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在 GIMEMA MM0305 随机对照试验中,循环细胞因子和血管生成因子对多发性骨髓瘤初始治疗的预后或预测价值。

Prognostic or predictive value of circulating cytokines and angiogenic factors for initial treatment of multiple myeloma in the GIMEMA MM0305 randomized controlled trial.

机构信息

Department of Biomedical Science and Human Oncology, University of Bari "Aldo Moro" Medical School, Bari, Italy.

Biothecnology Research Unit, Aprigliano, Cosenza, Italy.

出版信息

J Hematol Oncol. 2019 Jan 9;12(1):4. doi: 10.1186/s13045-018-0691-4.

Abstract

BACKGROUND

Several new drugs are approved for treatment of patients with multiple myeloma (MM), but no validated biomarkers are available for the prediction of a clinical outcome. We aimed to establish whether pretreatment blood and bone marrow plasma concentrations of major cytokines and angiogenic factors (CAFs) of patients from a phase 3 trial of a MM treatment could have a prognostic and predictive value in terms of response to therapy and progression-free and overall survival and whether these patients could be stratified for their prognosis.

METHODS

Blood and bone marrow plasma levels of Ang-2, FGF-2, HGF, VEGF, PDGF-β, IL-8, TNF-α, TIMP-1, and TIMP-2 were determined at diagnosis in MM patients enrolled in the GIMEMA MM0305 randomized controlled trial by an enzyme-linked immunosorbent assay (ELISA). These levels were correlated both reciprocally and with the type of therapy and patients' characteristics and with a group of non-MM patients as controls.

RESULTS

No significant differences were detected between the blood and bone marrow plasma levels of angiogenic cytokines. A cutoff for each CAF was established. The therapeutic response of patients with blood plasma levels of CAFs lower than the cutoff was better than the response of those with higher levels in terms of percentage of responding patients and quality of response.

CONCLUSION

FGF-2, HGF, VEGF, and PDGF-β plasma levels at diagnosis have predictive significance for response to treatment. The stratification of patients based on the levels of CAFs at diagnosis and their variations after therapy is useful to characterize different risk groups concerning outcome and response to therapy.

TRIAL REGISTRATION

Clinical trial information can be found at the following link: NCT01063179.

摘要

背景

有几种新药被批准用于治疗多发性骨髓瘤(MM)患者,但目前尚无可用的预测临床结局的有效生物标志物。我们旨在确定 3 期 MM 治疗试验中的患者的治疗前血液和骨髓血浆中主要细胞因子和血管生成因子(CAFs)浓度是否可以预测治疗反应、无进展生存期和总生存期,并在预后方面对这些患者进行分层。

方法

通过酶联免疫吸附试验(ELISA)在 GIMEMA MM0305 随机对照试验中确定诊断时 MM 患者的血液和骨髓血浆中 Ang-2、FGF-2、HGF、VEGF、PDGF-β、IL-8、TNF-α、TIMP-1 和 TIMP-2 的水平。这些水平既相互关联,也与治疗类型和患者特征相关联,并与一组非 MM 患者作为对照进行关联。

结果

未检测到血管生成细胞因子的血液和骨髓血浆水平之间存在显著差异。为每个 CAF 建立了一个截止值。与较高水平的 CAF 相比,CAF 血液水平低于截止值的患者的治疗反应更好,表现为反应患者的百分比和反应质量。

结论

诊断时的 FGF-2、HGF、VEGF 和 PDGF-β 血浆水平对治疗反应具有预测意义。基于诊断时 CAFs 水平及其治疗后变化对患者进行分层有助于根据结局和对治疗的反应来描述不同的风险组。

试验注册

临床试验信息可在以下链接中找到:NCT01063179。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cdb/6327520/e5838d823ca2/13045_2018_691_Fig1_HTML.jpg

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