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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Salvage High-dose Melphalan With Autologous Stem cell Transplantation as Bridge to Consolidation Therapy for Chemoresistant Aggressive B-cell Lymphoma.
Salvage High-dose Melphalan With Autologous Stem cell Transplantation as Bridge to Consolidation Therapy for Chemoresistant Aggressive B-cell Lymphoma.
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单药大剂量美法仑在化疗耐药、未控制的侵袭性 B 细胞淋巴瘤患者中产生高缓解率,并为巩固治疗提供机会窗口。
对挽救化疗无应答的难治性侵袭性B细胞淋巴瘤患者预后极差。CAR-T 细胞或异基因干细胞移植(SCT)可能具有根治潜力。然而,为使这两种巩固治疗长期有效,治疗前实现缓解并降低肿瘤负荷似乎至关重要。
本回顾性分析纳入两家三级医疗中心接受强化治疗的化疗耐药侵袭性B细胞淋巴瘤患者。化疗耐药定义为至少对二线挽救化疗无应答或疾病进展,包括自体干细胞移植(ASCT)前紧接的一种治疗方案。患者接受单药大剂量(HD)马法兰,以期在巩固治疗前获得缓解。
研究纳入36例患者,接受单药HD马法兰和ASCT诱导缓解,随后接受CAR-T 细胞治疗或异基因SCT。可评估患者中,13例(39.4%)达到部分缓解,9例(27.3%)达到完全缓解,总缓解率(ORR)为66.7%。各亚组缓解率均较高,包括原发难治性淋巴瘤患者(ORR 58.3%)以及疾病未控制、乳酸脱氢酶(LDH)升高的患者(LDH超过正常上限2倍者ORR 66.7%)。22例患者后续接受异基因SCT,5例接受CAR-T 细胞治疗。ASCT相关治疗死亡率为5.5%(2例,均死于感染)。全体患者两年总生存率为15.8%;主要原因是接受清髓性预处理化疗的异基因SCT患者非复发死亡率较高(45.5%)。
单药HD马法兰可使化疗耐药、疾病未控制的侵袭性B细胞淋巴瘤患者获得较高缓解率,为后续巩固治疗创造机会。 微摘要:挽救治疗后仍复发或难治的侵袭性B细胞淋巴瘤预后极差,是尚未满足的医疗需求。本研究回顾性分析36例患者,显示单药大剂量马法兰可获得较高缓解率(ORR 66.7%),即使疾病尚未控制也可能奏效,从而使后续异基因干细胞移植或CAR-T 细胞治疗等巩固方案成为可能。
Patients suffering from refractory aggressive B-cell lymphoma not responding to salvage chemotherapy have a dismal prognosis. CAR T-cells or allogeneic stem cell transplantation (SCT) are potentially curative approaches. However, obtaining a remission, and lowering tumor burden before consolidation seems crucial for long-term efficacy of both treatment modalities.
In this retrospective analysis, we reviewed patients with chemoresistant aggressive B-cell lymphoma, defined as being refractory or progressive to at least second line salvage chemotherapy including the regimen immediately preceding autologous stem cell transplantation (ASCT), treated at 2 tertiary centers, who were eligible for intensive treatment using single agent high-dose (HD) melphalan to obtain a remission before consolidating therapy.
We identified 36 patients that received single agent HD melphalan and ASCT as remission induction followed by CAR T-cells or allogeneic stem cell transplantation (SCT). Thirteen of the evaluable patients (39.4%) achieved a partial remission and 9 patients (27.73%) a complete remission, resulting in an overall response rate (ORR) of 66.7%. High remission rates were seen across all subgroups including patients with primary refractory lymphoma (ORR 58.3%), uncontrolled disease and high tumor burden as indicated by increased LDH levels (ORR 66.7% for patients with elevated LDH above 2 times upper limit of norm). 22 patients proceeded to allogeneic SCT and 5 to CAR T-cell therapy. Treatment related mortality of ASCT was 5.5% (2 patients, both due to infections). Two-year overall survival of all patients was 15.8%, primarily due to a high non-relapse mortality (45.5%) of allogeneic SCT patients treated with myeloablative conditioning chemotherapy.
Single agent HD melphalan produces high remission rates in patients with chemoresistant, uncontrolled aggressive B-cell lymphoma and provides a window of opportunity for consolidation therapy. MICROABSTRACT: Patient with refractory/relapsed aggressive B-cell lymphoma after salvage therapy are an unmet medical need because of their very poor prognosis. In our retrospective analysis of 36 patients we showed that single agent high-dose melphalan can achieve high response rates (ORR 66.7%) even in uncontrolled disease enabling consolidation therapy e.g. with allogeneic stem cell transplantation or CAR T-cell therapy.
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