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:Treatment and Prognosis of Newly Diagnosed Advanced-Stage Extranodal Natural Killer/T-Cell Lymphoma: A Single-Center Real-World Study across Two Decades.
Treatment and Prognosis of Newly Diagnosed Advanced-Stage Extranodal Natural Killer/T-Cell Lymphoma: A Single-Center Real-World Study across Two Decades.
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天冬酰胺酶和吉西他滨单药对 PFS 和 OS 产生了有利影响;天冬酰胺酶和吉西他滨联合化疗取得了最佳的疗效、缓解持续时间和生存结局。包括强效化疗辅以放疗和/或巩固性移植在内的综合治疗模式可改善新诊断晚期 ENKTCL 的预后。
尽管目前对于晚期结外NK/T细胞淋巴瘤(ENKTCL)采用以培门冬酶为基础的化疗方案已达成共识,但根据既往文献报道,真实世界中的患者生存情况仍不乐观,在综合治疗理念下最优化疗方案及不同治疗方法的整合仍需进一步探索和验证。
回顾性收集并分析中国国家癌症中心近二十年来新诊断的Ⅲ/Ⅳ期ENKTCL患者。总生存期(OS)和无进展生存期(PFS)被确定为主要终点。采用Log-rank检验和Cox比例风险模型检验亚组间的生存差异,并检验单变量和多变量关联。
该研究纳入83例新诊断的Ⅲ/Ⅳ期ENKTCL患者,报告中位OS为26.07个月,中位随访82.13个月时估计5年OS为41.3%。与不含培门冬酶的方案相比,一线含培门冬酶方案显著延长PFS(p = 0.007;HR = 0.48,p = 0.020),并显示出改善OS的趋势(p = 0.064;HR = 0.74,p = 0.359)。与不含吉西他滨的方案相比,含吉西他滨方案也显示出改善PFS(p = 0.048;HR = 0.59,p = 0.164)和OS(p = 0.008;HR = 0.67,p = 0.282)的趋势。培门冬酶与吉西他滨联合方案的5年OS为55.0%,与其余方案相比,PFS显著更优(p = 0.020;HR = 0.40,p = 0.022),OS略有改善(p = 0.054;HR = 0.79,p = 0.495)。与单纯化疗相比,整合化疗和放疗的一线联合模式治疗改善了PFS(p = 0.051)和OS(p = 0.036)。4例接受自体造血干细胞移植的受者中位OS达到58.34个月。
Newly diagnosed stage Ⅲ/Ⅳ ENKTCL patients from Chinese National Cancer Center in the last two decades were retrospectively collected and analyzed. Overall survival (OS) and progression-free survival (PFS) were determined as primary endpoints. Log-rank tests and Cox proportional hazard models were performed to test for survival differences between subgroups and examine the univariable and multivariable associations.
The study included 83 newly diagnosed stage Ⅲ/Ⅳ ENKTCL patients and reported a median OS of 26.07 months and an estimated 5-year OS of 41.3% with a median follow-up of 82.13 months. First-line asparaginase-based regimens compared to non-asparaginase-based regimens significantly prolonged PFS (p = 0.007; HR = 0.48, p = 0.020) and showed a tendency to improve OS (p = 0.064; HR = 0.74, p = 0.359). Gemcitabine-based regimens also exhibited a trend toward improved PFS (p = 0.048; HR = 0.59, p = 0.164) and OS (p = 0.008; HR = 0.67, p = 0.282) compared to non-gemcitabine-based ones. The asparaginase and gemcitabine combinations yielded a 5-year OS of 55.0% and led to significantly superior PFS (p = 0.020; HR = 0.40, p = 0.022) and slightly better OS (p = 0.054; HR = 0.79, p = 0.495) compared to the remaining regimens. First-line combined-modality treatment integrating chemotherapy and radiotherapy improved PFS (p = 0.051) and OS (p = 0.036) compared to chemotherapy alone. Four autologous hematopoietic stem cell transplantation recipients reached a median OS of 58.34 months.
Asparaginase and gemcitabine alone brought a favorable impact on PFS and OS; and the asparaginase and gemcitabine combination chemotherapy yielded the optimal efficacy, response duration, and survival outcomes. Combined-modality treatment including potent chemotherapy supplemented by radiotherapy and/or consolidative transplantation could improve prognosis in newly diagnosed advanced-stage ENKTCLs.
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