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硼替佐米联合地塞米松诱导治疗可改善 t(4;14) 骨髓瘤患者的预后,但不能改善 del(17p) 患者的预后。

Bortezomib plus dexamethasone induction improves outcome of patients with t(4;14) myeloma but not outcome of patients with del(17p).

机构信息

Centre Hospitalier Universitaire, Nantes, France.

出版信息

J Clin Oncol. 2010 Oct 20;28(30):4630-4. doi: 10.1200/JCO.2010.28.3945. Epub 2010 Jul 19.

Abstract

PURPOSE

Cytogenetics is an important prognostic parameter in multiple myeloma (MM). Patients presenting with either t(4;14) or del(17p) are known to have a short event-free survival (EFS) and overall survival (OS). Some preliminary data suggest that bortezomib is able to overcome these prognostic parameters.

PATIENTS AND METHODS

A series of 507 patients with newly diagnosed MM who received four cycles of bortezomib-dexamethasone induction therapy before high-dose melphalan were analyzed for both t(4;14) and del(17p).

RESULTS

We found that both t(4;14) and del(17p) remain prognostic parameters, even in the context of bortezomib treatment. However, it is important to note that bortezomib significantly improves the prognosis (in terms of both EFS and OS) of patients with t(4;14), compared with patients treated with vincristine, doxorubicin, and dexamethasone induction therapy. In contrast, no improvement was observed for del(17p) patients.

CONCLUSION

Short-term bortezomib induction improves outcome of patients with t(4;14) but not the outcome of patients with del(17p). However, both abnormalities remain prognostic factors predicting both EFS and OS despite bortezomib induction.

摘要

目的

细胞遗传学是多发性骨髓瘤(MM)的一个重要预后参数。已知具有 t(4;14)或 del(17p)的患者无事件生存(EFS)和总生存(OS)较短。一些初步数据表明硼替佐米能够克服这些预后参数。

患者和方法

对接受 4 个周期硼替佐米-地塞米松诱导治疗后再接受高剂量美法仑治疗的 507 例新诊断 MM 患者进行了 t(4;14)和 del(17p)分析。

结果

我们发现,即使在硼替佐米治疗的情况下,t(4;14)和 del(17p)仍然是预后参数。然而,值得注意的是,与接受长春新碱、阿霉素和地塞米松诱导治疗的患者相比,硼替佐米显著改善了 t(4;14)患者的预后(EFS 和 OS)。相比之下,del(17p)患者未观察到改善。

结论

短期硼替佐米诱导可改善 t(4;14)患者的预后,但不能改善 del(17p)患者的预后。然而,尽管进行了硼替佐米诱导,这两种异常仍然是预测 EFS 和 OS 的预后因素。

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