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硼替佐米诱导治疗后自体造血干细胞移植治疗多发性骨髓瘤

[Bortezomib-based induction therapy followed by autologous hematopoietic stem cell transplantation in multiple myeloma].

作者信息

Huang Beihui, Li Juan, Liu Junru, Gu Jingli, Zheng Dong, Xu Duorong, Zou Waiyi, Wang Hehua

机构信息

Department of Hematology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.

Department of Hematology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China. Email:

出版信息

Zhonghua Nei Ke Za Zhi. 2014 Nov;53(11):865-72.

Abstract

OBJECTIVE

To evaluate the short-term and long-term effect of novel agents followed by autologous hematopoietic stem cell (ASCT) in Chinese multiple myeloma(MM) patients in order to find out the optimal therapeutic regimen for transplant-eligible patients.

METHODS

Clinical data of 100 active MM patients receiving bortezomib-based induction regimens followed by high-dose melphalan and ASCT were retrospectively analyzed from June 1, 2006 to January 30, 2014.

RESULTS

The overall response rates(ORR) after induction therapy, transplantation and consolidation and maintenance therapy were respectively 90.0%, 97.0%, and 98.9%. The median progress free survival(PFS) was 42.3 months. The median overall survival(OS) was not reached. The cumulative near complete response (nCR)+complete respanse(CR) rate was no longer improved after 4 cycles of induction therapy for non-light chain type MM and two cycles for light-chain type. In newly-diagnosed light-chain type MM patients, the cumulative nCR+CR rate after 4 cycles of bortezomib plus dexamethasone (VD) regimen was similar to that of bortezomib, doxorubicin and dexamethasone (PAD). While for those non-light-chain types, three drug-based regimen was better than two drug-based. PFS of patients receiving early ASCT was longer than that of late ASCT (50.7 months vs 26.6 months, P = 0.023) . PFS in patients receiving autologous bone marrow stem cell transplantation (ABMSCT) was longer than that of autologous peripheral blood stem cell transplantation (APBSCT) (NA vs 36.1 months, P = 0.049) . Maintenance therapy was beneficial regardless of the response rate after ASCT. Patients with CR at any time during the therapy had longer PFS than those with nCR.

CONCLUSIONS

Bortezomib-based therapy followed by ASCT is the first line therapy for transplant-eligible MM patients. Patients with different types of M protein require different induction regimens. Maintenance is beneficial to patients after ASCT, no matter whether a CR is reached or not. Patients with CR after induction or ASCT tend to have longer survival.

摘要

目的

评估新型药物联合自体造血干细胞移植(ASCT)对中国多发性骨髓瘤(MM)患者的短期和长期疗效,以找出适合移植患者的最佳治疗方案。

方法

回顾性分析2006年6月1日至2014年1月30日期间100例接受以硼替佐米为基础的诱导方案、随后进行大剂量美法仑和ASCT的活动性MM患者的临床资料。

结果

诱导治疗、移植及巩固和维持治疗后的总缓解率(ORR)分别为90.0%、97.0%和98.9%。无进展生存期(PFS)的中位数为42.3个月。总生存期(OS)的中位数未达到。对于非轻链型MM患者,诱导治疗4个周期后,累积的近乎完全缓解(nCR)+完全缓解(CR)率不再提高;对于轻链型患者,诱导治疗2个周期后该比率不再提高。在新诊断的轻链型MM患者中,硼替佐米联合地塞米松(VD)方案4个周期后的累积nCR+CR率与硼替佐米、阿霉素和地塞米松(PAD)方案相似。而对于非轻链型患者,三药联合方案优于两药联合方案。早期接受ASCT患者的PFS长于晚期接受ASCT的患者(50.7个月对26.6个月,P = 0.023)。接受自体骨髓干细胞移植(ABMSCT)患者的PFS长于自体外周血干细胞移植(APBSCT)的患者(未获得数据对36.1个月,P = 0.049)。无论ASCT后的缓解率如何,维持治疗均有益。治疗期间任何时候达到CR的患者的PFS长于达到nCR的患者。

结论

以硼替佐米为基础的治疗联合ASCT是适合移植的MM患者的一线治疗方案。不同类型M蛋白的患者需要不同的诱导方案。维持治疗对ASCT后的患者有益,无论是否达到CR。诱导或ASCT后达到CR的患者往往生存期更长。

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