Division of Hematology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Cancer Res Treat. 2023 Oct;55(4):1355-1362. doi: 10.4143/crt.2023.271. Epub 2023 Mar 30.
This phase II, open-label, multicenter study aimed to investigate the efficacy and safety of a rituximab intensification for the 1st cycle with every 21-day of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP-21) among patients with previously untreated advanced-stage or bulky diffuse large B-cell lymphoma (DLBCL).
Ninety-two patients with stage III/IV or bulky DLBCL from 21 institutions were administered 8 cycles of R-CHOP-21 with an additional one dose of rituximab intensification on day 0 of the 1st cycle (RR-CHOP). The primary endpoint was a complete response (CR) rate after 3 cycles of chemotherapy.
Among the 92 DLBCL patients assessed herein, the response rate after 3 cycles of chemotherapy was 88.0% (38.0% CR+50.0% partial response [PR]). After the completion of 8 cycles of chemotherapy, the overall response rate was observed for 68.4% (58.7% CR+9.8% PR). The 3-year progression-free survival rate was 64.0%, and the 3-year overall survival rate was 70.4%. Febrile neutropenia was one of the most frequent grade 3 adverse events (40.0%) and 5 treatment-related deaths occurred. Compared with the clinical outcomes of patients who received R-CHOP chemotherapy as a historical control, the interim CR rate was higher in male patients with RR-CHOP (20.5% vs. 48.8%, p=0.016).
Rituximab intensification on days 0 to the 1st cycle of the standard 8 cycles R-CHOP-21 for advanced DLBCL yielded favorable response rates after the 3 cycles of chemotherapy and acceptable toxicities, especially for male patients. ClinicalTrials.gov ID: NCT01054781.
本 II 期、开放标签、多中心研究旨在评估在未经治疗的晚期或大肿块弥漫性大 B 细胞淋巴瘤(DLBCL)患者中,第 1 周期每 21 天使用利妥昔单抗强化治疗(第 1 周期第 0 天给予 1 次利妥昔单抗强化治疗)与标准的 8 周期利妥昔单抗+环磷酰胺+多柔比星+长春新碱+泼尼松(R-CHOP-21)相比的疗效和安全性。
21 个机构的 92 例 III/IV 期或大肿块 DLBCL 患者接受了 8 个周期的 R-CHOP-21 治疗,并在第 1 周期的第 0 天给予额外的 1 次利妥昔单抗强化治疗(RR-CHOP)。主要终点是 3 个周期化疗后的完全缓解(CR)率。
在本研究中评估的 92 例 DLBCL 患者中,化疗 3 个周期后的缓解率为 88.0%(38.0% CR+50.0%部分缓解[PR])。在完成 8 个周期的化疗后,总体缓解率为 68.4%(58.7% CR+9.8% PR)。3 年无进展生存率为 64.0%,3 年总生存率为 70.4%。发热性中性粒细胞减少症是最常见的≥3 级不良事件之一(40.0%),有 5 例治疗相关死亡。与接受 R-CHOP 化疗的历史对照患者的临床结局相比,RR-CHOP 治疗的男性患者的中期 CR 率更高(20.5% vs. 48.8%,p=0.016)。
在标准的 8 周期 R-CHOP-21 中,在第 1 周期的第 0 天给予利妥昔单抗强化治疗,用于治疗晚期 DLBCL,在化疗 3 个周期后可获得良好的缓解率,且毒性可接受,特别是对男性患者。临床试验注册号:NCT01054781。