Wang Yi, Yan Yuting, Shan Dandan, Chen Jiawen, Liu Wei, Wang Tingyu, An Gang, Sui Weiwei, Huang Wenyang, Xiong Wenjie, Liu Huimin, Sun Qi, Wang Huijun, Xiao Zhijian, Wang Jianxiang, Qiu Lugui, Zou Dehui, Yi Shuhua
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.
Tianjin Institutes of Health Science, Tianjin 301600, China.
Cancer Biol Med. 2025 Mar 12;22(2):177-89. doi: 10.20892/j.issn.2095-3941.2024.0200.
Our previous studies have indicated potentially higher proliferative activity of tumor cells in Chinese patients with mantle-cell lymphoma (MCL) than those in Western. Given the success and tolerability of R-DA-EDOCH immunochemotherapy in treating aggressive B-cell lymphomas, we designed a prospective, phase 3 trial to explore the efficacy and safety of alternating R-DA-EDOCH/R-DHAP induction therapy for young patients with newly diagnosed MCL. The primary endpoint was the complete remission rate (CRR) at the end of induction (EOI).
A total of 55 patients were enrolled. The CRR at the EOI was 89.1% [95% confidence interval (CI) 78%-96%], and the overall response rate was 98.1% (95% CI 90%-100%). Most patients with bone marrow involvement quickly attained minimal residual disease (MRD) negative status, with a 95.7% rate at the EOI.
The 3-year progression-free survival (PFS) and overall survival rates were 66.3% and 83.2%, respectively. No patients discontinued treatment because of adverse events. Univariate analysis identified pathologic morphology and TP53 mutations as risk factors for PFS. However, high tumor proliferative activity and certain cytogenetic abnormalities showed no significant adverse prognostic significance.
Intensive therapy based on a high cytarabine dose and continuously administered EDOCH achieved a high MRD-negative rate and provides an optional induction choice for young patients with MCL with high-risk factors.
我们之前的研究表明,中国套细胞淋巴瘤(MCL)患者肿瘤细胞的增殖活性可能高于西方患者。鉴于R-DA-EDOCH免疫化疗在治疗侵袭性B细胞淋巴瘤方面的成功及耐受性,我们设计了一项前瞻性3期试验,以探索交替使用R-DA-EDOCH/R-DHAP诱导疗法对新诊断的年轻MCL患者的疗效和安全性。主要终点是诱导结束时的完全缓解率(CRR)。
共纳入55例患者。诱导结束时的CRR为89.1%[95%置信区间(CI)78%-96%],总缓解率为98.1%(95%CI 90%-100%)。大多数骨髓受累患者迅速达到微小残留病(MRD)阴性状态,诱导结束时的比例为95.7%。
3年无进展生存期(PFS)和总生存率分别为66.3%和83.2%。没有患者因不良事件而停止治疗。单因素分析确定病理形态和TP53突变是PFS的危险因素。然而,高肿瘤增殖活性和某些细胞遗传学异常未显示出显著的不良预后意义。
基于高剂量阿糖胞苷和持续给予EDOCH的强化治疗实现了高MRD阴性率,并为有高危因素的年轻MCL患者提供了一种诱导治疗选择。