CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ibrutinib, lenalidomide, and rituximab in relapsed mantle cell lymphoma: Long-term follow-up of the Nordic Lymphoma Group MCL6 Philemon trial.
Ibrutinib, lenalidomide, and rituximab in relapsed mantle cell lymphoma: Long-term follow-up of the Nordic Lymphoma Group MCL6 Philemon trial.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
复发/难治性套细胞淋巴瘤(R/R MCL)仍然难以治疗,其结局取决于治疗方案和一线治疗后的缓解持续时间。多种非化疗方案正在R/R中进行评估,但很少有研究报告长期结局。
在本研究中,我们展示了北欧淋巴瘤组MCL6 Philemon 2期试验中50例接受伊布替尼、来那度胺和利妥昔单抗(IR2)治疗患者的长期结局。生存结局与来自瑞典MCL完整研究的匹配队列进行了比较。5年后,14例患者(28%)仍无复发,其中包括1例携带TP53突变。中位无进展生存期(PFS)为17.4个月,最长PFS为8.1年。32例患者已死亡,主要死于MCL(72%)。较差的生存与中危或高危套细胞淋巴瘤国际预后指数以及健康相关生活质量(HRQoL)受损相关。虽然TP53突变(n = 11)未显著影响生存,但在多变量Cox回归分析中观察到结局较差的趋势(PFS风险比:2.09,95%置信区间:0.95-4.62,p = 0.068)。与MCL完整队列相比,IR2方案在匹配前后均显示出更优的生存。
总之,本研究强调了非化疗药物在R/R MCL中的作用,并证明了HRQoL对总生存期的预后影响。尽管IR2在TP53突变患者中显示出初步活性,但并未完全克服其不良预后。
然而,IR2方案可作为异基因干细胞移植或CAR-T 细胞治疗的桥接。
Relapsed or refractory mantle cell lymphoma (R/R MCL) remains difficult to treat, with outcomes dependent on the treatment regimen and remission duration after first-line therapy. Several non-chemotherapeutic regimens are under evaluation in R/R, but few studies report long-term outcomes. In this study, we present the long-term outcomes of the 50 patients treated with ibrutinib, lenalidomide, and rituximab (IR2) in the Nordic Lymphoma Group MCL6 Philemon phase 2 trial. Survival outcomes were compared with a matched cohort from the Swedish MCL complete study. After 5 years, 14 patients (28%) remained relapse-free, including one with a TP53 mutation.
The median progression-free survival (PFS) was 17. 4 months, with the longest PFS of 8. 1 years. Thirty-two patients had died, primarily from MCL (72%). Poorer survival was associated with intermediate or high-risk Mantle Cell Lymphoma International Prognostic Index and impaired health-related quality of life (HRQoL).
While TP53 mutations ( n = 11) did not significantly impact survival, a trend toward poorer outcomes was observed in multivariable Cox regression analyses (PFS hazard ratio: 2. 09, 95% confidence interval: 0. 95-4. 62, p = 0. 068). The IR2 regimen demonstrated superior survival compared to the MCL complete cohort both before and after matching.
In conclusion, this study highlights the role of non-chemotherapeutic agents in R/R MCL and demonstrates the prognostic impact of HRQoL on overall survival. Although IR2 showed initial activity in TP53-mutated patients, it did not completely overcome their poor prognosis.
However, the IR2 regimen may serve as a bridge to allogeneic stem cell transplantation or chimeric antigen receptor T-cell therapy.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。