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首页> 外文期刊>Haematologica >Safety of obinutuzumab alone or combined with chemotherapy for previously untreated or relapsed/refractory chronic lymphocytic leukemia in the phase IIIb GREEN study
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Safety of obinutuzumab alone or combined with chemotherapy for previously untreated or relapsed/refractory chronic lymphocytic leukemia in the phase IIIb GREEN study

机译:在IIIb期GREEN研究中,单独使用obinutuzumab或联合化疗治疗先前未治疗或复发/难治的慢性淋巴细胞性白血病的安全性

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The safety of obinutuzumab, alone or with chemotherapy, was studied in a non-randomized, open-label, non-comparative, phase IIIb study (GREEN) in previously untreated or relapsed/refractory chronic lymphocytic leukemia. Patients received obinutuzumab 1000 mg alone or with chemotherapy (investigator’s choice of fludarabine-cyclophosphamide for fit patients, chlorambucil for unfit patients, or bendamustine for any patient) on days 1, 8 and 15 of cycle 1, and day 1 of cycles 2–6 (28-day cycles), with the cycle 1/day 1 dose administered over two days. The primary end point was safety/tolerability. Between October 2013 and March 2016, 972 patients were enrolled and 971 treated (126 with obinutuzumab monotherapy, 193 with obinutuzumab-fludarabine-cyclophosphamide, 114 with obinutuzumab-chlorambucil, and 538 with obinutuzumab-bendamustine). Grade ≥3 adverse events occurred in 80.3% of patients, and included neutropenia (49.9%), thrombocytopenia (16.4%), anemia (9.6%), and pneumonia (9.0%); rates were similar in first-line and relapsed/refractory patients, and in first-line fit and unfit patients. Using expanded definitions, infusion-related reactions were observed in 65.4% of patients (grade ≥3, 19.9%; mainly seen during the first obinutuzumab infusion), tumor lysis syndrome in 6.4% [clinical and laboratory; highest incidence with obinutuzumab-bendamustine (9.3%)], and infections in 53.7% (grade ≥3, 20.1%). Serious and fatal adverse events were seen in 53.1% and 7.3% of patients, respectively. In first-line patients, overall response rates at three months post treatment exceeded 80% for all obinutuzumab-chemotherapy combinations. In the largest trial of obinutuzumab to date, toxicities were generally manageable in this broad patient population. Safety data were consistent with previous reports, and response rates were high. ( clinicaltrials.gov identifier: 01905943 ).
机译:在非随机,开放标签,非对照,IIIb期研究(GREEN)中,对以前未治疗或复发/难治的慢性淋巴细胞白血病进行了单药或化学疗法治疗奥比妥单抗的安全性研究。患者在第1周期的第1、8和15天以及第2-6周期的第1天接受单独的奥比妥珠单抗1000 mg或化疗(研究人员选择适合患者的氟达拉滨-环磷酰胺,不适合患者的苯丁酸氮芥或任何患者的苯达莫司汀)。 (28天周期),其中周期1 /天1剂在两天内给药。主要终点是安全性/耐受性。在2013年10月至2016年3月之间,招募了972例患者并治疗了971名患者(奥比妥珠单抗单药治疗126例,奥比妥珠单抗氟达拉滨环磷酰胺治疗193例,奥比妥珠单抗-苯丁酸氮芥治疗114例,奥比妥珠单抗-苯达莫司汀治疗538例)。 ≥3级不良事件发生在80.3%的患者中,包括中性粒细胞减少症(49.9%),血小板减少症(16.4%),贫血(9.6%)和肺炎(9.0%);一线和复发/难治性患者以及一线适合和不适合患者的发生率相似。使用扩展的定义,在65.4%的患者中观察到与输注相关的反应(≥3,19.9%;主要在第一次obinutuzumab输注期间发生),在6.4%的患者中出现了肿瘤溶解综合征[临床和实验室研究;奥比妥珠单抗-苯达莫司汀的最高发生率(9.3%),感染率为53.7%(≥3,20.1%)。分别在53.1%和7.3%的患者中发现了严重和致命的不良事件。在一线患者中,所有obinutuzumab-化疗组合的治疗后三个月的总缓解率均超过80%。在迄今为止最大的obinutuzumab试验中,在这一广泛的患者人群中毒性通常是可控的。安全性数据与以前的报告一致,并且答复率很高。 (Clinicaltrials.gov标识符:01905943)。

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