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:Nutritional and immunologic scoring systems to predict complications and outcomes after anti-B-cell maturation antigen chimeric antigen receptor T-cell therapy in relapsed/refractory multiple myeloma.
Nutritional and immunologic scoring systems to predict complications and outcomes after anti-B-cell maturation antigen chimeric antigen receptor T-cell therapy in relapsed/refractory multiple myeloma.
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CAR-T 细胞免疫治疗前的 CONUT 评分、PNI 和 mGPS 为 R/R MM 患者的风险分层提供了新的见解。基线营养不良可能有助于临床医生识别脆弱患者,以预防或减少不良事件,并在早期提供个体化管理。
嵌合抗原受体(CAR)T细胞疗法在治疗复发/难治性多发性骨髓瘤(R/R MM)方面具有显著获益。尽管营养状态与血液系统恶性肿瘤不良预后之间的相关性已得到证实,但关于其对CAR-T 细胞免疫治疗结局及并发症的预测价值,目前仍知之甚少。
基于LEGEND-2临床试验(1期西安中心)开展了一项回顾性研究,旨在评估由三种营养与免疫评分系统——控制营养状态(CONUT)、预后营养指数(PNI)和改良格拉斯哥预后评分(mGPS)——得出的评分对CAR-T 细胞治疗后的结局和并发症的影响。
所有患者(N = 57)均符合 CONUT 和 PNI 的评估条件,其中 24 例患者可进行 mGPS 评估。接受 CAR-T 细胞免疫治疗的 R/R MM 患者的营养状态最初在最初 2 周内出现下降,随后在 CAR-T 细胞治疗后 3 周出现改善。我们发现,基线 CONUT 评分升高(>4)是严重早期中性粒细胞减少、弥散性血管内凝血、活化部分凝血活酶时间延长和纤维蛋白原降低的危险因素。低 PNI 水平(<36.5)与低丙种球蛋白血症发生率升高相关。最后,我们发现基线 mGPS 与无进展生存期之间存在关联。
A retrospective study was conducted based on the LEGEND-2 clinical trial (Xi'an site of phase 1) to evaluate the impact of scores derived from three nutritional and immunologic scoring systems-Controlling Nutritional Status (CONUT), prognostic nutritional index (PNI) and modified Glasgow Prognostic Score (mGPS)-on outcomes and complications after CAR T-cell therapy.
All patients (N = 57) were eligible for the CONUT and PNI, and 24 patients were available for the mGPS. The nutritional status of R/R MM patients who underwent CAR T-cell immunotherapy initially exhibited a decline within the first 2 weeks followed by an improvement 3 weeks after CAR T-cell therapy. We found that an elevated baseline CONUT score (>4) was a risk factor for severe early neutropenia, disseminated intravascular coagulation, prolonged activated partial thromboplastin time and decreased fibrinogen. Low PNI levels (<36.5) were associated with an elevated incidence of hypogammaglobulinemia. Finally, we found an association between baseline mGPS and progression-free survival.
The CONUT score, PNI and mGPS prior to CAR T-cell immunotherapy offer novel insights into risk stratification in R/R MM patients. Baseline malnutrition might facilitate clinicians in the identification of vulnerable patients to prevent or reduce adverse events and provide individualized management at an early stage.
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