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首页> 外文期刊>Haematologica >Rituximab plus subcutaneous cladribine in patients with extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue: a phase II study by the Arbeitsgemeinschaft Medikament?se Tumortherapie
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Rituximab plus subcutaneous cladribine in patients with extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue: a phase II study by the Arbeitsgemeinschaft Medikament?se Tumortherapie

机译:利妥昔单抗联合皮下克拉屈滨治疗黏膜相关淋巴组织结外边缘区B细胞淋巴瘤的患者:Arbeitsgemeinschaft Medikament?se Tumortherapie的II期研究

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Currently, there is no standard systemic treatment for extranodal marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue. Both rituximab and cladribine have shown some activity in this disease, but the combination has not been tested so far. In view of this, we initiated a phase II study to assess the activity and safety of rituximab and cladribine in patients with histologically verified mucosa-associated lymphoid tissue lymphoma. Treatment consisted of rituximab 375 mg/m~(2) i.v. day 1 and cladribine 0.1 mg/kg s.c. days 1 – 4 every 21 days. In case of complete remission after two courses, another two cycles of therapy were administered, while patients with a partial response or stable disease were scheduled to receive six cycles of treatment. Out of 40 evaluable patients (14 female, 26 male), 39 received treatment as scheduled while one patient died before initiation of therapy and was rated as having progressive disease in the intent-to-treat analysis. Twenty-one patients had gastric lymphoma, while 19 suffered from extragastric mucosa-associated lymphoid tissue lymphoma. Side effects consisted mainly of hematologic toxicity including leukopenia, lymphopenia, anemia and thrombocytopenia. Twenty-three patients had a complete remission (58%) and nine had a partial remission (23%) for an overall response rate of 81%, while five had stable disease (13%) and two progressed during therapy. After a median follow-up of 16.7 months (interquartile range: 15.9 – 18.7 months), 35 patients are alive (88%) while four patients have died and one patient withdrew consent and did not allow further follow up. Our data demonstrate that rituximab plus cladribine is active and safe in patients with mucosa-associated lymphoid tissue lymphoma.
机译:当前,对于粘膜相关淋巴组织的结外边缘区B细胞淋巴瘤尚无标准的全身治疗方法。利妥昔单抗和克拉屈滨都对这种疾病表现出一定的活性,但到目前为止尚未对该组合进行测试。有鉴于此,我们启动了一项II期研究,以评估经组织学证实为黏膜相关淋巴样组织淋巴瘤的患者利妥昔单抗和克拉屈滨的活性和安全性。静脉注射rituximab 375 mg / m〜(2)。第1天和克拉屈滨0.1 mg / kg s.c.每21天1-4天。如果在两个疗程后完全缓解,则需要再进行两个疗程,而部分缓解或疾病稳定的患者则计划接受六个疗程。在40位可评估患者(14位女性,26位男性)中,有39位按计划接受了治疗,而一位患者在开始治疗前死亡,在意向治疗分析中被评为患有进行性疾病。 21例患胃淋巴瘤,而19例患胃外黏膜相关淋巴样淋巴瘤。副作用主要包括血液毒性,包括白细胞减少症,淋巴细胞减少症,贫血和血小板减少症。 23例患者完全缓解(58%),9例部分缓解(23%),总缓解率为81%,5例疾病稳定(13%),2例在治疗期间进展。在中位随访16.7个月(四分位数范围:15.9 – 18.7个月)后,有35例患者还活着(88%),而4例患者死亡并且1例患者撤回了同意并且不允许进一步随访。我们的数据表明,利妥昔单抗加克拉屈滨在黏膜相关淋巴样组织淋巴瘤患者中是安全有效的。

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