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:Polatuzumab Vedotin Combined With R-ICE (PolaR-ICE) as Second-Line Therapy in Diffuse Large B-Cell Lymphoma.
Polatuzumab Vedotin Combined With R-ICE (PolaR-ICE) as Second-Line Therapy in Diffuse Large B-Cell Lymphoma.
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挽救性化学免疫治疗序贯自体干细胞移植(ASCT)仍是前线治疗后>1年复发的复发/难治性(r/r)弥漫大B细胞淋巴瘤(DLBCL)的标准治疗。
我们评估了维泊妥珠单抗(Pola)联合R-ICE挽救性化疗、随后ASCT后Pola维持治疗的安全性和疗效,旨在提高r/r DLBCL的完全缓解(CR)率并改善ASCT后的结局。
值得注意的是,该研究的入组期早于二线CAR-T 细胞疗法的获批。共入组41例患者并接受PolaR-ICE治疗。该联合方案的不良反应与Pola和R-ICE化疗中观察到的一致,未观察到新的毒性信号,最常见为血液学和胃肠道不良反应。挽救治疗后的总缓解率为88%,CR率为56%。22例患者(56%)随后接受了自体干细胞移植,16例(39%)接受了Pola巩固治疗。在中位随访25个月(范围:18-21)时,所有接受PolaR-ICE治疗的患者(n = 41)的2年PFS为49.9%(95% CI:31.7-65.7),2年OS为75.0%(95% CI:58.5-85.8)。初始治疗后12个月内复发的患者2年PFS为36.4%(90% CI:17.1-56.0),而12个月后复发的患者为80.0%(95% CI:40.9-94.6)。
我们的研究结果表明,Pola-RICE是r/r DLBCL一种安全有效的挽救方案,可考虑用于晚期复发患者或CAR-T 可及性可能有限的地区。试验注册:ClinicalTrials.gov标识符:NCT04665765。
Salvage chemoimmunotherapy followed by autologous stem cell transplantation (ASCT) remains a standard therapy for relapsed/refractory (r/r) diffuse large B-cell lymphoma (DLBCL) who relapse > 1 year after frontline treatment.
We evaluated the safety and efficacy of polatuzumab vedotin (Pola) combined with R-ICE salvage chemotherapy, followed by post-ASCT Pola maintenance, aiming to improve complete response (CR) rates and enhance post-ASCT outcomes in r/r DLBCL.
Notably, the study's accrual period predated the approvals of second-line CAR T cell therapies. Forty-one patients were enrolled and received PolaR-ICE. Adverse effects of the combination were consistent with those observed with Pola and R-ICE chemotherapy with no new toxicity signals observed and were most commonly hematologic and gastrointestinal. The overall response rate after salvage was 88% with a CR rate of 56%.
Twenty-two patients (56%) went on to receive autologous stem cell transplant and 16 (39%) received Pola consolidation. At a median follow-up of 25 months (range: 18-21), the 2-year PFS of all patients treated with PolaR-ICE (n = 41) was 49. 9% (95% CI: 31. 7-65. 7) and 2-year OS was 75. 0% (95% CI: 58. 5-85. 8). Patients with relapse 12 months of initial therapy achieved a 2-year PFS of 36. 4% (90% CI: 17. 1-56. 0) versus 80. 0% (95% CI: 40. 9-94. 6) among patients with relapse 12 months.
Our findings demonstrate that Pola-RICE is a safe and effective salvage regimen for r/r DLBCL, which can be considered for patients with late relapse or in areas where CAR T access may be limited. Trial Registration: ClinicalTrials. gov identifier: NCT04665765.
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