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老年套细胞淋巴瘤:生物学风险分层、体能适应性策略与未满足需求

英文原题:Mantle Cell Lymphoma in Geriatric Patients: Biologic Risk Stratification, Fitness-Adapted Strategies, and Unmet Needs.

PubMed 2026/07/21(内容时间) Eur J Haematol Q2 · IF 2.6(JCR 2025)

研究概要

以显著的生物学和临床异质性为特征,老年套细胞淋巴瘤(MCL)患者代表着日益严峻的临床挑战,其驱动因素包括人口老龄化、合并症负担增加以及对强化化疗耐受性降低。

中文摘要

以显著的生物学和临床异质性为特征,老年套细胞淋巴瘤(MCL)患者代表着日益严峻的临床挑战,其驱动因素包括人口老龄化、合并症负担增加以及对强化化疗耐受性降低。本文探讨老年及体能较差MCL患者的当代治疗策略。我们通过PubMed、Embase和Cochrane Library对英文文献进行了结构化综述,纳入2000年1月至2025年11月发表的研究。老年脆弱性与毒性增加和死亡率升高相关,并可能妨碍患者参与临床试验。作为一线治疗,以苯达莫司汀为基础的化学免疫治疗后续利妥昔单抗维持治疗仍是可行选择。第二代布鲁顿酪氨酸激酶抑制剂(BTKis)在初治和复发疾病中均为有效选择,在Ki-67高表达或化疗禁忌或拒绝化疗的患者中优先使用。在TP53突变型MCL中,第二代BTKi联合BCL2抑制及抗CD20治疗似乎具有前景,但需要更大规模的试验。在该年龄组中,自体干细胞移植和CAR-T治疗带来显著的发病风险。抗体药物偶联物和双特异性抗体可能在后线治疗中提供额外选择。最佳管理需要个体化、适应体能状态的策略,整合生物学风险和老年评估。持续开发耐受性良好的方案和合理的序贯治疗对于改善预后至关重要。

展开英文摘要原文

Marked by significant biological and clinical heterogeneity, mantle cell lymphoma (MCL) in older adults represents a growing clinical challenge, driven by an aging population, increasing burden of comorbidities, and reduced tolerance to intensive chemotherapy. This paper tackles contemporary therapeutic strategies for older and less fit patients with MCL. We conducted a structured review of the English literature using PubMed, Embase, and the Cochrane Library, including studies published between January 2000 and November 2025. Geriatric vulnerabilities are associated with increased toxicity and mortality and may preclude participation in clinical trials. As frontline, bendamustine-based chemoimmunotherapy followed by rituximab maintenance remains a feasible option. Second-generation Bruton tyrosine kinase inhibitors (BTKis) constitute valid options in both treatment-na ve and relapsed disease, being preferred in patients with high Ki-67 or when chemotherapy is contraindicated or refused. In TP53-mutated MCL, a second-generation BTKi combined with BCL2 inhibition anti-CD20 therapy appears promising, but larger trials are needed. In this age category, autologous stem cell transplantation and CAR-T therapy pose significant morbidity risks. Antibody-drug conjugates and bispecifics may offer additional options in later lines. Optimal management requires individualized, fitness-adapted strategies integrating biological risk and geriatric assessment. Continued development of well-tolerated regimens and rational sequencing is essential to improve outcomes.

论文信息

作者
Samperio VM、Hamoud M、Ike I、Dasanu CA
第一作者单位
Department of Medicine, Eisenhower Health, Rancho Mirage, California, USA.United States
通讯作者单位
Spohn Cancer Center, Christus Health, Corpus Christi, Texas, USA.United States
文献类型
综述
期刊
European journal of haematology2026 Jul 21
原文标识
PubMed 42482559 · DOI 10.1111/ejh.70272