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血清 CXCL13 水平与治疗反应相关,并可预测华氏巨球蛋白血症的疾病预后。

Serum CXCL13 level is related to treatment response and predicts disease prognosis in Waldenström macroglobulinemia.

机构信息

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Ann Hematol. 2024 Sep;103(9):3667-3675. doi: 10.1007/s00277-024-05690-3. Epub 2024 Mar 6.

Abstract

Waldenström macroglobulinemia (WM) is a type of B-cell lymphoma that produces IgM. Our study aimed to investigate the role of CXCL13, a chemokine essential for B lymphocytes, in the evaluation of treatment response and prognosis in WM. We collected serum samples and clinical data from 72 WM patients, with 69 patients receiving systemic therapy and 3 patients opting not to receive treatment. Serum CXCL13 levels at baseline and after six months of treatments were measured by enzyme-linked immunosorbent assay. The median serum level of CXCL13 was 1 539.2 pg/ml (range 10.0-21 389.9) at baseline and significantly decreased to 123.1 pg/ml (range 0.0-6 741.5) after 6 months of treatments. At baseline, higher CXCL13 levels were associated with lower hemoglobin levels (p = 0.001), higher β2-microglobulin levels (p = 0.001), lower albumin levels (p = 0.046), and higher IPSS-WM scores (p = 0.013). After 6 months of treatment, patients who achieved PR/VGPR had significantly lower CXCL13 levels compared to those with SD (70.2 pg/ml vs 798.6 pg/ml, p = 0.002). The median follow-up period was 40 months (range 4.2-188). Eight patients died during the follow-up period. Overall survival differed based on CXCL13 levels. When grouped by baseline CXCL13 levels, the median OS was 60.0 months in patients with serum CXCL13 > 2 000 pg/ml, while it was not reached in patients with low CXCL13 levels (p < 0.001). Based on CXCL13 levels after the treatments, the median OS was 74.0 months in patients with serum CXCL13 > 200 pg/ml, while it was not reached in patients with CXCL13 ≤ 200 pg/ml. In a subgroup of 28 patients with a series of serum samples, the increase of serum CXCL13 level was associated with disease progression or the start of next-line therapy (p < 0.001). Our study concludes that serum CXCL13 levels decrease in WM patients treated with various regimens and correlate with treatment response. Detecting serum CXCL13 at baseline or after treatment help in predicting prognosis.

摘要

华氏巨球蛋白血症(WM)是一种产生 IgM 的 B 细胞淋巴瘤。我们的研究旨在探讨趋化因子 CXCL13 在 WM 患者治疗反应和预后评估中的作用,该趋化因子对 B 淋巴细胞至关重要。我们收集了 72 名 WM 患者的血清样本和临床数据,其中 69 名患者接受了系统治疗,3 名患者选择不接受治疗。通过酶联免疫吸附试验测量了基线和治疗 6 个月后的血清 CXCL13 水平。基线时,中位血清 CXCL13 水平为 1539.2pg/ml(范围 10.0-21389.9),治疗 6 个月后显著下降至 123.1pg/ml(范围 0.0-6741.5)。基线时,较高的 CXCL13 水平与较低的血红蛋白水平(p=0.001)、较高的β2-微球蛋白水平(p=0.001)、较低的白蛋白水平(p=0.046)和较高的 IPSS-WM 评分(p=0.013)相关。治疗 6 个月后,与 SD 相比,获得 PR/VGPR 的患者 CXCL13 水平显著降低(70.2pg/ml 比 798.6pg/ml,p=0.002)。中位随访时间为 40 个月(范围 4.2-188)。8 名患者在随访期间死亡。总体生存情况因 CXCL13 水平而异。按基线 CXCL13 水平分组时,血清 CXCL13>2000pg/ml 的患者中位 OS 为 60.0 个月,而血清 CXCL13 水平较低的患者中位 OS 未达到(p<0.001)。根据治疗后 CXCL13 水平,血清 CXCL13>200pg/ml 的患者中位 OS 为 74.0 个月,而血清 CXCL13≤200pg/ml 的患者中位 OS 未达到。在 28 名具有一系列血清样本的患者亚组中,血清 CXCL13 水平的升高与疾病进展或开始下一线治疗相关(p<0.001)。我们的研究得出结论,接受各种方案治疗的 WM 患者的血清 CXCL13 水平下降,与治疗反应相关。检测基线或治疗后血清 CXCL13 有助于预测预后。

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