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首页> 外文期刊>Pediatric blood & cancer >Feasibility of a tandem autologous peripheral blood stem cell transplant regimen for high risk neuroblastoma in a cooperative group setting: A Pediatric Oncology Group study: A Report from the Children's Oncology Group
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Feasibility of a tandem autologous peripheral blood stem cell transplant regimen for high risk neuroblastoma in a cooperative group setting: A Pediatric Oncology Group study: A Report from the Children's Oncology Group

机译:在合作组中采用串联自体外周血干细胞移植方案治疗高危神经母细胞瘤的可行性:儿科肿瘤学研究:儿童肿瘤学组的报告

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摘要

Background: The Pediatric Oncology Group performed a pilot study to assess the feasibility of tandem high dose chemotherapy (HDC) with stem cell rescue (HDC/SCR). We report here the results of this single arm trial of induction chemotherapy, local control measures (surgery and local radiation), and tandem HDC/SCR. Procedure: Patients with high risk neuroblastoma (NBL) underwent five cycles of induction chemotherapy and resection of primary tumors. Peripheral blood stem cells (PBSC) were collected after Course 3 without exvivo manipulation. Myeloablative chemotherapy was performed in rapid sequence after induction chemotherapy and surgery. The ability of patients to complete both cycles of HDC/SCR was a primary endpoint. Transplant-related toxicity, progression-free survival (PFS) and overall survival (OS) were recorded. Results: A total of 33 patients were enrolled. Twenty-two patients completed at least one HDC/SCR procedure and 17 patients completed both. Only one patient had insufficient stem cells collected for both transplants. There was one transplant-related death; engraftment was rapid and toxicity was as expected. The PFS of the 33 patients treated on this study is 24.2%±7.5% and OS is 36.4%±8.4% at 5 years. For patients who received at least one transplant PFS is 36.4%±11.0% and OS is 45.5%±11.2% at 5 years. Conclusions: The treatment of high risk NBL with tandem HDC/SCR is feasible in terms of transplant-related mortality and the ability to collect adequate PBSC for two transplants. The outcomes from this intensified treatment have been used to design a Children's Oncology Group Phase III study testing the efficacy of tandem HDC/SCR.
机译:背景:儿科肿瘤学小组进行了一项初步研究,以评估串联高剂量化疗(HDC)与干细胞抢救(HDC / SCR)的可行性。我们在这里报告了诱导化疗,局部控制措施(手术和局部放疗)和串联HDC / SCR的单臂试验的结果。程序:高危神经母细胞瘤(NBL)患者经历了五个周期的诱导化疗和原发肿瘤切除。在第3疗程后无需进行离体操作即可收集外周血干细胞(PBSC)。诱导化疗和手术后快速进行清髓性化疗。患者完成HDC / SCR的两个周期的能力是主要终点。记录与移植相关的毒性,无进展生存期(PFS)和总生存期(OS)。结果:共纳入33例患者。 22名患者至少完成了一项HDC / SCR程序,而17名患者均完成了这两项。只有一名患者没有为两次移植收集足够的干细胞。有1例与移植相关的死亡。植入迅速,且毒性如预期。这项研究的33名患者在5年时的PFS为24.2%±7.5%,OS为36.4%±8.4%。对于至少接受过一次移植的患者,在5年时PFS为36.4%±11.0%,OS为45.5%±11.2%。结论:就串联移植相关的死亡率和为两次移植收集足够的PBSC的能力而言,串联HDC / SCR治疗高危NBL是可行的。这种强化治疗的结果已被用于设计儿童肿瘤学第三阶段研究,以测试串联HDC / SCR的疗效。

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