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:Case Report: CD19 CAR T-cell therapy following autologous stem cell transplantation: a successful treatment for R/R CD20-negative transformed follicular lymphoma with TP53 mutation.
Case Report: CD19 CAR T-cell therapy following autologous stem cell transplantation: a successful treatment for R/R CD20-negative transformed follicular lymphoma with TP53 mutation.
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。
本病例凸显了 ASCT 后 CD19 CAR-T 细胞疗法对 R/R tFL 的惊人疗效,从而为未来的治疗策略提供了新的见解。
滤泡性淋巴瘤(FL)是一种常见的惰性B细胞淋巴瘤,有可能转化为侵袭性淋巴瘤,如弥漫性大B细胞淋巴瘤(DLBCL)。转化性滤泡性淋巴瘤(tFL)患者的预后较差,尤其是化疗后转化的淋巴瘤患者和24个月内进展(POD24)的患者。嵌合抗原受体(CAR)T细胞疗法联合自体干细胞移植(ASCT)具有良好的抗肿瘤疗效。病例介绍:在此,我们描述了一名39岁男性患者,最初诊断为FL,在3线治疗后转化为DLBCL,伴有POD24、CD20阴性、TP53突变和巨大肿块,这些都是不良预后因素。我们采用了联合方案:ASCT后输注CD19 CAR-T 细胞。持续给予伊布替尼以增强疗效,DHAP作为挽救性化疗,ICE作为桥接方案。患者在第-7~-1天接受BEAM预处理,第01~02天输注总计3.8 10 6/kg CD34 + 干细胞,第03天输注总计10 8 CAR-T 细胞(relmacabtagene autoleucel,relma-cel,JWCAR029)。根据机构标准,患者出现2级细胞因子释放综合征(CRS),表现为发热和低血压。CAR-T 细胞输注后未出现免疫效应细胞相关神经毒性综合征(ICANS)。最终,患者在+1个月时达到CMR,并一直维持,未出现其他不良反应。
Follicular lymphoma (FL), a common indolent B-cell lymphoma, has the potential to transform into an aggressive lymphoma, such as diffuse large B-cell lymphoma (DLBCL). The outcome of patients with transformed follicular lymphoma (tFL) is poor, especially in patients with transformed lymphoma after chemotherapy and patients with progression within 24 months (POD24). Chimeric antigen receptor (CAR) T-cell therapy combined with autologous stem cell transplantation (ASCT) has promising antitumor efficacy. CASE PRESENTATION: Here, we described a 39-year-old male patient who was initially diagnosed with FL that transformed into DLBCL with POD24, CD20 negativity, TP53 mutation, and a bulky mass after 3 lines of therapy, all of which were adverse prognostic factors. We applied a combination approach: CD19 CAR T-cell infusion following ASCT. Ibrutinib was administered continuously to enhance efficacy, DHAP was administered as a salvage chemotherapy, and ICE was administered as a bridging regimen. The patient underwent BEAM conditioning on days -7~ -1, a total of 3.8 10 6/ kg CD34 + stem cells were infused on days 01~02, and a total of 10 8 CAR T cells (relmacabtagene autoleucel, relma-cel, JWCAR029) were infused on day 03. The patient experienced grade 2 cytokine release syndrome (CRS), manifesting as fever and hypotension according to institutional standards. There was no immune effector cell-associated neurotoxicity syndrome (ICANS) after CAR T-cell infusion. Finally, the patient achieved CMR at +1 month, which has been maintained without any other adverse effects.
This case highlights the amazing efficacy of CD19 CAR T-cell therapy following ASCT for R/R tFL, thus providing new insight on therapeutic strategies for the future.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。