不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Venetoclax plus dose-adjusted R-EPOCH (VR-DA-EPOCH) or G-EPOCH bridging to subsequent cellular therapy for the patients with transformed lymphoma a single center clinical experience.
Venetoclax plus dose-adjusted R-EPOCH (VR-DA-EPOCH) or G-EPOCH bridging to subsequent cellular therapy for the patients with transformed lymphoma a single center clinical experience.
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惰性淋巴瘤,包括慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)和滤泡性淋巴瘤(FL),可发生组织学转化,成为通常为弥漫性大B细胞淋巴瘤(DLBCL)的侵袭性亚型。转化淋巴瘤预后较差。
本研究报告了维奈克拉联合剂量调整的利妥昔单抗或奥妥珠单抗、依托泊苷、泼尼松、长春新碱、多柔比星和环磷酰胺(VR-DA-EPOCH或VG-DA-EPOCH)治疗11例活检证实转化为DLBCL患者的疗效和毒性,其中8例为Richter转化(RT),3例为转化型FL(tFL)。研究于2019年10月至2023年3月在单中心开展,入组患者中位年龄53岁。治疗结束时,6例患者(6/7,85.7%)达到完全缓解(CR);最佳总缓解率(ORR)和CR率均为72.7%。2例患者接受自体造血干细胞移植(ASCT),另有2例在ASCT同时接受CAR-T 巩固治疗。入组后中位随访13.5个月(范围2.4至29.8个月),中位无事件生存期、无进展生存期和总生存期分别为9.4、11.5和17.5个月。3级血液学毒性包括中性粒细胞减少(90.9%,10/11)、血小板减少(63.6%,7/11)和发热性中性粒细胞减少(54.5%,6/11)。
总之,VR-DA-EPOCH或VG-DA-EPOCH可能是帮助该人群早期缓解并过渡至细胞治疗的有前景策略。
Indolent lymphoma, including chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) and follicular lymphoma (FL), can undergo histological transformation into an aggressive subtype, typically diffuse large B-cell lymphoma (DLBCL). The prognosis of transformed lymphoma is poor. In this study, we reported the efficacy and toxicity of a combination of venetoclax, dose-adjusted rituximab or obinutuzumab, etoposide, prednisone, vincristine, doxorubicin, and cyclophosphamide (VR-DA-EPOCH or VG-DA-EPOCH) in 11 patients with biopsy-proven histology transformation into DLBCL, including 8 patients with RT and 3 with transformed FL (tFL). The study was conducted between October 2019 and March 2023 at our single center.
The median age of participants at enrolment was 53 years. Six patients (85. 7%, 6/7) achieved complete remission (CR) at the end of treatment. The best overall response rate (ORR) and CR rate were both 72. 7%, respectively. Two patients received autologous hemopoietic stem cell transplant (ASCT) while two patients received ASCT concurrently with CAR-T therapy for consolidation.
With a median follow-up of 13. 5 (range, 2. 4-29. 8) months after enrollment, the median event-free survival, progression-free survival, and overall survival were 9. 4, 11. 5, and 17. 5 months, respectively. Hematologic toxicities of grade 3 consisted of neutropenia (90. 9%, 10/11), thrombocytopenia (63. 6%, 7/11), and febrile neutropenia (54. 5%, 6/11).
In conclusion, VR-DA-EPOCH or VG-DA-EPOCH was a promising strategy to achieve an early remission, bridging to cellular therapy within this population.
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