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:Recent advances and future directions in newly diagnosed mantle cell lymphoma.
Recent advances and future directions in newly diagnosed mantle cell lymphoma.
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本综述将讨论这一棘手疾病初始治疗的最新进展,以及一套兼顾一线 cBTKi 可及与不可及情况的建议治疗流程。
引言:套细胞淋巴瘤(MCL)的管理和治疗近期取得重大进展。这种少见的成熟B细胞淋巴瘤亚型临床病程异质,涵盖惰性至侵袭性疾病谱。过去长期被认为无法治愈且远期预后不佳,但近期进展改善了患者结局。 综述范围:近期临床试验支持在初始治疗中应用共价布鲁顿酪氨酸激酶抑制剂(cBTKi),无论是否联合免疫化疗,均显示出令人鼓舞的疗效和安全性。可测量微小残留病(MRD)检测正成为指导治疗决策、改善结局并尽量减少毒性的有力工具。用于复发/难治性疾病的治疗,包括BCL2抑制剂及利用免疫效应的疗法(如T细胞衔接抗体和嵌合抗原受体[CAR]T细胞疗法),也正在初始治疗情境中接受评估。 专家观点:本综述讨论这一棘手疾病初始治疗管理的近期进展,并在一线cBTKi可用与不可用两种情况下提出治疗流程建议。将cBTKi纳入免疫化疗方案似乎有效且安全。不过,免疫化疗疗效不理想,因此高危患者可能需要新型治疗策略。
INTRODUCTION: There have been recent major advances in the management and treatment of mantle cell lymphoma (MCL). This uncommon subtype of mature B-cell lymphoma has a heterogeneous clinical course, including a spectrum of indolent and aggressive disease. While historically regarded as an incurable disease with a poor long-term prognosis, recent developments have improved outcomes. AREAS COVERED: The incorporation of targeted treatments, such as covalent Bruton's tyrosine kinase inhibitors (cBTKi), with or without chemo-immunotherapy in the upfront treatment setting is supported by recent clinical trials indicating encouraging efficacy and safety.
Measurable residual disease (MRD) testing is emerging as a potent tool in guiding treatment decision and improving outcomes while minimizing toxicities. Therapies utilized in relapsed/refractory disease, such as BCL2 inhibitors as well as immune-leveraging therapies, including T-cell engaging antibodies and chimeric antigen receptor (CAR) T-cells therapy, are being evaluated in upfront settings.
EXPERT OPINION: This review will discuss recent advances in the upfront management of this challenging disease as well as a suggested treatment algorithm considering both availability and unavailability of first-line cBTKi. The incorporation of cBTKi to chemo-immunotherapy regimens appears effective and safe.
However, patients with high-risk disease may require novel therapeutic approaches due to suboptimal outcomes with chemo-immunotherapy.
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