原发性结节性 Epstein-Barr 病毒阳性 T 细胞/NK 细胞淋巴瘤:真实世界的经验。

IF 1.7 4区 医学 Q3 HEMATOLOGY
Dae-Ho Choi, Sang Eun Yoon, Junhun Cho, Seok Jin Kim, Won Seog Kim
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引用次数: 0

摘要

PTCL-EBV是WHO-HAEMS5和成熟淋巴肿瘤国际协调委员会(ICC of Mature Lymphoid neoplasms)分类中新确认的一种疾病实体。以前,它被归类为 PTCL-NOS 中的一个亚型,预后较差。然而,其临床特征和治疗效果并不为人所知。这项回顾性观察研究的对象是 2000 年至 2020 年在三星医疗中心通过病理复查确诊为 PTCL-EBV 的患者。我们分析了 14 名患者的临床数据。我们对 PTCL-EBV 患者进行了免疫组化调查,并分析了每种治疗方案的生存结果。我们分析了每种治疗方案的总生存期和无进展生存期。25%的患者β-F1阳性,67%的患者TCRγ阳性。TIA-1和颗粒酶B在所有病例中均呈阳性,而NK细胞标记物CD56仅在11%的患者中呈阴性。在所有患者中都观察到了 CD3。CD4 阳性率为 43%。对 8 名患者进行了 CD8 检测,37.5% 呈阳性。55% 的患者出现肝脾肿大,70% 的患者在诊断时出现 B 型症状。接受CHOP或CVP治疗的患者中位PFS为2.2个月(95% CI为1.9-2.5个月),接受其他治疗的患者中位PFS为5.1个月(NA)。ICE/dexa作为一线或二线治疗的客观反应率(ORR)为100%(3例中有3例)。但是,CHOP或CVP作为一线治疗的客观反应率为33.3%(9例中有3例)。获得应答后接受造血干细胞移植组的中位总生存期(OS)为34.6个月(95% CI 0-74.6个月),未接受造血干细胞移植组的中位总生存期为5.0个月(95% CI 2.1-7.9个月)(P=0.04)。总之,在PTCL-EBV的研究中,尽管样本量有限,但ICE/Dexa方案在ORR和PFS方面显示出潜在的优势。此外,在获得完全应答后应用造血干细胞移植可能会被证明是有利的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary nodal Epstein-Barr virus-positive T-cell/NK-cell lymphoma: Real-world experience.

PTCL-EBV is a disease entity newly recognized in the WHO-HAEMS5 and the ICC of Mature Lymphoid neoplasms classification. Previously, it was classified as a subtype within PTCL-NOS and was known to have a poor prognosis. However, the clinical feature and treatment outcomes are not well known. This retrospective observational study was conducted on patients diagnosed with PTCL-EBV at Samsung Medical Center through a pathology review from 2000 to 2020. We analyzed clinical data from 14 patients. We conducted an investigation of patients with PTCL-EBV into immunohistochemistry and analysis of survival outcomes for each treatment regimen. We analyzed both overall survival and progression-free survival for each treatment regimen. 25% were beta-F1 positive, and 67% were TCRγ positive. TIA-1 and granzyme B exhibited positive results in all cases, whereas the NK cell marker CD56 was negative in only 11% of patients. The CD3 was observed in all of patients. And, the CD4 was 43% positive. The CD8 were investigated in 8 patients, with 37.5% positive. Hepatosplenomegaly was observed in 55% of patients, and 70% of patients displayed B symptoms at the time of diagnosis. Patients who received CHOP or CVP treatment had a median PFS of 2.2 months (95% CI 1.9-2.5 months), and patients who received other treatments had a median PFS of 5.1 months (NA). The objective response rate (ORR) for ICE/dexa as the first or second line treatment was 100% (3 out of 3). But, ORR of CHOP or CVP as the first line treatment was 33.3% (3 out of 9). The median overall survival (OS) for the group that received HSCT after achieving a response was 34.6 months (95% CI 0-74.6 months), and the median OS for the group that did not receive HSCT was 5.0 months (95% CI 2.1-7.9 months) (p=0.04). In conclusion, in the context of PTCL-EBV, despite a limited sample size, the ICE/Dexa regimen shows potential benefits in terms of ORR and PFS. Furthermore, the application of HSCT following the attainment of a complete response may prove advantageous.

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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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