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对于新诊断的多发性骨髓瘤患者,在进行大剂量美法仑和自体干细胞移植之前,环磷酰胺加地塞米松是一种有效的初始治疗方法:与长春新碱、阿霉素和地塞米松的随机对照结果

Cyclophosphamide plus dexamethasone is an efficient initial treatment before high-dose melphalan and autologous stem cell transplantation in patients with newly diagnosed multiple myeloma: results of a randomized comparison with vincristine, doxorubicin, and dexamethasone.

作者信息

Mellqvist Ulf-Henrik, Lenhoff Stig, Johnsen Hans E, Hjorth Martin, Holmberg Erik, Juliusson Gunnar, Tangen Jon Magnus, Westin Jan

机构信息

Department of Hematology, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Cancer. 2008 Jan 1;112(1):129-35. doi: 10.1002/cncr.23145.

Abstract

BACKGROUND

Today, intensive therapy that includes high-dose melphalan with autologous stem cell transplantation (ASCT) is considered standard therapy in younger patients with newly diagnosed myeloma. When the current trial was initiated, combined vincristine, doxorubicin, and dexamethasone (VAD) was the most commonly used induction therapy before ASCT and yielded rapid major responses without interfering with stem cell harvest. However, the administration of VAD demands a central venous access, and well-described toxicities are associated with the therapy. This randomized trial, which was initiated in 2001 by the Nordic Myeloma Study Group, was an attempt to bring a larger portion of patients to ASCT more quickly.

METHODS

Patients were randomized to receive either 3 cycles of VAD or 2 courses of cyclophosphamide plus dexamethasone (Cy-Dex) (cyclophosphamide at a dose of 1000 mg/m(2) on Day 1 and dexamethasone at a dose of 40 mg per day on Days 1-4 and 9-12, repeated on Day 22) as initial therapy followed by stem cell mobilization, harvest, and finally ASCT.

RESULTS

No significant difference was observed in the proportion of patients undergoing ASCT (VAD [86%] vs Cy-Dex [87%]). During the first 4 months after the initiation of therapy, the mortality rates were 5.8% for VAD and 1.9% for Cy-Dex (P = .08). The response rates after ASCT were comparable (partial response or better: VAD: 80% vs Cy-Dex: 81%). In both groups, the median event-free survival was 29 months, and the overall survival rate at 3 years was 75%.

CONCLUSIONS

The current results indicated that Cy-Dex before ASCT has efficacy comparable to that of VAD. It also demonstrated that a short course of alkylator therapy using cyclophosphamide does not affect stem cell harvest or transplantation.

摘要

背景

如今,包括大剂量美法仑联合自体干细胞移植(ASCT)的强化治疗被视为新诊断骨髓瘤年轻患者的标准治疗方法。在开展当前试验时,长春新碱、阿霉素和地塞米松联合方案(VAD)是ASCT前最常用的诱导治疗方法,能产生快速的主要反应且不干扰干细胞采集。然而,VAD的给药需要中心静脉通路,且该治疗存在诸多已明确的毒性反应。这项由北欧骨髓瘤研究组于2001年启动的随机试验,旨在更快地让更多患者接受ASCT。

方法

患者被随机分为两组,一组接受3个周期的VAD治疗,另一组接受2个疗程的环磷酰胺加地塞米松(Cy-Dex)治疗(环磷酰胺剂量为1000mg/m²,于第1天给药;地塞米松剂量为每日40mg,于第1 - 4天和第9 - 12天给药,第22天重复),作为初始治疗,随后进行干细胞动员、采集,最后进行ASCT。

结果

接受ASCT的患者比例无显著差异(VAD组[86%] vs Cy-Dex组[87%])。在治疗开始后的前4个月,VAD组的死亡率为5.8%,Cy-Dex组为1.9%(P = 0.08)。ASCT后的缓解率相当(部分缓解或更好:VAD组80% vs Cy-Dex组81%)。两组的无事件生存期均数为29个月,3年总生存率为75%。

结论

当前结果表明,ASCT前使用Cy-Dex的疗效与VAD相当。还表明使用环磷酰胺的短疗程烷化剂治疗不影响干细胞采集或移植。

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