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首页> 外文期刊>Annals of Hematology >Clinical outcomes of post-remission therapy using 90yttrium ibritumomab tiuxetan (Zevalin®) for high-risk patients with diffuse large B-cell lymphoma
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Clinical outcomes of post-remission therapy using 90yttrium ibritumomab tiuxetan (Zevalin®) for high-risk patients with diffuse large B-cell lymphoma

机译:90 伊波单抗泰坦坦(Zevalin®)缓解后治疗对弥漫性大B细胞淋巴瘤高危患者的临床疗效

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摘要

This phase II trial evaluated the efficacy and safety of tandem consolidation using 90yttrium ibritumomab tiuxetan (90Y-IT) and high-dose therapy (HDT) with autologous peripheral blood stem cell transplantation (PBSCT) in high-risk patients with diffuse large B-cell lymphoma (DLBCL) who were in primary remission. Eleven patients with high-risk DLBCL were enrolled. All patients had achieved complete or partial response after six to eight cycles of rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) as a frontline chemotherapy. Subsequently, the patients received one to two courses of ifosfamide-containing regimen for peripheral blood stem cell mobilization and harvesting. First consolidation with 90Y-IT was performed, followed by second consolidation using HDT with PBSCT. All patients received 90Y-IT therapy, but three patients did not undergo PBSCT. During the median follow-up period of 18.1 months, 9 of 11 patients exhibited disease progression, and 8 patients died. The estimated 2-year progression-free survival was 18.2%, and overall survival was 36.4%. Adverse events following 90Y-IT consolidation were primarily transient hematologic toxicities. The present pilot study suggests that tandem consolidation therapy using 90Y-IT followed by HDT with autologous PBSCT is not feasible for treatment of high-risk patients with DLBCL in remission after R-CHOP. In addition, this treatment failed to provide beneficial effects for the clinical outcome of subsequent PBSCT.
机译:这项II期临床试验评估了使用 90 伊波单抗tiritetan( 90 Y-IT)和高剂量疗法(HDT)进行自体外周血干的串联巩固的疗效和安全性原发性缓解的高危弥漫性大B细胞淋巴瘤(DLBCL)患者中进行细胞移植(PBSCT)。招募了11名高危DLBCL患者。在作为一线化疗的利妥昔单抗-环磷酰胺,阿霉素,长春新碱和泼尼松(R-CHOP)六至八个周期后,所有患者均获得了完全或部分缓解。随后,患者接受一到两个疗程的含异环磷酰胺的方案,以动员和采集外周血干细胞。使用 90 Y-IT进行第一次合并,然后使用HDT和PBSCT进行第二次合并。所有患者均接受了 90 Y-IT治疗,但三名患者未接受PBSCT。在中位随访期18.1个月中,11例患者中有9例表现出疾病进展,8例死亡。估计的2年无进展生存率为18.2%,总生存率为36.4%。 90 Y-IT合并后的不良事件主要是暂时性血液学毒性。目前的前期研究表明,采用 90 Y-IT联合HDT结合自体PBSCT进行串联巩固治疗对于R-CHOP缓解后的高危DLBCL患者不可行。另外,这种治疗不能为随后的PBSCT的临床结果提供有益的效果。

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