Clinical Benefit of Autologous Stem Cell Transplantation for Patients with Multiple Myeloma Achieving Undetectable Minimal Residual Disease after Induction Treatment

被引:3
|
作者
Liu, Jiahui [1 ,2 ,3 ]
Yan, Wenqiang [1 ,2 ]
Fan, Huishou [1 ,2 ]
Xu, Jingyu [1 ,2 ]
Li, Lingna [1 ,2 ]
Du, Chenxing [1 ,2 ]
Mao, Xuehan [1 ,2 ]
Yan, Yuting [1 ,2 ]
Xu, Yan [1 ,2 ]
Sui, Weiwei [1 ,2 ]
Deng, Shuhui [1 ,2 ]
Yi, Shuhua [1 ,2 ]
Anderson, Kenneth C. [4 ,5 ]
Qiu, Lugui [1 ,2 ]
Zou, Dehui [1 ,2 ]
An, Gang [1 ,2 ,6 ,7 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Hematol & Blood Dis Hosp, Natl Clin Res Ctr Blood Dis, State Key Lab Expt Hematol,Haihe Lab Cell Ecosyst, Tianjin, Peoples R China
[2] Tianjin Inst Hlth Sci, Tianjin, Peoples R China
[3] Fujian Med Univ, Fujian Inst Hematol, Fujian Prov Key Lab Hematol, Union Hosp, Fuzhou, Peoples R China
[4] Harvard Med Sch, LeBow Inst Myeloma Therapeut, Dana Farber Canc Inst, Boston, MA USA
[5] Harvard Med Sch, Dana Farber Canc Inst, Jerome Lipper Ctr Multiple Myeloma Ctr, Boston, MA USA
[6] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Blood Dis, State Key Lab Expt Hematol, Tianjin 300020, Peoples R China
[7] Chinese Acad Med Sci & Peking Union Med Coll, Inst Hematol & Blood Dis Hosp, Tianjin 300020, Peoples R China
来源
CANCER RESEARCH COMMUNICATIONS | 2023年 / 3卷 / 09期
基金
中国国家自然科学基金;
关键词
LENALIDOMIDE MAINTENANCE; SURVIVAL OUTCOMES; THERAPY; DEXAMETHASONE; MULTICENTER; BORTEZOMIB; PREDNISONE; NEGATIVITY; DYNAMICS; IMPACT;
D O I
10.1158/2767-9764.CRC-23-0185
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Attaining undetectable minimal residual disease (MRD) is the current therapeutic goal for multiple myeloma. But there is a current lack of data regarding the clinical benefit of autologous stem cell transplantation (ASCT) for patients with myeloma achieving early MRD-negative status after induction treatment, in addition to the interaction of longitudinal MRD status with ASCT. The current study included 407 patients with transplant-eligible multiple myeloma with available MRD status from the National Longitudinal Cohort of Hematological Diseases in China (NCT04645199), of whom 147 (34.4%) achieved early undetectable MRD and 182 (44.7%) received ASCT. Early MRD-negative status was associated with a lower risk of disease progression [HR = 0.447; 95% confidence interval (CI), 0.333-0.600; P < 0.001] and death (HR = 0.473; 95% CI, 0.320-0.700; P < 0.001). Of note, patients who achieved undetectable MRD early still benefitted from ASCT, with a remarkable improvement in the median MRD-negative duration (33.5-58.0 months, P < 0.001), progression-free survival (PFS; 46.0-88.3 months, P < 0.001), and overall survival (OS; 76.4 months to not reached, P = 0.003). These clinical benefits were more pronounced in patients with aggressive features (high-risk cytogenetic abnormalities or high tumor burden) compared with standard-risk patients. Similar results were observed in patients with detectable MRD after induction treatment. In addition, we identified four MRD-status transformation patterns following ASCT, which were strongly correlated with diverse survival outcomes (P < 0.001). Our study revealed the enhanced clinical significance of ASCT in patients with transplant-eligible myeloma, regardless of early MRD status, particularly for high-risk patients. Subsequent prospective trials are essential to validate these observations.
引用
收藏
页码:1770 / 1780
页数:11
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