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晚期结外 NK/T 细胞淋巴瘤首次完全缓解期前线自体干细胞移植:一项多中心回顾性研究

英文原题:Upfront Autologous Stem Cell Transplantation in First Complete Remission for Advanced-Stage Extra-Nodal NK/T-Cell Lymphoma: A Multicenter Retrospective Study.

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Upfront Autologous Stem Cell Transplantation in First Complete Remission for Advanced-Stage Extra-Nodal NK/T-Cell Lymphoma: A Multicenter Retrospective Study.

PubMed 2026/07/20(内容时间) Am J Hematol Q1 · IF 9.4(JCR 2025)

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中文摘要

本研究旨在评估一线自体干细胞移植(ASCT)对一线治疗后获得首次完全缓解(CR1)的晚期结外NK/T细胞淋巴瘤(NKTCL)患者预后的影响。为此,我们回顾性分析了2006年至2023年间在中国14个医疗中心诊断为III期或IV期NKTCL且在一线治疗后获得CR1的患者数据。

本研究共纳入107例患者。大多数患者(87%)接受了非蒽环类药物为基础的一线化疗,38例(36%)在CR1时接受了 upfront ASCT 巩固治疗。中位随访时间为39.8个月,ASCT组的无进展生存期(PFS)和总生存期(OS)率显著优于非ASCT组(3年PFS:78.2% vs. 54.6%,p = 0.005;3年OS:86.0% vs. 68.9%,p = 0.04)。

然而,在接受非蒽环类药物为基础化疗的患者亚组(N = 93)中,ASCT与更好的PFS显著相关(3年PFS:77.6% vs. 59.3%,p = 0.025),但与OS无关(3年OS:85.6% vs. 74.8%,p = 0.164)。在多因素分析中,调整NK细胞淋巴瘤基线预后指数(PINK)、一线化疗类型和局部放疗后,upfront ASCT是更好PFS的独立预测因素(风险比[HR] = 0.37,95%置信区间[CI]:0.15-0.88,p = 0.025),但不是OS的独立预测因素。经过倾向性评分匹配分析后,upfront ASCT仍与更好的PFS显著相关,但与OS无关。这些真实世界数据表明,upfront ASCT可延长CR1期晚期NKTCL患者的PFS,但其对OS的影响仍不明确。

展开英文摘要原文

The aim of this study was to evaluate the effect of upfront autologous stem cell transplantation (ASCT) on the prognosis in patients with advanced-stage extra-nodal NK/T-cell lymphoma (NKTCL) achieving first complete remission (CR1) after frontline therapy. To this end, we retrospectively reviewed data from patients diagnosed with stage III or IV NKTCL who achieved CR1 after frontline treatment between 2006 and 2023 at 14 medical centers in China.

A total of 107 patients were included in this study. The majority of patients (87%) received non-anthracycline-based first-line chemotherapy, and 38 (36%) received upfront ASCT consolidation at the time of CR1. With a median follow-up time of 39. 8 months, progression-free survival (PFS) and overall survival (OS) rates were significantly better in the ASCT group than in the non-ASCT group (3-year PFS: 78. 2% vs. 54. 6%, p = 0. 005; 3-year OS: 86. 0% vs. 68. 9%, p = 0. 04).

However, in the subgroup of patients receiving non-anthracycline-based chemotherapy (N = 93), ASCT was significantly associated with better PFS (3-year PFS: 77. 6% vs. 59. 3%, p = 0. 025) but not with OS (3-year OS: 85. 6% vs. 74. 8%, p = 0. 164). In multivariate analyzes, upfront ASCT was an independent predictor of better PFS (hazard ratio [HR] = 0. 37, 95% confidence interval [CI]: 0. 15-0. 88, p = 0.

025) but not OS after adjusting for baseline prognostic index of NK-cell lymphoma (PINK), types of first-line chemotherapy, and local radiotherapy. After propensity score matched analyzes, upfront ASCT remained significantly associated with better PFS but not with OS. These real-world data suggest upfront ASCT prolongs PFS in patients with advanced-stage NKTCL in CR1, yet its impact on OS remains unclear.

论文信息

作者
Hu S、Liu W、Zhao L、Huang W、Gu Z、Huang H、Su L、Zhou H
单位
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.China
文献类型
多中心研究
期刊
American journal of hematology2026 Sep
原文标识
PubMed 42475115 · DOI 10.1002/ajh.70415