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:Real-world outcomes after CAR T versus standard therapy in third-line or later relapsed or refractory follicular lymphoma in the United States.
Real-world outcomes after CAR T versus standard therapy in third-line or later relapsed or refractory follicular lymphoma in the United States.
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在这项真实世界分析中,与非 CAR-T 治疗相比,CAR-T 与更长的 TTNT、更长的 TFI 以及更低的下游 FL 相关费用相关,其解读需结合随访时间和治疗背景的差异。
复发/难治性(R/R)滤泡性淋巴瘤(FL)患者往往需要接受多线治疗。
比较接受CAR-T 与非CAR-T 治疗的R/R FL患者的至下次治疗时间(TTNT)、无治疗间隔(TFI)、医疗资源利用(HRU)及后续医疗费用。
既往接受过2线治疗的成人R/R FL患者按CAR-T 和非CAR-T 队列分组。CAR-T 组以CAR-T 输注日期作为索引日期,非CAR-T 组以三线治疗(3L)开始日期作为索引日期。结局包括TTNT、TFI、HRU和费用。采用描述性分析,并使用Kaplan-Meier方法及多变量模型。
研究纳入335例CAR-T 患者和4342例非CAR-T 患者。CAR-T 组TTNT中位数尚未达到,描述性分析显示其TFI较长。调整后分析显示,CAR-T 组在3L及以上治疗中的药品费用更低(比值[CR] 0.32;95% CI,0.21–0.48;p<0.0001),在4L及以上治疗中的药品费用亦更低(CR 0.26;95% CI,0.16–0.42;p<0.0001);CAR-T 后4L及以上的医疗费用也较低(CR 0.69;95% CI,0.51–0.94;p=0.017)。
这项真实世界分析显示,与非CAR-T 治疗相比,CAR-T 与更长的TTNT、更长的TFI及更低的后续FL相关费用有关;解释结果时需考虑随访时间和治疗情境差异。 通俗摘要:滤泡性淋巴瘤(FL)是一种常在治疗后复发的血液癌症,因此许多患者会先后接受多种治疗。CAR-T 细胞疗法是FL的一种较新治疗选择,可用于至少两种既往疗法失效后的患者。本研究使用医保理赔记录,比较接受CAR-T 的患者与接受其他常规疗法患者在疾病后期的情况。研究评估了患者无需再次治疗的时间、医疗服务使用频率,以及治疗后的医疗费用。总体而言,接受CAR-T 的患者通常更长时间无需追加治疗,CAR-T 治疗后的FL相关治疗费用也低于接受其他疗法者。由于本研究分析的是既有理赔记录而非随机分配治疗,两组患者并不完全相同,随访时长也不同。因此,结果应理解为总体趋势,而非确证性比较。
Relapsed/refractory (R/R) follicular lymphoma (FL) often requires multiple lines of therapy.
To compare time to next treatment (TTNT), treatment-free interval (TFI), healthcare resource utilization (HRU), and downstream costs among R/R FL patients treated with CAR T versus non-CAR T therapy.
Adult R/R FL patients with 2 prior lines of therapy were stratified into CAR T and non-CAR T cohorts. The Index Date was CAR T infusion (CAR T) or 3L initiation (non-CAR T). Outcomes included TTNT, TFI, HRU, and costs. Analyses were descriptive, incorporating Kaplan-Meier methods and multivariable models.
335 CAR T and 4,342 non-CAR T patients were included. Median TTNT was not reached for CAR T, with longer TFIs observed in descriptive analyses. Adjusted analyses showed lower pharmacy costs at both 3L+ (CR 0.32; 95% CI 0.21-0.48; p < 0.0001)and 4L+ (CR 0.26; 95% CI 0.16-0.42; p < 0.0001), and post-CAR T medical costs at 4L+ (CR 0.69; 95% CI 0.51-0.94; p = 0.017).
In this real-world analysis, CAR T was associated with longer TTNT, longer TFI, and lower downstream FL-related costs compared with non-CAR T therapy, with interpretation informed by differences in follow-up time and treatment context. Follicular lymphoma (FL) is a type of blood cancer that often returns after treatment. As a result, many patients receive several different treatments over time. Chimeric antigen receptor T-cell therapy (CAR T) is a newer treatment option for FL that can be used after at least two prior treatments have stopped working. This study used health insurance records to compare what happened to patients who received CAR T with patients who received other standard treatments in later stages of the disease. We looked at how long patients went without needing another treatment, how often they used healthcare services, and the costs of care after treatment. Patients who received CAR T generally went longer without needing additional treatment and had lower FL-related treatment costs after CAR T therapy compared with patients receiving other treatments. As this study looked at existing claims records than assigning treatments, the two patient groups were not exactly the same and were followed for different lengths of time. For this reason, results should be interpreted as showing overall trends rather than definitive comparisons.
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