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:When Timing Matters Most: Early Relapse Outweighs Baseline Risk in Myeloma.
When Timing Matters Most: Early Relapse Outweighs Baseline Risk in Myeloma.
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多发性骨髓瘤的结局差异很大,风险分层通常基于基线特征。功能性高危多发性骨髓瘤(FHRMM)定义为初始治疗或自体干细胞移植后12个月内早期复发,与不良预后相关。然而,在FHRMM队列中,基线高危特征的持续预后影响仍不明确。本研究分析了来自CoMMpass数据集的181例FHRMM患者,根据基线细胞遗传学和ISS分期分为标危组(SRG)和高危组(HRG)。尽管SRG患者具有更有利的基线风险特征,包括较低的SKY92评分,但其总生存期(OS)与HRG患者无显著差异(20.7 vs. 18.1个月,p = 0.059)。两组之间的治疗方案和缓解率相当。在FHRMM队列中,仅基线ISS I期对OS保留了预后意义。总之,FHR状态在决定预后方面超越了传统的基线风险因素。经历早期复发的患者应被视为统一的高危人群,这凸显了对有效挽救治疗的需求以及考虑CAR-T 细胞疗法等新型治疗的必要性。
Multiple myeloma outcomes vary widely, with risk stratification typically based on baseline characteristics. Functionally high-risk multiple myeloma (FHRMM), defined by early relapse within 12 months of initial therapy or autologous stem cell transplant, is associated with poor prognosis.
However, the continued prognostic impact of baseline high-risk features within the FHRMM cohort remains unclear.
This study analyzed 181 FHRMM patients from the CoMMpass dataset, categorized into standard-risk (SRG) and high-risk (HRG) groups based on baseline cytogenetics and ISS stage. Despite SRG patients possessing more favorable baseline risk profiles, including lower SKY92 scores, their overall survival (OS) was not significantly different from HRG patients (20. 7 vs. 18. 1 months, p = 0. 059). Treatment regimens and response rates were comparable between groups. Within the FHRMM cohort, only baseline ISS stage I retained prognostic significance for OS.
In conclusion, FHR status overrides traditional baseline risk factors in determining prognosis. Patients experiencing early relapse should be considered uniformly high-risk, highlighting the need for effective salvage therapies and consideration of novel treatments like CAR T-cell therapies.
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