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非分泌型多发性骨髓瘤的临床病程及预后

Clinical Course and Prognosis of Non-Secretory Multiple Myeloma.

作者信息

Chawla Sagar S, Kumar Shaji K, Dispenzieri Angela, Greenberg Alexandra J, Larson Dirk R, Kyle Robert A, Lacy Martha Q, Gertz Morie A, Rajkumar S Vincent

机构信息

Mayo Medical School, Mayo Clinic, Rochester, MN, USA.

出版信息

Eur J Haematol. 2015 Feb 16. doi: 10.1111/ejh.12534.

DOI:10.1111/ejh.12534
PMID:25690913
Abstract

OBJECTIVE

To determine the prognosis of patients with non-secretory myeloma. Methods: We studied 124 patients diagnosed with multiple myeloma who had no monoclonal protein detected on serum and urine immunofixation at diagnosis and on all subsequent follow up testing (non-secretory myeloma). The overall survival (OS) of patients with non-secretory myeloma was compared with 7075 patients with typical myeloma seen during the same time period in whom a monoclonal protein was detected at the time of diagnosis.

RESULTS

One hundred and twenty four patients met criteria for non-secretory multiple myeloma. The median follow-up was 102 months (range, 1-204 months). The median progression free survival with initial therapy was 28.6 months, and the median OS was 49.3 months. There was a significant improvement in OS since 2001; median survival 99.2 versus 43.8 months (prior to 2001) versus 99.2 months (2001-2012), P<0.001. OS was superior in patients with a normal baseline FLC ratio (n=10) compared to patients with an abnormal ratio (n=19), medians not reached in both groups. Prior to 2001, OS was similar in non-secretory myeloma (n=86) and secretory myeloma (n=4011), median 3.6 versus 3.5 years, respectively, P=0.63. However, among patients diagnosed between 2001-2012, OS was superior in non-secretory myeloma (n=36) compared to secretory myeloma (n=2942), median 8.3 versus 5.4 years, respectively, P=0.03.

CONCLUSIONS

Non-secretory myeloma is an uncommon subtype of multiple myeloma. In the last decade, there has been an improvement in the survival of non-secretory myeloma, and appears superior to secretory myeloma. This article is protected by copyright. All rights reserved.

摘要

目的

确定非分泌型骨髓瘤患者的预后。方法:我们研究了124例被诊断为多发性骨髓瘤的患者,这些患者在诊断时以及所有后续随访检测中血清和尿免疫固定电泳均未检测到单克隆蛋白(非分泌型骨髓瘤)。将非分泌型骨髓瘤患者的总生存期(OS)与同期诊断时检测到单克隆蛋白的7075例典型骨髓瘤患者进行比较。

结果

124例患者符合非分泌型多发性骨髓瘤标准。中位随访时间为102个月(范围1 - 204个月)。初始治疗后的中位无进展生存期为28.6个月,中位总生存期为49.3个月。自2001年以来总生存期有显著改善;中位生存期分别为99.2个月、2001年前的43.8个月以及2001 - 2012年的99.2个月,P<0.001。基线游离轻链(FLC)比值正常的患者(n = 10)的总生存期优于比值异常的患者(n = 19),两组均未达到中位生存期。2001年前,非分泌型骨髓瘤(n = 86)和分泌型骨髓瘤(n = 4011)的总生存期相似,中位生存期分别为3.6年和3.5年,P = 0.63。然而,在2001 - 2012年诊断的患者中,非分泌型骨髓瘤(n = 36)的总生存期优于分泌型骨髓瘤(n = 2942),中位生存期分别为8.3年和5.4年,P = 0.03。

结论

非分泌型骨髓瘤是多发性骨髓瘤的一种罕见亚型。在过去十年中,非分泌型骨髓瘤的生存率有所提高,且似乎优于分泌型骨髓瘤。本文受版权保护。保留所有权利。

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