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:Characteristics and treatment patterns of relapsed/refractory diffuse large B-cell lymphoma in patients receiving ≥3 therapy lines in post-CAR-T era.
Characteristics and treatment patterns of relapsed/refractory diffuse large B-cell lymphoma in patients receiving ≥3 therapy lines in post-CAR-T era.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
CAR-T 获批后,大多数患者在 3 L 和 4 L 接受了 CT/CIT 或靶向治疗,尽管所开具的大多数靶向治疗并未获批用于 DLBCL。
自CAR-T 细胞疗法问世以来,已有多种新型疗法获批用于复发/难治性弥漫性大B细胞淋巴瘤(R/R DLBCL)。本研究旨在描述CAR-T 获批后R/R DLBCL患者的特征和治疗模式。
利用IQVIA PharMetrics Plus行政理赔数据库,识别2017年10月18日后开始接受三线及以上治疗的成年R/R DLBCL患者,数据覆盖2014年1月1日至2020年3月31日。治疗分为化疗/化学免疫治疗(CT/CIT)、靶向治疗、CAR-T 及干细胞移植(SCT)。对接受三线治疗患者的治疗分布、CT/CIT和靶向治疗持续时间及启动下一线治疗的情况进行描述,并对四线治疗重复分析。
2017年10月18日至2020年3月31日,共145名患者接受三线治疗;平均年龄57岁,女性占34%。三线治疗中,44.9%接受CT/CIT,26.9%接受靶向治疗,17.2%接受CAR-T,11.0%接受SCT。CT/CIT和靶向治疗的中位持续时间合计为2.9个月。中位随访5.8个月内,31%的患者开始四线治疗。在接受四线治疗的55名患者中,靶向治疗最常用(36.4%),中位治疗持续时间为2.5个月。
CAR-T 获批后,多数患者在三线和四线治疗中接受CT/CIT或靶向治疗,但所用靶向药物大多尚未获批用于DLBCL。治疗持续时间较短,且相当多患者在短期随访内进入下一治疗线。这项研究凸显了三线及以上R/R DLBCL患者对更有效治疗的迫切需求。
Several novel treatments have been approved for relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) since chimeric antigen receptor T-cell (CAR-T) therapy became available. The objective of this study was to describe characteristics and treatment patterns in patients with R/R DLBCL post-CAR-T approval.
Adult patients with R/R DLBCL who initiated third-line treatment or later (3 L+) since 18 October 2017 were identified using administrative claims from IQVIA PharMetrics Plus (1 January 2014-31 March 2020). Treatments were categorized as chemotherapy/chemoimmunotherapy (CT/CIT), targeted therapies, CAR-T and stem cell transplant (SCT). Treatment distribution, treatment duration of CT/CIT and targeted therapies, and initiation of next-line therapy were described for patients receiving 3 L; analyses were repeated for 4 L.
A total of 145 patients received 3 L between 18 October 2017 and 31 March 2020. Mean age was 57 years, and 34% were female. CT/CIT (44.9%), targeted therapies (26.9%), CAR-T (17.2%) and SCT (11.0%) were administered in 3 L. The median treatment duration was 2.9 months for CT/CIT and targeted therapies combined. 31% of patients initiated 4 L within a median follow-up of 5.8 months. Among patients who received 4 L ( N = 55), targeted therapies were most commonly used (36.4%), and the median treatment duration was 2.5 months.
Post-CAR-T approval, the majority of patients were treated with CT/CIT or targeted therapies in 3 L and 4 L, though most of the targeted therapies prescribed are not indicated for DLBCL. Treatment duration was short. A high proportion of patients moved to the next line of therapy (LOT) during a short follow-up period. This study highlights the unmet need for more effective treatments for patients with R/R DLBCL in 3 L+.
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