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首页> 外文期刊>Haematologica >A phase II study of lenalidomide in patients with extranodal marginal zone B-cell lymphoma of the mucosa associated lymphoid tissue (MALT lymphoma) | Haematologica
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A phase II study of lenalidomide in patients with extranodal marginal zone B-cell lymphoma of the mucosa associated lymphoid tissue (MALT lymphoma) | Haematologica

机译:来那度胺在黏膜相关淋巴组织结外边缘区B细胞淋巴瘤(MALT淋巴瘤)患者中的II期研究血液学

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摘要

Mucosa associated lymphoid tissue lymphoma shares certain features with multiple myeloma. In view of this and the activity of lenalidomide in various B-cell lymphomas, we have initiated a phase II study of lenalidomide in patients with mucosa associated lymphoid tissue lymphoma. Patients with histologically verified advanced stages of this lymphoma were included in the study. Treatment consisted of oral lenalidomide 25 mg Days 1–21, with a 7-day break after each cycle. A total of 18 patients were included in the trial: 5 had gastric and 13 had extragastric mucosa associated lymphoid tissue lymphoma, but 2 discontinued therapy during the first course of therapy. In the intent to treat analysis, an overall response rate of 61% was seen (11 of 18; 6 complete and 5 partial remissions). Three patients had stable disease while 2 progressed. Side effects were manageable and included neutropenia (grade III in 3 patients) as the leading hematotoxicity. After a median follow up of 20.3 months, one patient has died from lymphoma while the remaining patients are alive and relapse-free. These data suggest activity of lenalidomide monotherapy in mucosa associated lymphoid tissue lymphoma. The study protocol had been approved by the Ethical Board of the Medical University Vienna (EK-No.: 146/09), and before opening the trial, it had been registered at www.clinicaltrials.gov. (identifier: NCT00923663).
机译:粘膜相关淋巴组织淋巴瘤与多发性骨髓瘤共有某些特征。考虑到这一点以及来那度胺在各种B细胞淋巴瘤中的活性,我们已经开始了来那度胺在粘膜相关淋巴样组织淋巴瘤患者中的II期研究。经组织学证实为该淋巴瘤晚期的患者纳入研究。治疗包括口服来那度胺25 mg第1–21天,每个周期后休息7天。该试验共纳入18例患者:5例患有胃癌,13例患有胃外黏膜相关淋巴样组织淋巴瘤,但有2例在治疗的第一个疗程中停药。就治疗分析而言,总体缓解率为61%(18例中有11例;完全缓解6例,部分缓解5例)。 3例患者病情稳定,2例进展。副作用是可控的,包括嗜中性白血球减少症(3例患者达到III级)是主要的血液毒性。中位随访20.3个月后,一名患者死于淋巴瘤,而其余患者仍活着且无复发。这些数据表明来那度胺单一疗法在粘膜相关淋巴组织淋巴瘤中具有活性。研究方案已获得维也纳医科大学伦理委员会的批准(EK-No .: 146/09),在开始试验之前,该方案已在www.clinicaltrials.gov上注册。 (标识符:NCT00923663)。

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