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基于直线加速器的调强全身骨髓照射与氟达拉滨/白消安清髓治疗的联合应用:一项I期研究。

Combination of linear accelerator-based intensity-modulated total marrow irradiation and myeloablative fludarabine/busulfan: a phase I study.

作者信息

Patel Pritesh, Aydogan Bulent, Koshy Matthew, Mahmud Dolores, Oh Annie, Saraf Santosh L, Quigley John G, Khan Irum, Sweiss Karen, Mahmud Nadim, Peace David J, DeMasi Vincenzo, Awan Azhar M, Weichselbaum Ralph R, Rondelli Damiano

机构信息

Division of Hematology/Oncology, University of Illinois Hospital and Health Sciences System, Chicago, Illinois; University of Illinois Cancer Center, Chicago, Illinois.

Department of Radiation Oncology, University of Illinois Hospital and Health Sciences System, Chicago, Illinois; Department of Cellular and Radiation Oncology, University of Chicago, Chicago, Illinois.

出版信息

Biol Blood Marrow Transplant. 2014 Dec;20(12):2034-41. doi: 10.1016/j.bbmt.2014.09.005. Epub 2014 Sep 16.

Abstract

Here we examined the addition of intensity-modulated total marrow irradiation (TMI) delivered using a linear accelerator to a myeloablative chemotherapy conditioning regimen before allogeneic hematopoietic stem cell transplantation (HSCT). In this phase I study, we enrolled 14 patients with high-risk hematologic malignancies who received escalating doses of TMI at 3 Gy (n = 3), 6 Gy (n = 3), 9 Gy (n = 6), and 12 Gy (n = 2) in combination with intravenous (i.v.) fludarabine 160 mg/m(2) and targeted busulfan (area under the curve, 4800 μM*minute). Peripheral blood mobilized stem cells were obtained from HLA-matched related (n = 9) or unrelated (n = 4) or 1 antigen-mismatched unrelated (n = 1) donors. All patients rapidly engrafted and recovered their immune cells. Overall, Bearman extrahematologic toxicity were limited to grades 1 or 2, with oral mucositis grade 1 in 64% and grade 2 in 36% of the patients. With a median follow-up of 1126 days (range, 362 to 1469) for living patients, the overall survival was 50% and relapse-free survival was 43%. Of 7 deaths, 3 were due to relapse and 4 to transplantation-related complications. We conclude that 9 Gy TMI can be combined with myeloablative chemotherapy in the design of new preparative regimens for HSCT. This study was registered at clinicaltrials.gov as NCT00988013.

摘要

在此,我们研究了在异基因造血干细胞移植(HSCT)前,将使用直线加速器进行的调强全身骨髓照射(TMI)添加到清髓性化疗预处理方案中的情况。在这项I期研究中,我们纳入了14例高危血液系统恶性肿瘤患者,他们接受了递增剂量的TMI,分别为3 Gy(n = 3)、6 Gy(n = 3)、9 Gy(n = 6)和12 Gy(n = 2),并联合静脉注射(i.v.)氟达拉滨160 mg/m²和靶向白消安(曲线下面积,4800 μM·分钟)。外周血动员干细胞来自人类白细胞抗原(HLA)匹配的亲属供者(n = 9)、非亲属供者(n = 4)或1个抗原不匹配的非亲属供者(n = 1)。所有患者均迅速植入并恢复了免疫细胞。总体而言,贝尔曼血液外毒性仅限于1级或2级,64%的患者出现1级口腔黏膜炎,36%的患者出现2级口腔黏膜炎。存活患者的中位随访时间为1126天(范围,362至1469天),总生存率为50%,无复发生存率为43%。在7例死亡病例中,3例死于复发,4例死于移植相关并发症。我们得出结论,在设计HSCT新的预处理方案时,9 Gy的TMI可与清髓性化疗联合使用。本研究已在clinicaltrials.gov上注册,注册号为NCT00988013。

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