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Evaluation of Different Treatment Regimens for Relapsed and Refractory NHL: Single Institute Experience

机译:复发和难治性NHL的不同治疗方案的评估:单一机构的经验

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Background and Aim: The treatment of choice for relapsed or refractory Non-Hodgkin Lymphoma (NHL) mainly, is High dose chemotherapy with autologous stem cell transplantation. However, its use is mostly restricted to patients responding to salvage chemotherapy. In this study, our aim was to evaluate outcome and toxicity of different treatment modalities of relapsed and refractory NHL. Patient and Methods: This retrospective study included 217 patients were diagnosed as refractory or relapsed NHL. Those patients received different treatment modalities as GDP (Gemcitabine, dexamethasone, cisplatin), DHAP (Dexamethasone, Cytarabine, and Cisplatin), MINE (Mitoxantrone, ifosfamide, etoposide and mesna), CHOP (Cyclophosphamide, Doxorubicin, Vincristine and Prednisone), and CVP (Cyclophosphamide, vincristine and prednisone). Results: The median age of patients in the study was 50 years. Patients who received DHAP showed ORR of 62%, which was the highest response. The most common adverse effects were hematological which were more noticed in patients, received CHOP. Sixty one patients (54.5%) had anemia, 54 patients (48.2%) had neutropenia and 55 patients (49.1%) had thrombocytopenia, but th e difference between the different lines of treatment wasn’t significant p value of 0.95. The median time to relapse is 10 months and the median survival time is 40 months. The 3-year PFS rates of all patients were 49.3%, while the 3 year OS rates were 54.8%. Conclusion: The overall and PFS didn’t show any difference betwee n different lines of treatment.
机译:背景与目的:复发或难治性非霍奇金淋巴瘤(NHL)的治疗选择主要是高剂量化学疗法与自体干细胞移植。但是,它的使用主要限于对挽救性化疗有反应的患者。在这项研究中,我们的目的是评估复发和难治性NHL不同治疗方式的结果和毒性。 患者和方法:这项回顾性研究包括217位被诊断为顽固性或复发性NHL的患者。这些患者接受了不同的治疗方式,包括GDP(吉西他滨,地塞米松,顺铂),DHAP(地塞米松,阿糖胞苷和顺铂),MINE(米托蒽醌,异环磷酰胺,依托泊苷和甲磺酸),CHOP(环磷酰胺,阿霉素,长春新碱和长春新碱和(环磷酰胺,长春新碱和泼尼松)。 结果:研究中患者的中位年龄为50岁。接受DHAP的患者的ORR为62%,是最高的反应。最常见的不良反应是血液学,在接受CHOP的患者中更为明显。患有贫血的患者为61名(54.5%),患有中性粒细胞减少症的患者为54名(48.2%),患有血小板减少症的患者为55名(49.1%),但不同治疗方案之间的差异无显着性,p值为0.95。中位复发时间为10个月,中位生存时间为40个月。所有患者的3年PFS率为49.3%,而3年OS率为54.8%。 结论:在不同的治疗方法之间,总体和PFS均无差异。

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