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新型药物引入后多发性骨髓瘤患者生存率的提高及国际分期系统(ISS)的适用性:希腊骨髓瘤研究组(GMSG)的分析

Improved survival of patients with multiple myeloma after the introduction of novel agents and the applicability of the International Staging System (ISS): an analysis of the Greek Myeloma Study Group (GMSG).

作者信息

Kastritis E, Zervas K, Symeonidis A, Terpos E, Delimbassi S, Anagnostopoulos N, Michali E, Zomas A, Katodritou E, Gika D, Pouli A, Christoulas D, Roussou M, Kartasis Z, Economopoulos T, Dimopoulos M A

机构信息

Department of Clinical Therapeutics, Alexandra Hospital, University of Athens School of Medicine, Athens, Greece.

出版信息

Leukemia. 2009 Jun;23(6):1152-7. doi: 10.1038/leu.2008.402. Epub 2009 Feb 19.

DOI:10.1038/leu.2008.402
PMID:19225533
Abstract

When the novel agents thalidomide, bortezomib and lenalidomide are administered to patients with myeloma in the context of clinical trials, they are associated with a significant improvement in response, progression-free survival and in some studies, overall survival (OS); however, their effect on the outcome of unselected myeloma patients has not been fully assessed. We compared the outcome of 1376 unselected patients with symptomatic myeloma, who started treatment before or after the introduction of thalidomide. The median OS in patients who started treatment after the introduction of novel agents increased by 12 months (48 vs 36 months, P<0.001). This improvement was more pronounced in patients < or =70 years (from 39 to 74 months, P<0.001), but less evident in patients >70 years (from 26 to 33 months, P=0.27). In patients treated after the introduction of novel agents, the international staging system (ISS) could discriminate three groups with significantly different outcomes (5-year survival for ISS stage I, II and III was 66, 45 and 18%, respectively, P<0.001). ISS was also valid in patients who actually received upfront treatment with novel drugs (4-year survival rate was 85, 61 and 26% for ISS stage I, II and III patients, P=0.001).

摘要

在临床试验中,当向骨髓瘤患者施用新型药物沙利度胺、硼替佐米和来那度胺时,它们与反应、无进展生存期的显著改善相关,并且在一些研究中还与总生存期(OS)的改善相关;然而,它们对未选择的骨髓瘤患者结局的影响尚未得到充分评估。我们比较了1376例有症状骨髓瘤未选择患者的结局,这些患者在沙利度胺引入之前或之后开始治疗。在引入新型药物后开始治疗的患者中,中位总生存期增加了12个月(48个月对36个月,P<0.001)。这种改善在年龄≤70岁的患者中更为明显(从39个月至74个月,P<0.001),但在年龄>70岁的患者中不太明显(从26个月至33个月,P=0.27)。在引入新型药物后接受治疗的患者中,国际分期系统(ISS)可以区分出三组结局显著不同的患者(ISS I期、II期和III期的5年生存率分别为66%、45%和18%,P<0.001)。ISS在实际接受新型药物一线治疗的患者中也有效(ISS I期、II期和III期患者的4年生存率分别为85%、61%和26%,P=0.001)。

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