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首页> 外文期刊>Annals of Hematology >Efficacy of continuous venovenous hemofiltration with chemotherapy in patients with Burkitt lymphoma and leukemia at high risk of tumor lysis syndrome
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Efficacy of continuous venovenous hemofiltration with chemotherapy in patients with Burkitt lymphoma and leukemia at high risk of tumor lysis syndrome

机译:持续性静脉血液滤过与化学疗法治疗Burkitt淋巴瘤和白血病患者合并肿瘤溶解综合征高风险的疗效

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摘要

Tumor lysis syndrome (TLS) is a potentially fatal metabolic complication of chemotherapy for Burkitt lymphoma. It has not been established whether chemotherapy should be delayed in patients with spontaneous TLS, and several studies have shown poor prognoses in this group. This retrospective study evaluated the efficacy and safety of continuous venovenous hemofiltration (CVVH) with prephase chemotherapy using the modified LMB-89 regimen in patients with Burkitt lymphoma and leukemia (BL/L) at a high risk of developing TLS from February 1998 to February 2007. The chemotherapy regimen was followed by the modified LMB-89 protocol. CVVH was applied to all patients before prephase chemotherapy or within 2 h of chemotherapy. The median follow-up was 19.7 months (range 1–97.8). Eight patients had Burkitt lymphoma and three had Burkitt leukemia; their median age was 48 years. The international prognostic indices were >3 for all patients. Seven patients had spontaneous TLS and four patients were at a high risk of TLS. CVVH was continued for 109 h (range 70.5–157.5). No patient had fatal metabolic complications related to TLS. Renal function had recovered fully before induction chemotherapy in all but one patient. The 1-year event-free survival and overall survival rates were both 82%. In conclusion, chemotherapy combined with CVVH might be effective and safe in patients with advanced Burkitt lymphoma and leukemia at a high risk of developing TLS.
机译:肿瘤溶解综合征(TLS)是Burkitt淋巴瘤化疗潜在的致命性代谢并发症。自发性TLS患者是否应延迟化疗尚无定论,一些研究表明该组患者预后较差。这项回顾性研究评估了1998年2月至2007年2月使用改良的LMB-89方案进行前期化疗的连续静脉静脉血液滤过(CVVH)在Burkitt淋巴瘤和白血病(BL / L)患者中发生TLS的高风险的有效性和安全性化疗方案之后是改良的LMB-89方案。在前期化疗之前或化疗后2小时内,将CVVH应用于所有患者。中位随访时间为19.7个月(范围1–97.8)。八名患者患有Burkitt淋巴瘤,三名患有Burkitt白血病;他们的中位年龄是48岁。所有患者的国际预后指数均> 3。 7例患者自发性TLS,4例患者发生TLS的高风险。 CVVH持续109小时(范围70.5–157.5)。没有患者发生与TLS相关的致命性代谢并发症。除一名患者外,其他所有患者在诱导化疗前肾功能均已完全恢复。 1年无事件生存率和总生存率均为82%。总之,化学疗法与CVVH结合可能对发展为高危TLS的晚期Burkitt淋巴瘤和白血病患者有效且安全。

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