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利妥昔单抗治疗 4 剂后微小反应对瓦尔登斯特伦巨球蛋白血症的临床价值:东部肿瘤协作组 E3A98 试验的随访。

Clinical value of minor responses after 4 doses of rituximab in Waldenström macroglobulinaemia: a follow-up of the Eastern Cooperative Oncology Group E3A98 trial.

机构信息

Division of Hematology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Br J Haematol. 2009 Dec;147(5):677-80. doi: 10.1111/j.1365-2141.2009.07892.x. Epub 2009 Sep 14.

Abstract

Waldenström macroglobulinaemia is a low-grade, lymphoplasmacytic lymphoma that is responsive to rituximab. We report the role of a minor response in predicting overall outcomes. We extended follow-up of a previously described cohort (n = 69) treated with 4 weekly doses of rituximab and observed durable responses (median time to progression, 30 months; 5-year survival rate, 66%). Patients achieving a minor response [25-50% immunoglobulin M (IgM) reduction] appeared to do as well as those achieving an objective response (>50% IgM reduction), which suggests that more aggressive or intensive therapy for minor responders is not required. Future studies of Waldenström macroglobulinaemia should report minor responses because they are associated with clinically meaningful benefits. This trial was registered at http://www.clinicaltrials.gov as #NCT00005609.

摘要

华氏巨球蛋白血症是一种低度的淋巴浆细胞淋巴瘤,对利妥昔单抗有反应。我们报告了次要反应在预测总体结果中的作用。我们延长了先前描述的队列(n=69)的随访时间,这些患者接受了 4 周剂量的利妥昔单抗治疗,并观察到了持久的反应(中位无进展时间为 30 个月;5 年生存率为 66%)。达到次要反应(IgM 减少 25-50%)的患者与达到客观反应(IgM 减少>50%)的患者一样,这表明不需要对次要反应者进行更积极或更强化的治疗。未来的华氏巨球蛋白血症研究应该报告次要反应,因为它们与具有临床意义的益处相关。该试验在 http://www.clinicaltrials.gov 上注册为 #NCT00005609。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0798/3548235/45e863c4526d/nihms429325f1.jpg

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