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首页> 外文期刊>Leukemia and lymphoma >Prognostic value of bone marrow microvessel density and angiogenic cytokines in patients with multiple myeloma undergoing autologous stem cell transplant.
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Prognostic value of bone marrow microvessel density and angiogenic cytokines in patients with multiple myeloma undergoing autologous stem cell transplant.

机译:骨髓微血管密度和血管生成细胞因子对多发性骨髓瘤患者自体干细胞移植的预后价值。

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Angiogenesis is important for the proliferation and metastasis of most malignant neoplasms including multiple myeloma (MM). The aim of this study was to evaluate the role of bone marrow angiogenesis and angiogenic cytokines in patients with MM prior to and after autologous stem cell transplant (ASCT). Twenty-nine patients with MM who underwent ASCT had serial samples of serum and bone marrow biopsies at diagnosis, prior to ASCT, and at the 3rd and 6th months post-transplant. Besides bone marrow microvessel density (MVD), serum angiogenic cytokines including vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF) and markers of disease activity such as interleukin-6 (IL-6), IL-1beta, C-reactive protein (CRP), beta(2)-microglobulin, and bone marrow plasma cells (BMPCs) were also determined. Bone marrow MVD, serum levels of IL-6, CRP, and beta(2)-microglobulin, and BMPCs decreased significantly from diagnosis to the 6th month post-transplant (p < 0.05). Serum FGF and IL-1beta levels decreased significantly until 3 months post-transplant, however lost this significance at the 6th month. Serum VEGF levels did not vary significantly during follow-up. MVD, serum angiogenic cytokine levels, and parameters reflecting disease activity were similar in responders and non-responders to induction chemotherapy. Cytokines and MVD both at diagnosis and prior to transplant did not show any correlation with overall survival (OS) and progression-free survival (PFS) after a median follow-up of 55 months after transplant (p > 0.05). Our findings suggest that bone marrow MVD decreases significantly with ASCT in MM, however without an impact on OS and PFS.
机译:血管生成对于包括多发性骨髓瘤(MM)在内的大多数恶性肿瘤的增殖和转移是重要的。这项研究的目的是评估自体干细胞移植(ASCT)之前和之后MM患者骨髓血管生成和血管生成细胞因子的作用。接受ASCT的29例MM患者在诊断时,ASCT之前以及移植后3个月和6个月进行了一系列血清和骨髓活检。除骨髓微血管密度(MVD)之外,血清血管生成细胞因子还包括血管内皮生长因子(VEGF)和成纤维细胞生长因子(FGF)以及疾病活动性标记物,例如白介素6(IL-6),IL-1beta,C反应性还确定了蛋白质(CRP),β(2)-微球蛋白和骨髓浆细胞(BMPC)。从诊断到移植后第6个月,骨髓MVD,血清IL-6,CRP和β(2)-微球蛋白水平以及BMPC均显着降低(p <0.05)。直到移植后3个月,血清FGF和IL-1beta的水平都显着下降,但是在第6个月时,这种重要性就消失了。随访期间血清VEGF水平无明显变化。在诱导化疗的反应者和非反应者中,MVD,血清血管生成细胞因子水平和反映疾病活动的参数相似。在移植后55个月进行中位随访后,诊断时和移植前的细胞因子和MVD与总生存期(OS)和无进展生存期(PFS)没有任何相关性(p> 0.05)。我们的发现表明,MM的ASCT可使骨髓MVD显着降低,而对OS和PFS却没有影响。

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