立体定向消融体放射治疗低转移癌患者肺或肝转移后外周血淋巴细胞的变化。

IF 1.8 Q3 ONCOLOGY Radiation Oncology Journal Pub Date : 2023-03-01 DOI:10.3857/roj.2022.00521
Sergey Nikolaevich Novikov, Irina Aleksandrovna Baldueva, Anton Yurievich Zozulya, Natalya Viktorovna Emelyanova, Dmitriy Viktorovich Girdyuk, Andrey Ivanovich Arsenyev, Elena Alexandrovna, Elena Ivanovna Tyuryaeva, E I Filip Evgenevich Antipov, Mikhail Markovich Girshovich, Sergey Vasilevich Kanayev
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引用次数: 1

摘要

目的:分析立体定向消融放疗(SABR)对低转移性肿瘤患者外周血淋巴细胞的影响。材料与方法:前瞻性评价46例经SABR治疗的肺(17例)或肝(29例)转移瘤患者外周血免疫状态动态。在SABR结束前、3-4周和6-8周分别进行外周血淋巴细胞亚群流式细胞术检测:15-20 Gy 3组和13.5 Gy 4组。治疗的病变数量从1例(32例)到2 ~ 3例(14例)不等。结果:SABR诱导t淋巴细胞(CD3+CD19-) (p = 0.001)、辅助t淋巴细胞(CD3+CD4+) (p = 0.004)、活化的细胞毒性t淋巴细胞(CD3+CD8+HLA-DR+) (p = 0.001)、活化的辅助t淋巴细胞(CD3+CD4+HLA-DR+) (p < 0.001)。SABR后t调节免疫抑制淋巴细胞(CD4+CD25brightCD127low) (p = 0.002)和nkt细胞(CD3+CD16+CD56+) (p = 0.007)显著减少。比较分析表明,低剂量的SABR (EQD2Gy(α/β=10) = 93.7 ~ 105.7 Gy)诱导t淋巴细胞、活化的细胞毒性t淋巴细胞和活化的CD4+CD25+ t辅助细胞显著增加,而高剂量的SABR (EQD2Gy(α/β=10) = 150 Gy)与这些作用无关。更有效的t淋巴细胞活化(p = 0.010)、活化的t辅助细胞(p < 0.001)和细胞毒性t淋巴细胞(p = 0.003)与单一病变的SABR相关。与肺病变SABR相比,SABR治疗肝转移后t淋巴细胞(p = 0.002)、辅助t淋巴细胞(p = 0.003)和活化的细胞毒性t淋巴细胞(p = 0.001)显著增加。结论:SABR后外周血淋巴细胞的变化可能与放疗转移部位、转移次数及SABR剂量有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Peripheral blood lymphocyte changes after stereotactic ablative body radiotherapy to lung or liver metastases in patients with oligometastatic cancers.

Purpose: To perform the analysis of the peripheral blood lymphocyte changes after stereotactic ablative radiotherapy (SABR) in patients with oligometastatic cancers.

Materials and methods: The dynamics of the immune status in peripheral blood was prospectively evaluated in 46 patients with lung (17 cases) or liver (29 cases) metastases treated by SABR. Flow cytometry of peripheral blood lymphocyte subpopulations was performed before SABR, 3-4 weeks and 6-8 weeks after the end of SABR: 3 fractions of 15-20 Gy or 4 fractions of 13.5 Gy. The number of treated lesions varied from 1 (32 patients) to 2-3 (14 patients).

Results: SABR induced a significant increase of T-lymphocytes (CD3+CD19-) (p = 0.001), T-helper (CD3+CD4+) (p = 0.004), activated cytotoxic T-lymphocytes (CD3+CD8+HLA-DR+) (p = 0.001), activated T-helpers (CD3+CD4+HLA-DR+) (p < 0.001). A significant decrease of T-regulated immune suppressive lymphocytes (CD4+CD25brightCD127low) (p = 0.002) and NKT-cells (CD3+CD16+CD56+) (p = 0.007) was recorded after the SABR. The comparative analysis demonstrated that lower doses of SABR (EQD2Gy(α/β=10) = 93.7-105.7 Gy) induced significant increase of T-lymphocytes, activated cytotoxic T-lymphocytes, and activated CD4+CD25+ T-helpers, while SABR with higher doses (EQD2Gy(α/β=10) = 150 Gy) was not associated with these effects. A more efficient activations of T-lymphocytes (p = 0.010), activated T-helpers (p < 0.001), and cytotoxic T-lymphocytes (p = 0.003) were associated with SABR to a single lesion. A significant increase of T-lymphocytes (p = 0.002), T-helpers (p = 0.003), and activated cytotoxic T-lymphocytes (p = 0.001) was observed after SABR for hepatic metastases in contrast to SABR for lung lesions.

Conclusion: Changes in peripheral blood lymphocytes after SABR could be influenced by the location or the number of irradiated metastasis, and the dose of SABR.

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