不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Retrospective study of chidamide-containing regimens as maintenance therapy among T- and NK-cell lymphoma patients.
Retrospective study of chidamide-containing regimens as maintenance therapy among T- and NK-cell lymphoma patients.
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生存期延长表明,含西达本胺的维持治疗在 TNKLs 患者中具有前景且耐受性良好。
评估含西达本胺方案作为 T 细胞和自然杀伤(NK)细胞淋巴瘤(TNKL)患者维持治疗的疗效。
纳入 51 例在诱导治疗后接受含西达本胺方案的 TNKL 患者。主要终点为无进展生存期(PFS),次要终点包括总生存期(OS)和安全性。
维持治疗中位持续时间为 14 个月(范围 1–24 个月)。多数患者诊断为结外 NK/T 细胞淋巴瘤(ENKTCL;24/51,47.1%),其次为血管免疫母细胞性 T 细胞淋巴瘤(AITL;14/51,27.5%)。PFS 和 OS 中位数分别为 21 个月和 29 个月。总体人群 2 年 PFS 和 OS 率分别为 45.1% 和 54.2%。诱导治疗后达到完全缓解(CR)的患者,相比未达到 CR 的患者(部分缓解/疾病稳定,PR/SD)生存结局更佳。一线诱导治疗后达到 CR 的患者生存也更佳,但挽救治疗组中未观察到类似的显著关联。尽管 86.3% 的患者发生西达本胺相关不良事件(AE),严重血液学不良事件(3 级)仅见于 11 例(21.6%),表明西达本胺的毒性特征可接受。
患者生存期延长提示,含西达本胺的维持治疗对 TNKL 患者具有前景且耐受性良好。
This study aimed to explore the efficacy of chidamide-containing regimens as maintenance therapy in patients with T- and natural killer (NK)-cell lymphomas (TNKLs).
A total of 51 patients with TNKLs who received chidamide-containing regimens after induction therapy were enrolled. The primary end point was progression-free survival (PFS), while the secondary end point was overall survival (OS) and safety.
The median duration of maintenance was 14 months (range = 1-24 months). Most of the patients were diagnosed with extranodal NK/T-cell lymphoma (ENKTCL; 24/51, 47.1%), followed by angioimmunoblastic T-cell lymphoma (AITL; 14/51, 27.5%). The median PFS and OS were 21 and 29 months, respectively. The 2-year PFS and OS among the overall population were 45.1% and 54.2%, respectively. Patients who experienced complete remission (CR) after induction therapy had favorable survival compared with non-CR patients (partial remission/stable disease, PR/SD). Patients who experienced CR after first-line induction treatment also had favorable survival, but similar significance was not observed in the salvage treatment group. Although 86.3% of the patients had chidamide-related adverse events (AEs), severe hematological AEs (grade 3) occurred in only 11 (21.6%) patients, indicating the safe toxicity profile of chidamide.
The prolonged survival indicated that chidamide-containing maintenance therapy is promising and well tolerated in patients with TNKLs.
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