Rituximab and Dose-Dense Chemotherapy in Primary Testicular Lymphoma

Agustin Avilés , M. Jesús Nambo , Sergio Cleto , Natividad Neri , Judith Huerta-Guzmán
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引用次数: 25

Abstract

Background

Treatment of primary testicular lymphoma (PTL) remains unsatisfactory even in patients with good prognosis, as < 30% of patients are alive at 3 years.

Patients and Methods

We began a phase II study to assess efficacy and toxicity of a dose-dense cyclophosphamide/epirubicin/vincristine/prednisone (CEOP14) regimen with rituximab (CEOP14R) in 38 previously untreated patients with PTL with early-stage (I or II) and low-risk disease, followed by adjuvant radiation therapy and central nervous system prophylaxis.

Results

Complete response was 86% (similar to historical controls), but improvement in outcome was observed; with actuarial curves at 5 years, event-free survival was 70%, and overall survival was 66%. Toxicity was mild, and the regimen was well tolerated.

Conclusion

The addition of rituximab to dose-dense chemotherapy improves outcome in this setting of patients who previously had been considered to have the poorest prognosis. It is important that these findings will be validated in multicentric, controlled clinical trials.

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利妥昔单抗和剂量密集化疗治疗原发性睾丸淋巴瘤
背景:原发性睾丸淋巴瘤(PTL)即使在预后良好的患者中,治疗仍然令人不满意。30%的患者存活3年。患者和方法我们开始了一项II期研究,以评估剂量密集环磷酰胺/表柔比星/长春新碱/泼尼松(CEOP14)方案联合利妥昔单抗(CEOP14R)对38例早期(I或II)低风险PTL患者的疗效和毒性,随后进行辅助放射治疗和中枢神经系统预防。结果完全缓解率为86%(与历史对照组相似),但观察到预后改善;根据5年的精算曲线,无事件生存率为70%,总生存率为66%。毒性轻微,治疗方案耐受性良好。结论:利妥昔单抗在高剂量化疗的基础上,改善了先前被认为预后最差的患者的预后。重要的是,这些发现将在多中心对照临床试验中得到验证。
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