首页> 美国卫生研究院文献>Haematologica >Rituximab plus gemcitabine and oxaliplatin in patients with refractory/relapsed diffuse large B-cell lymphoma who are not candidates for high-dose therapy. A phase II Lymphoma Study Association trial
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Rituximab plus gemcitabine and oxaliplatin in patients with refractory/relapsed diffuse large B-cell lymphoma who are not candidates for high-dose therapy. A phase II Lymphoma Study Association trial

机译:利妥昔单抗联合吉西他滨和奥沙利铂用于难治性/复发性弥漫性大B细胞淋巴瘤患者不适合大剂量治疗。 II期淋巴瘤研究协会试验

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摘要

A previous pilot study with rituximab, gemcitabine and oxaliplatin showed promising activity in patients with refractory/relapsed B-cell lymphoma. We, therefore, conducted a phase II study to determine whether these results could be reproduced in a multi-institutional setting. This phase II study included 49 patients with refractory (n=6) or relapsing (n=43) diffuse large B-cell lymphoma. The median age of the patients was 69 years. Prior treatment included rituximab in 31 (63%) and autologous transplantation in 17 (35%) patients. International Prognostic Index at enrollment was >2 in 34 patients (71%). The primary endpoint was overall response rate after four cycles of treatment. Patients were planned to receive eight cycles if they reached at least partial remission after four cycles. After four cycles 21 patients (44%) were in complete remission and 8 (17%) in partial remission, resulting in an overall response rate of 61%. Factors significantly affecting overall response rate were early (<1 year) progression/relapse (18% versus 54%; P=0.001) and prior exposure to rituximab (23% versus 65%; P=0.004). Five-year progression-free and overall survival rates were 12.8% and 13.9%, respectively. Rituximab, gemcitabine and oxaliplatin were well tolerated with grade 3–4 infectious episodes in 22% of the cycles. These results are the first confirmation from a multicenter study that rituximab, gemcitabine and oxaliplatin provide a consistent response rate in patients with refractory/relapsed diffuse large B-cell lymphoma. This therapy can now be considered as a platform for new combinations with targeted treatments. This trial was registered at under #.
机译:先前使用利妥昔单抗,吉西他滨和奥沙利铂进行的先期研究显示,难治性/复发性B细胞淋巴瘤患者的活性很有希望。因此,我们进行了II期研究,以确定这些结果是否可以在多机构环境中复制。该II期研究包括49例难治性(n = 6)或复发性(n = 43)弥漫性大B细胞淋巴瘤患者。患者的中位年龄为69岁。先前的治疗包括利妥昔单抗31例(63%)和自体移植17例(35%)。入组时国际预后指数在34例患者中大于2(71%)。主要终点是四个疗程后的总体缓解率。如果患者在四个周期后至少达到部分缓解,则计划接受八个周期。在四个周期后,21例患者(44%)完全缓解,8例(17%)部分缓解,总体缓解率为61%。显着影响总体缓解率的因素是早期(<1年)进展/复发(18%对54%; P = 0.001)和先前接触利妥昔单抗(23%对65%; P = 0.004)。五年无进展生存率和总生存率分别为12.8%和13.9%。在22%的周期中,利妥昔单抗,吉西他滨和奥沙利铂具有3-4级感染发作的良好耐受性。这些结果是一项多中心研究的首次证实,即利妥昔单抗,吉西他滨和奥沙利铂在难治性/复发性弥漫性大B细胞淋巴瘤患者中提供一致的缓解率。现在可以将这种疗法视为针对性治疗新组合的平台。该试用版在#下注册。

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