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 of extranodal NK/T-cell lymphoma: From past to future.
Treatment of extranodal NK/T-cell lymphoma: From past to future.
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结外NK/T细胞淋巴瘤(ENKTCL)是亚洲和拉丁美洲最常见的T/NK细胞淋巴瘤亚型,但在北美和欧洲极为罕见。过去20年患者生存显著改善。
然而,尽管已开展数十项前瞻性试验,标准治疗方案仍未确立。为了解ENKTCL治疗的演变及未来趋势,我们全面综述了这种侵袭性恶性肿瘤的治疗,特别关注一些被忽视或尚无答案的问题,如最佳分期方法、天冬酰胺酶(Asp)的最佳联合药物、Asp的个体化给药,以及化疗(CT)和放疗(RT)的优选顺序等。
总体而言,Ann Arbor I/II期患者的5年总生存率从20世纪初不足50%提升至近年来超过80%;Ann Arbor III/IV期患者的总生存期中位数从不足1年延长至3年以上。患者生存改善主要归因于放疗技术进步,以及Asp和抗PD-1/PD-L1免疫疗法应用于临床。早期患者治疗离不开放疗,而基于Asp的化疗和PD-1/PD-L1抑制剂显著改善了晚期患者预后。ENKTCL治疗正朝着方案更简洁、毒性更低、疗效更高的方向发展。工程化T细胞、单克隆抗体和小分子抑制剂等新药正在得到深入研究。鉴于除Asp外ENKTCL对细胞毒药物高度耐药,而强化化疗只会增加毒性、未能改善结局,我们认为没有必要再投入额外资源比较Asp与不同细胞毒药物的联合方案。更应加大力度优化Asp和免疫疗法的使用,以最大限度提高疗效并降低毒性;探索克服Asp和免疫疗法耐药的方法;识别新治疗靶点;并确定更可能从特定治疗中获益的亚群。
Extranodal NK/T-cell lymphoma (ENKTCL) is the most common subtype of T/NK-cell lymphoma in Asia and Latin America, but very rare in North American and Europe. Patient survival has improved significantly over the past two decades.
However, standard treatment has not yet been established, although dozens of prospective trials have been conducted. To help understand how the treatment of ENKTCL has evolved in the past and what trends lie ahead, we have comprehensively reviewed the treatment of this aggressive malignancy, with a particular focus on neglected or unanswered issues, such as the optimal staging method, the best partner of asparaginase (Asp), the individualized administration of Asp, the preferred sequence of CT and RT and so on.
Overall, the 5-year overall survival (OS) of patients with Ann Arbor stage I/II disease increased from < 50% in the early 20th century to > 80% in recent years, and the median OS of patients with Ann Arbor stage III/IV disease increased from < 1 year to more than 3 years. The improvement in patient survival is largely attributable to advances in radiation technology and the introduction of Asp and anti-PD-1/PD-L1 immunotherapy into practice. Radiotherapy is essential for patients with early-stage disease, while Asp-based chemotherapy (CT) and PD-1/PD-L1 inhibitors significantly improved the prognosis of patients with advanced-stage disease. ENKTCL management is trending toward simpler regimens, less toxicity, and higher efficacy.
Novel drugs, such as manufactured T cells, monoclonal antibodies, and small molecule inhibitors, are being intensively investigated. Based on the fact that ENKTCL is highly resistant to cytotoxic drugs except Asp, and aggressive CT leads to higher toxicity rather than better outcomes, we recommend it is unnecessary to expend additional resources to compare different combinations of Asp with cytotoxic agents.
Instead, more efforts should be made to optimize the use of Asp and immunotherapy to maximize efficacy and minimize toxicity, explore ways to overcome resistance to Asp and immunotherapy, identify novel treatment targets, and define subpopulations who may benefit more from specific treatments.
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