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MCL01 期临床试验的长期结果:利妥昔单抗联合 HyperCVAD 交替高剂量阿糖胞苷和甲氨蝶呤用于初治套细胞淋巴瘤患者。

Long-term results of the MCL01 phase II trial of rituximab plus HyperCVAD alternating with high-dose cytarabine and methotrexate for the initial treatment of patients with mantle cell lymphoma.

机构信息

Hematology, AUSL/IRCCS Reggio Emilia, Reggio Emilia, Italy.

PhD Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, Italy.

出版信息

Br J Haematol. 2021 Mar;192(6):1011-1014. doi: 10.1111/bjh.16714. Epub 2020 May 14.

Abstract

Mantle cell lymphoma is a rare and incurable lymphoproliferative disorder. In the MCL01 trial, patients were treated with the R-HCVAD regimen [rituximab plus HyperCVAD (hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone; R-CVAD) alternating with high-dose methotrexate and cytarabine (AM)] for four cycles followed by autologous stem cell transplantation (ASCT) for those who reached only a partial response. After a median follow-up of 10·5 years, we reported 10-year progression-free and overall survival rates of 35% and 61% respectively, with a 10-years cumulative incidence rate of second malignancies of 10·6%. Mature results of the MCL01 trial confirmed the efficacy of HyperCVAD-AM as a frontline regimen for younger patients (≤65 years).

摘要

套细胞淋巴瘤是一种罕见且无法治愈的淋巴增生性疾病。在 MCL01 试验中,患者接受了 R-HCVAD 方案(利妥昔单抗联合 HyperCVAD[高剂量环磷酰胺、长春新碱、多柔比星、地塞米松;R-CVAD,与大剂量甲氨蝶呤和阿糖胞苷(AM)交替])治疗四个周期,然后对仅部分缓解的患者进行自体干细胞移植(ASCT)。中位随访 10.5 年后,我们报告的 10 年无进展生存率和总生存率分别为 35%和 61%,10 年累积第二恶性肿瘤发生率为 10.6%。MCL01 试验的成熟结果证实了 HyperCVAD-AM 作为年轻患者(≤65 岁)一线治疗方案的疗效。

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