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首页> 外文期刊>Leukemia and lymphoma >Phase II study of low-grade non-Hodgkin lymphomas with fludarabine and mitoxantrone followed by rituximab consolidation: promising results in marginal zone lymphoma.
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Phase II study of low-grade non-Hodgkin lymphomas with fludarabine and mitoxantrone followed by rituximab consolidation: promising results in marginal zone lymphoma.

机译:低度非霍奇金淋巴瘤伴氟达拉滨和米托蒽醌继之利妥昔单抗合并治疗的II期研究:边缘区淋巴瘤的前景广阔。

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The majority of patients with indolent lymphomas relapse due to minimal residual disease (MRD). In the present study, we sought to determine whether by using rituximab consolidation, for eradication of MRD, following induction chemotherapy with fludarabine and mitoxantrone (FN) combination could improve the outcome of indolent lymphomas. Patients with indolent lymphoma received fludarabine 25 mg/m2 Day 1-3 and mitoxantrone 10 mg/m2 on Day 1 every 28 days. Patients who attained a response (complete response, CR or partial response, PR) received four weekly doses of Rituximab 375 mg/m2 1 month and 3 months after completion of treatment. Forty-five patients were entered into this Phase II trial. The median follow-up time was 39 months. The median number of delivered cycles was 6. Fifty-three percent of patients attained a CR and 38% a PR for an overall response rate of 91%. One patient had stable disease, one had progression of the disease, whereas 2 were non-evaluable. After a median follow-up of 39 months, 32 of 46 patients (74%) are alive and disease-free. Grade III and IV toxicities included leucopenia (37%), neutropenia (28%), thrombocytopenia (7%), anemia (4%), and diarrhea (2%). Grade V toxicities included septic death in one patient and death due to hepatitis B reactivation 6 months after the last Rituximab dose in another patient. FN followed by R consolidation is a well-tolerated and active regimen in the treatment of patients with indolent lymphomas. Further follow-up is required to determine if these remissions are maintained.
机译:惰性淋巴瘤的大多数患者由于最小残留病(MRD)而复发。在本研究中,我们试图确定氟达拉滨和米托蒽醌(FN)联合诱导化疗后,通过使用利妥昔单抗巩固治疗根除MRD是否可以改善惰性淋巴瘤的预后。惰性淋巴瘤患者在第1-3天接受氟达拉滨25 mg / m2,在第1天每28天接受米托蒽醌10 mg / m2。达到缓解(完全缓解,CR或部分缓解,PR)的患者在治疗完成后1个月和3个月每周接受4剂利妥昔单抗375 mg / m2。四十五名患者进入了该II期试验。中位随访时间为39个月。分娩周期的中位数为6。53%的患者获得CR,PR的患者为38%,总缓解率为91%。一名患者病情稳定,一名患者病情进展,而两名则无法评估。在中位随访39个月后,46例患者中有32例(74%)仍然活着并且没有疾病。 III级和IV级毒性包括白细胞减少症(37%),中性粒细胞减少症(28%),血小板减少症(7%),贫血(4%)和腹泻(2%)。 V级毒性包括一名患者的败血病死亡和另一名患者在最后一次利妥昔单抗给药后6个月因乙型肝炎再活化而死亡。 FN继之以R巩固是治疗惰性淋巴瘤患者的良好耐受且积极的方案。需要进一步的随访以确定这些缓解是否得以维持。

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