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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >A phase 1 dose escalation study of bortezomib combined with rituximab, cyclophosphamide, doxorubicin, modified vincristine, and prednisone for untreated follicular lymphoma and other low-grade B-cell lymphomas
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A phase 1 dose escalation study of bortezomib combined with rituximab, cyclophosphamide, doxorubicin, modified vincristine, and prednisone for untreated follicular lymphoma and other low-grade B-cell lymphomas

机译:硼替佐米联合利妥昔单抗,环磷酰胺,阿霉素,改良长春新碱和泼尼松治疗未经治疗的滤泡性淋巴瘤和其他低度B细胞淋巴瘤的1期剂量递增研究

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BACKGROUND: Bortezomib has demonstrated efficacy in patients with relapsed B-cell non-Hodgkin lymphoma (NHL) both alone and in combination with other agents; however, limited data exist regarding its toxicity in combination with common frontline therapies for indolent NHL. A phase 1 study of bortezomib combined with rituximab, cyclophosphamide, doxorubicin, modified vincristine, and prednisone (R-CHOP) was conducted in patients with untreated follicular lymphoma (FL) and other indolent NHLs. METHODS: Nineteen patients, including 10 patients with FL, were enrolled. The median patient age was 59 years (range, 29-71 years). Seven patients had a FL International Prognostic Index score ≥3. R-CHOP with the vincristine dose capped at 1.5 mg was administered on a 21-day cycle for 6 to 8 cycles, and 1 of 3 dose levels of bortezomib (1.0 mg/m 2 [n = 1], 1.3 mg/m 2 [n = 6], or 1.6 mg/m 2 [n = 12]) was administered on days 1 and 8 of each cycle using a Bayesian algorithm for dose escalation. RESULTS: The maximum tolerated dose (MTD) of bortezomib with modified R-CHOP was reached at 1.6 mg/m 2. Dose-limiting toxicity was observed in 5 patients (1 patient at a bortezomib dose of 1.0 mg/m 2, 1 patient at a bortezomib dose of 1.3 mg/m 2, and 3 patients at a bortezomib dose of 1.6 mg/m 2). Neuropathy occurred in 16 patients (84%), including 2 patients (11%) who experienced grade 3 sensory neuropathy. Grade 4 hematologic toxicity occurred in 4 patients. Of 19 evaluable patients, 100% responded, and the complete response rate was 68%. At a median follow-up of 32 months, the 3-year progression-free survival rate was 89.5%. CONCLUSIONS: Bortezomib combined with modified R-CHOP produced high response rates without substantial increases in toxicity. A phase 2 study of R-CHOP and bortezomib given at this established MTD is currently ongoing.
机译:背景:硼替佐米已证明对单独或与其他药物联合治疗的复发性B细胞非霍奇金淋巴瘤(NHL)患者有效。然而,关于其毒性与惰性NHL的常用一线治疗相结合的数据尚有限。在未经治疗的滤泡性淋巴瘤(FL)和其他惰性NHL患者中进行了硼替佐米联合利妥昔单抗,环磷酰胺,阿霉素,改良长春新碱和泼尼松(R-CHOP)的1期研究。方法:入选19例患者,包括10例FL患者。患者的中位年龄为59岁(范围29-71岁)。 7名患者的FL国际预后指数得分≥3。长春新碱剂量上限为1.5 mg的R-CHOP在21天周期内进行6至8个周期,并使用3种剂量水平的硼替佐米(1.0 mg / m 2 [n = 1],1.3 mg / m 2)中的一种[n = 6]或1.6 mg / m 2 [n = 12])在每个周期的第1天和第8天使用贝叶斯算法进行剂量递增。结果:改良R-CHOP的硼替佐米的最大耐受剂量(MTD)达到1.6 mg / m2。在5例患者中观察到剂量限制性毒性(1例硼替佐米剂量为1.0 mg / m 2的患者2例,硼替佐米剂量为1.3 mg / m 2的患者; 3例硼替佐米剂量为1.6 mg / m 2的患者)。神经病发生在16例患者中(84%),其中2例经历了3级感觉神经病。 4名患者发生4级血液学毒性。在19例可评估患者中,100%缓解,完全缓解率为68%。在中位随访32个月时,3年无进展生存率为89.5%。结论:硼替佐米联合修饰的R-CHOP产生了高响应率,而毒性没有实质性增加。目前正在对该MTD进行R-CHOP和硼替佐米的2期研究。

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