Avilés Agustin, Nambo M Jesús, Cleto Sergio, Neri Natividad, Huerta-Guzmán Judith
Oncology Research Unit, Oncology Hospital, National Medical Center, IMSS, D.F. Mexico.
Clin Lymphoma Myeloma. 2009 Oct;9(5):386-9. doi: 10.3816/CLM.2009.n.075.
Treatment of primary testicular lymphoma (PTL) remains unsatisfactory even in patients with good prognosis, as < 30% of patients are alive at 3 years.
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.
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.
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.
即使对于预后良好的原发性睾丸淋巴瘤(PTL)患者,其治疗效果仍不尽人意,因为3年生存率低于30%。
我们开展了一项II期研究,以评估剂量密集型环磷酰胺/表柔比星/长春新碱/泼尼松(CEOP14)方案联合利妥昔单抗(CEOP14R)对38例既往未接受过治疗、处于疾病早期(I期或II期)且低风险的PTL患者的疗效和毒性,随后进行辅助放疗和中枢神经系统预防。
完全缓解率为86%(与历史对照相似),但观察到预后有所改善;5年精算曲线显示,无事件生存率为70%,总生存率为66%。毒性轻微,该方案耐受性良好。
在剂量密集型化疗中加入利妥昔单抗可改善这类既往被认为预后最差的患者的预后。重要的是,这些发现需在多中心对照临床试验中得到验证。