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RD-CODOX-M/IVAC 联合利妥昔单抗和鞘内脂质体阿糖胞苷治疗成人伯基特淋巴瘤和“未分类”高度侵袭性 B 细胞淋巴瘤。

RD-CODOX-M/IVAC with rituximab and intrathecal liposomal cytarabine in adult Burkitt lymphoma and 'unclassifiable' highly aggressive B-cell lymphoma.

机构信息

Haematology-Oncology and Stem Cell Transplantation Unit, Fondazione 'G. Pascale,' IRCCS, Naples, Italy.

出版信息

Br J Haematol. 2012 Jan;156(2):234-44. doi: 10.1111/j.1365-2141.2011.08947.x. Epub 2011 Nov 21.

DOI:10.1111/j.1365-2141.2011.08947.x
PMID:22098541
Abstract

Specific trials on adult Burkitt lymphoma (BL) and 'unclassifiable' lymphomas with features intermediate between BL and diffuse large B-cell lymphoma (BL/DLBCL) are advocated which include substantial numbers of older patients, to improve treatment feasibility, while countering risks of systemic and central nervous system (CNS) recurrences. We prospectively evaluated a modified CODOX-M/IVAC (CODOX-M: cyclophosphamide, vincristine, doxorubicin, high-dose methotrexate; IVAC: ifosfamide, etoposide and high-dose cytarabine) regimen by the addition of rituximab (R) and liposome-encapsulated cytarabine (D) to increase antitumour activity and halve the number of intrathecal treatments. Thirty adults (40% >60years) with BL (n=15) and BL/DLBCL (n=15) were accrued. Primary endpoints were progression-free survival (PFS), CNS recurrence, and liposomal cytarabine-associated toxicity. Eighty percent of patients received the whole treatment programme, the remaining cases received at least three full courses. Application of the RD-CODOX-M/IVAC regimen resulted in remarkable 4-year PFS (78%) and complete remission (CR) rates (93%). However, PFS was significantly lower in patients older than 60years as compared to younger ones (49%vs 93%, P=0·03; median, 36months), despite high actual dose-intensity, CR rate and tolerability. Reduced-intensity intratechal prophylaxis through liposomal cytarabine was effective because the CNS failure rate was low (3·4%) and without severe neurological toxicities. The RD-CODOX-M/IVAC strategy is feasible and highly effective, but improving outcomes in elderly patients remains a priority.

摘要

建议进行专门针对成人伯基特淋巴瘤(BL)和具有 BL 和弥漫性大 B 细胞淋巴瘤(BL/DLBCL)之间特征的“未分类”淋巴瘤的临床试验,包括大量老年患者,以提高治疗可行性,同时降低全身和中枢神经系统(CNS)复发的风险。我们前瞻性地评估了一种改良的 CODOX-M/IVAC(CODOX-M:环磷酰胺、长春新碱、多柔比星、高剂量甲氨蝶呤;IVAC:异环磷酰胺、依托泊苷和高剂量阿糖胞苷)方案,通过添加利妥昔单抗(R)和脂质体阿糖胞苷(D)来提高抗肿瘤活性并将鞘内治疗次数减半。共入组了 30 名 BL(n=15)和 BL/DLBCL(n=15)成人患者(40%>60 岁)。主要终点是无进展生存期(PFS)、CNS 复发和脂质体阿糖胞苷相关毒性。80%的患者接受了整个治疗方案,其余患者接受了至少三个完整疗程。应用 RD-CODOX-M/IVAC 方案后,4 年 PFS(78%)和完全缓解(CR)率(93%)非常显著。然而,与年轻患者相比,年龄大于 60 岁的患者 PFS 明显较低(49%比 93%,P=0·03;中位数,36 个月),尽管实际剂量强度高、CR 率和耐受性好。通过脂质体阿糖胞苷进行低强度鞘内预防是有效的,因为 CNS 失败率低(3·4%)且无严重神经毒性。RD-CODOX-M/IVAC 策略是可行且非常有效的,但改善老年患者的预后仍是当务之急。

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