。

研究思路结论见上方概要

成人T细胞白血病/淋巴瘤(ATL)由人类T细胞白血病病毒1型(HTLV-1)在长期潜伏感染后引起。HTLV-1可在5%的HTLV-1携带者中诱导惰性或侵袭性白血病。ATL,尤其是侵袭性类型,对多药化疗耐药。惰性类型常进展为侵袭性类型。即使在最惰性的类型,即冒烟型ATL中,平均生存时间也为55.0个月。病例介绍:5例ATL患者在接受扩增NK 细胞(ANK)治疗后随访其临床病程。4例接受ANK治疗作为一线治疗的患者获得完全缓解,并显示长期生存,超过5年无侵袭性转化或复发。1例患者因急性加重接受多药化疗,但2个月后复发。她随后接受放疗和ANK治疗,生存超过6年。此外,ANK治疗将ATL患者的免疫功能增强至高于正常个体的水平。

展开英文摘要原文

Adult T-cell leukemia/lymphoma (ATL) is caused by human T-cell leukemia virus type 1 (HTLV-1) after a long latent infection. HTLV-1 induces the indolent or aggressive type of leukemia in 5% of HTLV-1 carriers. ATL, especially the aggressive type, is resistant to multi-agent chemotherapy. The indolent type often progresses to the aggressive type. Even in the most indolent-type cases, that is, smoldering ATL, the average survival time is 55.0 months. CASE PRESENTATION: Five patients with ATL were followed up for their clinical course after amplified natural killer cell (ANK) therapy. Four patients who received ANK therapy as first-line therapy achieved complete remission and showed long-term survival without aggressive conversion or relapse for more than 5 years. One patient was treated with multiagent chemotherapy due to acute exacerbation but relapsed 2 months later. She was subsequently treated with radiation and ANK therapy and survived for more than 6 years. Furthermore, ANK therapy enhanced the immune function of ATL patients to a level higher than that of normal individuals.

ANK therapy has great potential as first-line treatment for ATL.

论文信息

作者
Okubo Y、Nagai S、Katayama Y、Kitamura K、Hiwaki K、Teshigawara K
单位
Higashinotohin Clinic, 338 Empukuji, Nakagyo, Kyoto 604-8175, Japan.Japan
文献类型
病例报告
期刊
Reports (MDPI)2024 Sep 19
原文标识
PubMed 40729303 · DOI 10.3390/reports7030080