第二周期诱导前化疗治疗危重儿童伯基特淋巴瘤的效果

E. Moussa, A. Hamoda, S. Semary, Marwa Romeih, R. Amin, Omneya Hassanin
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摘要

晚期伯基特淋巴瘤(BL)与肿瘤负荷相关。强化治疗的毒性是显著的。本研究的目的是分析不能按时接受诱导化疗并给予第二期预期(CVP)的患者的结局,并测量延迟对疾病结局的影响。这是一项回顾性非随机研究,纳入了患有伯基特淋巴瘤超过8年的儿童患者。结果显示,2007年7月至2015年10月诊断为Burkitt淋巴瘤的448例患者中,286例(70.1%)患者按方案按时接受诱导化疗,122例(29.9%)患者不适合按时接受诱导化疗。延迟时间从6-45天不等。延迟患者中45例(36.88%)接受第二次CVP治疗,16例(13.1%)出现复发/进展。延迟接受第二次CVP的患者与延迟接受完全诱导化疗的患者的OS分别为(76.1%)和(88.7%)。延迟患者与未延迟患者的OS分别为(84%)和(85.9%)。综上所述,危重患者在诱导期延迟化疗对降低发病率和死亡率至关重要。延迟化疗对伯基特淋巴瘤儿童的OS无影响。我们认为,不应该对所有在早期治疗阶段不能耐受强化治疗的危重患者采用第二次前期治疗,而是建议在器官毒性恢复后开始强化治疗(COPADM),而不是在仔细监测疾病进展的情况下给予第二次CVP。
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Effect of Second Cycle Pre-induction Chemotherapy in Critically Ill Burkitt’s Lymphoma Children
Advanced stage Burkiit’s lymphoma (BL) is associated with tumor burden. Toxicities from intensive therapies are significant. The objectives of this study were to analyze the outcome of patients who could not receive induction chemotherapy on time, and were given a 2nd pre-phase (CVP), and to measure the impact of delay on disease outcome. It is a retrospective non randomized study included pediatric patients, suffering from Burkitt’s Lymphoma over 8 years period in CCHE. The result showed that, four hundred and eight patients were diagnosed as Burkitt’s Lymphoma from July 2007 till October 2015, 286 patients (70.1%) received induction on time as per protocol, while 122 patients (29.9%) were not fit to receive their induction chemotherapy on due time. The delay ranged from 6-45 days. While forty five patients (36.88%) out of the delayed patients received 2nd CVP, 16 patients (13.1%) showed relapse/progression. OS among delayed patients who received 2nd CVP versus those who were delayed and were able to receive full induction chemotherapy was (76.1%), (88.7%) respectively. OS in patients who were delayed versus those who were not delayed was (84%), (85.9%) respectively. In conclusion, in critically ill patients delay of chemotherapy in induction phase is important to reduce morbidity and mortality. The delay of chemotherapy has no impact on OS in Burkitt’s lymphoma children. A second pre-phase therapy in our opinion should not be adopted for all critical ill patients who will not tolerate intensive therapy during early phases of treatment, but instead we recommend a recovery from organ toxicity and starting intensive therapy (COPADM) rather than giving 2nd CVP with careful surveillance of disease progression.
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