首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Combination therapy with fludarabine and rituximab followed by alemtuzumab in the first-line treatment of patients with chronic lymphocytic leukemia or small lymphocytic lymphoma: a phase 2 trial of the Minnie Pearl Cancer Research Network.
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Combination therapy with fludarabine and rituximab followed by alemtuzumab in the first-line treatment of patients with chronic lymphocytic leukemia or small lymphocytic lymphoma: a phase 2 trial of the Minnie Pearl Cancer Research Network.

机译:一线治疗与氟达拉滨和利妥昔单抗联合阿仑单抗联合治疗慢性淋巴细胞性白血病或小淋巴细胞性淋巴瘤患者:Minnie Pearl Cancer Research Network的2期试验。

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BACKGROUND: The purpose of the current study was to evaluate the efficacy and toxicity of the combination of fludarabine and rituximab, followed by alemtuzumab, as first-line treatment for patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). METHODS: In a nonrandomized phase 2 trial, 41 patients who had previously untreated CLL or SLL and required treatment received 4 cycles of the fludarabine and rituximab combination followed 5 weeks later by 4 weeks (12 doses) of intravenous alemtuzumab therapy. The response to treatment was evaluated after completion of treatment with fludarabine and rituximab, and again after the completion of alemtuzumab consolidation. RESULTS: Initial treatment with the combination of fludarabine and rituximab was well tolerated, and produced a 71% overall response rate (13% complete response). Thirty-four patients began treatment with intravenous alemtuzumab, but this drug was relatively poorly tolerated when given at a short interval after fludarabine and rituximab, and only 20 patients (49% of total) were able to complete the prescribed course. Five patients had an improvement in their response with alemtuzumab; the final complete response rate was 21%. The median progression-free survival for the entire group was 42 months. Toxicity with alemtuzumab included infusion-related toxicity, myelosuppression, and opportunistic infections. CONCLUSIONS: The intravenous schedule of alemtuzumab employed in the trial was relatively poorly tolerated in this community-based trial. The relatively low complete response rates after treatment with the combination of fludarabine and rituximab and after the completion of treatment suggest that these abbreviated courses may compromise efficacy. The generalized use of alemtuzumab as consolidation therapy cannot yet be recommended for community practice. However, optimization of the route of administration, duration of treatment, and interval after completion of induction therapy may improve efficacy, and further investigation is ongoing. Cancer 2008. (c) 2008 American Cancer Society.
机译:背景:本研究的目的是评估氟达拉滨与利妥昔单抗联合阿仑单抗联合治疗慢性淋巴细胞性白血病(CLL)或小淋巴细胞性淋巴瘤(SLL)患者的一线治疗的疗效和毒性。方法:在一项非随机的2期临床试验中,先前未接受过CLL或SLL治疗且需要治疗的41例患者接受了4个周期的氟达拉滨和利妥昔单抗联合治疗,随后5周后进行了4周(12剂)静脉注射Alemtuzumab治疗。在用氟达拉滨和利妥昔单抗治疗完成后,以及在完成阿仑单抗巩固后再次评估对治疗的反应。结果:氟达拉滨和利妥昔单抗联合治疗的初始治疗耐受性良好,总体缓解率达71%(完全缓解率为13%)。 34例患者开始接受静脉注射Alemtuzumab治疗,但在氟达拉滨和利妥昔单抗治疗后短期内给予这种药物耐受性相对较差,只有20例患者(占总数的49%)能够完成规定的疗程。 5例患者对alemtuzumab的反应有所改善;最终的完全答复率为21%。整个组的无进展生存期中位数为42个月。阿仑单抗的毒性包括与输注相关的毒性,骨髓抑制和机会性感染。结论:在这项基于社区的试验中,该试验所用的alemtuzumab的静脉给药方案相对较差。氟达拉滨和利妥昔单抗联合治疗后和治疗完成后相对较低的完全缓解率表明,这些简短的疗程可能会损害疗效。尚不建议将alemtuzumab普遍用于巩固治疗以用于社区实践。但是,优化给药途径,治疗时间和诱导治疗完成后的间隔可能会提高疗效,并且正在进行进一步的研究。癌症2008。(c)2008美国癌症协会。

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