Tom Baker Cancer Centre, University of Calgary, Calgary, Alberta, Canada.
University Health Network, Princess Margaret Cancer Center, Toronto, Ontario, Canada.
Br J Haematol. 2024 Sep;205(3):881-890. doi: 10.1111/bjh.19555. Epub 2024 May 27.
The Canadian Cancer Trials Group (CCTG) LY.17 is an ongoing multi-arm randomized phase II trial evaluating novel salvage therapies compared with R-GDP (rituximab, gemcitabine, dexamethasone and cisplatin) in autologous stem cell transplantation (ASCT)-eligible patients with relapsed/refractory diffuse large B-cell lymphoma (RR-DLBCL). This component of the LY.17 trial evaluated a dose-intensive chemotherapy approach using a single cycle of inpatient R-DICEP (rituximab, dose-intensive cyclophosphamide, etoposide and cisplatin) to achieve both lymphoma response and stem cell mobilization, shortening time to ASCT. This report is the result of the protocol-specified second interim analysis of the 67 patients who were randomized to either 1 cycle of R-DICEP or to 3 cycles of R-GDP. The overall response rate (ORR) was 65.6% for R-DICEP and 48.6% for R-GDP. The ASCT rate was 71.9% versus 54.3%, and 1-year progression-free survival rate was 42% versus 32%, respectively, for R-DICEP versus R-GDP. Although the improvement in ORR for R-DICEP versus R-GDP exceeded the pre-specified 10% threshold to proceed to full accrual of 64 patients/arm, higher rates of grade 3-5 toxicities, and the need for hospitalization led to the decision to stop this arm of the study. CCTG LY.17 will continue to evaluate different salvage regimens that incorporate novel agents.
加拿大癌症临床试验组(CCTG)LY.17 是一项正在进行的多臂随机 II 期试验,评估了新型挽救治疗方案与 R-GDP(利妥昔单抗、吉西他滨、地塞米松和顺铂)在适合自体干细胞移植(ASCT)的复发/难治性弥漫性大 B 细胞淋巴瘤(RR-DLBCL)患者中的疗效比较。LY.17 试验的这一部分评估了一种剂量密集型化疗方法,即使用单次住院 R-DICEP(利妥昔单抗、剂量密集环磷酰胺、依托泊苷和顺铂)来实现淋巴瘤缓解和干细胞动员,从而缩短 ASCT 的时间。本报告是根据方案规定对随机分为 R-DICEP 组或 R-GDP 组的 67 例患者的第二次中期分析结果。R-DICEP 的总缓解率(ORR)为 65.6%,R-GDP 的 ORR 为 48.6%。ASCT 率分别为 71.9%和 54.3%,R-DICEP 组和 R-GDP 组 1 年无进展生存率分别为 42%和 32%。虽然 R-DICEP 组的 ORR 较 R-GDP 组的改善超过了预定的 10%阈值,可继续招募 64 例/臂的全部患者,但较高的 3-5 级毒性发生率和住院需求导致决定停止该研究臂。CCTG LY.17 将继续评估包含新型药物的不同挽救治疗方案。