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拓展研究:利妥昔单抗马罗替尼作为门诊或住院治疗用于社区机构的复发/难治性大B细胞淋巴瘤的2期研究。

OUTREACH: phase 2 study of lisocabtagene maraleucel as outpatient or inpatient treatment at community sites for R/R LBCL.

作者信息

Linhares Yuliya, Freytes Cesar O, Cherry Mohamad, Bachier Carlos, Maris Michael, Hoda Daanish, Varela Juan C, Bellomo Courtney, Cross Scott, Essell James, Fanning Suzanne, Terebelo Howard, Yimer Habte, Courtright Jay, Sharman Jeff P, Kostic Ana, Vedal Min, Ogasawara Ken, Avilion Ariel, Espinola Ricardo, Yuan Brenda, Mattar Bassam

机构信息

Baptist Health, Miami Cancer Institute, Miami, FL.

Sarah Cannon Transplant & Cellular Therapy Program at Methodist Hospital, San Antonio, TX.

出版信息

Blood Adv. 2024 Dec 10;8(23):6114-6126. doi: 10.1182/bloodadvances.2024013254.

Abstract

Lisocabtagene maraleucel (liso-cel) is an autologous, CD19-directed, 4-1BB chimeric antigen receptor (CAR) T-cell product approved for relapsed/refractory (R/R) large B-cell lymphoma (LBCL). We present the OUTREACH primary analysis, evaluating the safety and efficacy of outpatient monitoring after liso-cel treatment at community sites in the United States. Adults with R/R LBCL after ≥2 prior lines of therapy received liso-cel. Outpatient vs inpatient monitoring was per investigator discretion. The primary end points were incidences of grade ≥3 cytokine release syndrome (CRS), neurological events (NEs), prolonged cytopenia, and infections. Efficacy was a secondary end point. Eighty-two patients received liso-cel (outpatient monitored, 70%; inpatient monitored, 30%). The median follow-up was 10.6 months (range, 1.0-24.5). In outpatients and inpatients, grade ≥3 CRS occurred in 0% and 0%, NEs in 12% and 4%, infections in 12% and 8%, and prolonged cytopenia in 33% and 32%, respectively. Among outpatients, 25% were never hospitalized after infusion, and 32% were hospitalized ≤72 hours after the day of infusion; the median time to hospitalization was 5.0 days (range, 2-310). The median initial hospitalization duration after liso-cel was 6.0 days (range, 1-28) for outpatients and 15.0 days (range, 3-31) for inpatients. Objective response rate was 80%, complete response rate was 54%, and the median duration of response was 14.75 months (95% confidence interval, 5.0 to not reached). OUTREACH is, to our knowledge, the first and largest study to prospectively assess CAR T-cell therapy with outpatient monitoring in community-based medical centers. Liso-cel demonstrated meaningful efficacy with favorable safety in patients with R/R LBCL. Data support the feasibility of liso-cel administration at community sites with outpatient monitoring. This trial was registered at www.ClinicalTrials.gov as #NCT03744676.

摘要

利妥昔单抗(liso-cel)是一种自体、靶向CD19、4-1BB嵌合抗原受体(CAR)T细胞产品,已被批准用于复发/难治性(R/R)大B细胞淋巴瘤(LBCL)。我们展示了OUTREACH的初步分析结果,评估了美国社区机构中利妥昔单抗治疗后门诊监测的安全性和有效性。接受过≥2线先前治疗的R/R LBCL成年患者接受了利妥昔单抗治疗。门诊还是住院监测由研究者自行决定。主要终点是≥3级细胞因子释放综合征(CRS)、神经系统事件(NE)、长期血细胞减少和感染的发生率。疗效是次要终点。82例患者接受了利妥昔单抗治疗(门诊监测,70%;住院监测,30%)。中位随访时间为10.6个月(范围1.0 - 24.5个月)。门诊患者和住院患者中,≥3级CRS的发生率分别为0%和0%,NE的发生率分别为12%和4%,感染的发生率分别为12%和8%,长期血细胞减少的发生率分别为33%和32%。在门诊患者中,25%在输注后从未住院,32%在输注当天后≤72小时住院;住院的中位时间为5.0天(范围2 - 310天)。利妥昔单抗治疗后门诊患者的初始住院中位时长为6.0天(范围1 - 28天),住院患者为15.0天(范围3 - 31天)。客观缓解率为80%,完全缓解率为54%,中位缓解持续时间为14.75个月(95%置信区间,5.0至未达到)。据我们所知,OUTREACH是第一项也是规模最大的前瞻性评估在社区医疗中心进行门诊监测的CAR T细胞疗法的研究。利妥昔单抗在R/R LBCL患者中显示出有意义的疗效且安全性良好。数据支持在社区机构进行门诊监测下给予利妥昔单抗的可行性。该试验已在www.ClinicalTrials.gov上注册,编号为#NCT03744676。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be5b/11652776/35558e30a926/BLOODA_ADV-2024-013254-ga1.jpg

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