Possibility of long-term remission in patients with advanced hematologic malignancies after reduced intensity conditioning regimen (RIC) and allogeneic stem cell transplantation.

Alessandra Picardi, Paolo de Fabritiis Pd, Laura Cudillo, Teresa Dentamaro, Luca Cupelli, Giovanna Ballatore, Adriano Venditti, Tommaso Caravita, Maria Cristina Cox, Gianfranco Catalano, Sergio Amadori
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引用次数: 3

Abstract

High-dose chemotherapy and radiation used as a preparative regimen for allogeneic stem cell transplantation (SCT) produces a considerable morbidity and mortality. An alternative strategy, developed to reduce transplant-related toxicity and to induce graft versus malignancy effect in the presence of full hematopoietic engraftment, includes the application of RIC that provide sufficient immunosuppression. We studied the efficacy and toxicity of RIC followed by allogeneic SCT in elderly patients or with relative contraindications to conventional SCT. In all, 22 patients with hematologic malignancies and HLA-identical sibling donors were included in this study. All patients were either refractory to therapy or beyond first complete remission (CR). The majority of patients received fludarabine 120 mg/m(2)+thiotepa 10 mg/kg as conditioning regimen and cyclosporine as graft versus host disease (GVHD) prophylaxis. Organ toxicity was acceptable and all evaluable patients achieved engraftment. Three patients (15%) showed grade >II aGVHD; extensive chronic GVHD occurred in three out of 15 evaluable patients (20%). With median follow-up of 63.5 months, survival was 31%, disease-free survival (DFS) was 23%. All the durable responses occurred in patients who developed GVHD. Transplant related mortality (TRM) at 100 days was 27.3%, 67% of that caused by infections, while 6-year cumulative incidence of TRM was 38%. Our data show that RIC: (1). allows the engraftment of HLA-matched hematopoietic stem cells (2). provide durable responses in patients not eligible for conventional SCT exploiting the graft-versus-malignancy effect and (3). is loaded by an high rate of fatal infections.

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降低强度调节方案(RIC)和同种异体干细胞移植后晚期血液恶性肿瘤患者长期缓解的可能性。
大剂量化疗和放疗作为同种异体干细胞移植(SCT)的准备方案产生相当高的发病率和死亡率。另一种策略是在完全造血植入的情况下减少移植相关的毒性和诱导移植物抗恶性肿瘤效应,包括应用提供足够免疫抑制的RIC。我们研究了RIC后同种异体SCT对老年患者或对常规SCT有相对禁忌症的患者的疗效和毒性。总共有22名血液学恶性肿瘤患者和hla相同的兄弟姐妹供体被纳入本研究。所有患者要么对治疗难治,要么超过首次完全缓解(CR)。大多数患者接受氟达拉滨120 mg/m(2)+硫替帕10 mg/kg作为调节方案,环孢素作为移植物抗宿主病(GVHD)预防方案。器官毒性是可接受的,所有可评估的患者都获得了移植。3例(15%)表现为>II级aGVHD;15例可评估患者中有3例(20%)发生了广泛的慢性GVHD。中位随访63.5个月,生存率31%,无病生存率(DFS) 23%。所有持久的反应都发生在GVHD患者中。100天移植相关死亡率(TRM)为27.3%,其中感染引起的占67%,而6年累计TRM发生率为38%。我们的数据显示RIC:(1)允许移植hla匹配的造血干细胞(2)为不符合常规SCT条件的患者提供持久的应答,利用移植物抗恶性肿瘤效应(3)致命感染的高发生率。
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