James P. Wilmot Cancer Center, University of Rochester, Rochester, NY, USA.
Br J Haematol. 2014 Aug;166(3):382-9. doi: 10.1111/bjh.12906. Epub 2014 Apr 18.
Radiolabelled antiCD-20 antibodies have demonstrated single agent activity in relapsed diffuse large B-cell lymphoma (DLBCL). The S0433 clinical trial enrolled patients with newly diagnosed, advanced stage or bulky stage II, histologically confirmed DLBCL. Patients received six cycles of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone), two cycles of CHOP, then iodine-131 tositumomab radioimmunotherapy consolidation 30-60 d after completion of chemotherapy. The primary endpoint was 2-year progression-free survival (PFS). Eighty-four eligible patients were enrolled, and 56 patients completed the entire course of protocol treatment. Of the 84 patients evaluable for treatment response, 72 [86%, 95% confidence interval (CI): 76-92%] achieved a partial response (n = 21) or a confirmed (n = 41) or unconfirmed (n = 10) complete response to therapy. With a median follow-up of 3·9 years, the 2-year PFS estimate is 69% and the 2-year overall survival estimate is 77%. Rituximab levels at time of radioimmunotherapy did not correlate with toxicity or outcome. Twenty percent of patients had double hit features (MYC+; BCL2+) by immunohistochemistry, and had inferior outcome. These current results suggest that the incorporation of novel agents earlier in therapy may ultimately have greater impact in DLBCL, as early progressions, deaths and declining performance status during CHOP chemotherapy limited the number of patients who ultimately could benefit from radioimmunotherapy consolidation.
放射性标记的抗 CD-20 抗体在复发性弥漫性大 B 细胞淋巴瘤(DLBCL)中显示出单药活性。S0433 临床试验纳入了新诊断的、晚期或大块 II 期、组织学证实的 DLBCL 患者。患者接受了 6 个周期的 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松)、2 个周期的 CHOP,然后在化疗完成后 30-60 天接受碘-131 托西莫单抗放射性免疫治疗巩固。主要终点是 2 年无进展生存率(PFS)。共纳入 84 例符合条件的患者,其中 56 例完成了整个方案治疗。84 例可评估治疗反应的患者中,72 例(86%,95%置信区间[CI]:76-92%)达到部分缓解(n=21)或确认(n=41)或未确认(n=10)完全缓解。中位随访 3.9 年后,2 年 PFS 估计值为 69%,2 年总生存率估计值为 77%。放射性免疫治疗时的利妥昔单抗水平与毒性或结果无关。20%的患者通过免疫组化具有双打击特征(MYC+;BCL2+),结局较差。这些目前的结果表明,在治疗中更早地加入新型药物可能最终对 DLBCL 产生更大的影响,因为在 CHOP 化疗期间的早期进展、死亡和下降的表现状态限制了最终能够从放射性免疫治疗巩固中获益的患者数量。