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硼替佐米诱导治疗伴随后续大剂量美法仑和自体干细胞移植用于治疗AL淀粉样变性:一项单机构回顾性研究

Induction bortezomib in Al amyloidosis followed by high dose melphalan and autologous stem cell transplantation: a single institution retrospective study.

作者信息

Scott Emma C, Heitner Stephen B, Dibb William, Meyers Gabrielle, Smith Stephen D, Abar Farnoush, Kovacsovics Tibor, Perez-Avraham Galit, Stentz Alex, Frires Rachel, Dibb James, Maziarz Richard T

机构信息

Center for Hematologic Malignancies, Oregon Health and Science University Knight Cancer Institute, Portland, OR.

Oregon Health and Science University Knight Cardiovascular Institute, Portland, OR.

出版信息

Clin Lymphoma Myeloma Leuk. 2014 Oct;14(5):424-430.e1. doi: 10.1016/j.clml.2014.02.003. Epub 2014 Feb 16.

Abstract

INTRODUCTION/BACKGROUND: High-dose melphalan (HDM) followed by autologous stem cell transplant (ASCT) for light chain amyloidosis (AL) was performed in 31 patients at Oregon Health and Science University between 2005 and 2012. Fifteen patients had cardiac involvement.

PATIENTS AND METHODS

Patients received melphalan 200 mg/m(2) or dose-adjusted HDM (100-140 mg/m(2)) depending on high risk features. Thirteen patients proceeded directly to ASCT after diagnosis, 12 patients received a bortezomib-containing regimen, and 6 received a variety of other induction regimens.

RESULTS

The day 100 treatment-related mortality was 9.6%. Overall hematologic (ORR) and organ response rates (OR) in the whole cohort after ASCT were 77% and 58%. ORR and OR in the bortezomib pretreated group were 92% and 75% vs. 69% and 54% in the group that received no pretreatment. The median time to maximum hematologic response after ASCT was reduced in the group that received bortezomib induction (3 vs. 14 months). Overall cardiac response rate was 60%; 100% in patients pretreated with bortezomib and 43% in those without induction treatment. With a median follow-up of 2.9 years, the 3-year progression-free and overall survival rates in the entire cohort were 66% and 73% and in those with cardiac involvement, 73% and 80%.

CONCLUSION

We observed that bortezomib-based induction is well tolerated in patients with and without cardiac involvement and suggest that this approach be studied in prospective multi-institutional trials.

摘要

引言/背景:2005年至2012年期间,俄勒冈健康与科学大学对31例轻链淀粉样变性(AL)患者进行了大剂量美法仑(HDM)治疗,随后进行自体干细胞移植(ASCT)。15例患者有心脏受累。

患者与方法

根据高危特征,患者接受200mg/m²美法仑或剂量调整的HDM(100 - 140mg/m²)。13例患者诊断后直接进行ASCT,12例患者接受含硼替佐米的方案,6例接受各种其他诱导方案。

结果

第100天的治疗相关死亡率为9.6%。ASCT后整个队列的总体血液学缓解率(ORR)和器官反应率(OR)分别为77%和58%。硼替佐米预处理组的ORR和OR分别为92%和75%,而未预处理组为69%和54%。接受硼替佐米诱导的组ASCT后达到最大血液学反应的中位时间缩短(3个月对14个月)。总体心脏反应率为60%;硼替佐米预处理患者为100%,未接受诱导治疗患者为43%。中位随访2.9年,整个队列的3年无进展生存率和总生存率分别为66%和73%,有心脏受累者分别为73%和80%。

结论

我们观察到,无论有无心脏受累,基于硼替佐米的诱导治疗患者耐受性良好,并建议在多机构前瞻性试验中研究此方法。

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