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骨髓瘤患者可溶性CD86的循环水平及临床意义

Circulating levels and clinical significance of soluble CD86 in myeloma patients.

作者信息

Hock B D, Drayson M, Patton W N, Taylor K, Kerr L, McKenzie J L

机构信息

Haematology Research Group, Christchurch School of Medicine, PO Box 4345, Christchurch, New Zealand.

出版信息

Br J Haematol. 2006 Apr;133(2):165-72. doi: 10.1111/j.1365-2141.2006.05983.x.

Abstract

Circulating soluble CD86 (sCD86) levels are elevated in a number of leukaemias and are an independent prognostic factor in acute myeloid leukaemia. We investigated the clinical significance of circulating sCD86 in 299 patients from the UK Medical Research Council myeloma VIth trial, where patients received ABCM [adriamycin, carmustine (BCNU), cyclophosphamide, melphalan] either alone or with prednisolone (ABCM + P). Serum levels of sCD86 were significantly elevated (P = 0.0001) in myeloma patients and using the median normal donor level (0.621 ng/ml) as a cut-off point, 70% of patients had elevated levels (range = 0.015-15.87 ng/ml, median = 1.1 ng/ml). In univariate analysis elevated sCD86 levels were associated with significantly shorter (P < 0.001) survival (median = 22 vs. 51 months) and event-free survival (median = 14 vs. 31 months) in ABCM + P but not ABCM patients. Multivariate analysis demonstrated that sCD86 was a significant, independent prognostic marker of both overall [risk ratio (RR) = 2.04, P = 0.0006] and event-free (RR = 1.95, P = 0.0004) survival in ABCM + P patients. In conclusion, this study demonstrated that sCD86 levels are a significant independent prognostic marker in at least some myeloma treatment groups and its biological role and prognostic value should be further investigated.

摘要

在多种白血病中,循环可溶性CD86(sCD86)水平升高,且是急性髓系白血病的一个独立预后因素。我们在英国医学研究委员会骨髓瘤VI期试验的299例患者中研究了循环sCD86的临床意义,这些患者接受了单独的ABCM[阿霉素、卡莫司汀(BCNU)、环磷酰胺、美法仑]或联合泼尼松龙(ABCM + P)治疗。骨髓瘤患者的血清sCD86水平显著升高(P = 0.0001),以正常供体水平中位数(0.621 ng/ml)为界值点,70%的患者水平升高(范围 = 0.015 - 15.87 ng/ml,中位数 = 1.1 ng/ml)。单因素分析显示,在接受ABCM + P治疗的患者中,sCD86水平升高与显著缩短的生存时间(P < 0.001)(中位数 = 22个月对51个月)和无事件生存时间(中位数 = 14个月对31个月)相关,但在接受ABCM治疗的患者中无此关联。多因素分析表明,sCD86是ABCM + P治疗患者总生存[风险比(RR) = 2.04,P = 0.0006]和无事件生存(RR = 1.95,P = 0.0004)的显著独立预后标志物。总之,本研究表明,sCD86水平是至少部分骨髓瘤治疗组中的一个显著独立预后标志物,其生物学作用和预后价值应进一步研究。

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